Mitarbeiterin Personalwesen, Teilzeit 50 % (20 Std/Wo) (Freiburg, DE, 79108)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

As a Charles River employee, you will be part of an industry-leading, customer-focused company at the forefront of drug development. Your skills will play a key role in bringing life-saving therapies to market faster through simpler, quicker, and more digitalized processes. Whether you are in lab operations, finance, IT, sales, or another area, when you work at Charles River, you will be the difference every day for patients across the globe.

Zur Verstärkung unseres Teams in Freiburg suchen wir

Mitarbeiter*in Personalwesen, Teilzeit 50 % (20 Std/Wo)

*Charles River setzt sich für Chancengleichheit ein und ist stolz auf seine vielfältige Kultur. Wir lehnen jegliche Diskriminierung ab, ungeachtet des Geschlechts, Alters, der Herkunft oder Behinderung.

Charles River Laboratories ist führend im Bereich der Auftragsforschung in der präklinischen Entwicklung und wir haben an über 80% der Medikamente gearbeitet, die in den letzten 5 Jahren auf dem Markt gekommen sind. Charles River hat derzeit über 20.000 Mitarbeitende weltweit und ist mit mehr als 150 Einrichtungen in 21 Ländern tätig. In Freiburg arbeiten wir im Bereich der Krebsforschung.

Ihr Aufgabengebiet:

Erstellung und Betreuung von Stellenausschreibungen, Koordinieren und Führen von Vorstellungsgesprächen und das Einstellungsmanagement
Betreuung eines definierten Mitarbeitenden-Bereichs
Betreuung des Zeiterfassungssystems
Vorbereitung der Gehaltsabrechnungen
Erstellung von Zeugnissen
Organisation von Firmenevents, Mitarbeiterveranstaltungen und gesundheitsfördernden Maßnahmen
Organisation von inhouse Events und Betreuung der Teilnehmenden
Mitbetreuung der SOX-Kontrollen

Was Sie mitbringen sollten:

Erfolgreich abgeschlossene kaufmännische Ausbildung
Idealerweise Kenntnisse/Berufserfahrung im Personalbereich, wir freuen uns aber auch über Quereinsteiger, denn alle nötigen Kenntnisse können Sie bei uns erwerben
Englischkenntnisse und Hands-on Mentalität
Kommunikationsstarke Persönlichkeit mit Lust auf Teamwork
Selbstständige und zielorientierte Arbeitsweise

Was uns als Arbeitgeber ausmacht:

Einarbeitung | Ab dem ersten Tag bekommen Sie eine/n Mentor/in an deine Seite die/der langjährige Arbeitserfahrung mitbringt und dich begleitet
Entwicklung | Wir führen jährliche Gespräche zur individuellen Weiterentwicklung und finanzieren verschiedene Schulungen & Weiterbildungen, um Sie zu unterstützen.
Finanzen | Kindergarten- und Kita-Zuschüsse, Kinderferiengeld, Urlaubsgeld, Firmenrabatte, vermögenswirksame Leistungen, Zuschuss zur betriebliche Altersvorsorge

About Corporate Functions
The Corporate Functions provide operational support across Charles River in areas such as Human Resources, Finance, IT, Legal, Sales, Quality Assurance, Marketing, and Corporate Development. They partner with their colleagues across the company to develop and drive strategies and to set global standards. The functions are essential to providing a bridge between strategic vision and operational readiness, to ensure ongoing functional innovation and capability improvement.

With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

For more information, please visit www.criver.com.

Tierpfleger*in in der Krebsforschung (Freiburg, DE, 79108)

.

Zur Verstärkung unseres Teams in Freiburg suchen wir

Tierpfleger*in Krebsforschung*

Dein Aufgabengebiet

Pflege der Tiere (Füttern und Tränken, Käfigwechsel, Führen von Versorgungsnachweisen und artgerechte Beschäftigung der Tiere, Training)
Instandhaltung der Tierhaltungsräume (Kontrolle der Tierställe, Reinigung, Desinfektion von Käfigen und Gestellen, Autoklavierung)
Gesundheitskontrolle (Beobachtung des Gesundheitszustandes und des Verhaltens der Tiere, um Auffälligkeiten zu erkennen und Krankheiten vorzubeugen)
Elektronische Dokumentation und Datenverarbeitung

Was Du mitbringen sollten

Eine abgeschlossene Berufsausbildung egal in welchem Bereich bevorzug, aber Neueinsteiger sind bei uns herzlich willkommen, denn bei uns können Sie alle notwendigen Kenntnisse erwerben
Verantwortungsbewusstsein im Umgang mit Tieren
Strukturierte und sorgfältige Arbeitsweise
Gute Team- und Kommunikationsfähigkeit

Was uns als Arbeitgeber ausmacht

Mentoring | Ab dem ersten Tag bekommen Sie eine/n Mentor/in an deine Seite die/der langjährige Arbeitserfahrung mitbringt und dich begleitet
Einarbeitung | Sie erhalten eine detaillierte Einarbeitung durch Ablaufpläne für die ersten Monate
Entwicklung | Wir führen jährliche Gespräche zur individuellen Weiterentwicklung und finanzieren verschiedene Schulungen & Weiterbildungen, um Sie zu unterstützen.
Finanzen | Kindergarten- und Kita-Zuschüsse, Urlaubsgeld, Firmenrabatte, vermögenswirksame Leistungen, Zuschuss zur betriebliche Altersvorsorge
Benefits | Fahrrad/E-Bikeleasing über Businessbike, Sportangebot mit HanseFit, Food Trucks, One-Day Aktionen (soziales Engagement), Umzugskostenpauschale und vieles mehr …
Verantwortung | Wir sind uns unserer wichtigen Aufgabe bewusst und leben Tierschutz jeden Tag. Unsere Mitarbeitenden sind umfangreich geschult und halten eine Vielzahl an Regularien ein, um das Tierwohl immer vorne anzustellen.

Unser Bewerbungsprozess
1. Erstes Kennenlernen & Erklärung Ihrer Aufgaben (online)
2. Praktische Einblicke vor Ort
3. Dein Start bei Charles River Freiburg

Befristeter Vertrag: 18 Monate -Human Resources Business Partner (m/w/d) (Sulzfeld, Bavaria (Bayern), DE, 97633)

For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

An unserem Standort in Sulzfeld bieten wir eine Stelle als Human Resources Business Partner (HRBP) an. Sie verstärken unser HR-Team und unterstützen und beraten bei HR-relevanten Themen und Prozessen.

Zu den Hauptaufgaben dieser Position gehören:
- Enge Zusammenarbeit mit dem line-Management, um die korrekte Anwendung von HR-Richtlinien und -Praktiken sicherzustellen. Bei Bedarf sollen Änderungsvorschläge für Richtlinien und Praktiken unterbreitet werden.
- Coaching und Zusammenarbeit mit Führungskräften bei der Lösung komplexer Probleme im Bereich der Mitarbeiterbeziehungen; bei Bedarf soll rechtliche Beratung eingeholt werden.
- Vorbereitung von Betriebsratsinformationen und der erforderlichen Dokumente.
- Sicherstellung der zeitnahen Bearbeitung von Dokumenten und Transaktionen, Übermittlung relevanter Vertragsinformationen, zeitnahe Eingabe von Änderungen in das HR-System, Digitalisierung und Aktualisierung der Personalakten. Aktualisierung und Aufrechterhaltung der SOX-Kontrollen und Gewährleistung der vollständigen Compliance/Prüfung von HR-Daten.
- Sicherstellung der Einhaltung lokaler, staatlicher und bundesstaatlicher Vorschriften und Pflege der erforderlichen Dokumentation zu Compliance-Zwecken; Überwachung und Prüfungen der HR-Dokumentation nach Bedarf.
Unterstützung der Führungskräfte bei der Analyse ihrer Profilanforderungen zur Personalbeschaffung, Erstellung und Veröffentlichung von Stellenanzeigen; Auswahl und Durchführung von Vorstellungsgesprächen, Bewertung von Kandidaten, Beratung der Führungskräfte und Unterbreitung von Stellenangeboten.
- Analysieren und Bearbeiten von Änderungen der Vergütung und der Zusatzleistungen, Durchführung des jährlichen Lohnerhöhungsprozesses und der Bonusauszahlungen und Erstellen der entsprechenden Dokumentation.
- Unterstützen bei den Onboarding- und Offboarding-Prozessen und Sicherstellen, dass alle erforderlichen Dokumentationen und Systemaktualisierungen vollständig sind. Führen von Onboarding-Meetings und Kündigungsgesprächen.
-Sie kommunizieren aktiv vor Ort, um Führungskräfte und Mitarbeiter über HR-relevante Themen zu informieren.

Für diese Position erwarten wir folgende Mindestqualifikationen:
-Bachelor-Abschluss im Bereich Personalmanagement (People & Culture Studies);
-3 Jahre einschlägige Berufserfahrung als HR-Generalist/HRBP oder in einer ähnlichen Funktion.
-Gute Englischkenntnisse sind für die Position erforderlich.
-Proaktiver Teamplayer, sowohl abteilungsintern als auch unternehmensweit.

Rollenspezifische Informationen:
• Befristeter Vertrag: 18 Monate
• Standort: 97633 Sulzfeld; Kostenlose Parkplätze.
Arbeitszeit: Montag bis Freitagmittag, Vollzeitbeschäftigung bevorzugt, Teilzeit ist jedoch möglich.
Ein Arbeitstag zu Hause nach 6 Monaten in der Position ist möglich.

About Research Models & Services
Fundamental to basic research and discovery is the use of in vivo models to help identify disease targets and determine potential biological pathways that regulate the condition. As the world’s leader in the production and distribution of the highest quality research animal, with 1 out of 2 animal models produced for preclinical research globally, we understand the importance of this step. With seven decades of experience, our expertise is unmatched, allowing us to provide you with the perfect model, including disease-specific and preconditioned options, for basic research and beyond.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Mitarbeiter für den internen Produktions- und Logistikbereich (Sulzfeld, Bavaria (Bayern), DE, 97633)

Seit fast 75 Jahren arbeiten die Mitarbeiter von Charles River zusammen, um bei der Entdeckung, Entwicklung und sicheren Herstellung neuer Arzneimitteltherapien zu helfen. Wenn Sie sich unserer Familie anschließen, haben Sie einen bedeutenden Einfluss auf die Gesundheit und das Wohlbefinden der Menschen auf der ganzen Welt. Ob Ihr Hintergrund in Life Sciences, Finanzen, IT, Vertrieb oder einem anderen Bereich ist, Ihre Fähigkeiten werden eine wichtige Rolle bei der Arbeit spielen, die wir durchführen. Im Gegenzug helfen wir Ihnen, eine Karriere zu bauen, die Sie begeistern wird.

Wir suchen ab sofort

eine/n Mitarbeiter/in (m/w/d)

für Außenbereichstätigkeiten

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld.

Ihre Aufgaben:

· Warenannahme und -lagerung

· Bau, Wartung und Abbau von Isolatoren

· Bestückung des Autoklaven mit Materialien für Reinräume

· Abfallbeseitigung gemäß Vorschrift

· Reinigung und Desinfektion von Außenbereich, Lagerhallen

Die Anforderungen:

Körperliche Belastbarkeit
Ordentlichkeit
Personalhygiene
Einsatzbereitschaft
Sorgfalt
Technisches Verständnis

Unser Angebot:

· eine ausführliche und betreute Einarbeitung

· ein leistungsgerechtes Einkommen

· eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team

· Teilnahme an diversen Unternehmensveranstaltungen

· zahlreiche soziale Leistungen und Zuschüsse (z.B. zur Kinderbetreuung, Tankgutschein, VWL-Förderung u.v.m.)

Dann freuen wir uns über die Zusendung Ihrer ausführlichen Bewerbungsunterlagen an:

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

Email: BewerbungenRMS@crl.com, www.criver.com

Vorabinfos unter: 09761/406-11 oder 09761/406-280

Über Research Models & Services

Für die Grundlagenforschung ist die Verwendung von In-vivo-Modellen zur Identifikation von Zielkrankheiten und potentieller biologischer Pfade, welche Krankheiten bestimmen, notwendig. Als eines der weltweit führenden Unternehmen für die Produktion und den Vertrieb von Versuchstieren der höchsten Qualität, welches die Hälfte aller Versuchstiermodelle weltweit für die präklinische Forschung liefert, verstehen wir, wie wichtig dieser Schritt ist. Mit sieben Jahrzehnten Erfahrung ist unser Know-how unerreicht, sodass wir das perfekte Modell liefern können, einschließlich krankheitsspezifischer und konditionierter Optionen, für die Grundlagenforschung und darüber hinaus.

Über Charles River

Charles River ist ein auf die Frühphase der Wirkstoffentwicklung spezialisiertes Auftragsforschungsunternehmen (CRO). Wir haben auf der Grundlage unserer Erfahrungen mit Versuchstiermedizin und -wissenschaft ein vielseitiges Portfolio von Discovery- und Sicherheitsprüfungsdienstleistungen aufgebaut, sowohl mit Good Laboratory Practice (GLP) und ohne GLP, um Kunden von der Wirkstoffidentifikation bis zur präklinischen Entwicklung zu unterstützen. Charles River bietet auch eine Reihe von Produkten und Dienstleistungen für klinische Labortestbedürfnisse und Herstellungsaktivitäten. Die Nutzung dieses breiten Portfolios von Produkten und Dienstleistungen ermöglicht unseren Kunden, ein flexibleres Medikamentenentwicklungsmodell zu entwickeln, wodurch die Kosten gesenkt, die Produktivität erhöht und die Markteinführung beschleunigt wird.

Mit über 20.000 Mitarbeitern in 110 Standorten in 20 Ländern rund um den Globus sind wir strategisch positioniert, weltweite Ressourcen zu koordinieren und multidisziplinäre Projekte für die Entwicklung und Herausforderungen unserer Kunden zu entwickeln. Unsere Kundenbasis umfasst globale Pharmaunternehmen, Biotechnologieunternehmen, Behörden und Krankenhäuser sowie akademische Institutionen in der ganzen Welt.

Charles River setzt sich leidenschaftlich für die Verbesserung der Lebensqualität ein. Unsere Mission, unsere exzellente Wissenschaft und unser Engagement für einen sinnvollen Einsatz unserer Kapazitäten leiten uns in allem, was wir tun. Wir beginnen jeden Tag in dem Wissen, dass unsere Arbeit die Gesundheit und das Wohlergehen von vielen Menschen weltweit nutzt. Wir sind stolz darauf, dass wir die Entwicklung von rund 80% der von der FDA in den letzten fünf Jahren zugelassenen Arzneimittel unterstützt haben.

Bei Charles River Laboratories erkennen wir alle Talente an und stellen sie ein. Wir sind ein Unternehmen, das sich dem Grundsatz der Vielfalt und Inklusion verpflichtet hat und täglich in diese Richtung arbeitet.

Weitere Informationen finden Sie unter www.criver.com.

Mitarbeiter/in in der Tierpflege (m/w/d) (Sulzfeld, Bavaria (Bayern), DE, 97633)

Zum nächstmöglichen Zeitpunkt suchen wir Sie als

Tierpfleger / Mitarbeiter in der Tierbetreuung (m/w/d)

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld.

Ihre Aufgaben:

Betreuung, Zucht und Haltung unserer Labornager
Einhaltung der internen Qualitätsvorgaben und Arbeit unter sterilen Bedingungen
Dokumentationserstellung
Mitarbeit an der Verbesserung von Arbeitsabläufen

Die Anforderungen:

Freude am professionellen Umgang mit Tieren
Teamgeist
Einsatzbereitschaft und Sorgfalt
Körperliche Belastbarkeit
EDV-Kenntnisse erwünscht

Unser Angebot:

· eine ausführliche und betreute Einarbeitung im Rahmen unseres Trainingskonzepts

· ein leistungsgerechtes Einkommen

· eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team

· Teilnahme an diversen Unternehmensveranstaltungen

· zahlreiche soziale Leistungen und Zuschüsse (z.B. zur Kinderbetreuung, Tankgutschein, VWL-Förderung u.v.m.)

Auch Bewerber ohne spezifische Vorkenntnisse/ Quereinsteiger sind uns willkommen!

Sie sind interessiert?

Dann freuen wir uns über die Zusendung Ihrer ausführlichen Bewerbungsunterlagen an:

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

Email: BewerbungenRMS@crl.com, www.criver.com

Für Vorabinformationen stehen wir Ihnen gerne unter der Telefonnummer 09761 406-11 zur Verfügung.

Über Research Models & Services

Über Charles River

Charles River setzt sich leidenschaftlich für die Verbesserung der Lebensqualität ein. Unsere Mission, unsere exzellente Wissenschaft und unser Engagement für einen sinnvollen Einsatz unserer Kapazitäten leiten uns in allem, was wir tun. Wir beginnen jeden Tag in dem Wissen, dass unsere Arbeit die Gesundheit und das Wohlergehen von vielen Menschen weltweit nutzt. Wir sind stolz darauf, dass wir die Entwicklung von etwa 86% der von der FDA in 2021 zugelassenen Medikamente unterstützt haben.

Weitere Informationen finden Sie unter www.criver.com.

Veterinary Technician Assistant I (Reno, NV, US, 89511)

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Summary

We are seeking a Veterinary Technician Assistant for our Safety Assessment site located in Reno, Nevada.

The Veterinary Technician Assistant will assist veterinary staff in the documentation and triage of all laboratory animal health cases In addition, this individual will may also perform technical in-life procedures.

Job Qualifications

MINIMUM QUALIFICATIONS:

Education: High School Diploma or G.E.D.
Experience: 1-2 years related experience in a laboratory animal facility. related experience working with animals in pre-clinical laboratory or clinical setting; experience working with a CRO with multi-species preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: ALAT preferred
Other: None.

PREFERRED QUALIFICATIONS:

LVT license or CVT/RVT certification.
AALAS certification.

The pay range for this position starts at $20.50 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Group Housing Technician I (Reno, NV, US, 89511)

Job Summary

We are seeking a Group Housing Technician for our Safety Assessment site located in Reno, Nevada.

Responsible for performing operational, administrative and technical tasks to provide comprehensive care for all nonhuman primates at the site, including: daily health observations, feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint, generating and recording data and related tasks. Assist with the movement of animals and stocking of supplies.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform in-life technical procedures (e.g., handling, body weight).
Input and edit computer entries (e.g., LIMS data capture for husbandry and animal health)
Observe animals for general health and overall well being.
Clean primary enclosure and enclosure area for animals.
Sanitize group housing units, enrichment devices and other related equipment.
Measure and distribute feed to animals in accordance with established procedures.
Prepare and provide environmental enrichment.
Collect monthly animal bodyweights.
Assist with handling and restraint habituation activities.
Inspect feeding and watering devices for proper function.
Review documentation of functions performed as part of quality control requirements.
Stocking of supplies for group housing.
Retrieve and view Standard Operating Procedures using appropriate database.
Use GLPs, SOPs, processes and company policies when performing all job functions.
Handle, restrain, and provide care for all nonhuman primates at the site.
Maintain clean work areas (e.g.: laboratory area, primary enclosures, animal exam areas).
Receive animals (e.g., general health observation, sexing and identification).
May perform basic veterinary technical and husbandry tasks with guidance, including the following:
Administration of various therapeutic veterinary treatment as needed.
Assist with animal receipt processing; sedation, animal handling, and physical exam recording.
Proficient animal restraint techniques.
Veterinary Rounds and behavior treatments.

Job Qualifications

•    Education: High school diploma or General Education Degree (G.E.D.) required.
•    Experience: None.
•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•    Certification/Licensure: None.

***The pay range for this position starts at $19.75. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Group Housing Technician I (Reno, NV, US, 89511)

Job Summary

We are seeking a Group Housing Technician for our Safety Assessment site located in Reno, Nevada.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform in-life technical procedures (e.g., handling, body weight).
Input and edit computer entries (e.g., LIMS data capture for husbandry and animal health)
Observe animals for general health and overall well being.
Clean primary enclosure and enclosure area for animals.
Sanitize group housing units, enrichment devices and other related equipment.
Measure and distribute feed to animals in accordance with established procedures.
Prepare and provide environmental enrichment.
Collect monthly animal bodyweights.
Assist with handling and restraint habituation activities.
Inspect feeding and watering devices for proper function.
Review documentation of functions performed as part of quality control requirements.
Stocking of supplies for group housing.
Retrieve and view Standard Operating Procedures using appropriate database.
Use GLPs, SOPs, processes and company policies when performing all job functions.
Handle, restrain, and provide care for all nonhuman primates at the site.
Maintain clean work areas (e.g.: laboratory area, primary enclosures, animal exam areas).
Receive animals (e.g., general health observation, sexing and identification).
May perform basic veterinary technical and husbandry tasks with guidance, including the following:
Administration of various therapeutic veterinary treatment as needed.
Assist with animal receipt processing; sedation, animal handling, and physical exam recording.
Proficient animal restraint techniques.
Veterinary Rounds and behavior treatments.

Job Qualifications

Equal Employment Opportunity

For more information, please visit www.criver.com.

Veterinary Technician I - $5,000 Sign On Bonus! (Reno, NV, US, 89511)

Job Summary

***Position is eligible for a $5,000 sign on bonus!***

The Veterinary Technician 1 is responsible for assisting the veterinarians in documentation, triage, and management of laboratory animal health cases. Also responsible for daily health observations, preventive health care, environmental enrichment and handling and restraining of laboratory animals.

Assist veterinary staff in the documentation and triage of all animal health cases noted by technical staff and/or Attending Veterinarian.
Perform routine veterinary technical skills including the following:
Assess and follow-up on animal health concerns
Generate animal treatment records and perform, track and schedule follow-ups
Administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc.
Bandage/wrapping techniques.
Nail/teeth clipping/trimming.
Venipuncture techniques.
Perform radiographs as required.
Daily walk through of animal rooms
Proficient animal restraint techniques.
Monitor critical care animals (i.e., place IVs, monitor fluids, etc.).
Participate in colony management (new NHP processing, TB testing, collection of biological samples, routine health monitoring, etc.)
Monitor animal health, visually, and by following detailed schedules.
Generate animal treatment records and perform, track and schedule follow-ups.
Maintain appropriate medical records for each animal in accordance with study and regulatory requirements. Assist in maintaining accurate record keeping procedures for the veterinary department.
Maintain and follow complex procedures to ensure appropriate animal health and treatment.
Assist in providing leadership, animal health training, and guidance to other laboratory personnel.
Assist in keeping inventory and stocking the vet rooms (i.e., drugs and supplies). Assist in organizing and maintaining the vet exam rooms.
Responsible for tissue sampling, routine animal manipulations and administration of fluids or other treatments as required.

Job Qualifications

Graduate of a collegiate veterinary technology program accredited by the American Veterinary Medical Association Committee on Veterinary Technician Education and Training Activities or equivalent program in veterinary technology.
0-2 years related experience working with animals in a pre-clinical laboratory or clinical setting; experience working in a CRO with multi-species preferred. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above if the individual is credentialed as a Certified Veterinary Technician.
LVT license or CVT/RVT certification preferred. Uncertified candidates must have Vet Tech in Training (VTIT) and will be required to receive certification within 12-18 months or show that certification has been substantially completed. AALAS certification desired.

The pay range for this position is $28.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Analyst I -Bioanalytical Sciences (Reno, NV, US, 89511)

Job Summary

We are seeking a Research Analyst I for our Safety Assessment site located in Reno, NV.

This position will be responsible for handling and processing samples and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies.

Job Qualifications

The following are minimum requirements related to the Research Analyst 1 position.

Associate's degree (A.A. / A.S) or equivalent in biological science or related discipline required. Bachelor’s degree (B.A. / B.S.) preferred.
6 Months minimum related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Proficient in basic technical skills and the operation of data collection equipment.
Knowledge of GLPs and other federal regulations and guidelines.
Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information.
Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors.
Able to quickly learn and utilize computer programs as needed.

The pay for this position starts at $24/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Clinical Pathology Team Lead (Reno, NV, US, 89511)

Job Summary

Job Qualifications

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Senior HVAC Technician (Reno, NV, US, 89511)

Job Summary

We are seeking a Senior HVAC Technician for our Safety Assessment site located in Reno, Nevada.

Perform a variety of master-level mechanical and pressure/temperature equipment repairs and maintenance requiring close interface with other trade/craft functions. Perform other semi-skilled tasks in the general maintenance of the physical plant and provide work direction to others performing HVAC projects.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Monitor and maintain HVAC systems including high/low temperature, water and electricity. Isolate and identify malfunctioning equipment for repair, adjustment, and replacement. Interpret instructions as required
•   Observe and interpret readings on gauges, meters, and charts to ensure correct functioning of systems. May calibrate equipment.
•   Perform adjustments, repairs and replacement of parts and equipment following written specifications such as blueprints, drawings and schematics.
•   Dismantle equipment fixtures and plan systematic replacement or repair of accessories and parts and return equipment to operation.
•   Oversee HVAC-related tasks being performed by other department personnel.
•   Inspect completed work for quality, safety, and proper operation.
•   Coordinate maintenance work with other departments and divisions; maintain accurate records of maintenance and repair work.
•   Periodically perform preventative maintenance programs as required.
•   Perform other semi-skilled tasks as assigned to assist in the general maintenance of the physical plant.
•   Respond to emergencies as needed. Provide 24-hour on-call maintenance coverage, as scheduled in rotation
•   May perform waste vacuum maintenance.
•   Take proper safety precautions and utilize appropriate safety gear/equipment in the performance of all duties.
•   Perform all other related duties as assigned.

Job Qualifications

•   Education: High school diploma or General Education Degree (GE.D.). Completion of trade school or formal apprenticeship program.
•   Experience: Five or more related experience.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: Valid EPA 608 certification.
•   Other: None

The pay range for this position starts at $39.00/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Security Officer - Part Time (Reno, NV, US, 89511)

Job Summary

***This position covers weekends, Saturday - Sunday from 6:00pm to 6:00am****

We are seeking a Security Officer for our Safety Assessment site located in Reno, NV.

Ensures the protection of organizational personnel and company property against fire, theft, vandalism, illegal entry, and other hazards. Inspects credentials and facilities, and reports irregularities, alarm activation and tampering. Develops, implements and administers programs designed to protect organizational personnel and property. Ensures compliance with government and organization security policies and procedures and protects and safeguards intellectual property. Conducts investigations to identify and document instances of noncompliance and possible breaches in law.

The following are responsibilities related to the Security Officer:

•   Greet, screen, record and allow visitors and employees admittance to the site in accordance with company procedures.
•   Monitor security systems and/or environmental systems and investigate and/or report any incidents.
•   Report all unauthorized persons to the proper authorities and initiate action to protect employees, animals, products, and physical site. In so doing, the incumbent should not place him or herself in harm’s way.
•   Ensure the physical safety and security of the facility by enforcing company policies and procedures; provide a deterrent and detection factor for wrongful activity; conducts patrols and monitors the status of the physical security measures; and monitors the critical building systems.
•   Physically walk the facility grounds to complete visual inspection of site security on regularly scheduled tours.
•   Document all security department activity and generates incident reports as necessary.
•   Monitor facility equipment during tours and report equipment failure, reset alarms as instructed and/or assist in minor repair as directed. Provides effective secondary communication during business hours; and primary communications during non-business hours.
•   Contact emergency personnel as required and in accordance with
•   Assist in directing appropriate emergency response efforts when required.
•   Perform all other related duties as assigned.
•   We are also seeking an individual to work on the weekends but may be available to provide coverage for others during the week, during vacation, and sick leaves

Job Qualifications

The following are minimum qualifications related to the Security Officer position:

Education: High school diploma, General Education Degree (G.E.D.) or the equivalent. Associates degree preferred.
Experience: 2 -3 years experience with at least Six to twelve months of related security experience and/or training.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Valid Drivers license
Other: None

The pay for this position starts at $19/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (Reno, NV, US, 89511)

Job Summary

The Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support study conduct which may include cage change out, animal handling, husbandry, observations, basic physiological indices, and data collection/recoding to support each skill.

Essential Functions (The fundamental Duties & Responsibilities of the role products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include animal husbandry needs, animal handling, cage manipulation, and movement, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Vivarium PPE stocking, and facility cleaning.
Use and maintain instrumentation and equipment.
Skill plan completed for this role based on department training plan.
Perform all other related duties as assigned.

The pay for this position is $19.00 USD per hour.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High School Diploma, General Education Degree (G.E.D) preferred, but not required.
Experience: No previous experience required
An equivalent combination of education and experience may be accepted as a satisfactory
substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.

Preferred Qualifications:

Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evening, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician - Group Housing (Reno, NV, US, 89511)

Job Summary

We are seeking a Group Housing Technician for our Safety Assessment site located in Reno, Nevada.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform in-life technical procedures (e.g., handling, body weight).
Input and edit computer entries (e.g., LIMS data capture for husbandry and animal health)
Observe animals for general health and overall well being.
Clean primary enclosure and enclosure area for animals.
Sanitize group housing units, enrichment devices and other related equipment.
Measure and distribute feed to animals in accordance with established procedures.
Prepare and provide environmental enrichment.
Collect monthly animal bodyweights.
Assist with handling and restraint habituation activities.
Inspect feeding and watering devices for proper function.
Review documentation of functions performed as part of quality control requirements.
Stocking of supplies for group housing.
Retrieve and view Standard Operating Procedures using appropriate database.
Use GLPs, SOPs, processes and company policies when performing all job functions.
Handle, restrain, and provide care for all nonhuman primates at the site.
Maintain clean work areas (e.g.: laboratory area, primary enclosures, animal exam areas).
Receive animals (e.g., general health observation, sexing and identification).
May perform basic veterinary technical and husbandry tasks with guidance, including the following:
Administration of various therapeutic veterinary treatment as needed.
Assist with animal receipt processing; sedation, animal handling, and physical exam recording.
Proficient animal restraint techniques.
Veterinary Rounds and behavior treatments.

Job Qualifications

Equal Employment Opportunity

For more information, please visit www.criver.com.

Surgical Laboratory Technician I (Reno, NV, US, 89511)

Job Summary

Job Qualifications

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Account Development Representative - Initial 6 Month FTC (Cambridge, GB, CB23 6DP)

Job Summary

Are you a great communicator?

Have you got customer service / account manager experience?

Do you have good organisation skills?

We are recruiting for a remote Account Development Representative.

Initially, on a 6 month fixed term contract, the Account Development Representative is responsible for driving Microbial Solutions sales in UK / IRE & Nordics.

The role will enable you to administer the sales process for specific products, services, accounts and/or sales opportunities via phone and
e-mail while supporting a Regional Account Manager team. You also have the opportunity to work cross functionally with the Microbial
Solutions Commercial team to meet and exceed sales quotas for a specific territory.

Essential Duties and Responsibilities:

Drives sales in specified region.
Point of contact for customer inquiries and outbound prospecting.
Engage with existing customers and generating sales opportunities.
Lead projects such as dormant account reimplementation, next generation products and end of life campaigns.
Establish new customers and maintain/grow existing customer accounts.
Establish and nurture positive, productive relationships with customer accounts end-users, management and purchasing contacts.
Assist with territory opportunities and product lifecycle management.
Partner with regional Account Managers to meet shared sales goals and manage territory opportunities.
Work collaboratively with Marketing to drive product promotions and provide feedback on ROI.
Share customer problems/concerns with relevant departments for quality resolution.
Maintain a CRM database via updates to sales opportunities, sales stages, marketing statuses, and customer intelligence data.
Provide pricing, create and submit individualised quotes and support price renewal price process in region.
Client communications.

Job Qualifications:

Education: Degree in marketing or equivalent
Experience: Some related experience in sales or customer services.
This position requires regular domestic and occasional international travel.

About Microbial Solutions
Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Commis aux soins des animaux (St. Constant, Quebec, CA, J5A 2E7)

Pendant 75 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication sûre de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous aurez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences joueront un rôle important dans le travail que nous effectuons. En retour, nous vous aiderons à bâtir une carrière dont vous pouvez vous sentir passionné.

Sommaire de l'emploi

En tant que Commis aux soins des animaux pour notre site d’élevage situé à St-Constant, vous serez responsable du bien-être de nos animaux de recherche. Votre réussite assurera la santé de nos animaux.

Dans ce poste, les principales responsabilités incluront:

Assurer la propreté de l’environnement de vie des animaux selon les plus hauts standards de bien-être de l'industrie (nettoyer les salles d’animaux ainsi que les cages);
Manipuler les animaux avec soins;
Participer aux activités physiques/sociales des animaux.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

AEP en soins animaliers (atout);
Apte à travailler physiquement (soulever jusqu’à 20-25kg, marcher, rester debout, s’accroupir, etc.);
Avoir un bon esprit d’équipe;
Passion pour les animaux.

Informations spécifiques au poste:

Localisation : 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport : Stationnement gratuit;
Salaire : 18$/hrs;
Horaire : Du lundi au vendredi, entre 6h00 et 14h15. Selon les besoins de l’entreprise, vous pourriez avoir à faire du temps supplémentaire ainsi que des fin de semaine;
Poste temps plein, 40 heures par semaine;
Poste temporaire à l’embauche & après la période de probation de 6 mois, poste permanent.

Pourquoi Charles River?

Aucune expérience préalable requise;
Des heures garanties, car le milieu de la recherche est très en demande;
Excellent programme de formation continue;
Opportunités de développement professionnel.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

À propos des modèles et services de recherche
Indispensable dans la recherche fondamentale et la découverte, l'utilisation de modèles in vivo nous aide à cibler certaines maladies et à déterminer les voies d'intervention biologiques potentielles qui permettent de contrôler l'évolution de la maladie. En notre qualité de leader mondial dans la production et la distribution d'animaux de recherche de qualité supérieure, avec un modèle sur deux produit pour la recherche préclinique à l'échelle mondiale, nous sommes bien placés pour comprendre l'importance de cette étape. Grâce à nos sept décennies d'expérience, notre expertise est inégalée, ce qui nous permet de mettre à votre disposition le modèle parfait, y compris des options spécifiques à une maladie et pré-conditionnées, pour la recherche fondamentale et au-delà.

À propos de Charles River
Charles River est une organisation internationale de recherche de phase initiale sous contrat (ORC). Nous avons tiré parti de nos solides fondations dans le domaine de la médecine et de la science vétérinaire de laboratoire pour créer un portefeuille diversifié de services d'évaluation de découverte et de sécurité, conformes aux bonnes pratiques de laboratoire et autres, dans le but d'apporter à nos clients un soutien complet, de l'identification de cible au développement pré-clinique. Charles River propose également une gamme de produits et de services à l'appui des besoins en matière d'essais cliniques en laboratoire et des activités de fabrication de ses clients. Ce portefeuille considérable de produits et de services permet à nos clients de créer un modèle de développement de médicament plus flexible réduisant leurs coûts, accroissant leur productivité et améliorant leur efficacité, pour une mise sur le marché plus rapide.

Avec plus de 20 000 collaborateurs sur 110 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 86 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Animal Care Clerk (St. Constant, Quebec, CA, J5A 2E7)

Job Summary

As an Animal Care Clerk for our Husbandry facility located in St-Constant, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals.

In this role, primary responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry (clean the animal rooms and the cages);
Handle animals with care;
Participate in the physical/social activities of the animals.

Job Qualifications

If you possess the following qualifications, we will train you in the rest:

AEP in Animal Care (asset);
Able to work physically (lift up to 20-25 kg, walk, stand, stoop, etc.);
Have a good team spirit;
Passion for animals.

Role Specific Information:

Location: 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport: Free parking;
Salary: $18/hrs;
Schedule: Monday to Friday, between 6:00 am to 2:15 pm. Depending on the needs, you may have to do weekends and/or overtime;
Full-time position, 40 hours per week;
Temporary position at the hiring & after the probation period of 6 months, permanent position.

Why Charles River ?

No experience needed;
Guaranteed hours - The research field is in high demand;
Paid development training;
Professional development opportunities.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Étudiant.e - Commis aux soins des animaux (St. Constant, Quebec, CA, J5A 2E7)

Sommaire de l'emploi

Emploi étudiant - 15hrs par semaine lors de la période scolaire et 40hrs par semaine cet été

Dans ce poste, les principales responsabilités incluront:

Nettoyer les salles d’animaux;
Nettoyer les cages d’animaux;
Manipuler les animaux avec soins.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Apte à travailler physiquement (soulever jusqu’à 20-25kg, marcher, rester debout, s’accroupir, etc.);
Avoir un bon esprit d’équipe;
Passion pour les animaux.

Informations spécifiques au poste:

Localisation : 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport : Stationnement gratuit;
Salaire : 18$/hrs;
Horaire : Tous les samedis et dimanches, horaire entre 6h00 et 14h15;
Poste temps partiel, 15 heures par semaine – 40hrs par semaine cet été.

Pourquoi Charles River?

Aucune expérience préalable requise;
Des heures garanties, car le milieu de la recherche est très en demande;
Excellent programme de formation continue;
Opportunités de développement professionnel.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Student - Animal Care Clerk (St. Constant, Quebec, CA, J5A 2E7)

Job Summary

Student job - 15hrs per week during school term and 40hrs per week this summer

In this role, primary responsibilities include:

Cleaning the animal rooms;
Cleaning the animal cages;
Animals handling.

Key Elements

If you possess the following qualifications, we will train you in the rest:

Able to work physically (lift up to 20-25 kg, walk, stand, stoop, etc.);
Have a good team spirit;
Passion for animals.

Role Specific Information:

Location: 324 Rang St-Régis Nord, St-Constant, J5A 2E7;
Transport: Free parking;
Salary: $18/hrs;
Schedule: Saturday and Sunday, schedule between 6:00 am to 2:15 pm;
Part-time position, 15 hours per week – 40hrs per week this summer.

Why Charles River ?

No experience needed;
Guaranteed hours - The research field is in high demand;
Paid development training;
Professional development opportunities.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animalier.ière (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire du poste

Technicien.ne en Soins aux Animaux – Formation sur place

En tant que Technicien.ne en Soins aux Animaux pour notre équipe de Toxicologie à notre site situé dans la ville de Sherbrooke (QC), vous aurez la charge de veiller au bien-être de tous nos animaux ainsi qu’à intégrité de nos études pré-cliniques.

Dans ce rôle, les principales responsabilités incluront:

Assurer la propreté de l’environnement de vie des animaux selon les plus hauts standards de bien-être de l'industrie
Assister les techniciens dans leurs tâches quotidiennes
Manipuler les animaux;
Participer aux activités physiques/sociales des animaux

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Capable de suivre des instructions précises.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
Bonne compréhension de l’anglais écrit.
Diplôme d'étude Secondaire (DES) requis - Diplôme AEP en soins animaliers est un atout.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Information spécifique au poste :

Localisation : 1580 Rue Ida-Métivier, Sherbrooke (Qc), J1E 0B5.
Transport: Facilement accessible par le transport en commun (Rabais avec la Société des Transport de Sherbrooke). Stationnement gratuit. Borne de recharge pour voiture électrique.
Salaire : À partir de 18.50$/HR. Possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche.
Horaire : Poste temps plein et permanent (37.5HR/semaine), selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire. Travail de fin de semaine par rotation et Prime de quart (2.75$/HR).

Pourquoi Charles River?

3 semaines de vacances et des congés personnels.
Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire).
Accès à un programme d’épargne et de retraite qui comprend une contribution de l’employeur.
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne.
Gym gratuit sur place.
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine).

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe.C'est Votre Moment!

À propos de l'évaluation de la sécurité
Charles River est une société engagée dans une démarche visant à aider ses partenaires à accélérer le développement préclinique de leurs médicaments avec des services d'évaluation de l'innocuité exceptionnels, des locaux utilisant des équipements à la pointe de la technologie et des conseils d'experts en matière de réglementation. Depuis la toxicologie spécialisée individuelle et les études permettant le dépôt d'une demande d'autorisation de nouveau médicament expérimental jusqu'aux formules sur mesure et à l'assistance totale pour les laboratoires, notre équipe chevronnée peut concevoir et exécuter des programmes qui anticipent les difficultés et évitent les blocages pour un parcours sans encombre et efficace jusqu'à la mise sur le marché. Chaque année, environ 300 études d'autorisation de nouveau médicament expérimental (dans le cadre du programme IDN, de l'anglais Investigational New Drug) sont réalisées dans nos centres d'évaluation de l'innocuité.

Pour plus d'information, consultez www.criver.com.

Animal Care Technician (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Animal Care Technician – On site training

As an Animal Care Technician for our Toxicology team for our site located in the city of Sherbrooke (QC), you will be responsible of ensuring the welfare of the animals and the integrity of our pre-clinical studies.

In this role, key responsibilities include:

Ensure the cleanliness of the living environment of the animals according to the highest standards of welfare in the industry.
Assist the technicians in their daily tasks .
Handle animals.
Participate in the physical/social activities of the animals.

Key Elements

If you possess the following qualifications, we will train you in the rest:

Able to follow precises instructions.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English.
Passionate about animals.
High School Diploma (DES) required - Having an AEP in Animal Care is an asset.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Job specific information:

Location: 1580 Ida Métivier, Sherbrooke (Qc), J1E 0B5.
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station.
Salary: Starting at 18.50$/hrs. Opportunity to start at higher level and higher salary with specific research experience.
Schedule: Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime. Weekend work (rotation) and bonus ($2.75/hour).

Why Charles River?

3 weeks’ vacation & Personal days.
Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
Access to a savings and retirement program that includes an employer contribution.
Excellent welcome program for new employees as well as in-house advancement and career development opportunities.
Access to a doctor and various health professionals (telemedicine).
Free gym on site.

If you want to contribute to the wellbeing of our communities across the country and around the world, join our team. This is Your Moment!

Equal Employment Opportunity

For more information, please visit www.criver.com.

Mechanical Engineer (Margate, GB, CT9 4LT)

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly.

Salary D.O.E + On Call Allowance

Mechanical Engineer

Rota - 35 Hrs per week

Monday - Thursday 8.00 am - 4.30 pm

Friday 8.00 am - 1.00 pm

Out of hours callouts - rostered - 1 in 4 weeks (Paid at additional rate)

* Please not due to nature of role flexibilty surrounding core hours is essential.

Overall responsibility

To be responsible for site steam systems and the maintenance, modification of all site mechanical services and equipment as directed by the Facilities Manager. To carry out mechanical repairs, tests and reports as and when necessary.

Main duties/responsibilities

To carry out mechanical repairs and improvements to Company properties, both on a responsive basis and strategic basis.
To carry out Mechanical tests and reports on company property and carry out the necessary repairs.
To carry out preventative planned maintenance and complete relevant job documentation
To respond to reactive work orders and complete as necessary
To promote customer satisfaction through the repair and improvements process
To advise the facilities Manager re. future mechanical maintenance requirements, and any changes to Mechanical practice and legislation.
Installation of pipe work throughout site both copper and iron
Responsible for the operation and monitoring of site boilers both oil and steam ( steam training can be provided)
Responsible for the operation and upkeep of this site biomass boiler
Assist with training of new team members on department procedures.
Responsible for monitoring stock levels for all plumbing and pipe fitting and assist with stock takes.
Provide on call cover to ensure correct operation of systems and equipment out of normal working hours.
Complete specific tasks or projects as requested by the Facilities Manager or Maintenance Manager.
Promote good work practices and enhance working relationships.
Contribute to continuous improvement with an enthesis on sustainability.
Ensure that all Health and Safety regulations are always adhered to.
Where appropriate, be able to report leading and lagging indicators with regards to safety and health to the EHS team.
Ensure a safe and tidy work area.
Provide cover for other members of the team as and when necessary.
Carry out other reasonable duties that may or may not be related to the job as requested by the management.
Must at all times adhere to the Company’s Equal Opportunities Policy in the planning and execution of their duties.

Qualifications, Skills & Abilities

At a minimum City& Guilds Mechanical installation
5 years’ work experience
Steam qualification / or equivalent time served
Some IT literacy
Experience of working in a busy environment to tight deadlines.
Maintaining Steam Boilers
Planned preventive maintenance
HVAC
LTHW Boilers
Some controls experience
Installation experience
Fault finding

Benefits: Life assurance, bonus, career development, training opportunities, free onsite parking, subsidised staff room, pay for participation on volunteer days, on-site team building, charity fundraising days, employee engagement programs.

Pension plan: 1st year employee -Company contribution 5% - Employee 4%, After 3 years: Company contribution 9% and employee 1%

Holidays - 26 days + 8 for Public holidays

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Clinical Veterinary Surgeon (Tranent, GB, EH33 2NE)

Job Summary

An exciting opportunity has arisen for a veterinarian to join our dedicated team passionate about animal welfare. We are a growing group of 5 vets plus dedicated support staff.

At Charles River, we take a passionate approach to improving human and animal health. Our motivating force is the knowledge that our high quality of work provides people with the potential to live healthier and better lives. Scientific excellence and outstanding customer service are the hallmarks of Charles River.

As one of the world’s largest Contract Research Organisations with more than 7000 employees and a market leader in the development of novel human and veterinary medicines, Charles River can offer you the chance to build on your skills and knowledge and work with world-class experts. With more than 60 facilities in 16 countries, we have built a company uniquely designed to meet the needs of our clients in the Pharmaceutical, Biotechnology, Veterinary Medicine, and Agrochemical sectors.

At our world class preclinical facility in Elphinstone, Tranent (close to Edinburgh), our Department of Veterinary Services provides expert advice on animal health and welfare in a diverse mix of laboratory and farm animal species.

Acting as a deputy Named Veterinary Surgeon in accordance with the Animals (Scientific Procedures) Act, you will provide clinical care services to the broad range species at our site in Tranent. As a laboratory animal veterinarian, you are the advocate for the animals, you will use your clinical and interpersonal skills to ensure delivery of the highest standards of welfare, ethical consideration, and compliance in association with the Animal Welfare and Ethical Review Body.

You will assist in the conduct of clinical work across site, including medical and surgical case management, as well as supporting our studies by provision of specialist veterinary services in fields such as anaesthesia, surgery, and ophthalmology.

Due to high volume of applications we are receiving if you have not heard anything from Charles River Laboratories Edinburgh regarding the next steps of our recruitment process within 3 weeks of the closing date then please conclude you have been unsuccessful.

Job Qualifications

Eligibility for membership of the Royal College of Veterinary Surgeons and a relevant clinical work experience is essential.

You will have graduated with a Veterinary degree and have good observational and fine motor skills. You will have established skills in medicine and surgery translatable to the species you will be working with and the drive to expand your skillset. You will have the confidence and ability to communicate effectively with internal and external clients, as well as regulatory bodies. Previous experience in the laboratory animal field would be advantageous, although full training will be provided.

Participation in an out of hours on-call rota will be required although this is not onerous.

In return we offer a competitive salary and benefits package and a real commitment to your training and development needs. This includes the opportunity for undertaking, publishing and presenting relevant personal research, as we support and encourage you to develop your veterinary career.

About Charles River

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

For more information, please visit www.criver.com.

Senior Data Scientist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Senior Data Scientist, you will play a critical role in the process to help unlocking the value of data.

In this role, primary responsibilities include:

Lead and execute end to end data science projects, including problem formulation, data exploration, model development, validation, deployment and ongoing optimization for mission critical applications;
Collaborate closely with the Data Analysts team, Data Engineering team and DataOps team to automate and integrate data science solutions seamlessly into production pipelines;
Work collaboratively, in a consultative way, across the business units, advising on best approaches to leveraging data science in the most effective and efficient manner, including utilizing Generative AI technologies where applicable to develop cutting-edge solutions.

Key Elements

We are looking for the following minimum qualifications for this role:

Master’s with a minimum of 5 years’ experience or Bachelor’s with a minimum of 7 years’ experience in Data science, Computer science, Statistics, Operations research, applied mathematics, applied physics or any related field;
Excellent analytical and problem-solving skills with the ability to approach challenges creatively;
Strong communication skills to translate the findings into actionable business recommendations through rich data visualization;
Familiar with Agile methodologies and tools;
Self-driven and capable of working both independently and collaboratively within a team setting.

Technical Expertise required:

Minimum of 5 years’ hands-on experience processing and analyzing large data sets;
Minimum of 3 years’ experience with the full Machine Learning product lifecycle process and able to take the initiative in making sure deadlines and requirements are met proactively;
Minimum of 5 years’ experience working with development toolsets such as SQL, PySpark, Python, Pandas, Scala;
Minimum of 2 years’ experience in data science projects focused on marketing, sales, or customer experience, delivering insights that drive business impact.

Role Specific Information:

Location: Remote
Annual bonus based on performance;
Schedule: Daytime between Monday and Friday;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Scientifique de données sénior (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Scientifique de données sénior, vous allez jouer un rôle essentiel dans le processus visant à libérer la valeur des données.

Dans ce poste, les principales responsabilités incluront:

Diriger et exécuter des projets de science des données de bout en bout, y compris la formulation de problèmes, l'exploration de données, le développement de modèles, la validation, le déploiement et l'optimisation continue pour les applications critiques;
Collaborer étroitement avec l'équipe d'analystes de données, l'équipe d'ingénierie de données et l'équipe DataOps afin d'automatiser et d'intégrer les solutions de science des données de manière transparente dans les pipelines de production;
Travailler en collaboration, de manière consultative, avec les unités opérationnelles, en donnant des conseils sur les meilleures approches pour tirer parti de la science des données de la manière la plus efficace et la plus efficiente, y compris en utilisant les technologies d'IA générative, le cas échéant, pour développer des solutions de pointe.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Maitrise avec un minimum de 5 ans d'expérience ou Baccalauréat avec un minimum de 7 ans d'expérience en science des données, informatique, statistiques, recherche opérationnelle, mathématiques appliquées, physique appliquée ou tout autre domaine connexe;
Excellentes compétences en matière d'analyse et de résolution de problèmes, avec la capacité d'aborder les défis de manière créative;
Solides compétences en communication pour traduire les résultats en recommandations commerciales exploitables par le biais d'une riche visualisation des données;
Familiarité avec les méthodologies et les outils Agile;
Autonome et capable de travailler à la fois de manière indépendante et en collaboration au sein d'une équipe.

Expertise technique requise :

Au moins 5 ans d'expérience pratique dans le traitement et l'analyse de grands ensembles de données;
Au moins 3 ans d'expérience avec le processus complet du cycle de vie d'un produit d'apprentissage automatique et capacité à prendre l'initiative pour s'assurer que les délais et les exigences sont respectés de manière proactive;
Au moins 5 ans d'expérience dans l'utilisation d'outils de développement tels que SQL, PySpark, Python, Pandas, Scala;
Minimum 2 ans d’expérience dans des projets de science des données axés sur le marketing, les ventes, ou l’expérience client, fournissant des informations qui ont un impact sur les affaires.

Informations spécifiques au poste:

Localisation: Télétravail
Bonus annuel basé sur la performance;
Horaire: De jour en semaine, du lundi au vendredi;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel.

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Veterinary Technician (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Veterinary Technician for our Medicine & Surgery team located in Senneville, you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Evaluate and follow the health status of animals under veterinary supervision;
Work closely with our veterinarians to prepare and perform treatment plans;
Perform medical treatments, interventions, and diagnostic tests under veterinary supervision;
Identify potential animal welfare issues and find solutions.

Key Elements

We are looking for the following minimum qualifications for this role:

College Diploma in Animal Health;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.);
Good observation skills;
Problem solving skills.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: Starting at $20/hrs. Opportunity to start at higher level and higher salary with specific research experience;
Annual bonus based on performance;
Schedule: Weekdays, between Monday to Friday. Depending on the needs, you may have to do overtime and weekend rotations;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien.ne vétérinaire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Technicien.ne vétérinaire pour notre équipe de Médecine & Chirurgie situé à notre site de Senneville, vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce rôle, les principales responsabilités incluront:

Évaluer et suivre l’état de santé des animaux sous la supervision vétérinaire;
Travailler en étroite collaboration avec nos vétérinaires afin de préparer et d’exécuter les plans de traitement;
Exécuter des traitements, procédures médicales et tests de diagnostic sous la supervision vétérinaire;
Identifier des problèmes potentiels reliés au bien-être animal et trouver des solutions.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme collégial en Santé animale;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.);
Bon sens de l’observation;
Compétence en résolution de problème.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au rôle:

Localisation : 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire : à partir de 20$/hrs. Possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche;
Bonus annuel basé sur la performance;
Horaire : Horaire de jour en semaine du lundi au vendredi. Selon les besoins de l’entreprise vous pourriez avoir à effectuer des rotations de fin de semaine;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Animalier.ière (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Animaler.ère - Aucune Experience requise

Tu as toujours rêvé de travailler avec les animaux dans une compagnie qui participe à la recherche de médicament pour sauver des vies? Bonne nouvelle! Nous cherchons actuellement un.e Animalier.ère à temps-plein pour notre site de Senneville (QC). Tu n’as pas besoin d’expérience préalable car nous avons une équipe de formation exceptionnelle qui va tout t’apprendre!

En tant qu’Animalier.ère pour notre équipe de Toxicologie situé au site de Senneville (QC), vous serez responsable du bien-être de tous nos animaux de recherche. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Nettoyer les salles d’animaux;
Nettoyer les cages d’animaux;
Manipuler les animaux.

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Tu aimes travailler physiquement (lever des charges de 20-25 lbs);
Tu es capable de suivre des instructions précises;
Tu aimes les animaux.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 18.50 $ de l’heure avec des primes de :
- Soirée : 2.50$;
- Fin de semaine : 2.75$;
- Heure supplémentaire : Temps et demi;
- Fériés : Temps Double.
Horaire: Majoritairement le jour, la fin de semaine en rotation et les jours fériés. Selon les besoins, il pourrait y avoir du temps supplémentaire de soir ou de nuit;
Poste permanent, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Animal Care Attendant (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Animal Care Attendant - No Experience needed

Have you always dreamed of working with animals in a company that participates in drug research to save lives? Good news! We are currently looking for a full-time Animal Care Attendant for our Senneville (QC) site. You don't need any previous experience because we have an exceptional training team who will teach you everything!

As an Animal Care Attendant for our Toxicology team at the Senneville (QC) site, you will be you will be responsible for the well-being of our laboratory animals. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Cleaning the animal rooms;
Cleaning the animal cages;
Handling animals.

Key Elements

If you have the following qualifications, we'll train you for the rest:

You like to work physically (lifting loads of 20-25 lbs);
You are able to follow precises instructions;
You like animals;

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: $18.50 per hour with primes of :
- Evenings: $2.50;
- Weekend: $2.75;
- Overtime: Time and a half;
- Holidays: Double time;
Schedule: Mostly days, weekend rotations and holidays with overtime on evenings or nights when needed;
Permanent position, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Spécialiste de laboratoire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que spécialiste de laboratoire pour notre site de Senneville, vous aurez à gérer les produits et fournitures nécessaires au bon fonctionnement des départements.

Dans ce poste, les principales responsabilités incluront:

Responsable de la réception, de l’inventaire et de la distribution de produits (substances d’essai, produits chimiques, consommables et colonnes chromatographiques, par exemple), ainsi que de tous les documents qui y sont reliés.
Responsable de faire les commandes du département.
Participer au maintien de l’inventaire des produits et fournitures en quantité suffisante.
Effectuer toute autre tâche connexe, telle qu’assignée.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Posséder un Diplôme d’études secondaires ;
Une combinaison équivalente d’éducation et d’expérience peut être considérée comme substitut acceptable pour l’éducation et l’expérience spécifique telle qu’énumérée ci-dessus
Posséder un excellent sens de l’organisation et capacité à s'adapter aux changements;
Être capable de travailler en équipe.

Informations spécifiques au poste

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire : 24.25$/hrs;
Bonus annuel basé sur la performance;
Horaire : Du lundi au vendredi, de jour.
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River ?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Laboratory Specialist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Laboratory specialist for our Senneville site, you will manage products and supplies necessary for the proper functioning of departments.

In this role, primary responsibilities include:

In charge of the reception, inventory and the distribution of products (test items, chemicals, consumable products, chromatographic columns, for example), as well as all the related documentation.
Responsible for placing the orders for the department.
Participate in maintaining inventory of products and supplies in sufficient quantity.
Perform all other related duties as assigned.

Key Elements

We are looking for the following minimum qualifications for this role:

Possess a high school diploma;
An equivalent combination of education and experience may be considered an acceptable substitute for the specific education and experience listed above.
Flexible and able to adapt quickly to change
Ability to work as part of a team.

Role Specific Information

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: 24.25$/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, day schedule.
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career; development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you want to contribute to the well-being of our communities, not only across the country, but around the world, join the team. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Regional Biosafety Officer (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Regional Biosafety Officer for our Health and Safety team, you will be coordinating the Regional Biosafety Program to ensure our program meets federal, local and corporate requirements.

In this role, primary responsibilities include:

Coordinates the Regional Biosafety network; maintains appropriate memberships and licenses, coordinates/manages a regular meeting cadence, drives regional objectives, and maintains records.
Promotes and monitors compliance with applicable legislation, conditions of license, animal pathogen import permits, biosafety and biosecurity standards, the Biosafety Manual and standard operating procedures;
Arrange and document appropriate biosafety and biosecurity training for personnel
Develop/maintain supporting document management systems and tools to support the program including local risks assessments and inventories of regulated material.
Conduct periodic inspections and biosafety audits. Report audit findings to the license holder and animal pathogen import holder in writing of any non-compliance and drive resulting action plans to closure
Communicate with the Public Health Agency of Canada (PHAC) and the Canadian Food Inspection Agency (CFIA) on behalf of the license holder and animal pathogen import permit holder, as applicable.
Supports the review and approval of proposed work involving infectious and biological safety work conducted at site level
Collaborates with Global/ Regional EHS&S team to establish assessment and inspection tools to identify Biosafety risks associated with operations and creates solutions for gaps or opportunities for program improvement.

Key Elements

We are looking for the following minimum qualifications for this role:

Technical or Bachelor’s degree in biological sciences;
3-5 years experience in biosafety work;
Experience working with NHP and asset;
Ability to inspire trust and confidence through strong interpersonal skills and effective collaboration;
Ability to effectively manage multiple projects simultaneously;
Bilingual (French & English).

Role Specific Information:

Locations (3):
- 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3(1-2x per week);
- 22022 route Transcanadienne, Senneville, QC, H9X 1C1 (3-4x per week);
- 580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5 (1x per month);
Annual bonus based on performance;
Schedule: Monday to Friday, Day schedule, On site;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Officier.e Biosécurité Régional (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant qu’ Officier.e Biosécurité Régional pour notre équipe de Santé et Sécurité, vous coordonnerez le programme régional de biosécurité pour garantir que notre programme répond aux exigences fédérales, locales et corporatives.

Dans ce poste, les principales responsabilités incluront:

Coordonner le réseau régional de biosécurité ; maintenir les adhésions et les licences appropriées, coordonner/gérer la fréquence des réunions, piloter les objectifs régionaux et tenir les dossiers à jours;
Favoriser et surveiller le respect de la législation applicable, des conditions de licence, des permis d'importation d'agents zoopathogènes, des normes de biosécurité et de biosûreté, du Manuel de biosécurité et des procédures opérationnelles normalisées;
Organiser et documenter la formation appropriée du personnel en matière de biosécurité et de biosûreté;
Élaborer et maintenir des systèmes et des outils de gestion des documents justificatifs pour soutenir le programme, notamment les évaluations des risques locaux et les inventaires de matières réglementées;
Effectuer des inspections et des audits de biosécurité périodiques. Signaler par écrit les constatations d'audit au titulaire de licence et au titulaire du permis d'importation d'agents zoopathogènes de toute non-conformité et met en œuvre les plans d'action qui en découlent jusqu'à leur résolution;
Communiquer avec l'Agence de la santé publique du Canada (ASPC) et l'Agence canadienne d'inspection des aliments (ACIA) au nom du titulaire de licence et du titulaire du permis d'importation d'agents zoopathogènes, le cas échéant.
Soutenir l'examen et l'approbation des projets de travaux de sécurité infectieuse et biologique menés sur site.
Collaborer avec l'équipe SST mondiale/régionale pour mettre en place des outils d'évaluation et d'inspection afin d'identifier les risques de biosécurité associés aux opérations et crée des solutions pour combler les lacunes ou améliorer les programmes.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

DEC ou BAC en sciences biologiques;
3-5 années d’expérience en de travail avec la biosécurité;
Experience de travail avec les NHP est un atout;
Capacité à inspirer confiance grâce à de solides compétences interpersonnelles et à une collaboration efficace ;
Capacité à gérer efficacement plusieurs projets simultanément;
Bilingue (français et anglais).

Informations spécifiques au poste:

Localisations (3):
- 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3 (1-2x par semaine);
- 22022 route Transcanadienne, Senneville, QC, H9X 1C1 (3-4 x par semaine);
- 580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5 (1x par mois);
Bonus annuel basé sur la performance;
Horaire: Lundi au vendredi de jours, sur site;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Technicien.ne en Laboratoires Cliniques (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Technicien.ne – Laboratoires cliniques

En tant que Technicien.ne pour notre équipe de Laboratoires cliniques située au site de Senneville, vous devrez accomplir les tâches techniques et suivre les directives des plans d’étude/phase et des PNO.

Dans ce poste, les principales responsabilités incluront:

Effectue les préparations ainsi que les analyses des échantillons;
Effectue le control de qualité ainsi que les maintenances sur les différents instruments;
Accomplis les activités en temps opportun en suivant les horaires établis;
Assure l’intégrité des études et satisfait les exigences des agences réglementaires en exécutant les activités et recueillant les données conformément aux Bonnes Pratiques de Laboratoires (BPL), aux Procédures Normalisées d’Opération (PNO) et aux règles de santé sécurité.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études collégiales en sciences;
Une expérience connexe est un atout;
Une combinaison équivalente d’éducation et d’expérience peut être considérée comme substitut acceptable pour l’éducation et l’expérience spécifique telle qu’énumérée ci-dessus;
Avoir la capacité de travailler sous la contrainte de temps et de s'adapter aux changements;
Lire et écrire en anglais est requis. Le bilinguisme est préférable;
Faire preuve de flexibilité et être capable de travailler de manière autonome.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 20$/hrs avec prime de soir et possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche;
Bonus annuel basé sur la performance;
Horaire: Lundi au vendredi de 3h PM à 11h15 PM après la formation de 3 à 6 mois de 8 AM à 4h15 PM;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Technician in Clinical Laboratories (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Technician – Clinical Laboratories

As a Technician for our Clinical Laboratories team at the Senneville location, you will perform technical activities and follows directives from the study/phase plan and the SOP.

In this role, primary responsibilities include:

Perform the preparation and the analysis of samples;
Perform the quality control procedure and maintenances on the different instruments;
Perform the activities in a timely fashion by adhering to preset schedules;
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the GLP, SOP and health and safety rules.

Key Elements

We are looking for the following minimum qualifications for this role:

College diploma in science;
Relevant experience is an asset;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Reading and writing English is required. Bilingualism is preferred;
Ability to work under time constraint and adapt to change;
Demonstrate flexibility and ability to work independently.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: 20$/per hour, evening premiums and opportunity to start at higher level and higher salary with specific research experience;
Schedule: Monday to Friday (3h PM-11h15PM) after 3-6 months of training from (8h AM-4h15 PM);
Annual bonus based on performance;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

• Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
• Free gym on site;
• Employee and family assistance program;
• Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
• Access to a doctor and various health professionals (telemedicine);
• 3 weeks’ Vacation & 5 Personal day policy;
• Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

Competencies

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Reviseur.e de données-Immunochimie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Depuis plus de 75 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous avez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences jouent un rôle important dans le travail que nous effectuons. En retour, nous vous aidons à bâtir une carrière passionnante à nos côtés.

Résumé du travail

En tant que Réviseur.e de données pour notre équipe de Toxicologie génétique situé au site de Ville Saint-Laurent, vous serez responsable de la vérification des données en conformité avec les Bonnes Pratiques de Laboratoire (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Garantir l’intégrité de la révision et des corrections en conformité avec les Bonnes Pratiques de Laboratoires (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude;
S’assurer que toutes les données pertinentes soient révisées;
Être en mesure de finaliser la révision et les corrections à temps, selon les dates prédéterminées;
Être proactif.ve dans ses démarches pour obtenir les réponses aux erreurs décelées;
Être responsable de documenter tout commentaire toujours en suspens à la fin du processus de révision.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un DEC en sciences (biotechnologie, laboratoire médical ou l’équivalent) ou d’un BAC en sciences (immunologie, biologie, biochimie) ;
Habileté à travailler avec des contraintes de temps;
Posséder un excellent sens de l’organisation;
Travailler avec précision, faire attention aux détails et s’appliquer à réaliser un travail de qualité.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Salaire: 22,50$/H
Horaire: Du lundi au vendredi, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à effectuer du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

À propos de l'évaluation de sécurité

Charles River est une société engagée dans une démarche visant à aider ses partenaires à accélérer le développement préclinique de leurs médicaments avec des services d'évaluation de l'innocuité exceptionnels, des locaux utilisant des équipements à la pointe de la technologie et des conseils d'experts en matière de réglementation. Depuis la toxicologie spécialisée individuelle et les études permettant le dépôt d'une demande d'autorisation de nouveau médicament expérimental jusqu'aux formules sur mesure et à l'assistance totale pour les laboratoires, notre équipe chevronnée peut concevoir et exécuter des programmes qui anticipent les difficultés et évitent les blocages pour un parcours sans encombre et efficace jusqu'à la mise sur le marché. Chaque année, environ 300 études d'autorisation de nouveau médicament expérimental (dans le cadre du programme IDN, de l'anglais Investigational New Drug) sont réalisées dans nos centres d'évaluation de l'innocuité.

Au sein des laboratoires Charles River, nous reconnaissons et recrutons tous les talents. Nous sommes une entreprise attachée au principe de mixité, de diversité et d’inclusion et œuvrons quotidiennement en ce sens

Les Laboratoires Charles River France sont engagés dans une politique en faveur de l’intégration et du maintien dans l’emploi des personnes en situation de handicap. Tous nos postes sont ouverts aux travailleurs handicapés et une attention particulière sera portée aux candidats en situation de handicap qui postuleront auprès de Charles River.

Pour plus d'information, consultez www.criver.com.

Data Reviewer - Immunochemistry (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Data Reviewer for our Genetic Toxicology team at the Ville Saint-Laurent location, you will be responsible for the verification of raw data according to Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), and study plans.
Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Guarantee accurate review and corrections in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP) and study plans.
Ensure that all pertinent data is reviewed.
Ensure that the review and corrections are finalized according to established due dates.
Proactive in obtaining answers to findings.
Responsible for documenting any remaining issues at data review clearance.

Job Qualifications

We are looking for the following minimum qualifications for this role:

Holder of a DEC in Science (Biotechnology, Medical Laboratory, or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry);
Ability to work under time constraints;
Outstanding organizational skills;
Work with precision, pay attention to detail and strive for quality work.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Annual bonus based on performance;
Salary: 22,50$/H
Schedule: Monday to Friday, 8am to 4:15pm. Depending on business needs, you may have to do overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career; development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Reviseur.e de données-Immunochimie (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Dans ce poste, les principales responsabilités incluront:

Garantir l’intégrité de la révision et des corrections en conformité avec les Bonnes Pratiques de Laboratoires (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude;
S’assurer que toutes les données pertinentes soient révisées;
Être en mesure de finaliser la révision et les corrections à temps, selon les dates prédéterminées;
Être proactif.ve dans ses démarches pour obtenir les réponses aux erreurs décelées;
Être responsable de documenter tout commentaire toujours en suspens à la fin du processus de révision.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un DEC en sciences (biotechnologie, laboratoire médical ou l’équivalent) ou d’un BAC en sciences (immunologie, biologie, biochimie) ;
Habileté à travailler avec des contraintes de temps;
Posséder un excellent sens de l’organisation;
Travailler avec précision, faire attention aux détails et s’appliquer à réaliser un travail de qualité.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Salaire: 22,50$/H
Horaire: Du lundi au vendredi, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à effectuer du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Reviseur.e de données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Résumé du travail

En tant que Réviseur.e de données pour notre équipe de Immunologie situé au site de Senneville, vous serez responsable de la vérification des données en conformité avec les Bonnes Pratiques de Laboratoire (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Garantir l’intégrité de la révision et des corrections en conformité avec les Bonnes Pratiques de Laboratoires (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude;
S’assurer que toutes les données pertinentes soient révisées;
Être en mesure de finaliser la révision et les corrections à temps, selon les dates prédéterminées;
Être proactif.ve dans ses démarches pour obtenir les réponses aux erreurs décelées;
Être responsable de documenter tout commentaire toujours en suspens à la fin du processus de révision.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un DEC en sciences (biotechnologie, laboratoire médical ou l’équivalent) ou d’un BAC en sciences (immunologie, biologie, biochimie) ;
Habileté à travailler avec des contraintes de temps;
Posséder un excellent sens de l’organisation;
Travailler avec précision, faire attention aux détails et s’appliquer à réaliser un travail de qualité.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à effectuer du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

À propos de l'évaluation de sécurité

Pour plus d'information, consultez www.criver.com.

Reviseur.e de Données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Dans ce poste, les principales responsabilités incluront:

Garantir l’intégrité de la révision et des corrections en conformité avec les Bonnes Pratiques de Laboratoires (BPL), les Procédures Opératoires Normalisées (PON), les Procédures Analytiques (PA) et les plans d’étude;
S’assurer que toutes les données pertinentes soient révisées;
Être en mesure de finaliser la révision et les corrections à temps, selon les dates prédéterminées;
Être proactif.ve dans ses démarches pour obtenir les réponses aux erreurs décelées;
Être responsable de documenter tout commentaire toujours en suspens à la fin du processus de révision.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Titulaire d’un DEC en sciences (biotechnologie, laboratoire médical ou l’équivalent) ou d’un BAC en sciences (immunologie, biologie, biochimie) ;
Habileté à travailler avec des contraintes de temps;
Posséder un excellent sens de l’organisation;
Travailler avec précision, faire attention aux détails et s’appliquer à réaliser un travail de qualité.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi, de 8h à 16h15. Selon les besoins de l’entreprise, vous pourriez avoir à effectuer du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Data Reviewer (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Data Reviewer for our Immunology team at the Senneville location, you will be responsible for the verification of raw data according to Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP), and study plans.
Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Guarantee accurate review and corrections in accordance with Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Analytical Procedures (AP) and study plans.
Ensure that all pertinent data is reviewed.
Ensure that the review and corrections are finalized according to established due dates.
Proactive in obtaining answers to findings.
Responsible for documenting any remaining issues at data review clearance.

Job Qualifications

We are looking for the following minimum qualifications for this role:

Holder of a DEC in Science (Biotechnology, Medical Laboratory, or equivalent) or a BAC in Science (Immunology, Biology, Biochemistry);
Ability to work under time constraints;
Outstanding organizational skills;
Work with precision, pay attention to detail and strive for quality work.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Monday to Friday, 8am to 4:15pm. Depending on business needs, you may have to do overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career; development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Analyste en Immunologie (LBA) (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant qu’Analyste pour notre équipe d’Immunologie situé au site de Laval, vous serez responsable d’effectuer l'analyse des données pour déterminer si les résultats sont conforme aux attentes. Vous allez également enregistrer les données conformément aux politiques et aux normes de l'entreprise pour répondre aux exigences de qualité et d'exactitude.

Dans ce poste, les principales responsabilités incluront:

Effectuer des travaux d'analyse d'échantillons dans un laboratoire multidisciplinaire en utilisant une vaste gamme de techniques;
Documenter, effectuer et analyser des essais;
Recevoir, entreposer, vérifier et préparer les échantillons biologiques à des fins d'analyse;
Participer aux tâches quotidiennes du laboratoire telles que la préparation de réactifs, calibration des instruments et réception des produits.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’étude secondaire – Aucune expérience requise;
AEC en Biotechnologie ou dans tout autres domaines reliés aux science biologique est un atout;
Habileté à effectuer des essais de manière autonome;
Avoir l'esprit d'équipe et une approche collaborative et positive.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire: 23$/hrs;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de 8h à 16h15. Selon les besoins de l’entreprise vous pourriez avoir à faire du temps supplémentaire;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Veterinary Pathology Certified (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Veterinary Pathologist for our team at the Laval location, you will mainly be responsible for tissue evaluation and interpretation of assigned studies. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies;
Record Histopathology findings in data capturing system;
Prepare complex reports delineating pathological findings and detailing all test article effects;
Interact with clients to assure satisfaction and to market services;
Assist with necropsy supervision and may conduct necropsies, including gross pathology interpretation, sample collection and fixation;
Work with study directors to ensure data is accurately integrated into study reports;
Provide training, technical guidance and leadership to laboratory staff and to less experienced pathologists;
Provide advanced scientific expertise for experimental design and other aspects of research studies;
Collaborate with other units within the Pathology teams and other departments within the site.

Key Elements

We are looking for the following minimum qualifications for this role:

Doctorate degree (D.V.M/V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine;
Working knowledge of clinical pathology preferred;
Board certification with the American College of Veterinary Pathologists (A.C.V.P.) or European College of Veterinary Pathologists (E.C.V.P) required to enter the level grade;
Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought;
Ability to work on problems of diverse scope in which analysis of data requires evaluation of multiple factors;
Ability to exercise judgement within generally defined practices and policies in selecting methods or techniques for obtaining solutions;
Working knowledge of related computer applications;
Special interest in digital Pathology & Molecular Pathology as well as digital image analysis is preferred;
Bilingualism in French and English is mandatory. Good communication skills in both languages is required.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Annual bonus based on performance;
Schedule: Monday to Friday, daytime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid ACVP / ECVP yearly license;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
4 weeks’ Vacation & 10 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Pathologiste vétérinaire avec certification (Laval, Quebec, CA, H7V 4B3)

Sommaire de l'emploi

En tant que Pathologiste Vétérinaire pour notre équipe située au site de Laval, vous serez principalement responsable de l'évaluation des tissus et de l'interprétation des études assignées. Votre contribution assurera la santé de nos animaux ainsi que l'intégrité de nos études précliniques.

Dans ce poste, les principales responsabilités incluront:

Effectuer l'évaluation et l'interprétation macroscopes et microscopiques des tissus des études assignées;
Enregistrer les résultats d'histopathologie dans le système de capture de données;
Préparer des rapports complexes décrivant les résultats pathologiques et détaillant tous les effets des articles de test;
Interagir avec les clients pour assurer leur satisfaction et promouvoir les services;
Aider à la supervision des nécropsies et peut réaliser des nécropsies, y compris l'interprétation de la pathologie macroscopique, la collecte et la fixation des échantillons;
Travailler avec les directeurs d'études pour s'assurer que les données sont intégrées avec précision dans les rapports d'études;
Fournir formation, orientation technique et leadership au personnel de laboratoire et aux pathologistes moins expérimentés;
Apporter une expertise scientifique avancée pour la conception expérimentale et d'autres aspects des études de recherche;
Collaborer avec d'autres unités au sein des équipes de Pathologie et d'autres départements sur le site.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme de doctorat (D.V.M/V.M.D.) d'une école vétérinaire accréditée, ou équivalent international acceptable en médecine vétérinaire;
Connaissance pratique de la pathologie clinique préférée;
Certification par le American College of Veterinary Pathologists (A.C.V.P.) ou le European College of Veterinary Pathologists (E.C.V.P) requise pour accéder au grade de niveau;
Succès démontré en compétence technique, créativité scientifique, collaboration avec les autres et pensée indépendante;
Capacité à travailler sur des problèmes de portée diverse où l'analyse des données nécessite une évaluation de multiples facteurs;
Capacité à exercer un jugement dans le cadre de pratiques et politiques généralement définies lors de la sélection des méthodes ou techniques pour obtenir des solutions;
Connaissance pratique des applications informatiques connexes;
Un intérêt particulier pour la Pathologie numérique et la Pathologie moléculaire ainsi que l'analyse d'image numérique est préféré;
Le bilinguisme en français et en anglais est obligatoire. De bonnes compétences en communication dans les deux langues sont requises.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au poste:

Localisation: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport: Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Bonus annuel basé sur la performance;
Horaire: Du lundi au vendredi de jour;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Licence annuelle ACVP / ECVP payée;
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
4 semaines de vacances et 10 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Senior Formulation Scientist (Harlow, GB, CM19 5TR)

Job Summary

Are you a skilled formulator looking to take the next step in your career?

Have you got experience of working in an industrial R&D setting, developing formulations for novel small molecule API’s?

Do you want to join a global contract research organisation that improves health and lives?

Our expanding pharmaceutical development team in Harlow, Essex are recruiting for an experienced formulation scientist. In this role you will apply formulation expertise to guide formulation projects through pre-clinical development.

This leadership role in a small but far-reaching team is an excellent opportunity to help shape the future direction of the Pharmaceutical Development group at Charles River. You will have the opportunity to work on a variety of client projects spanning oral, inhaled, dermal and parenteral administration routes. This role encompasses project management and ownership of client relationships, as well as supporting lab work when required.

Main Tasks:

Advise as a subject matter expert for Integrated Drug Discovery and Development projects, guiding formulation strategy to ensure successful outcomes.
Design and execute formulation study plans, based on client needs.
Manage client formulation projects to agreed timelines and budgets.
Act as the scientific point of contact for clients, from initial discussion through to project delivery.
Mentor junior scientists in formulation techniques and strategies.

Skills and Experience

The ideal candidate has a pro-active can-do approach, pays attention to detail, and has the ability to adapt to changing demands and requirements. They use PK data and the Developability Classification System to drive formulation strategy and is comfortable communicating complex scientific data to stakeholders with varying degrees of expertise.

A working knowledge of solid form characterisations techniques, non-oral dosage routes and formulation of “Beyond Rule of 5” compounds is desirable. Experience of scientific project management would also be advantageous.

Minimum BSc. Qualification in a relevant subject (Chemistry, Pharmaceutical Sciences or related subject). Post-graduate qualifications desirable.
Extensive experience of working in an industrial R&D setting, developing formulations for novel small molecule APIs.
Strong knowledge of the drug discovery and development process.
Experience of mentoring junior colleagues.
Experience in designing and executing preformulation studies, including:- Physicochemical assessment, Solubility Assessment and Biorelevant Dissolution studies.
Expertise in at least one of the following enabling oral formulation techniques:- Spray Drying, Wet milling for particle size reduction or Emulsion development.

What We Offer You

A very comprehensive benefits package from day one, including a generous pension contribution, and flexible health benefits.
Parental leave.
Group Life Assurance and Group Income Protection.
Remote GP access 24/7.
Wellbeing support and initiatives.
Access to great discounts via our CREDS discount scheme.
Global opportunities and strong career progression.
The chance to work on several varied projects and liaise globally and nationally with other business areas.
To be able make a difference to health and wellbeing of people.
To continue your own career growth.
Cycle to work scheme and much much more!

About Discovery
Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Immunology Analyst (LBA) (Laval, Quebec, CA, H7V 4B3)

Job Summary

As an Analyst for our Immunology team at the Laval location, you will perform analysis of data for quality and completeness and determines if results are as expected. You will also record data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements.

In this role, primary responsibilities include:

Carry out sample analysis in a multidisciplinary laboratory, using a wide variety of techniques;
Prepare technical worksheets and procedures;
Receive, store, verify and process biological samples for analysis;
Take part in the routine duties of the laboratory such as preparation of reagents, instrument calibration, product reception.

Key Elements

We are looking for the following minimum qualifications for this role:

High school diploma - No experience required;
AEC in Biotechnology or other bioscience related field is an asset;
Ability to perform tests independently;
Team player with a collaborative and positive approach.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: $23/hrs;
Annual bonus based on performance;
Schedule: Monday to Friday, 8am to 4:15pm. Depending on the business needs, you may have to do overtime;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career; development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Associate (Raleigh, NC, US, 27610)

JOB SUMMARY

As an Animal Care Associate for our production site in Raleigh, NC, you will be responsible for the well-being of our research animals. Your contribution will ensure the health of our animals, as well as impact the lives of patients across the world. You will perform routine animal husbandry and other production duties. You will also maintain supplies and environment of environmentally-controlled work area(s).

* This is a temporary opportunity with the potential to be hired as a full-time, employee.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform routine animal husbandry duties and monitor daily health and welfare to maintain quality and health of animals.
Handle, transfer, and distribute animals, supplies and waste as needed to and from work area(s).
Monitor animal health by observing animal behavior, physical appearance, and physical environment. Identify and report any abnormal findings.
Responsible for collecting health monitoring swabs and following health monitoring schedules.
Perform physical environment housekeeping duties and production operations according to Good Manufacturing Practices (GMPs) and/or Standard Operating Procedures (SOPs).
Maintain recordkeeping pertaining to animal or supply area inventories.
Strictly follow all procedures necessary to maintain the barrier room barrier.
Use supplies according to safety guidelines. Perform all job-related duties in accordance with company safety procedures.
Colony Management
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS:

No experience required. On the job training will be provided.

ROLE SPECIFIC INFORMATION:

Location: Raleigh, NC
Pay: $17.75 - $19.00 / hour
Schedule: Start times fall between 4:00am - 6:00 am, working 9 hour shifts Monday - Thursday and a 4 hour shift on Friday. Weekend rotation is required.

PHYSICAL DEMANDS

Regularly required to utilize a computer/tablet.
Regularly required to stand, use hands to finger, handle or feel objects, tools or controls; and reach with hands and arms.
Regularly required to stand and ascend/descend rolling platform ladder (up to six steps) to perform all tasks and procedures related to the job.
Regularly transports supplies, removes waste, and/or laboratory equipment while ascending/descending rolling platform stairs (up to six steps).
Regularly positions self (stoop, crouch, squat, sit, reach) to access and inspect small models and be able to assess their conditions and environment from various distances.
Regularly lifts and/or moves materials weighing up to 10 pounds and occasionally lifts and/or moves materials weighing up to 50 pounds.
May occasionally lift and/or move equipment and materials weighing 30-50 pounds, and equipment and materials weighing over 50 pounds with assistance.
Specific vision abilities required by this job include close vision, depth perception, and the ability to differentiate colors.
Regularly works with chemicals that require the use of respirators. Medical clearance is required prior to using respirators.

The pay range for this position is $17.75-$19.00 / hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Operaio stabularista - Categorie protette (Lg 68/99) (CALCO, IT, 23885)

Da 75 anni, i dipendenti di Charles River hanno lavorato insieme per assistere alla scoperta, allo sviluppo e alla produzione sicura di nuove terapie farmacologiche. Quando si unisce alla nostra famiglia, avrai un impatto significativo sulla salute e il benessere di persone in tutto il mondo. Se il tuo background è in scienze della vita, finanza, IT, vendite o in un'altra area, le tue abilità avranno un ruolo importante nel lavoro che svolgiamo. In cambio, ti aiuteremo a costruire una carriera che puoi sentirti appassionata.

Job Summary

Per la nostra sede di Calco/Milano ricerchiamo uno stabularista.

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro part-time e week-end

Buona conoscenza del pacchetto office

Essere iscritto alle categorie protette Lg 68/99

Di cosa si occupa la Charles River

Charles River è un’organizzazione di ricerca a contratto (CRO) per le fasi precoci della ricerca farmacologica. Sulla base della nostra scienza e medicina degli animali da laboratorio abbiamo costituito e sviluppato un portafoglio diversificato di servizi di scoperta e di valutazione della sicurezza, sia GLP che non-GLP, per supportare i clienti a partire dall’identificazione del bersaglio fino allo sviluppo preclinico. Charles River offre inoltre una gamma di prodotti e servizi a supporto delle esigenze di analisi cliniche di laboratorio e delle attività di produzione dei nostri clienti laboratorio. L’utilizzo di questo portafoglio variegato di prodotti e servizi permette ai nostri clienti di creare modello di sviluppo dei farmaci più flessibile, che riduce i costi e migliora la produttività e l’efficienza al fine di ridurre i tempi di immissione sul mercato.

Con oltre 20.000 dipendenti in 90 strutture dislocate in 20 paesi in tutto il mondo, siamo posizionati strategicamente per coordinare le risorse a livello mondiale e applicare prospettive multidisciplinari per risolvere le sfide particolari dei nostri clienti. La nostra base clienti include aziende farmaceutiche di livello mondiale, aziende operanti nel settore delle biotecnologie ed enti governativi, nonché ospedali e istituzioni accademiche di tutto il mondo.

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosamente ha collaborato allo sviluppo di ~85% dei farmaci approvati dalla FDA nel 2021.

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Operaio stabularista - Categorie protette (Lg 68/99) (CALCO, IT, 23885)

Da quasi 75 anni, i dipendenti di Charles River hanno lavorato insieme per assistere alla scoperta, allo sviluppo e alla produzione sicura di nuove terapie farmacologiche. Quando si unisce alla nostra famiglia, avrai un impatto significativo sulla salute e il benessere di persone in tutto il mondo. Se il tuo background è in scienze della vita, finanza, IT, vendite o in un'altra area, le tue abilità avranno un ruolo importante nel lavoro che svolgiamo. In cambio, ti aiuteremo a costruire una carriera che puoi sentirti appassionata.

Riepilogo del lavoro

Di cosa si occupa la Charles River

Con oltre 20.000 dipendenti in 110 strutture dislocate in 20 paesi in tutto il mondo, siamo posizionati strategicamente per coordinare le risorse a livello mondiale e applicare prospettive multidisciplinari per risolvere le sfide particolari dei nostri clienti. La nostra base clienti include aziende farmaceutiche di livello mondiale, aziende operanti nel settore delle biotecnologie ed enti governativi, nonché ospedali e istituzioni accademiche di tutto il mondo.

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

Per ulteriori informazioni, visita il sito www.criver.com.

Inventory Warehouse Tech (Charleston, SC, US, 29407)

Job Summary

We are seeking an Inventory Warehouse Inventory Tech for Microbial Solutions at our site in Charleston, SC.

The primary responsibilities of the Warehouse Inventory Tech are as follows:

Receive, sort, and distribute incoming shipments and raw materials
Maintain inventory levels in computer platforms and place requisitions for supplies as needed
Store and identify materials according to quality guidelines
Complete documentation as required by SOPs and regulatory agencies
Assist with Production support duties as needed
Ensure warehouse environment is kept in a clean and safe working condition
Perform all other duties as assigned

Job Qualifications

The primary qualifications for the Warehouse Inventory Tech position are as follows:

Education: High school diploma or equivalent required
Experience: 1-2 years of related experience
An equivalent combination of education and experience may be accepted as a satisfactory substitute
Other: Must be computer literate; collaboration with internal and external customers is key; efficient verbal and written communication skills; ability to prioritize multiple tasks

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

With over 17,000 employees within 90 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Automation Engineer I (Charleston, SC, US, 29407)

Job Summary

This position will work with both hardware and software aspects of automation to determine the best way to implement the Microbial Solutions automation roadmap, including conceptual design, capital expenditure approval, management of integration and suppliers, testing, and validation. This role will monitor existing automation for end of life/replacement/repair and identify, justify, and implement technology and equipment upgrades, process technologies, and process improvements. Additionally, the Automation and Controls Engineer will provide project leadership and support for assigned automation, equipment, and software projects.

Essential Duties and Responsibilities

Investigates, analyze, and prepare justification for the purchase of automation equipment and other capital equipment purchases
Identify, lead, and support continuous improvement/new projects, developing detailed specifications, electrical drawings, implementation plans, and other appropriate documentation
Collaborate with functional experts, operations personnel, and site management to shape the future state of the manufacturing facility and the plant software architecture that adheres to automation standards and regulations
Review, quality check, and provide final approval for all control system hardware drawings, including network architecture, panel drawings, communications wiring diagrams, etc.
Troubleshoot existing hardware and software and provide programming assistance to maintain current equipment and software/control systems.
Validation, Qualification and FAT/SAT experience a plus
Perform all other related duties as assigned

Qualifications

Education:
⦁ B.S or equivalent in Mechatronics, Industrial Engineering, Mechanical Engineering, Electrical Engineering, Computer/Computer Systems Engineering, Electronics

Experience:
⦁ At least 3 years in a cGMP environment
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above

Skills and Abilities:
Working knowledge and experience with PLC, HMI, and SCADA; working knowledge of vision systems (Cognex, Keyence, etc.); ability to work on multiple projects simultaneously, good interpersonal skills, quality mindset with focus on risk management and mitigation; technical writing and communication

PHYSICAL DEMANDS:
⦁   Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer.
⦁   Regularly interfaces with lab equipment and associated test equipment (meters, scopes, etc.).
⦁   Must be able to lift 40 lbs on occasion

WORK ENVIRONMENT:
⦁ Office and production environment.

Comments:
⦁ Occasional Travel may be required

Compensation Data

The pay range for this position is $80,000 to $100,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Equal Employment Opportunity

Shipping Technician I (Charleston, SC, US, 29407)

Job Summary

Pack and ship products to customers and complete all associated paperwork.
Check orders prepared by others for shipment to customers; monitor for accuracy of lot numbers, quantities, certificate of analysis, and agreement between customer order and content of package.
Move finished goods to released storage area after QA release.
Perform inspection of final product as necessary; verify count, package insert, that label and vial meets standards described in SOPs and product specs.\
Perform Kit production: assemble packaging, components and necessary paperwork for Kit release.
Maintain retention storage area, retrieve samples for QC testing, and fill out appropriate paperwork.
Maintain customer returns by inspecting and quarantining the product until QA release.Create freight shipping labels; must perform measurement and weighing and document shipping specifications.
Maintain documentation as required by FDA, company policy, and cGMP.Share responsibility for inventory control to prevent stock-out situations.
Clean and maintain work and storage areas and adhere to established safety procedures.
Perform seasonal duties associated with processing crude LAL, as needed.
Assist other areas of the facility when needed.
Remain proficient in all SOPs in areas of responsibility.
Perform all other related duties as assigned.

Job Qualifications

• Education: High school diploma or General Education Degree (G.E.D.).
• Experience: Zero to twelve months related experience in and/or training in a GMP manufacturing environment.

PHYSICAL DEMANDS:
•   Tasks require full range of motion of arms.
•   While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel objects, tools, or controls.
•   The employee is frequently required to stand while performing duties; sit; reach with hands and arms; and stoop, kneel, crouch, or crawl.
•   The employee is occasionally required to work/type at a computer.
•   The employee must frequently lift and/or move up to 50 pounds.
•   Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:
•   While performing the duties of this job, the employee regularly wears protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots)
•   The employee occasionally works near moving mechanical parts, works with sharp objects, works with or near toxic or caustic chemicals, works with biohazards, works with live animals (small, medium, large) with risk of exposure to allergens, is exposed to fumes or airborne particles, is exposed to unpleasant odors, is exposed to wet, humid and/or extreme temperature conditions, is exposed to vibration.
•   The noise level in the work environment is usually low / moderate

Compensation Data

The pay for this position is $19.25 hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

For more information, please visit www.criver.com.

Celsis Technical Support Specialist I (Charleston, SC, US, 29407)

Job Summary

The Microbial Solutions Business Located in Charleston SC, is seeking Celsis Technical Support Specialist.
The working hours for this position are Monday - Friday 830a - 5pm located in the office onsite.
The Celsis Technical Support Specialist will provide technical support to customers on Celsis instrumentation, sample preparation, and data interpretation. Assist customers regarding Celsis reagent questions, software questions and testing issues or product complaints. Process microbial samples in the laboratory utilizing various technology platforms. Perform LAL testing as needed.

ESSENTIAL DUTIES AND RESPONSIBILITIES
• Communicate with customers providing support for testing questions and resolution of issues for the Celsis and LAL product lines.
• Perform Celsis testing as needed for investigation or special studies as assigned.
• Utilizes Salesforce application for customer communication.
• Answers incoming phone calls and live chats.
• Assist with product returns and Complaints for the applicable product lines. Document product complaints as required by the SOP. Perform investigational testing for complaints.
• Assist with training to global technical staff, distributors, and customers regarding technical support issues.
• Perform laboratory activities necessary to isolate, grow and maintain cultures of bacteria.
• Perform LAL testing as needed for contract testing or special studies as assigned.
• Receipt of customer samples following applicable procedures. Contacts customer for discrepancies.
• May occasionally travel to customer site for troubleshooting assistance.
• Responsible for proficiency in all SOPs in areas of responsibility.
• Responsible for documentation as required by company policy, cGMP and FDA.
• Perform all other related duties as assigned.

Job Qualifications

• Education: Bachelor’s Degree (B.A. /B.S.) in Microbiology biology or a related discipline.
• Experience: 3+ years of customer interfacing, documentation practices.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experiencelisted above.
• Certification/Licensure: None
• Other:
•Computer literacy with Windows Office Suite programs including data entry.
• Attention to detail in all aspects of work is essential.
• Excellent interpersonal skills.
• Strong written and oral communication skills.
• Pipetting and use of basic lab equipment, microbial testing experience, making dilutions.
• Math literacy

The pay range for this position is $57,500-75,800. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Manager - Field Customer Support, Nexus (Charleston, SC, US, 29407)

Job Summary

Manage activities of a team of US Nexus Field Service Technicians to provide customers (internal and external) technical service in repair, trouble shoot and training for Endosafe Brand products. Coordinate efforts with Field Service Manager(s) as well as individual contributors to meet customer expectations and company needs. Manage the development and training of team members for existing as well as new product offerings. Provide insight on customer expectations to the appropriate department management groups.

ESSENTIAL DUTIES AND RESPONSIBILITIES: The following statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified.

• Manage team to meet customer needs (internal and external)
• Oversight of teams and on-going development to ensure growth and retention
• Identify development opportunities for team and help implement and complete career growth as you and team members agree on
• Manage customer-facing technical repair and maintenance services for endotoxin and microbial detection laboratory instruments on site at customer locations.
• Provide technical assistance and problem resolution for instrumentation to team members as well as customers via telephone, email, or on-site communication to team or customers.
• Manage all required field service activities and documentation as assigned based on specific product, customer and/or standard operating procedural requirements.
• Collaborate with leadership in identifying and developing service contract sales opportunities through up-selling; promoting the customers’ conversion from billable to contract coverage.
• Assisting field sales personnel in product demonstrations, customer training, and product validations.
• Responsible for team member training to complete all service and compliance documentation as required by company policy, cGMP and FDA.
• Responsible for resolving client testing laboratory instrument service issues.
• Oversee and maintain training documentation and global harmonization of these procedures where possible.
• Monitoring and evaluating Instrument Service department meeting customer expectation and internal metrics.
• Work with sales management to evaluate and, where applicable, improve service offerings.
• Monitor service software to ensure metrics are being met. Evaluate and improve metrics and KPIs as necessary.
• Provide feedback and collaborate with service software vendor for improvements to product and/or workflow.
• Work with internal and external teams to introduce and implement technology solutions for improving service and processes.
• Forecast service workload, carve territories and add headcount based on current and future service offerings.
• Triage urgent customer issues and provide necessary support for team to resolve issue as quickly as possible.
• Monitor team expenses.
• Perform all other related duties as assigned.

Job Qualifications

The following are the minimum qualifications related to the Field Service Supervisor:

• Education: Bachelor's degree (B.A./B.Sc.) or equivalent in Engineering or Life Sciences; Microbiology, Biology or Chemistry
• Experience: 5+ years of related experience (technical, laboratory or research); or
Equivalent combination of education and experience.

The pay for this position is $110K - $130K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

For more information, please visit www.criver.com.

Technicien de Laboratoire en Immunologie - H/F - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le site Charles River d’Evreux est un site unique de 2 hectares, situé aux portes de la Normandie. Il offre un environnement scientifique innovant, dynamique et convivial où près de 500 personnes travaillent chaque jour dans l'objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Le département Biomarkers recrute un Technicien en Immunologie pour intégrer son équipe composée de 15 techniciens.

Les missions

Au sein du Département Biomarkers, vous aurez pour principales missions sous la responsabilité du responsable du service :
•   Réaliser progressivement certaines techniques de laboratoire comme des dosages ELISA, des développements de méthode mais aussi des études de cultures cellulaires comme Elispot dans le cadre d’études dites de Cells based assays,
•   Assurer la saisie informatique des résultats et leurs conformités,
•   Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,
•   Lire les protocoles, avenants et notices en anglais.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique et possédez au minimum 3 ans d’expérience sur un poste similaire.
Connaissances en culture cellulaire (Elispot).
Vous maitrisez l’anglais et possédez une aisance relationnelle et un sens du contact et du service.
Vous êtes organisé(e), vous appréciez de travailler en équipe.
Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.

Les modalités

•   Convention collective de l’industrie pharmaceutique, groupe : 3
•   Contrat : CDI Non-cadre (accord de modulation 35h)
•   Salaire : A compter de 24 500 € bruts / an sur 13 mois
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Primes de transport, d’intéressement/participation, accord d’ancienneté
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Avec plus de 20 000 collaborateurs sur 90 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com

Associate Director Biomanufacturing (Memphis, TN, US, 38118)

Job Summary

Reporting to the Site Director, the Associate Director, Biomanufacturing Operations is responsible for managing a cross functional work cell team that provides for the manufacture of drug substance and drug product. The Associate Director is responsible for ensuring that all staff is appropriately trained and follows the appropriate SOPs. This role will work closely with the Site Director and Manufacturing Leadership Team to ensure manufacturing activities are fully supported. This role will also work closely with Tech Transfer and Manufacturing Leadership to assess incoming processes and advise site leadership and business development on compatibility of incoming technologies and manufacturing facility.

Participate in overall account governance, facilitate leadership review as required.
Provide strategic context for objectives and decisions to team, senior leadership, and the broader organization as appropriate
Drive collaboration with internal cross-functional teams necessary for delivery on the project including Process Sciences, Manufacturing Sciences & Technologies, Quality Control, Quality Assurance, Supply Chain to ensuring alignment on project objectives and priorities.
Facilitate internal project team meetings and external client meetings including delivery and management of a project objectives, meeting agendas, integrated project schedules, key performance measures, risk registrar, timely meeting minutes & action items.
Assist in development of budget and budget planning, forecasting, etc
Assist in strategic planning and development of projections for business needs required to meet production goals
Advise and inform leadership of any potential impacts to production, production timelines, or CQA
Build, train, and develops highly skilled teams by identifying opportunities for improvement, coaching/mentoring reports towards growth, and provided goals and challenges to stretch capabilities
Oversees and approves nonconformance investigations, including root cause analysis, and CAPA development

Job Qualifications

A minimum of a BS in science or engineering or advanced degree (MS preferred), with at least 7 years of biologics manufacturing experience or equivalent cGMP experience is required
A minimum of 5 years cGMP manufacturing leadership experience required
Exhibits exceptional leadership skills and deep knowledge of GMP
Possess effective written and oral communication skills
Demonstrates initiative to remain apprise of relevant industry and regulatory trends

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

For more information, please visit www.criver.com.

Production Technician (m/f/d) 1 (Kaarst, DE, 41564)

Wir suchen eine Person in Vollzeit, die Teil unseres Produktionsteams für Reagenzien werden möchte.

Ihre Tätigkeit:

• Sie arbeiten direkt an den Produktionsmaschinen zur Abfüllung und Etikettierung von Reagenzien und dokumentieren die Tätigkeiten nach Vorgabe.

• Sie unterstützen beim Reinigen und Einrichten der Maschinen nach externen (GMP, ISO 9001) und internen Standards

• Sie helfen beim Reinigen von Hilfsmitteln und Vorbereiten von Rohmaterialen für die Produktion

• Sie stellen die Ausführung der übertragenen Aufgaben und Aufträge gemäß den vorliegenden Arbeitsstandards sicher.

Gerne mit einer abgeschlossenen Berufsausbildung, gleich welcher Branche, gerne Quereinsteiger (m/w/d) mit oder ohne produktionstechnische Kenntnisse.

Sie verfügen über:

• Interesse und Verständnis für technische Zusammenhänge und unsere hohen Hygieneanforderungen.

• Sichereren Umgang mit automatisierten Maschinen, handwerkliches Geschick.

• Hohes Sicherheitsempfinden und Verantwortungsbewusstsein

• Strukturiertes, zielorientiertes Arbeiten, hohe Verlässlichkeit und Flexibilität,

• Team- und Kommunikationsfähigkeit, Serviceorientierung

• Gute Deutschkenntnisse sind unerlässlich. Englischkenntnisse sind wünschenswert.

Wir bieten:

• Eine befristete Vollzeitstelle mit abwechslungsreichen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen

• Aktive Mitgestaltung Ihres Aufgabengebietes in einem hoch motivierten Team mit flachen Hierarchien

• Weiterentwicklung und die Möglichkeit, mehr Verantwortung zu übernehmen und innerhalb des Unternehmens zu wachsen

• Eine intensive Einarbeitung

• Flexible Arbeitszeiten

• Wettbewerbsfähige Vergütung

We are looking for a full-time person to become part of our reagent production team.

Your Tasks:

• You work directly on the production machines for filling and labelling reagents and document the activities according to specifications.

• You assist in cleaning and setting up the machines according to external (GMP, ISO 9001) and internal standards.

• You assist in cleaning auxiliary materials and preparing raw materials and for production.

• You ensure the execution of the assigned tasks and orders in accordance with the present work standards.

A completed vocational training is desirable, regardless of the industry, we welcome career changers (m/f/d) with or without technical production knowledge.

You have:

• Interest in and understanding of technical interrelationships and our high hygiene requirements.

• Confident handling of automated machines, manual dexterity.

• High sense of safety and responsibility

• Structured, goal-oriented work, high reliability and flexibility,

• Team and communication skills, service orientation

• Good German language skills are essential. Knowledge of English is desirable.

We offer:

• A full-time position (2 year fixed term contract) with varied, challenging activities in a future-oriented company

• Active participation in shaping your area of responsibility in a highly motivated team with flat hierarchies.

• Further development and the opportunity to take on more responsibility and grow within the company.

• An intensive induction

• Flexible working hours

• Competitive remuneration

For more information, please visit www.criver.com.

Production Technician (m/w/d) 1 1 1 1 1 1 (Kaarst, DE, 41564)

Wir suchen eine Person in Vollzeit mit chemisch/biologischem Hintergrund (BTA,CTA,PTA, auch B.Sc. oder M.Sc.) die Teil unseres Produktions-Teams unserer Reagenzien werden möchte.

Unterstützen Sie uns bei:
•   der Bulk-Herstellung der Reagenzien (im 1-200 L Maßstab),
•   In-Prozess-Kontrollen und Freigabe-Prüfungen
•   der Aufreinigung einiger unserer Rohstoffe mittels HPLC
•   weiteren Prozessschritten (Abfüllung, Gefriertrocknung, Autoklavieren etc.)
•   der Aufrechterhaltung unseres ISO Systems und der Einhaltung der Vorgaben der Guten Herstellungspraxis (GMP)

Überzeugen Sie uns durch:
•   gute Team- und Kommunikationsfähigkeit
•   strukturiertes und auf das Ziel fokussiertes Arbeiten, Verantwortungsbewusstsein, Organisationsfähigkeit, hohe Verlässlichkeit und Flexibilität
•   Gute Deutsch- und Englisch Sprachkenntnisse

Wir bieten:
•   eine unbefristete Vollzeitstelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen
•   eine aktive Mitgestaltung Ihres Tätigkeitsfeldes in einem sehr motivierten Team mit flachen Hierarchien
•   Weiterentwicklung uns Spezialisierung
•   eine intensive Einarbeitung
•   flexible Arbeitszeiten
•   eine angemessene Vergütung

Haben wir Ihr Interesse geweckt?
Wenn ja, bewerben Sie sich bitte unter Angabe der Referenz „Production Technician“ mit Ihren aussagekräftigen Bewerbungsunterlagen, Ihrem frühestmöglichen Eintrittstermin sowie Ihren Gehaltsvorstellungen. Wir freuen uns auf Ihre Bewerbung.

Über Microbial Solutions

Unsere Gruppe „Microbial Solutions“ verfügt über ein umfassendes Portfolio für Endotoxin-Tests, mikrobielle Detektion sowie mikrobielle Identifikationsprodukte und -dienstleistungen, das seinesgleichen sucht und das gezielt entwickelt wurde, um die komplexen und sich ständig ändernden Anforderungen der Branche zu erfüllen. Wir helfen unseren Kunden, die Produktsicherheit und -qualität durch einfach zu verwendende und robuste Testlösungen sicherzustellen, die behördliche Anforderungen erfüllen, kritische Entscheidungsfindung ermöglichen und die operative Effizienz verbessern.

Über Charles River

Mit über 20.000 Mitarbeitern in 90 Standorten in 20 Ländern rund um den Globus sind wir strategisch positioniert, weltweite Ressourcen zu koordinieren und multidisziplinäre Projekte für die Entwicklung und Herausforderungen unserer Kunden zu entwickeln. Unsere Kundenbasis umfasst globale Pharmaunternehmen, Biotechnologieunternehmen, Behörden und Krankenhäuser sowie akademische Institutionen in der ganzen Welt.

Charles River setzt sich leidenschaftlich für die Verbesserung der Lebensqualität ein. Unsere Mission, unsere exzellente Wissenschaft und unser Engagement für einen sinnvollen Einsatz unserer Kapazitäten leiten uns in allem, was wir tun. Wir beginnen jeden Tag in dem Wissen, dass unsere Arbeit die Gesundheit und das Wohlergehen von vielen Menschen weltweit nutzt. Wir sind stolz darauf, dass wir die Entwicklung von etwa 85% der von der FDA in 2021 zugelassenen Medikamente unterstützt haben.

Weitere Information en finden Sie unter www.criver.com.

Animal Care Technician I (Cambridge, MA, US, 02139)

Job Summary

We are looking for an Animal Care Technician I to join our Insourcing Solutions team, located in Cambridge, MA.

In the Animal Care Technician 1 role, you will use existing SOPs and quality assurance standards to monitor, observe, and record animal health and welfare daily, as well as complete various standard animal husbandry duties.

Maintain accurate records of animal breeding, health, and housing.
Follow all procedures to maintain housing areas, including room or facility personnel entry; personnel protective equipment use, spraying in all equipment and materials into controlled areas.
Receive, inspect, and put away incoming animals; and operating equipment following all safety guidelines. 
 You may also be involved in the breeding and weaning program, performing various duties from weaning and sexing, to ensuring appropriate production levels are met.
Work cooperatively with the on-site supervisor and/or facility veterinarian to assist with restraint, handling and manipulation of various animal species to include mice, rats and other rodents and possibly rabbits.

Job Qualifications

High school diploma, General Education Degree (G.E.D.) or equivalent required.
Six (6) to twelve (12) months related experience in animal husbandry.
Interest in achieving ALAT certification upon eligibility

The pay range for this position is $23-25 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Vaccine Mandate

This position services client(s) that requires us to ensure our employees are fully vaccinated against COVID-19. We will require proof of vaccination from all employees servicing client(s) with COVID-19 Vaccination requirements.

About Insourcing Solutions
Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Central Services Technician I (Cambridge, MA, US, 02139)

Job Summary

We are seeking an experienced Central Services Technician I to join our Insourcing Solutions team located in Cambridge, MA.

As the Central Services Technician I, you will provide cleaning and maintenance of laboratory animal caging, equipment, and cage preparation areas, as well as cleaning of animal support areas.

Additional responsibilities include:

Transport caging and equipment between animal areas and cage washrooms.
Receive and store feed, bedding, and supplies.
Provide quality assurance to the cagewash area.
Ensure that all logbooks, checklists, and other records are completed in a timely fashion.
Conduct and collect various aseptic sampling for the monitoring of water quality, sanitized animal racks, and equipment.
Inspect enrichment devices, cages, and other items, and perform all other related duties as assigned.

Job Qualifications

The following are minimum requirements related to the Central Services Technician I position:

High school diploma, general education degree (G.E.D.) or equivalent
Minimum of six months experience working in a laboratory animal facility performing cage wash duties, or working with glassware cleaning or a commercial dishwashing operation.

The pay range for this position is $20.00-22.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Vaccine Mandate

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician II (Cambridge, MA, US, 02139)

Job Summary

We are seeking an experienced Animal Care Technician II to join our Insourcing Solutions team, located in Cambridge, MA.

As the Animal Care Technician II, Observe, monitor, and document the health and physical environment within the client’s animal facility. Perform animal care and husbandry.

Additional responsibilities include:
• Review, comprehend and comply with all SOPs and quality assurance standards pertaining to laboratory animals for research.
• Monitor daily animal health and welfare while performing daily animal health observations. Perform animal husbandry duties to maintain quality and health of research animals, to include: perform daily water bottle /automatic water line and cage checks; provide appropriate food and water; perform cage changing and/or cage cleaning as required; record animal health concerns per SOP and/or specified protocols.
• Perform daily cage wash duties and sanitation.
• Maintain accurate records of animal breeding, health, and housing/isolator or support areas as required by Institute and facility.
• Assist with restraint, handling and manipulation of various animal species as assigned by the on-site supervisor or facility veterinarian.
• Dispose of animal carcasses following established procedures.
• Receive, inspect and put away incoming animals; ensure and provide for sentinel animals in each rodent housing area.
• May be involved in strictly maintaining and following breeding and weaning procedures to ensure appropriate production levels.
• Operate equipment and use supplies according to safety guidelines; perform general housekeeping and adheres to safety procedures.
• Maintain required attendance level and adherence to work schedule in accordance with required staffing levels in order to ensure that assigned duties are completed.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician II position:

• High school diploma or GED and 2 years related research husbandry experience, or Associates degree in Life Sciences or related field and 1.5 years related research husbandry experience, or Bachelor's degree in Life Sciences or related field and 1 year related research husbandry experience.
• AALAS certified as ALAT within 18 months of hire

The pay range for this position is $22-24 USD an hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technical Service Research Supervisor (Cambridge, MA, US, 02142)

Job Summary

We are seeking an experienced Technical Services & Research Supervisor to join our Insourcing Solutions team, located in Cambridge, MA.

As the Technical Services & Research Supervisor, you will provide direct supervision of Charles River Accelerator & Development Labs (CRADL) in vivo technical service and research group. Provides supervision and training for employees. Maintains performance and service levels consistent with and according to company standards, the CRADL organization and client contractual requirements. Recommend new or innovative techniques to improve productivity, increase efficiencies, and maintain quality standards Prioritizes and completes on-going tasks independently following established policies and guidelines. Liaises with clients to ensure satisfaction with technical staff’s performance.   

Additional responsibilities include:

Supervises the daily activities of technical services and study team comprising of research associate/study technicians and study coordinators, ensuring all services meets organizational standards & client expectations.
Schedules, assign and balance workload among the technical staff for research and tech services.
Interacts with clients as required to address client inquiries and complaints.
Maintain an awareness of the financial status and impacts of ongoing studies.
Proactive resolution of operational and quality issues; continuously guiding and training staff to improve processes, and operational efficiencies. 
Ensure in vivo study applications are performed in accordance with currently defined protocols and in a manner consistent with the Guide for the Care and Use of Laboratory Animals and all local, state, and federal requirements. 
Ensure creation and maintenance of accurate study records, and delivery of study data to clients.
Partner with the veterinarians, veterinary technicians, trainers, and the IACUC office to ensure compliance with biosecurity policies and procedures, IACUC required training, IACUC non-compliance and/or animal welfare concerns.
Responsible for personnel management activities such as: mentorship, hiring, promotions, training & development.

Job Qualifications

The following are minimum requirements related to the Technical Services & Research Supervisor position.

Bachelor's degree (B.A./B.S.) or equivalent in animal or laboratory science, business, or related discipline.
Minimum 4 years in the laboratory animal industry of which 2 years is supervisory or lead technician experience.
AALAS certification at the Laboratory Animal Technologist level (LATG) preferred.

The pay range for this position is $100-103k USD annually Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

Vaccine Mandate

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technicien maintenance 3*8 - F/H -CDI 1 (Saint Germain Nuelles, FR)

Le poste

Vous aimez travailler en autonomie dans un contexte exigeant et avec des défis techniques ambitieux ?

Nous recherchons un Technicien 3×8 – F/H en CDI pour rejoindre notre service maintenance, au sein d’une équipe dynamique de 14 personnes sur notre site basé à l’Arbresle (69) dans le nord-ouest lyonnais. Directement rattaché au Responsable maintenance, vous devez répondre à 4 principales missions :

Assurer la maintenance de 1er niveau.
Assurer la surveillance des paramètres environnementaux des bâtiments de production
Garantir la bonne distribution des énergies sur l’ensemble du site
Contribuer à la surveillance du site face à différents risques (intrusion, incendie, sécurité des biens et des personnes) essentiellement en dehors des horaires de journée

Missions principales

GTC

Prise en compte des alarmes GTC et interventions techniques si nécessaire, avec les moyens mis à sa disposition en fonction des difficultés à apprécier
Prise en compte et transmission des informations et consignes
Mise à jour des relevés sur documents d’enregistrement
Appel de l’astreinte en cas de panne

CHAUFFERIES

Maintenance curative et préventive sur les chaudières vapeur et matériels annexes
Essais journaliers des sécurités chaudières et des matériels annexes
Analyse des eaux et relevé des consommations
Mise à jour des différents relevés sur cahier de chaufferie

MAINTENANCE

Prise en charge du préventif hebdomadaire effectué sur l’ensemble des Centrales de Traitement d’Air
Réalise les interventions de maintenance curatives ( 1er niveau ) sur l’ensemble des installations techniques du site

G.M.A.O

Prise en charge des appels 24h/24 du numéro d’urgence
Rédaction des Demandes de Service sur le logiciel GMAO pour intervention de l’équipe de maintenance en journée

SECURITE du site et des personnes

Prise en compte des alarmes intrusion
Assurer la première intervention en cas d’accident en dehors des heures ouvrées
Premier intervenant dans le cadre du déclenchement du Plan d’Opérations Interne de l’entreprise

Profil recherché

Issu d’une formation Maintenance ou d'une formation type CAP, vous avez une première expérience similaire.
Vous disposez idéalement des habilitations suivantes : Conducteur de chaudière (niveau 2) et électrique avec le niveau BE Manoeuvre-BS-HOV.
Vous disposez du permis B
Vous êtes rigoureux, dynamique et vous avez le sens des responsabilités et savez être méthodique et faire preuve de sang-froid.
Vous êtes à l’aise avec l’utilisation des outils informatiques.
Esprit d’équipe nécessaire et flexibilité appréciée.

Modalités

Convention collective de l’industrie pharmaceutique : Groupe 3
Rémunération selon le profil à partir de 27 K€ sur 14 mois + prime forfaitaire 3x8 sur 12 mois + intéressement et participation
Prise en charge de la mutuelle à 60%, restaurant d’entreprise, indemnité de transport, accord d’ancienneté, CE

Site non accessible en transport en commun. Moyen de locomotion indispensable.

Pour plus d'information, consultez www.criver.com.

Soigneur animalier / Assistant vétérinaire - F/H - Missions temporaires (Paris, FR)

Pendant de 70 ans, les employés de Charles River ont travaillé ensemble pour aider à la découverte, au développement et à la fabrication sûre de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous aurez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences joueront un rôle important dans le travail que nous effectuons. En retour, nous vous aiderons à bâtir une carrière dont vous pouvez vous sentir passionné.

Notre société, de dimension internationale, partenaire de l’industrie pharmaceutique, est leader dans la vente de produits et services précliniques.

L'activité Insourcing désigne la prestation de gestion d'animalerie, dans laquelle le client confie à Charles River le soin de réaliser les prestations définies dans un contrat au sein de ses installations adaptées à l'hébergement des animaux de laboratoire.

Au sein de plusieurs animaleries de laboratoire, implantées dans plusieurs départements, principale à Paris et Marseille (75, 91, 92, 13, 34, 33), nous recherchons des Animaliers / ASV - F/H pour renforcer nos équipes dans le cadre de missions intérimaires de remplacement de courte durée.

Missions principales

Réception des animaux (rongeurs)

Vérification des animaux à l’arrivée
Installation des animaux dans les cages
Etiquetage des cages, suivi journalier des mouvements de cages et de leur nombre

Entretien et soins des animaux

Observation des animaux et vérification de l’état clinique, application du programme d’enrichissement
Distribution de l’aliment, vérification de l’abreuvement
Préparation des animaux et du matériel (cages, biberons, couvercles) pour les transferts
Opérations de change des litières et nettoyage des cages, distribution de l’alimentation et de la boisson

Entretien du matériel et des locaux

Désinfection du matériel et des produits
Nettoyage des locaux en respectant les règles de prophylaxie et de biosécurité

Votre profil

De formation ASV ou équivalent, vous possédez une expérience dans ce domaine ou dans une activité en lien avec les rongeurs.
Vous aimez les animaux, êtes rigoureux, autonome et assidu(e) et appréciez le travail en équipe.

Avec plus de 17 000 collaborateurs sur 90 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2019.

Pour plus d'information, consultez www.criver.com.

Scientific Research In Vitro - Associate (Szeged, HU)

A Charles River munkatársai 75 éve dolgoznak azon, hogy új gyógyszeres terápiák felfedezésében, fejlesztésében és biztonságos előállításában segédkezzenek. Ha csatlakozol ehhez a nagy családhoz, lehetőséged nyílik arra hogy jobbá tedd az emberek egészségét és jóllétét világszerte. Minannyiunk tudása és képessége fontos szerepet játszik a munkánkban függetlenül attól, hogy eddigi tapasztalataidat élettudományi, pénzügyi, informatikai, értékesítési vagy más területen szerezted. Cserébe segítünk egy sikeres karrier felépítésében.

Job Summary

Főbb feladatok:

- Validálásokhoz, kutatásokhoz kapcsolódó in-vitro mérések elvégzése (elsődleges feladat)
- Emlős sejtek fenntartása és kezelése, steril munkavégzés
- Laboratóriumi munka technikai előkészítése
- Oldatok, pufferek, törzsoldatok készítése
- Laboreszközök, műszerek használata, karbantartása
- Adminisztratív jellegű laboratóriumi feladatok ellátása

Job Qualifications

Az álláshoz tartozó elvárások:

- Legalább középfokú szakirányú végzettség
- Hasonló területen szerzett laboratóriumi tapasztalat - min. 2 év
- Jártasság általános laboreszközök használatában
- Önálló, precíz, felelősségteljes munkavégzés
- Dinamikus, nyitott, rugalmas, csapatjátékos személyiség
- Angol nyelvismeret
- Felhasználói szintű MS Office alkalmazások ismerete (Word, Excel)
- ISO 9001 minőségbiztosítási rendszerben való jártasság előny

A Discovery részlegről

A Charles River Discovery részlege az ipar által is bizonyítottan sikeres új terápiák fejlesztése terén. Az elmúlt 17 évben 320 új szabadalmat és 74 preklinikai gyógyszerkészítményt állítottunk elő megbízóink részére. Több mint 650 tudós által kidolgozott átfogó, integrált portfóliónk a legújabb technológiákat és platformokat alkalmazza, hogy kémiai, biológiai és farmakológiai szolgáltatásokat nyújtson, ezzel támogatva ügyfeleinket a preklinikai gyóyszerfejlesztési folyamaton át. Ügyfélközpontúak vagyunk, és együttműködéssel érjük el a valódi partnerkapcsolatok kialakulását, melyek során felmérjük az esetleges kihívásokat, legyőzzük az akadályokat és együtt haladunk azon az úton mely során új gyógyszereket juttatunk a piacra.

A Charles Riverről

A Charles River egy szolgáltató cég, mely a gyógyszerfejlesztés korai fázisára nyújt megoldásokat. Építkezve a laboratóriumi állatgyógyászati és tudományos alapjainkra egy széleskörű portfóliót hoztunk létre a gyógyszerfejlesztés preklinikai fázisaira koncentrálva (discovery és safety). Mind GLP és non-GLP rendszerben kínálunk vizsgálatokat a kezdeti lépésektől (target identification) a preklinikai fejlesztésekig. A Charles Rivernél termék- és szolgáltatáscsomagot is kínálunk, hogy segítsük ügyfeleink klinikai vizsgálatait és gyártási tevékenységüket. Ennek a széles termék- és szolgáltatás portfóliónak köszönhetően ügyfeleink egy rugalmasabb gyógyszerfejlesztési modellt hozhatnak létre, mely csökkenti a költségeiket, növeli a termelékenységüket és hatékonyságukat, hogy ezáltal gyorsabban léphessenek piacra.

A világ 20 országában, 110 telephelyen több, mint 20.000 munkavállalónkkal stratégiai helyzetben vagyunk, hogy összehangoljuk az erőforrásainkat és multidiszciplináris szempontokat alkalmazzunk ügyfeleink egyedi kihívásainak megoldásában. Ügyfélkörünk globális gyógyszergyárakból, biotechnológiai cégekből, kormányszervekből, klinikákból és akadémiai intézményekből áll szerte a világon.

A Charles Rivernél elkötelezettek vagyunk hogy javítsuk az emberek életminőségét. Küldetésünk, kitűnő tudományos hátterünk és erős céltudatosságunk vezérel minket mindenben amit teszünk, és minden napot azzal a nézettel közelítünk meg, hogy a munkánk segít az emberek egészségén és jóllétének javításán világszerte. Büszkék vagyunk arra, hogy az elmúlt öt évben az FDA által jóváhagyott gyógyszerek mintegy 80%-át mi fejlesztettük ki.

További információért látogass el a honlapra www.criver.com

Cagewash Technician (Baltimore, MD, US, 21224)

Job Summary

We are seeking a Cagewash Technician for our Insourcing Solutions site located in Baltimore, MD.

As the Cagewash Technician, you will Provide cleaning and maintenance of laboratory animal caging, equipment and cage preparation areas as well as cleaning of animal support areas under minimal supervision. Provide quality assurance to the cagewash area.

Additional responsibilities include:

Dumps and scrapes soiled bedding from caging and prepares caging for cagewash under minimal supervision.
Sanitizes caging and related equipment using cage washers, pressure washer or hand washing as required.
Properly disposes of soiled bedding and waste in specified receptacles.
Cleans and sanitizes cage preparation and storage areas.
Monitors and records results of cagewash water temperature and cleaning results using provided supplies such as temperature dots/strips, cultures.
Ensures that all logbooks, checklists and other records are completed in a timely fashion.

Job Qualifications

The following are minimum requirements related to the Cagewash Technician position.

Experience and/or training working with animal husbandry preferred
High school diploma/GED preferred

The pay for this position is $18.47 per hour.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Caretaker (Baltimore, MD, US, 21224)

Job Summary

We are seeking an Animal Caretaker to join our Insourcing Solutions team located in Baltimore, MD

As the Animal Caretaker, you will provide basic husbandry to rodents and lagomorphs, monitor environmental parameters for abnormalities and provide customer assistance to the investigative staff.

Additional responsibilities include:

- Perform daily animal husbandry duties to maintain quality and health of research animals, including: perform daily water bottle /automatic water line and cage checks; provide appropriate food and water; perform cage changing and/or cage cleaning.

- Monitor environmental parameters and maintain written records

- Assist with restraint and handling of various animal species.

- Receive, inspect, and put away incoming animals; as well as provide for sentinel animals in each rodent housing area.

- Operate equipment and perform general housekeeping.

Job Qualifications

The following are minimum requirements related to the Animal Caretaker position:

- AALAS certification at the ALAT level within one year of eligibility

- 1 year of related experience in animal care

- 3 months working with lab animal species (rodents), preferred

- High school diploma/ GED preferred

The pay for this position is $18.47 USD per hour.

For more information, please visit www.criver.com.

Cagewash Technician (Poolesville, MD, US, 20837)

Job Summary

We are seeking a Cagewash Technician for our Insourcing Solutions site located in Poolesville, MD.

Why work at Charles River?

We offer an excellent onboarding program for our new employees, internal career development, and competitive benefits.

What you will do!

In this role, you will provide cleaning and maintenance of laboratory animal caging, equipment and cage preparation areas as well as cleaning of animal support areas.

Additional responsibilities include:

Operates equipment and uses supplies according to safety guidelines; performs general housekeeping and adheres to safety procedures.
Sanitizes, maintains, and repairs caging materials as needed. Maintains cagewash and animal holding facilities in a clean and organized manner, in adherence with all SOP and facility requirements.
Disposes of waste materials in a safe and thorough manner as required.
Maintains facility equipment and performs routine preventative maintenance on cagewash and autoclaves, including routine inspection of cleaning filters and roto-arms.
Assists with the receipt, stocking and maintenance of supply inventories.
Assist with animal care activities to include, but not limited to; animal health observations, cage cleaning, water/feed checks, providing water/feed/enrichment.
Prepares and submits required written records, charts, logs and inventories.
Actively interacts with customers as required to resolve customer requests, inquiries, and complaints and to provide technical assistance.
Maintains consistent practice of general company and safety policies and procedures and MSDS guidelines, including those related to biohazards and radioactive substances. Performs all duties in compliance with local, state, and federal regulations.

Job Qualifications

The following are minimum qualifications related to the Cagewash Technician position:

Education: High school diploma or general education degree (GED) preferred.
Experience: Experience and/or training working with mechanical equipment preferred.
Certification/Licensure: none required.

The pay rate for this position is $20 USD per hour. If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us and BE THE DIFFERENCE!

With over 14,000 employees within 80 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2018, revenue increased by 22% to $2.27 billion from $1.86 billion in 2017.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

Technical Trainer I (Poolesville, MD, US, 20837)

Job Summary

We are seeking an experienced Technical Trainer I to join our Insourcing Solutions team, located in Poolesville, Maryland.

As the Technical Trainer I, you will develop, deliver, document, and report technical skills training programs involving both small and large laboratory animal species in accordance with client’s facility SOPs, Charles River policy and applicable Federal regulations.

Additional responsibilities include:

Direct, schedule, perform and document all relevant Task-specific technical, husbandry and administrative training for all contract positions in coordination with management and supervisors.
Perform continuing education and training to maintain and enhance employee skills and capabilities, including SOP or ASP revisions, animal welfare topics, operations and maintenance, and technical advancements.
Conduct AALAS certification training, monthly health & safety training; conduct and/or coordinate ASP-directed training.
Select or develop teaching aids such as training handbooks, demonstration models, multimedia visual aids, computer tutorials, and reference works.
Conduct training sessions covering specified areas such as on-the-job training, refresher training, in laboratory animal techniques.
Test trainees to measure progress and to evaluate effectiveness of technical training.
Provide didactic and hands-on technical training on SOPs Monitor technical methods used by employees and make on the spot corrections.
Perform quality assurance responsibilities for the contract site, including:
- Inspecting procedures, reports, facilities, equipment and data for on-going administrative, husbandry and technical-related functions relevant to contract performance and research mission support for adherence to CDC protocols and SOPs.
- Scheduling and conducting phase inspections and personnel performance audits to determine compliance with internal SOPs and study protocols.
Actively interact with customers as required to solve customer requests, inquiries, and complaints and to provide technical assistance.
Occasionally provide technical support, animal husbandry, and assist with research procedures as necessary to respond to surge in work load or personnel shortages.

Job Qualifications

The following are minimum requirements related to the Technical Trainer I position.

Associate degree or bachelor’s degree in animal science, veterinary technology or equivalent college level program required.
Minimum of three (3) years related animal care and handling experience required. One (1) year technical experience performing the duties and responsibilities detailed above preferred. Previous training and successful "hands -on" performance of animal care technical procedures required. Related technical experience includes, but not limited to:
- Rodents: Handling and restraint, identification methods, sexing, tissue collection (blood, tails, various organs), administration of medications and treatment.
- Non-human Primates: Utilization of squeeze cages, transferring, TB tests, blood collection, basic injections / administration of medications, treatments and anesthesia, identification (tattoo) proper use of bite/scratch kits.
- Farm Species: Handling and restrain, identification methods, blood collection, basic injections/administration of medications and treatment.
- General techniques: Surgical pack preparation, proper scrub-in technique, proper physical/physiological observation, gas and/or autoclave sterilization (use of machines and rationale for use of each type), drug dosage calculation, pre-surgical animal prep, gestation periods of various species, proper use of anesthesia machine (portable & fixed), anesthesia monitoring, safe handling and restraint techniques, proper use of PPE, euthanasia, blood collection and injection techniques - all species, all sites.
AALAS certification at the Laboratory Animal Technologist (LATG) level preferred.

The pay range for this position is $35-38 USD per hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Manufacturing Specialist (Rockville, MD, US, 20850)

Job Summary

The Manufacturing Specialist is a key technical contributor responsible for process optimizations, manufacturing troubleshooting, continuous improvement initiatives to ensure Manufacturing consistently produces quality product. This role sits at the intersection of operational excellence, quality, training & development, and MSAT supporting efficient, compliant, and ever improving operations.

The ideal candidate will have a strong understanding of cGMP compliance, quality event investigation, lean production methodologies, and process technology to drive reliability in operations.

Key Responsibilities and Duties:

Process Improvement & Optimization

Identify and implement continuous improvement projects using Lean methodologies to improve and stabilize yield, efficiency, and process success.
Partner with MS&T and Process Development to monitor process performance to identify data-driven solutions and enhancements.
Support technology transfer, process scale-up, and process validation to ensure smooth transitions into manufacturing.
Partner with MS&T and Engineering to optimize equipment utilization, automation strategies, and data analytics for real time adjustments and support.

Compliance & Manufacturing Support

Conduct timely batch record reviews and deviation investigations, ensuring long term resolution of documentation/instructional issues.
Lead root cause analysis and corrective/preventive action (CAPA) for process deviations, non-conformances, and quality issues.
Work close with Quality and Manufacturing teams to ensure documentation supports data integrity & good documentation practices (GDP) incompliance with FDA, EMA, guidelines.

Training and Documentation Management

Develop and maintain SOPs, training materials, and documentation systems for manufacturing compliance and process improvements.
Partner with MS&T and Training to conduct training programs for manufacturing staff to ensure adherence to cGMP, process guidelines, and quality requirements.
Work cross-functionally to ensure employees remain qualified and up to date on process and compliance expectations.

Job Qualifications

Bachelor’s degree in relevant Science or Engineering discipline preferred.
Minimum 3 years working within industry. Strong technical writing capabilities a plus.
Experience within cell/gene therapies, biologics, and/or cGMP regulated environment preferred
Knowledge of process improvement and lean methodologies preferred.
Ability to interpret and present complex scientific data in a clear and concise manner.
Proficient in Microsoft office suite and document management systems.
Strong organizational and project management skills.

Compensation Data

The pay range for this position is $68,712 - $87,200 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

QC Associate I - Environmental Monitoring - Shift is 1pm - 9:30pm (Rockville, MD, US, 20850)

Job Summary

At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate).

Key Responsibilities and Duties:

Performs viable and non-viable environmental monitoring in a static and dynamic environment.
Perform water quality analysis testing such as TOC and conductivity testing
Demonstrate excellent aseptic technique and clean room gowning practices required for working in Grade C, B and A spaces
Perform bioburden testing per current cGMP guidelines to facilitate in process product development and raw material release
Perform growth promotion, microbial identification, pure colony streak plate isolation, biological indicator testing in a controlled BSL2 environment.
Complete relevant data entry requirements in accordance with current data integrity expectations and the ALCOA principals
Assist in laboratory investigations, environmental monitoring excursions and deviations.
Participate and facilitate on-going lab excellence initiatives as directed by the Senior QC Analyst or area management.
Work may be required outside of normal business hours
Additional duties as needed

Job Qualifications

B.S in Biology or related field
1-2 years working in a GMP facility is preferred, although not required.
Able to lift up to 40 pounds
Able to work in a clean room suite while wearing appropriate gowning and PPE
Excellent verbal and written communication skills
Ability to work independently or within a team setting
Team-player
Good organizational skills
General computer skills including Microsoft Office software
General lab skills or science background desired

Compensation Data

The pay range for this position is $24.00 - $26.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Biomanufacturing Associate I - Upstream (Rockville, MD, US, 20850)

Job Summary

The Biomanufacturing Associate I will play an integral role within CRL’s gene therapy manufacturing function by understanding and applying biological, bioprocess, manufacturing, and mechanical principles, processes, procedures, inputs, and outputs, for designated production processes and handovers, within a cGMP and GLP environment. This will ensure the timely production and release of quality products, based on client specifications.

This role will perform a range of routine and semi-routine tasks, some of which are moderately difficult, requiring judgment in resolving issues or making recommendations, with guidance as needed, in order to proficiently execute manufacturing protocols in a regulated environment.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Under guidance, apply and adhere to SOPs, cGMP, GLP, Quality, and basic Safety standards and requirements when completing tasks.
Basic Upstream Activities (e.g., assist with solutions, media aliquot, and buffer preparation and autoclave materials for cell culture, staging of raw materials, seed train, bioreactor set up, fermentation monitoring and/or harvest).
Follow verbal and written instructions (e.g., SOPs), when performing planned manufacturing activities, in alignment with the batch record, and under guidance.
With guidance, use basic quality documents and apply Good Documentation Practices.
Ensure data integrity by accurately documenting, reviewing, and correcting work prior to submission.
Identify, record, and report observed process variances and deviations in real time.
Apply and adhere to SOPs, safety guidelines, and manufacturing instructions when completing process tasks and when operating equipment. Prepare, clean, maintain, and operate equipment and tools.
Recognize common safety issues and report all injuries and safety incidents immediately.
Adhere to safe working practices and comply with site-based guidelines to avoid the consequences of error by applying:
Cleanroom and aseptic behaviors and procedures.
Proper Personal Protective Equipment (PPE) and gowning requirements.
Proper preparation, disinfection, sterilization, and sanitation methods and processes for equipment, etc.
The safe handling, transport, storage, and disposal of biological specimen, chemical, and hazardous materials.
Universal precautions with respect to OSHA guidelines.
Appropriate organization, sanitizing, and stocking of work area to avoid unsafe situations.
Perform other responsibilities as required.

Job Qualifications

Education: High School Diploma or equivalent with high grades in science courses, or an Associates or Bachelors degree in biology/life sciences, bioengineering, or related discipline.
Experience: 2 years of related experience with a High School Diploma. 1 year of related experience with an Associates degree. 0-1 year of related experience with a Bachelors degree.
Related experience may include prior experience in a technical role and/or within a cGMP and/or biotech manufacturing environment or other related industry, etc.
Other:
Able to work in accordance with the Charles River Values.
Able to be a team player, have a positive attitude, professional tone and demeanor, and work effectively in a collaborative environment.
Willing and able to continuously learn and improve.
Strong attention to detail and ability to recognize deviations from accepted practices.
Good documentation and GDP skills.
Must possess good analytical, critical thinking, and problem-solving skills.
Able to hold oneself accountable by following up and doing what they say they will do.
Able to complete work accurately and on time.
Good listening, clear written, and verbal communication skills.
Working knowledge of computer software (MS Word, MS Excel, Teams, database systems, etc.).

Compensation Data

The pay range for this position is $25.00 - $27.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Quality Operations Supervisor (Rockville, MD, US, 20850)

Job Summary

This leadership role is responsible for a team of Quality Operations Specialists, which will require providing oversight of quality documentation and operations in adherence to cGMPs and SOP regulations. QOps Supervisors will represent Quality at cross-functional meetings, providing Quality input and decision making in Quality events and deviations. They will provide training to groups and departments when needed.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Assume supervisory responsibility for a team of Quality Operations (QOps) Specialists, including scheduling, work assignment, and productivity monitoring
• Coordinate review of manufacturing Batch Production Records (BPRs) and associated supporting documentation including logbooks, Quality Control (QC) testing reports, environmental monitoring reports, etc.
• Support Internal Management System by engagement in Work Center Team activities
• Serve as owner of assigned nonconformances, CAPA, change controls, or other quality system documents and collaborate to drive completion
• Create, review and approve documents in electronic document management systems
• Serve as QOps representative for client project teams as assigned by management
• Coordinate performance of key QOps functions by team members, including line clearances, general manufacturing support, product shipment, raw material receipt and release, etc.
• Participate in departmental and cross-functional continuous improvement efforts
• Train and mentor assigned QOps Specialists and Leads
• Consistently set a high standard for quality of work
• Promote a safety mindset through daily actions and communication with team members
• Manage risk and escalate issues to QOps management in a timely manner
• Communicate professionally, effectively, and efficiently with all clients, internal and external
• Demonstrate flexibility when confronted with high stress/emergency situations, shifting
• Perform all other duties as necessary

Job Qualifications

• Bachelors degree in a life science or related field preferred
• Minimum of 5 year GMP related experience in biopharmaceutical/pharmaceutical or related industry or a combination of 5 years of education and related work experience required
• Demonstrated leadership capability
• Experience with GMP regulatory requirements
• Ability to multi-task effectively
• Excellent written and verbal communication skills
• Ability to prioritize daily activities in order to meet client needs on time of established time lines in a fast-paced environment
• Proficient in computer system use, including but not limited to Microsoft Office (Word, Excel, Power Point)

Compensation Data

The pay range for this position is $83,380 to $105,200. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

QA Specialist II - Shift is 12pm - 10:30pm, Sun - Wed (Rockville, MD, US, 20850)

Job Summary

The Quality Assurance Specialist II is responsible for supporting Quality Systems, including investigation/deviation management, CAPA tracking, Effectiveness Verification, change control, internal and external audits. This position will facilitate the compiling, trending (as required), and reporting key quality metrics for management, and other quality system functions, as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products.

Key Responsibilities and Duties:

•   Establishes and maintains Investigation, Deviation, CAPA, EV systems, and internal and external audit. This task includes collaborating with cross-functional departments to ensure timely implementation and closure of quality records
•   Provides guidance and advice on methods, procedures, standardization, and requirements associated with these systems.
•   Responsible for tracking and trending (as required) aspects of the Quality System and provide reports to management identifying risks and trends on a routine basis
•   Performs CAPA effectiveness evaluation based on quantitative and qualitative measurements
•   Administers the Change Control process for the site and conduct effectiveness verification for changes implemented.
•   Maintains tracking mechanisms to support various Quality Systems elements and ensures visibility throughout the organization
•   Continuously monitors and review systems and procedures for adherence to regulatory compliance, quality improvements, efficiency, and industry best practices. Provide compliance support and expertise for QA department
•   Compiles and reports site monthly corporate Quality metrics
•   Supports the Quarterly Management Review (QMR)
•   Supports audits (internal, external) to verify the regulatory requirements, internal and CRL procedures and quality requirements have been met. Prepares annual audit plan, conducts the audit per the schedule, writes the relevant audit reports and keeps CAPA monitored to ensure compliance with the applicable regulations
•   Supports Deviation system and ensure proper investigation and root cause analysis are performed
•   Supports CAPA/EV system to ensure proper corrective actions are implemented and effective
•   Supports Change Control system to ensure proper change and impact assessments are performed and tasks are implemented
•   Develops, implements, and delivers training content for Deviation, CAPA, EV and Change Control processes and procedures
•   Responsible for procedure reviews and facilitating procedure updates for the Deviation, CAPA, EV and Change Control systems
•   Assures that personnel are adequately trained in the principles, policies, and procedures of the Deviation, CAPA, EV and Change Control systems
•   Identifies and escalates compliance gaps across quality systems
•   Maintains customer complaint and suspect sample management system and ensure its implementation
•   Additional duties as assigned

Job Qualifications

•   BS required; MS preferred in scientific/technical discipline
•   5+ years of experience in a GMP environment
•   Strong knowledge of GMP, SOPs and quality system processes
•   Excellent organizational skills and ability to review and update processes or procedures
•   Proficient in MS Word, Excel, Power Point, Adobe Pro, and electronic quality management systems. Previous experience in TrackWise, Pilgrim is preferable
•   Certification from American Society for Quality on certified quality audit is a plus
•   Experience in pharmaceutical or bio-pharmaceutical field
•   Education or training in cell culture and gene therapy manufacturing environment is a plus
•   Proficient in drafting and completing technical documents and presentations
•   Expertise in document management processes
•   Works on multiple assignments in collaboration with various department system owners
•   Quality systems demonstrated knowledge in areas such as Deviation, CAP A, EV, and Change Control system management practices/strategies
•   Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211/600/820, ICH and EMA)
•   Demonstrates basic understanding of training, instructional design, communication and/or education
•   Demonstrates knowledge and understanding of pharmaceutical manufacturing and quality assurance, aseptic and packaging processes, and product transfer
•   Demonstrates presentation skills with the ability to conduct training sessions

Compensation Data

The pay range for this position is $87,733 - $116,978 annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Project Manager I (Cagewash Manager) (Bethesda, MD, US, 20892)

Job Summary

We are looking for a Cagewash Manager to join our Insourcing Solutions team, located in Bethesda, MD.

In the CWM role, you can do that by planning, organizing, and directing the activities of the cagewash program, which directly contributes to the integrity of the research.

Additional responsibilities include:

Use existing SOPs and quality assurance standards to provide daily direction and supervision to cagewash technicians to maintain facility operation, condition, security, and sanitation levels, as well as coordinate personnel scheduling.
Ensure staff operates and maintains equipment and supplies; develop projections for equipment, personnel
Conduct routine inspections to determine if standards are being met.
Evaluate and adjust the workflow to ensure efficiency and effectiveness of cagewash operations
Conduct/participate in training activities and ongoing learning, including improvement planning.
Develop and implement new or updated SOPs. Additional duties include coordinating and communicating special projects/procedures, supervising record maintenance, as well as generating/submitting reports to management on operations-related issues.
Coordinate preventative maintenance on all cagewash machinery, equipment, and materials; in addition to organization and up-keep of physical environments.
Troubleshooting equipment issues, performing minor repairs, and coordinating service visits would also be a responsibility of this position.
Identify, document, and/or report environmental or cagewash abnormalities.
Use of computer programs to maintain data and reporting is required; in addition to actively interacting with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Job Qualifications

The following are minimum requirements related to the Cagewash Manager position:

A.A. in Animal Science or a related field plus 4 years lab animal experience or
B.A./B.S. degree or higher in Animal Science or related field plus 3 years lab animal experience
Minimum of 1 year supervisory experience in a multi-labor category rodent facility
AALAS certification at the Laboratory Animal Technologist level (LATG) required.

Additional requirements

Customer service experience preferred
Cagewash equipment maintenance experience preferred

The pay range for this position is $38.00 - 42.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us and BE THE DIFFERENCE!

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Vaccine Mandate

For more information, please visit www.criver.com.

Animal Care Technician II (50) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Animal Care Technician II to join our Insourcing Solutions team located in Bethesda, MD.

As the Animal Care Technician II, you will maintain, monitor, and document the health, breeding colony production, technical support, and physical environment within the animal facility. Your role will be to maintain the quality and health of the research animals.

Additional duties:

-Perform Animal Health assessments and send notifications to clinical veterinarians and investigative lab staff
-Animal health observations across multiple species; perform basic animal husbandry
-Perform breeder set-ups, vaginal plug checks and weaning
-Perform blood collection via various routes for technical service requests
-Perform ear tag/ID placement; sample/tissue collection for genotyping and other technical service request and facility sentinel program
-Administer topical, injectable, and oral treatments
-Maintain and update all related records, logs, forms, cage cards
-Applying quality assurance/quality control standards to ensure Statement of Work expectations are fulfilled

Job Qualifications

The following are minimum requirements related to the Animal Care Technician II position:

High school diploma or GED required.

One or more years of related animal care and handling experience

ALAT certification, or become certified within one year of eligibility

Schedule: Monday through Friday 7AM-3:30PM. Must be available some weekends and holidays.

The hourly range for this position is $22.00- $24.00 USD per hour. Please note that salaries vary within the range based on factors including skills, certifications, and location. 

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (50) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team located in Bethesda, MD.

As the Animal Care Technician I, you will work with our research animals to ensure they are well cared for.

Additional responsibilities include:
•   Providing food & water.
•   Ensuring cages are clean.
•   Performing and recording daily animal health checks.
•   Handing & restraining animals for injections
•   Learning & applying quality assurance standards
•   Examining new animals that arrive at the site & helping them to settle in
•   Learn & become involved in breeding of multiple animal species.

Job Qualifications 
The following are minimum requirements related to the Animal Care Technician I position:
•   Six months of animal experience (e.g., dog walking, pet sitting, kennel attendant, vet assistant, farm hand, 4-H background, pet store worker)
•   Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1-2 years of eligibility

• High school diploma/GED preferred
 
The pay for this position is $20-22/hour USD per hour. Please note that salaries vary within the range based on factors including, but not limited to skills, certifications and locations. Schedule: Monday through Friday 7AM-3:30PM. Must be available some weekend and holidays if necessary

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (50) (Bethesda, MD, US, 20892)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team located in Bethesda, MD.

As the Animal Care Technician I, you will work with our research animals to ensure they are well cared for.

Additional responsibilities include:
•   Providing food & water.
•   Ensuring cages are clean.
•   Performing and recording daily animal health checks.
•   Handing & restraining animals for injections
•   Learning & applying quality assurance standards
•   Examining new animals that arrive at the site & helping them to settle in
•   Learn & become involved in breeding of multiple animal species.

Job Qualifications 
The following are minimum requirements related to the Animal Care Technician I position:
•   Six months of animal experience (e.g., dog walking, pet sitting, kennel attendant, vet assistant, farm hand, 4-H background, pet store worker)
•   Must be successful in obtaining the ALAT (Assistant Lab Animal Technician) Certification within 1-2 years of eligibility

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (BLDG 35) (Bethesda, MD, US, 20892)

Job Summary

We are looking for an Animal Care Technician I to join our Insourcing Solutions team, located in Bethesda, MD.

The responsibilities of the Animal Care Technician I are to perform daily animal health observations, animal husbandry duties, to maintain the quality and health of research animals, to include performing daily water bottle and cage checks, cage changing and/or cage cleaning as required; providing food and water; and recording health concerns.

In addition:

Maintain accurate records of animal breeding, housing, or support areas.
Receive, inspect, and house incoming animals.
Assist with restraint, handling, and manipulation of various animal species.
May become involved in breeding and weaning procedures.
Monitor personnel and equipment entry into various rooms.
Operate required equipment and performs general housekeeping.

Job Qualifications

A candidate that possesses a high school diploma or general education degree is preferred; experience performing basic animal care desired. Interest in achieving ALAT certification upon eligibility.

The pay for this position is $18.50 USD per hour.

For more information, please visit www.criver.com.

Project Manager I (Animal Husbandry) Bldg 35 1 (Bethesda, MD, US, 20892)

Job Summary

We are seeking a Project Manager 1 (husbandry) Bldg 35 for our Insourcing Solutions site located in Bethesda, MD.

The following are responsibilities related to the Project Manager 1:

Review, comprehend and comply with all SOP's and quality assurance standards pertaining to specific area. Cares for and maintains laboratory animals
Oversees and coordinates the daily activities of the animal facility to include scheduling of staff for both workdays and weekends.
Oversees all aspects of husbandry support, to include related paperwork, cage change scheduling, and supplies.
Actively interacts with Project Officers, facility veterinarian(s) and investigators as required to solve customer requests, inquiries, and complaints.
Works with subordinate employees to ensure that all work is performed according the task Statement of Work.
Participates in interviewing applicants for open positions, developing performance improvement plans, and writing employee performance evaluations.
Assists in assessing training needs, as well as, developing and presenting training for staff and investigators
Oversees the animal surveillance program related to the husbandry staff.
Occasionally provides technical support (e.g. restraining animals, weaning, etc.).
Provides animal husbandry and environmental enrichment for colony animals.
Provides quality assurance to include animal health surveillance, monitoring of the effectiveness of facility sanitation, autoclaving procedures, monitoring of incoming animal shipments for container integrity and animal health, monitor the heating, ventilation and air conditioning (HVAC), internal facility reports for monitoring deviations from pre-established parameters, other quality assurance services as deemed necessary (e.g., water cultures) by the Project Officer.
Provides data entry/data base report generation for computerized systems which monitor facility internal environmental parameters, security, or other animal facility monitoring and management requirements.
Assist training department and supervisors in the development of course content and materials for training and continuing education of the animal care staff to achieve AALAS certification. Assists in assessing training needs, as well as, developing and presenting training for staff and investigators.
Will be required to rotate weekend coverage.

Qualifications

The following are minimum qualifications related to the Project Manager 1 position:

Education: AA/AS degree in Animal Science or related field required plus four years lab animal experience. Or BA/BS degree or higher in Animal Science or related field and 3 years same experience.
Experience: Minimum of one (1) year of experience of supervisory experience in a multiple labor category rodent facility.
Certification/Licensure: AALAS certification at the Laboratory Animal Technologist level (LATG).

The pay range for this position $38.50 to $42.25 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Vaccine Mandate
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19 by December 8, 2021. Our main priority is the wellbeing, health, and safety of our people. We will be requiring proof of vaccination from all employees.

Anyone with requests for disability-related and/or religious exemptions should contact Talent Acquisition (crrecruitment_US@crl.com) so that information can be provided about the accommodation process at Charles River.

With over 18,000 employees within 100 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

For more information, please visit www.criver.com.

Lead Cagewash Technician (Bethesda, MD, US, 20892)

Job Summary

We are seeking an experienced Lead Cagewash Technician to join our Insourcing Solutions team, located in Bethesda, MD.

As the Lead Cagewash Technician, you will provide quality assurance and control, in addition to coordinating preventative maintenance of equipment, as well as prioritizing workload on the assigned side to ensure daily goals are met and the integrity of the research is maintained.

Additional responsibilities include:

Maintains facility equipment and performs routine preventative maintenance on cagewash and autoclaves, including routine inspection of cleaning filters and roto-arms.
Responsible for conducting trouble shooting on the equipment and reporting any problems to the Cagewash Supervisor. If necessary, communicating directly with the manufacturers on problems with the equipment.
In the absence of the Cagewash Supervisor, is responsible for scheduling the staff, ensuring work and all related paperwork is completed.
Sanitize, maintain, and repair animal caging materials as needed and ensure cagewash facilities are kept clean and organized
Other tasks may include assisting with the receipt, stocking, and maintenance of supply inventories
Prepare and submit required written records, charts, logs, and inventories.
Assist with training and redirection of workload as necessary to ensure a cohesive team and that daily goals are met.

Qualifications

The following are minimum requirements related to the Lead Cagewash Technician position:

High school diploma or GED
Minimum six months of successful performance in cagewash facility operations

The pay range for this position is $19.00 - $19.50 per hour.  Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Cagewash Technician I (Bldg 35) (Bethesda, MD, US, 20892)

Job Summary

We are looking for a Cagewash Technician I to join our Insourcing Solutions team, located in Bethesda, MD.

The duties of the Cagewash Technician I are to maintain facility equipment and perform routine preventative maintenance on cagewash and autoclaves.

You will also perform the following duties:

Sanitize, maintain, and repair animal caging materials as needed.
Ensure cagewash and animal holding facilities are kept in a clean and organized manner.
Assist with the receipt, stocking, and maintenance of supply inventories.
Prepare and submit required written records, charts, logs, and inventories.
Actively interact with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Other duties will include general housekeeping, in addition to reviewing, comprehending and complying with all SOPs and quality assurance standards pertaining to specific areas.

Who are we looking for?

A candidate that possesses a high school diploma or general education degree is preferred. Experience and/or training working with mechanical equipment preferred.

The pay for this position is $17.50-18.47 USD per hour.

For more information, please visit www.criver.com.

Sr. Supply Chain Coordinator (Hanover, MD, US, 21076)

Job Summary

As a Senior Supply Chain Coordinator for Charles River, your role involves efficiently managing materials to support testing and meet client demands. Responsible for updating the Supply Chain Database or any other Warehouse Management System, documenting raw material movements and contributing to the completion of raw material request and submission of purchase requisitions. Your attention to detail and analytical skills contribute to Charles River’s operational efficiency and success in delivering high-quality products. This position reports onsite to the facility director.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Support Receiving, Shipping & Purchasing operations as needed.
Analyze and manage current inventory needs and levels, replenishment schedules, and order quantities.
Maintain accurate records of inventory levels, track material consumption and generate reports to provide insights into material usage patterns and identify areas for improvement.
Contribute to Raw Material Request completion and Purchase requisition submission.
Coordinate physical material movements for the picking of material and supply to testing.
Issue materials to testing by completing goods issue to material requisitions in inventory database.
Coordinate physical material movements for the picking of material and supply to testing
Maintain accurate daily records of good receipts and shipments made.
Manages and maintains inventory system; facilities upgrade to related database and/or software under the direction of the purchasing or inventory manager.
Conduct cycle counts as needed.
Execute timely inventory adjustments.
Reconcile and conduct root cause analysis to determine reasons for needed inventory adjustments and transactions.
Ensure materials meet specifications, standards, cost-efficient, with adequate supply for testing.
Document inventory properly and communicate any issues with upper management immediately
Ensures adherence to Approved Supplier List for all cGMP purchases.
Manage, log, assign lot numbers (as applicable) and appropriately document all Receipt (incoming) and Shipment (outgoing) of materials, documents, testing samples and product for the facility.
Create and process purchase requisitions.
Process invoices for payment in ERP SAP for the facility.
Create and assign material part numbers.
Develops/updates facility specific standard operating procedures and internal policies for material movement and delivery flow activities and documentation requirements.
Establishes inventory categorization and storage locations within facility.
Support negotiations and problem resolution with internal and external customers to ensure all issues are addressed and countermeasures are implemented and tracked.
Optimize inbound freight routes and timing to achieve company/client expectations.
Monitor and report performance metrics including (but not limited to) misses associated with on-time deliveries, quality metrics, and cost (including overtime).

Job Qualifications

Bachelor’s degree required
Minimum 3 to 4 years of experience performing Enterprise Resource Planning (ERP) inventory transactions.
Enterprise Resource Planning (ERP) or Warehouse Management System (WMS) experience required; SAP preferred
4+ years working around manufacturing and warehousing environments including logistics, materials handling, inventory control, and shipping/receiving in a lead or senior position.
3 years working in a GMP environment including transacting inventory in ERP system preferred
Demonstrated attention to detail and accuracy
Experience with ERP cycle counting
Familiarity with inventory batch management
Experience with Quality System/Standard (ISO, TQM, Six Sigma) Good Manufacturing Practices (cGMP) preferred.
Experience with Scheduling International shipments and drafting of Pro Forma Invoices
Experience with revising or creating Standard Operating Procedures
Proficiency with office technology including Microsoft Office Applications (Outlook, Excel, Word)
Strong written and verbal communication skills
Ability to lift 35 pounds without assistance.
Ability to read, analyze, and interpret documentation.
Ability to work independently, with a team, and different departments to improve processes for improved performance.
Adaptable and able to work within a fast-paced, changing environment.

The pay range for this position is $64,700 - $71,500. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Behavioral Management Technician II (Frederick, MD, US, 21701)

Job Summary

ESSENTIAL DUTIES AND RESPONSIBILITIES:

· Provide appropriate enrichments to the animals’ structural and social environments and provide opportunities for species-typical activities.

· Monitor colony behavioral health, and provide care for animals needing special attention and/or treatment.

· Observe animals and report behavioral abnormalities.

· Assist in performing behavioral assessments in response to reports of behavioral abnormalities.

· Work with other departments to coordinate animal psychological/behavioral enrichment, including the acclimation and socialization of study animals.

· Review animal approval documentation and submit approval forms to appropriate personnel.

· Work with other Behavioral staff to precondition animals for study procedures.

· Work closely with the veterinary and animal care staff to ensure proper animal care standards are maintained.

· Order fruit, enrichment foodstuffs and enrichment devices for the animals.

· Assist with evaluation of new enrichment devices and provide input on strategies for individually and socially housed animals.

· Research and review current literature regarding animal behavior and environmental enrichment as assigned.

· Assist with revisions to relevant SOPs as needed to ensure accordance with the Animal Welfare Act and accepted professional standards.

· Routinely handle animals as required for duties.

· Maintain and track data related to social housing, exemptions to social housing, and abnormal behavior.

· Maintain documentation for the Behavioral Management Program.

· Assist with training animal care staff and other site personnel on aspects of animal behavior and enrichment as needed.

· May serve as IACUC committee member.

Job Qualifications

· Education: Bachelor’s degree (B.A./B.S.) or equivalent in scientific related discipline.

· Experience: 4-6 years related experience in animal science, biology, chemistry/pharmacy, or similar lab environment or must have fully satisfied technical and experience requirements for the previous level. GLP experience preferred.

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

· Certification/Licensure: AALAS certification at the LAT level strongly preferred.

· Other: Demonstrated advanced technical and analytical skills. Effective communication and leadership skills. Ability to handle a variety of laboratory animals. Proficient in technical skills and the operation of data collection equipment. Knowledge of GLP’s and other federal regulations and guidelines relating to the care of laboratory animals required. Understanding of basic, intermediate, and complex study design and protocols. Ability to organize and prioritize work to meet deadlines. Computer literacy including word processing, spreadsheet and database programs.

The pay range for this position is $31-$36/hour. Please note that compensation varies based on factors including, but not limited to, experience, skills, education, and certifications.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Principal Scientist I - Discovery Bioanalysis (Worcester, MA, US, 01608)

Job Summary

We are seeking a Principal Scientist 1 for our Discovery site located Worcester, MA

We are seeking a highly-motivated individual with extensive hands-on experience in developing large and small molecule bioanalytical assays by LC-MS/MS to join our discovery bioanalytical team. The scientist will be responsible for method development and execution of quantitative assays, critical review of data, mentoring junior staff, and maintaining analytical equipment. Individuals in this role will also serve as primary point of communication with the clients. The scientist is expected to work independently to deliver high-quality non-GLP data in a fast-paced environment.

The successful candidate in this position will have:

A solid understanding of analytical approaches and experience of LC-MS bioanalysis.
Experience in extraction and analysis of biological samples, data generation, review of results and scientific presentation
Excellent scientific communication and interpersonal skills
Demonstrated ability to work collaboratively in a team environment with colleagues at various levels
Attention to detail and the ability to critically analyze and verify data prior to data release
Exceptional method development and assay troubleshooting skills
Technical proficiency in operation of analytical instrumentation including chromatography and mass spectrometry systems.

Other: Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs, as appropriate. Knowledge of applicable international guidelines for all types of studies. Demonstrate leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and analytical instrumentation software.

Job Qualifications

The following are minimum qualifications related to the Principal Scientist 1 position:

Education: Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline. Related Master's degree (M.S./M.A.) or Ph.D. preferred.
Experience: Minimum of 7 years related experience in the contract research, academic, or pharmaceutical industry.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Certification as appropriate for specialty preferred.
Other: Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs, as appropriate. Knowledge of applicable international guidelines for all types of studies. Demonstrate leadership skills as they pertain to intra- and interdepartmental initiatives, Sponsor interactions, and business development. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and analytical instrumentation software.

Compensation Data

The pay range for this position is between $100,000/yr. -$110,000/yr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Competencies

Care - We show we care when we respect each other, our animals and the communities where we work and live, when we create a positive healthy workplace, when we are mindful of our compliance standards, and when we choose to do the right thing.

Collaborate -We collaborate when we partner with each other and promote teamwork, when we communicate clearly and effectively across the hall or around the globe, and when we welcome all forms of diversity and encourage inclusiveness.

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

Own - We act like owners when we hold ourselves accountable for our actions, when we respond to internal and external client needs with speed and accuracy, when we set and achieve meaningful goals, and when we strive towards continuous improvement.

About Discovery
Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 320 patents and 74 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.

For more information, please visit www.criver.com.

Lab Coordinator I - In Vivo (Worcester, MA, US, 01608)

Job Summary

We are seeking a Lab Coordinator I for our Discovery site located in Worcester, MA.

The individual in this position will be responsible for supporting the operation of a in vivo laboratory. This position requires attention to detail and the ability to interact and communicate effectively with a wide variety of people. The position operates in a fast paced environment where the commitment to teamwork, quality, and speed is essential. This is a non-Scientific role supporting the labs and ensuring they have all equipment and materials.

Some of the responsibilities for this position include:

•   Handling of hazardous and flammable chemicals during preparation of laboratory solutions.
•   Moving, monitoring and general maintenance of temperature chambers (freezers/refrigerators) containing study samples.
•   Stocking laboratories and delivering consumables/chemicals/reagents to lab scientists.
•   Some shipping and receiving responsibilities, DOT training for hazardous materials shipping a plus.
•   Managing hazardous and biohazardous waste streams.

The pay for this position is $20/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

The following are minimum requirements related to the Lab Coordinator I position.

•   Education: High school diploma or General Education Degree (G.E.D.). Associate’s degree (A.A./A.S.) preferred.
•   Experience: 1 year related laboratory experience in a pharmaceutical or contract laboratory environment preferred but not required. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Ability to work effectively as a member of a team
•   Familiarity with Microsoft Office software (such as Word, Excel)
•   Ability to interact with others in a calm and professional manner
•   Ability to effectively communicate orally and in writing
•   Ability to organize and prioritize work while meeting timelines.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Technician I - In Vivo PK (Worcester, MA, US, 01608)

Job Summary

This position is working Full Time - Sunday - Thursday

Collect and record data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Perform in-life technical procedures (e.g., clipping, handling, binding, removals, body weight, dosing).
• Administer test substances by various basic methods (e.g., oral gavage).
• Input, print and edit computer entries (e.g., in life numbers, body weights, food consumption and clinical observation).
• Under supervision may act as lead/primary technician on basic studies.
• Observe animals for general health and overall well being. • Collect and record research data and biological specimens in compliance with applicable guidelines and regulations (GLPs, SOPS). • Read basic study protocols and extract pertinent information.
• Review documentation of functions performed as part of quality control requirements.
• Retrieve and view SOPs using appropriate database.
• Use applicable GLPs, SOPs, processes and company policies when performing all job functions.
• Handle, restrain, and provide care for all species of laboratory animals at the site.
• Perform study preparation activities including collection tube labeling and room setup.
• Maintain clean work areas (e.g.: laboratory area, primary enclosures, animal exam areas).
• Receive animals (e.g., general health observation, sexing and identification) of all species, if applicable for the site.
• Perform all other related duties as assigned.

Job Qualifications

Qualifications:

Education: High school diploma or General Equivalent Degree (G.E.D.). Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline.
Experience: 6 months related experience in animal research and/or husbandry or must have fully satisfied technical and experience requirements for the previous level.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: ALAT preferred.
Other: Ability to handle common laboratory species. Proficient in basic technical skills and the operation of data collection equipment. Knowledge of guidelines relating to the care of laboratory animals. Basic understanding of study design and protocols.

The pay for this position is $22.50/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

In-Vivo Scientist I - Oncology (Worcester, MA, US, 01608)

Job Summary

We are seeking an experienced Scientist I, Oncology for our Discovery site located in Worcester, MA.

We are seeking a motivated, skilled scientist to work within the Oncology team in our Worcester site. While retaining an element of hands-on responsibility, this position is also largely focused upon leveraging the individual’s scientific strengths through the mentoring of more junior staff. This position requires competency of all aspects of oncology studies including the skills and techniques necessary to satisfy the overall study objectives.

Successful candidates in this position will:

Possess strong interpersonal skills with strong scientific curiosity, initiative and resourcefulness
Possess exceptional organizational and planning skills enabling management of multiple, concurrent tasks & priorities
Careful attention to detail and the accurate, organized and timely documentation of study data and report generation
Team orientation, highly collaborative and results-oriented focus
Self-driven and enthusiastic with the ability to thrive in a dynamic environment
Design and plan projects/protocols with occasional direction from senior staff.
Follow company BOPs and guidelines.
Mentor and train technicians.

The pay range for this position is $70,000 to $74,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

The following are minimum requirements related to the Scientist I position.

Education: Bachelor’s Degree (B.S./B.A) or equivalent in a scientific related discipline. Master's degree (M.S./M.A.) or Ph.D. preferred.
Experience: Minimum of 5 years previous directly related laboratory experience in a pharmaceutical or contract laboratory environment. Animal handling in lab setting is required. Experience with cancer tumor models and imaging is preferred.
Other: Exceptional analytical and problem solving capabilities. Full understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and Good Laboratory Practices (GLPs), as appropriate. Excellent written and verbal communication skills in a team environment. Able to prioritize work and meet deadlines under minimal direction. Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations. Proficiency in the use of analytical instrumentation software with the ability to troubleshoot for routine and non-routine work.

Compensation Data

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

For more information, please visit www.criver.com.

Medical Technologist I (Shrewsbury, MA, US, 01545)

Job Summary

Perform basic medical technology procedures according to protocol, SOP and GLP. Operate, maintain, and perform basic troubleshooting procedures on analyzers. Biological sample processing. Perform and review study ordered parameters and computer input of raw data.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Perform all tasks in compliance with Standard Operating Procedures (SOP) and Good Laboratory Practice (GLP) regulations.
Read study protocols and extract pertinent information with guidance.
Maintain proficient knowledge of hematology, clinical chemistry, coagulation, urinalysis, and fecal analysis.
Operate, maintain, and troubleshoot clinical pathology analyzers with guidance.
Perform basic medical technology procedures such as blood slide differentials, reticulocyte counts and urinalysis with guidance.
Perform all specialized processing under supervision.
Prepare materials needed: labeling tubes, study books and appropriate paperwork prior to bleeding days.
Inventory and package differential and reticulocyte blood slides for each study for shipment or storage.
Manual entry of raw data into the computerized systems and review of data as needed.
Perform all other related duties as assigned.

The pay range for this position is between $30.00 - $35.00/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
Education: Associate’s degree (A.A./A.S.) or equivalent in medical laboratory technology (MLT) or related field required. Bachelor’s degree (B.A./B.S.) or equivalent in medical technology (MT) preferred.
Experience: 0-2 years of experience in a clinical pathology laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MT or MLT with certification or certification-eligible (ASCP or HEW) preferred.
Other: Experience with computer software programs is required. GLP environment requires attention to detail, strong organizational skills, and accurate record keeping competencies.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Director, Pharmacology (Shrewsbury, MA, US, 01545)

Job Summary

Provide senior level business, scientific, and strategic leadership for Pharmacology (Oncology and Metabolism) locally with input globally:

o Manage and scale the Pharmacology (Oncology and Metabolism) business responsibly, with a balanced approach of prioritizing employees, client satisfaction, and operational efficiency while growing topline revenues and maintaining consistently high margins.

o Identify and foster science-related initiatives and capabilities.

o Provide a focal point for assessing program related needs and proposals for improvement and effect their implementation.

o Identify key science-based issues needing discussion at the appropriate meeting venue and contribute exemplary leadership in determining resolution of issues and advancement of scientific programs.

o Contribute to problem resolution of study related science-based issues.

o Provide scientists with guidance in the interpretation and reporting of data.

o Support key business financial, operational, client service, employee, quality goals and achieve targets.

o Encourage and support global collaboration across all sites involved in Pharmacology.

· Scope of work, report and protocol scientific review: Contribute to the interactions of the study directors, clients, and sponsors and provide scientific oversight for study design, preparation of protocols, interpretation of data, and preparation of reports. Interact with study directors and their supervisors to ensure reports are of high quality.

· Functional area(s) of expertise: Provide scientific oversight through both direct and indirect management of the Pharmacology (Oncology and Metabolism) functional areas including PDX, CDX, syngeneic tumor models, DIO, Type I and Type II diabetes, NASH, and new therapies. Identify and recommend innovative technologies, techniques, and/or cross-functional management of staff responsible for the specialty area. Work directly with operations staff in the functional area to resolve scientific and technical issues.

· Responsible for personnel management activities such as: macro scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing regular direction and feedback on performance, disciplinary actions and preparing and delivering annual performance and salary reviews.

· Work effectively with technical operations groups and direct activities of assigned group(s) to ensure optimal performance of the group/function. Identify and implement collaborative projects and synergies with other departments and sites.

· Support strategic planning in the functional area of Pharmacology (Oncology and Metabolism).

· Business development: Engage clients directly and as part of co-travel with Charles River commercial teams. Identify and evaluate new capabilities to expand the scientific base of the company. Represent Charles River at scientific meetings and support sales and marketing at local Charles River sponsored meetings on request.

· Preclinical function: Participate in cross-site initiatives related to scientific initiatives, harmonization of procedures, and standardization of Pharmacology processes, templates for protocols, and reports. Provide scientific and regulatory advice to the Pharmacology group and interact with colleagues in Laboratory Sciences and Toxicology.

The pay for this position is between $185,000 - $230,000 annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: Veterinary or Medical degree (DVM/VMD, MD) and/or Ph.D. in Pharmacology- (Oncology and Metabolism) related discipline is preferred. Post-doctoral experience in a related discipline is a plus.
An equivalent combination of education and experience with documentation as a subject matter expert in the discipline of Pharmacology (Oncology and Metabolism) may be accepted as a satisfactory substitute for the requirements listed above.
Experience: Minimum of 10 years related experience in research or pharmaceutical environment. Management experience is essential.
Certification/Licensure: None required.
Other: Experience in use of desktop applications (word processing, spreadsheets, databases) and network navigation required.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Analyst 1, Bioanalytical Chemistry (Shrewsbury, MA, US, 01545)

Job Summary

Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Perform basic laboratory procedures and collect and record/document research data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), study protocols and company policies/practices.
•   Under supervision may act as lead/primary technician on basic studies.
•   Input, print and edit computer entries (e.g., laboratory data).
•   Prepare materials and data for shipment and archiving.
•   Receive samples and complete tracking documentation.
•   Review documentation of functions performed as part of quality control requirements.
•   Perform study preparation activities including collection tube labeling and room setup.
•   Maintain clean work areas.
•   Perform all other related duties as assigned.

The pay range for this position is between $24.00 and $25.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

MINIMUM QUALIFICATIONS:
•   Education: Bachelor’s degree (B.A. / B.S) or equivalent in laboratory science or related discipline required.
•   Experience: Zero to two years related experience in biology, chemistry/pharmacy, or similar lab environment GLP experience preferred.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: None
•   Other: Proficient in basic technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines. Basic understanding of study design and protocols; able to read basic study protocols and extract pertinent information. Must be able to perform effectively as a team member, accurately record data, follow verbal and written instructions, communicate effectively, and interact in a professional manner with management, coworkers, and sponsors. Able to quickly learn and utilize computer programs as needed; previous computer experience preferred.

WORKPLACE REQUIREMENTS:
•   Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or supplies.
•   Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
•   Must be able to frequently hold and manipulate work materials while utilizing fine motor skills.
•   Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.
•   Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
•   The employee is occasionally exposed to live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
•   The noise level in the work environment ranges from low to moderate depending upon the task being performed.

COMMENTS:
• This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Analyst 1- Immunology (Shrewsbury, MA, US, 01545)

Job Summary

Responsible for performing basic to moderately complex laboratory work in collaboration with departmental staff.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Analyze basic to moderately complex laboratory assays based on protocols and in compliance with SOPs and GLP regulations.
Record project data in accordance with GLP regulations.
Adhere to current Health and Safety regulations.
Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:
Education: Bachelor's Degree (B.S./BA) or equivalent in a scientific related discipline.
Experience: Zero to two years related laboratory experience, preferably in a pharmaceutical or contract laboratory environment.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Demonstrated analytical and problem solving capabilities. Understanding of regulatory requirements of study types assigned, as well as Testing Facility SOPs and the Good
Laboratory Practices (GLPs), as appropriate. Written and verbal communication skills. Ability to prioritize work and meet deadlines. Proficiency in the use of standard software including Microsoft@ Excel, Word, PowerPoint, etc. and with standard laboratory calculations.
PHYSICAL DEMANDS:

While performing the duties of this job, the employee is regularly required to sit, stand and walk, work/type at computer and repetitive use of hands.
Specific vision abilities required by this job include close vision.

WORK ENVIRONMENT:

General office and lab working conditions, the noise level in the work environment is usually quiet.
While performing the duties of this job the employee is regularly required to wear protective clothing (i.e. goggles, face shield, cap, gloves, scrubs, shoe covers), work near toxic or caustic chemicals, work with biohazards.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors and extreme temperature conditions.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Director - Lab Sciences (Shrewsbury, MA, US, 01545)

Job Summary

This is a senior management position within the company with overall responsibilities for the operations and management of all Lab Sciences group within Charles River Massachusetts Shrewsbury facility. Scope includes both regulated and non-regulated work (nGLP; GLP; Clinical).
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Management
•Manage capacity, flexibility, organizational structure and scalability of assigned services including personnel, instrumentation and laboratory space
•Manage allocation of resources to satisfy and exceed client expectations and requirements while also meeting company objectives
•Identify required resources, functional roles and organizational structure necessary to meet site and enterprise objectives
Commercial
•Lead as appropriate client interactions with SHR Lab Sciences clients, consultants and CRL colleagues, Including onsite visitations.
•Responsible for establishing pricing and ensuring alignment with that of other CRL locations as appropriate. Lead person responsible for all material decisions and negotiations regarding pricing discounts as applicable
•Responsible for monitoring financial performance versus plan, including commercial revenue; intercompany revenue; and operating income. Working with CRL colleagues, provide financial forecasting information for the assigned services and communicating and collaborating with colleagues to develop plans when necessary to address material shortfalls
Regulatory
•Ensure that processes fully satisfy regulatory requirements as applicable with company policies
•Serve as Test Facility/Site management
•Serve as Lab Sciences representative in regulatory agency visits and audits
Technical
•Provide scientific direction, oversight, and guidance to staff
•Ensure that new technologies and processes, applications, software, equipment and other initiatives are evaluated to improve the quality and/or value of the service to our clients
•Lead in the evaluation of new technologies in adjacent areas to assigned responsibilities with the objective of expanding service offerings to our clients
Personnel
•Develop and maintain a positive work environment supported by effective communication to inform employees of plans and progress
•Responsible for the development of all direct reports, providing regular coaching and feedback
•Ensuring that all staff have adequate training and education to do their jobs and when necessary
•Ensure the recruitment and retention of personnel necessary to meet departmental objective

The pay range for this position is between $219,000.00 and $245,000.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: Master’s degree in chemistry, biochemistry or a related scientific discipline required. PhD preferred.

Experience: 10 years relevant laboratory experience in a contract research organization (CRO), biotechnology, or pharmaceutical environment, working to Good Laboratory Practice (GLP) standards. 5 years management experience, including staff management and development, and financial responsibility including budgets.

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Other Computer proficiency in MS Office suite. Excellent verbal and written communication and organizational skills required. Demonstrated independent analytical and problem-solving abilities. Knowledge of GLP regulations. Ability to develop and maintain productive vendor, site, and company relationships. Ability to interact appropriately with all levels of employees and work effectively as a member of a team.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Associate (GEMS) - No Experience Needed - EG (Wilmington, MA, US, 01887)

Job Summary

As an Animal Care Associate for our GEMS Breed Group in Wilmington, MA. The GEMS Animal Care Associate will learn how and continue to maintain and monitor the health, production, and physical environment of client or Charles River Laboratories (CRL) animals housed at CRL facilities. These environments may include isolators or individual ventilated cages (IVC).

* This is a temporary opportunity with the potential to be hired as a full-time, employee*

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Perform entry-level husbandry tasks, including supplying food, bedding, water and environmental enrichment.
Maintain rat and mouse colonies, including setting up matings, weaning and sexing of offspring, genetic sampling of animals.
Handle rodents (mice and rats), including restraining of animals for collection of fecal pellets, ear/tail sampling as well as tagging animals for identification.
Observe animals for any abnormalities or common health issues.
Identify and select specific animals for customer shipments, genotyping, health monitoring, matings, transfers or other various tasks as needed.
Learn, understand, and comply with all Standard Operating Procedures (SOPs) with direct supervision and instruction for most processes/tasks.
Learn and strictly follow all animal welfare standards and biosecurity procedures necessary to maintain isolator integrity and animal health status, including the proper sterilization and entry of supplies/animals into isolators.
Be detailed-oriented and enter accurate data entry into Internet Colony Management (ICM).
Ensure compliance with all local, state and federal laws governing the use of research animals.
Ability to prioritize and execute daily tasks with guidance from supervisor(s).
Perform general housekeeping and adhere to EHS, safety, and ergonomic procedures.
General computer skills and ability to quickly learn required computer programs, databases and other applications (i.e. ICM and Microsoft Office)
Be able to learn to identify issues and communicate to management and learn the importance of our CRL DNA and core values.
Perform all other related duties as assigned.

Role Specific Information:

Location: Wilmington, MA
Schedule: Monday - Friday - 1st shift, no weekends required
Benefits: Paid Sick Time/Volunteer Time Off and use of our gym onsite

MINIMUM QUALIFICATIONS

Experience: Entry-level, no previous experience required.
Sufficient computer knowledge to use a tablet computer and communicate using Microsoft Applications.
The ability to develop knowledge of, respect for, and skills to engage with those of other cultures or backgrounds.
The ability to communicate clearly and effectively.

PREFERRED QUALIFICATIONS

Certification/Licensure: AALAS certification at the ALAT or above.

The hourly pay rate for this position is $18.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technologist - EG (Wilmington, MA, US, 01887)

Job Summary

We are seeking an Animal Care Technologist for our GEMS-Breed Department located in Wilmington, MA.

The Technologist performs specialized production duties to maintain and monitor the health, production and physical environment of animals within isolators, micro-isolator cages or barrier rooms. Provides training to departmental staff on all technical skills and Standard Operating Procedures (SOPs).

This is temporary opportunity with the potential to become a regular Charles River Labs employee.

Some benefits include:

Paid sick time
401K participation with a company match
Paid volunteer time off
Use of our onsite gym

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Has substantial understanding and knowledge to perform husbandry tasks, including supplying food, bedding, water and environmental enrichment.
Proficient at maintaining rat and mouse colonies, including setting up matings, weaning and sexing of offspring, genetic sampling of animals, processing samples and other technical tasks as required.
Proficient at handling rodents (mice and rats), including restraining of animals for collection of fecal pellets, ear/tail sampling as well as tagging animals for identification.
Has substantial understanding and knowledge to observe animals for any abnormalities or common health issues.
Has substantial understanding and knowledge to identify and select specific animals for customer shipments, genotyping, health monitoring, matings, transfers or other various tasks as needed.
Learn, understand, and comply with all Standard Operating Procedures (SOPs). Able to complete new processes/tasks with minimal instruction.
Strictly follow all animal welfare standards and biosecurity procedures necessary to maintain isolator integrity and animal health status, including the proper sterilization and entry of supplies/animals into isolators.
Workload contains complex projects and requires judgement in resolving issues and/or in making recommendations. Be detailed-oriented and enter accurate data entry into Internet Colony Management (ICM).
Ensure compliance with all local, state and federal laws governing the use of research animals.
Ability to collaborate with others to train and mentor on knowledge and skills learned.
Ability to self-organize, plan and execute daily tasks.
Perform general housekeeping and adhere to EHS, safety, and ergonomic procedures.
Has substantial understanding of using general computer skills and ability to quickly learn and master required computer programs, databases and other applications (i.e. ICM and Microsoft Office)
Engage in studies, special projects, efficiency improvements, engagement opportunities, etc.
Identify issues and recommend potential solutions to management.
Able to effectively apply and incorporate CRL DNA into day-to-day work.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

High school graduation diploma or General Education Degree (G.E.D.), higher educational experience preferred.
Two (2) to four (4) years related experience and/or training.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Competent with using a tablet computer for data entry and communication (emails, IM’s, etc)
The ability to develop knowledge of, respect for, and skills to engage with those of other cultures or backgrounds is required.
The ability to communicate clearly and effectively is required.
Must possess a high level of initiative and ability to work with minimal supervision
Proficient in computers (IE: MS Office Suite).

PREFERRED QUALIFICATIONS

AALAS certification at the ALATG.

The hourly pay rate for this position is $21.25. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Security Officer - Wilmington/Shrewsbury, MA (Sat & Sun, 6p-6a) (Wilmington, MA, US, 01887)

Job Summary

Charles River Laboratories is seeking a PART TIME (24 hrs. per week, benefit eligible) Security Officer for their Wilmington and Shrewsbury, MA sites.

Shift is overnights, Saturday & Sunday, 6pm-6am (12hrs) + 15% Differential

Following established procedures and guidelines, monitor and ensure compliance with company security and safety policies. Monitor all access activities to the facility by checking and issuing security badges. Monitor security, safety and integrity of buildings and environs and respond to any unusual circumstances. Protect facility from unwanted actions or espionage. Provide a safe and secure environment for employees, clients, visitors and animals.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Greet, screen, record and allow visitors and employees admittance to the site in accordance with company procedures.
Monitor security systems and/or environmental systems and investigate and/or report any incidents.
Report all unauthorized persons to the proper authorities and initiate action to protect employees, animals, products, and physical site. In so doing, the incumbent should not place him or herself in harm’s way.
Ensure the physical safety and security of the facility by enforcing company policies and procedures; provide a deterrent and detection factor for wrongful activity; conducts patrols and monitors the status of the physcial security measures; and monitors the critical building systems.
Physically walk the facility grounds to complete visual inspection of site security on regularly scheduled tours.
Document all security department activity and generates incident reports as necessary.
Monitor facility equipment during tours and report equipment failure, reset alarms as instructed and/or assist in minor repair as directed. Provides effective secondary communication during business hours; and primary communications during non-business hours.
Contact emergency personnel as required and in accordance with adherence to pertinent departmental policies, practices, and procedures.
Assist in directing appropriate emergency response efforts when required.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma, General Education Degree (G.E.D.) or the equivalent. Associates degree preferred.
Experience: 2 -3 years experience with at least six to twelve months of related security experience and/or training.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Valid Drivers license
Must be willing to work on a Part time schedule – 24hrs per week (position will be Benefits Eligible)
Shift: Sat & Sun 6pm-6am (12hrs) + 15% Differential.

Compensation Data

The base pay for this position is $22/hr. + 15% shift differential. Please note that salaries vary within the range (if applicable) based on factors including, but not limited to, experience, skills, education, certifications, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

For more information, please visit www.criver.com.

Isolator Technician (Animal Housing) (Wilmington, MA, US, 01887)

JOB SUMMARY

We are seeking an Isolator Technician for our GEMS-Breed Department located in Wilmington, MA.

In this role you will be working both indoors and outdoors with our animal housing (isolators).

This is a temporary opportunity with the potential to become a full time employee.

$17.75/Hour
Paid Sick time / 401K Participation / Volunteer Time Off
Use of our onsite gym
Monday-Friday work week schedule

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Assist with isolator moves between different locations.
Remove soiled caging and other materials from isolators.
Disassemble the isolators’ component parts.
Inspect the isolator, noting any damage.
Wash, rinse, and dry the isolator box/bag.
Replace isolator gloves.
Operate industrial cage and rack washer.
Order, assemble, sterilize and manage storage of supplies.
Performs all job-related duties in accordance with company safety procedures.

MINIMUM QUALIFICATIONS:

No experience required, we will train.
Valid driver's license required.
Will be required to get certifications on personal lift, forklift and power jack (paid by CRL)

PREFERRED QUALIFICATIONS:

Mechanical experience
Forklift experience

The hourly pay rate for this position is $17.75. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Executive Director DSA Commercial Finance (REMOTE) (Wilmington, MA, US, 01887)

Job Summary

ROLE SUMMARY:

Accountable for establishing sustainable and accurate forecasting and reporting, STRAT, budget development and delivery, and financial analysis, in addition to providing financial leadership, direction, and advice to the DSA Commercial team
The role requires leadership, strategic mindset, team performance management, along with strong influencing and negotiating skills.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Build, develop and lead a high-performing team
Focus on customer centricity and work closely with internal business partners, providing financial expertise and value-added services to support them in achieving their objectives
Initiate and maintain positive business partnerships and collaboration across operations, business finance and corporate accounting teams
Ensure data integrity and quality in both internal and external reporting/analysis
Drive the development of management reporting and planning systems and tools
Promote standardization and simplification

Commercial Finance

Partner in developing and implementing commercial strategies, ensuring alignment with overall business and financial strategies.
Work alongside the commercial team, supporting and advising strategic and operational decision making resulting in better business performance
Interpret, explain and drive performance in the industry, competitor and economic context.
Support and influence key commercial and strategic decisions.
Advise on key commercial planning opportunities
Perform commercial analytics, such as pricing, customer segmentation, service line profitability and price/volume/mix.
Prepare and present financials and key indicators for business reviews, management reporting, budget and strategic planning.
Prepare analysis of monthly, quarterly and annual financials compared to forecast, budget and prior year, including market impacts, currency fluctuations, etc.
Perform complex analyses including year-to-year comparisons and margins on new services for forecasting and pricing purposes.
Analyze appropriate key performance indicators optimally to improve commercial performance

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent required.
Experience: 20+ years related experience in accounting or finance, with a minimum of 10 years’ experience in financial analysis.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MBA, CPA or CMA designation preferred.
Other: Comprehensive understanding of operational, sales and financial issues for business unit required

COMMENTS:

This position may require domestic and international travel.

Compensation Data

The pay range for this position is $230,000/yr - $260,000/yr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Client Project Management - Administrative (Chaoyang District, BJ, CN, 100012)

Job Summary

Job Qualifications

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

研究模型饲养- 支持类 1 1 1 1 (Changping District, BJ, CN, 100107)

近七十年来，查尔斯河员工一起努力协助新药治疗的发现，开发和安全生产。当您加入我们的家庭时，您将对全球人民的健康和福祉产生重大影响。无论您的背景是生命科学，金融，IT，销售还是其他领域，您的技能将在我们所执行的工作中发挥重要作用。作为回报，我们将帮助您建立一个您可以感受到激情的职业。

工作总结

关于企业职能部
企业职能部门为Charles River的运营提供了各领域的专业支持（如人力资源、财务、IT、法律、销售、质量保证、营销和企业发展）。他们与公司全球范围内的同事合作，制定和推动战略，并设立全球标准。这些职能对于衔接战略愿景和实际运营就绪度至关重要，能够确保持续性职能创新和能力改进。

关于Charles River
Charles River是一家早期药物研发授权研究机构（CRO）。我们的业务是建立在实验室动物医学和科学基础之上，我们开发多样化的发现和安全评估服务组合，包括与实验室管理规范（GLP）和非实验室管理规范有关的服务，以在从靶标鉴定到临床前开发的整个流程中为客户提供支持。Charles River还提供一套支持客户的临床实验室测试需求和制造活动的产品和服务。利用广泛的产品和服务组合，我们的客户可以创建更灵活的药物开发模式，从而降低成本、提高效率和功效，并加快上市速度。

我们在全球各地20个国家和地区拥有110家设施及20000多名员工，我们在战略上能够协调全球资源并采取多学科视角来解决客户面对的独特挑战。我们的客户群包括世界各地的全球性制药公司、生物技术公司、政府机构、医院和学术机构。

在Charles River，我们对在提高人们的生活质量方面所起的作用充满激情。我们的使命、优秀的科学专长和强烈的目标意识指导我们开展的所有业务，我们每天开展工作时都知道，我们在帮助改善世界各地人们的健康和安康。我们支持了2021年FDA批准的所有药物中约86％的药物的开发工作，我们为此感到自豪。

欲了解更多信息，请访问www.criver.com。

研究模型饲养- 支持类-DIRECT LABOR 1 (Changping District, BJ, CN, 100107)

工作总结

关于研究模型与服务
基础研究和发现的基本方法是使用体内模型来帮助寻找疾病靶标并确定调节相应病症的潜在生物学通路。作为世界上生产和销售最优质研究动物的领军企业，其中全球临床前研究中使用的动物模型中有一半是我们生产的，我们了解这一步的重要性。凭借七十年的经验和无与伦比的的技术专长，我们能够为您提供完美的动物模型，包括特定疾病模型和预处理模型，可用于基础研究等等。

欲了解更多信息，请访问www.criver.com。

生产副主管 (Changping District, BJ, CN, 100107)

近七十年来，查尔斯河员工一起努力协助新药治疗的发现，开发和安全生产。当您加入我们的家庭时，您将对全球人民的健康和福祉产生重大影响。无论您的背景是生命科学，金融， IT，销售还是其他领域，您的技能将在我们所执行的工作中发挥重要作用。作为回报，我们将帮助您建立一个您可以感受到激情的职业。

工作总结

在Charles River，我们对在提高人们的生活质量方面所起的作用充满激情。我们的使命、优秀的科学专长和强烈的目标意识指导我们开展的所有业务，我们每天开展工作时都知道，我们在帮助改善世界各地人们的健康和安康。在过去五年中，美国食品和药物管理局 (FDA) 批准的药品中有 80% 都与我们合作，我们为此感到自豪。

欲了解更多信息，请访问www.criver.com。

Scientific Manager, Bioassay (Wayne, PA, US, 19087)

Job Summary

Serve as the Scientific Manager responsible for the management and scientific oversight of assigned studies within the Bioassay laboratory including development and execution of highly complex method development and characterization studies related to the testing characterization and analysis of biotherapeutics using analytical instrumentation and methodologies. Independently responsible for method feasibility, method development, method optimization, method transfers, method qualifications, method validations and routine testing under both R&D and cGMP environments. Responsible for guidance and oversight of junior Staff. Additionally, serve as subject matter expert for key Clients, Business Development and Management.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Functioning independently as the technical expert on highly complex studies, develop, perform, and troubleshoot laboratory experiments, tests, and procedures within accepted regulatory compliance for the characterization and analysis of biotherapeutics through use of cell culture and analytical testing techniques and methodologies.
Maintain a safe working environment by adhering to Company policies or procedures. Actively participate in laboratory experiments and maintenance.
Provide oversight of laboratories and mentor and/or supervise research staff in areas such as protocol interpretation, method development and refinement, study related problem resolution, and technique validation, as well as providing scientific expertise in study conduct, design, and interpretation.
Oversee Sponsor interactions, including scientific program development, consulting on study and program design, scheduling, conduct, and reporting. Communicate and provide guidance for client issue resolution and interaction concerning regulatory issues.
Generate and finalize high quality method and study protocols for sponsor and internal characterization and sample testing programs.
Ensure that study protocols are amended to accurately reflect any changes in scope of work or deliverables in a timely fashion.
Provide mentoring and technical guidance to resolve Bioassay challenges in a timely fashion.
Implement techniques to improve productivity, increase efficiencies and maintain laboratory state-of-the-art practices.
Perform routine testing techniques, such as the following, with a high degree of reliability, efficiency, accuracy, and a well-versed skill set in regulatory compliance
Cell culture and various cell handling techniques including expertise with: Adherent Cell Lines, Non-Adherent Cell Lines and Lightly Adherent cell lines
Experience and comfort with plate reader platforms including but not limited to: Softmax Pro, Tecan Magellan, Biotek Gen-5, and/or Stegmann PLA
High level of capability with ADC, ADCC, CDC assays
High level of capability with Potency assays
ELISA/ Immunoassay Analyses – Experience in kit and custom ELISA
RT-PCR – Experience with general methods
Independently review, interpret, analyze, evaluate, integrate, present, and discuss experimental data with research staff and Sponsor.
Independently perform tabulation and statistical analyses of study data, as required.
Prepare high quality final reports appropriate for assigned study, including integration of supporting subcontractor(s)’s reports into final reports as required, independently.
Perform all other related duties as required.

Job Qualifications

Education: Bachelor’s degree (B.A. /B.S.) or equivalent in Cellular/Molecular Biology or related scientific discipline. M.S. or Ph.D. strongly preferred.
Experience: Minimum 7 year’s relevant experience within a contract research, academic or pharmaceutical industry, including experience in the core competencies of characterization and analysis of biotherapeutics.
An equivalent combination of education and experience with contract research or the pharmaceutical industry may be accepted as a satisfactory substitute for the specific education and experience listed above.

Compensation Data

Pay rate for this role is $128,500 - $140,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Sample Management Technician I (Horsham, PA, US, 19044)

Job Summary

Perform a variety of activities related management of study samples including, sample processing, storage, and client support and inventory management.

ESSENTIAL DUTIES AND RESPONSIBILITIES:Protocol Interpretation with guidance.
Complete Watson inventory training.
Perform daily tasks including sample receipt, processing, and storage of samples.
Label creation
Labelling of collection tubes and/or vials.
Train on blood related procedures/techniques.
Communicate sample discrepancies with appropriate parties involved within the Test Facility.
Maintain blood supply inventory closet.
Notify appropriate personnel when supplies require ordering.
Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
Assist with appropriate storage placement conditions for all incoming samples per protocol requirements.
Clean/Maintain blood processing area including but not limited to centrifuges, countertops, blood processing associated equipment/tools and coolers.
Perform data-entry/documentation to maintain accurate status of all sample processing.
Retrieve/Restock study materials as needed.
Maintain appropriate documentation to demonstrate positive control of study-related materials with guidance.
Manage sample processing.
Maintain processing records and inventory of required samples per protocol requirements.
Complete training requirements as applicable.
Perform all other related duties as assigned.

The pay range for this position is between $21.00 and $23.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
Education: High School Diploma or General Education Degree (G.E.D. or equivalent) required; Associates preferred. GLP experience preferred.
Experience: 0-1 years experience in a life science laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Other: Must be detailed oriented and have general familiarity with lab procedures. Good verbal and written communication skills required. Basic computer skills; familiarity with Microsoft Office, Excel software and Smartsheets required. Ability to organize and prioritize work and meet timelines efficiently.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Technician - Milano (MILANO, Milan, IT, 20122)

Job Summary

Per nostro cliente sito in Milano e Calco ricerchiamo un Animal Technician

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli;
Effettuare attività e procedure tecniche sugli animali

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full time

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Animal Technician - Milano (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Di cosa si occupa la Charles River

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

Per ulteriori informazioni, visita il sito www.criver.com.

Animal Caretaker - contratto a chiamata (Milano) (MILANO, Milan, IT, 20122)

Job Summary

Per nostro cliente sito in Milano ricerchiamo un operaio stabularista

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full time

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Animal Caretaker - contratto a chiamata (Milano) (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Per nostro cliente sito in Milano ricerchiamo un operaio stabularista

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full time

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

Per ulteriori informazioni, visita il sito www.criver.com.

Operaio stabularista - Firenze (MILANO, Milan, IT, 20122)

Job Summary

Per nostro cliente sito in Firenze ricerchiamo uno stabularista.

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione del laboratorio

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nel controllo delle procedure sperimentali;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature automatiche e carrelli

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro full time e trasferta a Milano per un periodo iniziale di training

Disponibilità a lavoro nel week-end

Buona conoscenza del pacchetto office

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Allevamento animali da ricerca - Collaboratore (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Attività aviaria

La nostra attività aviaria offre a ricercatori e produttori di vaccini la sicurezza che deriva dalla consapevolezza che i materiali impiegati per il loro processo di produzione sono esenti da agenti estranei. Charles River ha stabilito procedure per la manipolazione degli uccelli e la produzione di uova che hanno fissato lo standard d’industria a livello mondiale.

Di cosa si occupa la Charles River

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

Per ulteriori informazioni, visita il sito www.criver.com.

Maintenance Technician IV Automation - Mon - Friday 3:00pm - 11:30pm (Mattawan, MI, US, 49071)

Job Summary

Note: This position is 3:00pm - 11:30pm EST Monday thru Friday with w/e rotation every 2 months

A Building Automation System Operator is responsible for: maintaining the building environment, environmental monitoring systems and controls; performing maintenance functions; and recommending improvements. The individual in this role works with minimal supervisor on complex projects and handles work orders for facility equipment control issues in a highly regulated environment.

Essential Duties & Responsibilities:

Maintain the building environment, environmental monitoring systems and controls.
Perform equipment maintenance functions associated with monitoring of a laboratory research environment.
Make recommendations to improve efficiency or operations.
Assist with the design of new facility heating, ventilation, and air conditioning (HVAC) and other monitored systems.
Remediate routine/nonroutine work orders and facility equipment control issues.
Coordinator correspondence for corrective action preventative action (CAPA) issues for Good Laboratory Procedures (GLP) documentation of errors and deviations.
Remediate HVAC deviations and repairs encountered in the facility.
Other duties as assigned.

Job Qualifications

Education & Experience:

HS/GED/Associate's/Bachelor's degree with 2 or more years of relevant experience; contract research organization experience preferred.
Building control system experience required.
Commercial HVAC and systems experience preferred.
EPA Certified preferred.
Demonstrated ability to problem-solve, make decisions, work effectively independently and as part of a team.
Demonstrated knowledge of plant mechanical functions, Standard Operating Procedures (SOPs), policies, GLPs and associated requirements.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate wit Essential Duties and Responsiblities, including the ability to learn a validated systems.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under time constraints.
Ability to push, pull, lift 50lbs +.

The pay range for this position is $28-35/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I, Animal Care Services (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Animal Care Technician I at our Safety Assessment site located in Mattawan, MI. The pay for this position is $19/hour plus benefits.

A Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to support a study which may include animal husbandry needs, animal handling, cages, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. The technician is working under close supervision to gain proficiency.

Potential Permanent Schedules: May vary based on business need and available roles to include:

Monday – Friday with weekend and holiday rotations 07:00AM* – 3:30PM*
Saturday - Wednesday with holiday rotations 07:00AM* – 3:30PM*
Wednesday - Saturday with holiday rotations 07:00AM* – 3:30PM*

All roles and shifts require flexibility to work extended hours outside of scheduled shift based on business need, sometimes with short notice.

Essential Duties and Responsibilities

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding skills which may include animal husbandry needs, animal handling, cages, equipment storage/tracking, wash systems, and water delivery system maintenance for various species throughout the site. Specific skills will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

Job Qualifications

Education: High school diploma, General Education Degree (G.E.D.), preferred.
Experience: No previous experience required.

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Certification/Licensure: None.
Other:

Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and
Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Research Technician (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Technician I at our Safety Assessment site located in Mattawan, MI. The pay for this position is $20/hour plus benefits.

A Technician 1 – In Vivo Technical Operations is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis. The technician is working under close supervision to gain proficiency.

Successful Candidates will possess the 6 Cs of Success:

Character – Unquestionable integrity. Respect for all.
Coachable – Eager to receive feedback. Open to making improvements.
Commitment – Dedicated to our animals, our clients/studies, our team.
Collaborative – Team player. Eager to help.
Communicative – Proactively asks questions. Provide complete answers.
Competent – Continuously and proactively hones and expands skill sets.

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals worked with through gentle, positive human animal interactions.
Train in on-boarding skills which may include animal handling, husbandry, observations, basic physiological indices, and data collection/recording to support each skill. Specific tasks will be based on each area's training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Maintain appropriate communication with other personnel.
Use and maintain instrumentation and equipment according to SOPs.
Capable of repetitive gripping, pinching, lifting, carrying, pushing, and pulling. Job requires ability to independently routinely lift or carry up to 50lbs, or team lift weights exceeding 50lbs.
Ability to perform repeated twisting, bending, and reaching; exposure to hot and/or humid environments.

QUALIFICATIONS:

Education: High school diploma or General Education Degree (G.E.D.), required. Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred.
Experience: No previous experience required.
Excellent written and verbal communication skills.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule includes evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to ensure that a safe working environment is maintained observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Facilities Engineer 1 (Mattawan, MI, US, 49071)

Job Summary

The Facilities Engineer is responsible for supporting the facilities/engineering for the building utilities and equipment that supports office, laboratory, and vivarium operations; responsible for capital project efforts and supporting facilities operations. The individual in this position will also monitor facility conditions, support the site master plan associated with reliability and maintenance engineering functions. This individual is expected to be an expert in their discipline while serving as a CRL representative on advanced projects. This individual will act as an advisor to Facilities leadership and external customers on advanced technical projects.

Essential Duties and Responsibilities:

Provide Engineering / Project Management activities supporting the execution capital projects and support of facilities operations.
Provide oversite and voice of the customer for onsite third-party engineering support.
Act as Subject Matter Expert (SME) to review and approve drawing packages provided by internal or external engineering support.
Prepare and review bid packages from external suppliers and A&E firms.
Assist in development and implementation Engineering department capital budget for the facility.
Work closely with local facilities departments, corporate project managers and site operations management to coordinate design efforts; compile user requirements in alignment with design guidelines, commissioning, validation, and operational delivery of small to large-scale capital projects to meet project objectives.
Assist Facilities team with engineering oversight of distribution of chilled water, steam, power, gas and other utilities.
Ensuring compliance with national and local safety codes and regulations
Work with leadership in developing site master plans; prepare maintenance and engineering plans to support master plan objectives.
Monitor the condition of the facilities through assessments and condition evaluations.
Compile and maintain information on plant facilities; establish and maintain engineering and construction standards and drawings.
Support reliability / maintenance engineering functions.
Implement and oversee site energy savings strategies to align with corporate sustainability initiatives.
Support local and corporate safety program.
Leverage engineering expertise (i.e., automation/BMS, CQV, GxP, HVAC/Electrical, LEED and maintenance) throughout the CRL Engineering network.
Other duties as assigned.

Job Qualifications

Bachelor’s degree (BA/BS) or equivalent in mechanical or chemical engineering or related discipline required.
Eight to ten years related experience in managing multiple capital projects / supporting utilities equipment (central utilities) up to $25MM
Certifications: Plant Engineering and or Building trades license helpful.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Demonstrated working knowledge of LEED, Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMPs), AAALAC, FDA/EU and government regulatory requirements and guidelines.
Demonstrated ability to handle multiple projects, prioritize work and meet deadlines.
Demonstrated ability to assess and troubleshoot facility systems.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite, knowledgeable with Microsoft Project, AutoCAD, Bluebeam (REVU CAD).
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ensure project timelines and Budgets are maintained
Ability to work under specific time constraints.

The pay range for this position is $115K - 135k/year. Please note that salaries vary within the range based on experience and education.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Electrical and Controls Engineer (Mattawan, MI, US, 49071)

Job Summary

This role is responsible for the design, start-up, commissioning, and maintenance of the electrical systems (480V and below), Building Automation System (BAS), and stand-alone Process Logic Controllers (PLC’s). This position will oversee electrical and controls projects, troubleshoot systems, and be the lead point of contact for electrical and controls systems used throughout the facility.

Essential Functions

Responsible for the site’s electrical and Building Automation System (BAS), including changes, upgrades, programming, installations, and overall proper operation.
Generate and review reports from the Building Automation System (BAS) to maintain proper system health and ensure data capture to maintain GLP compliance.
Plan and perform preventative maintenance and repair of controls-related HVAC and plant equipment.
Analyze plant electrical and automation/control systems; design and implement improvements.
Provide remote support as needed to troubleshoot and maintain the Building Automation System and other control systems.
Work with Engineering and Facilities personnel to design and implement control sequences for the Building Automation System that improve plant efficiency.
Basic familiarity with Microsoft Office Suite, knowledgeablewith Microsoft Project, AutoCAD, Bluebeam (REVU CAD).
Oversee the programing of various standalone PLC platforms for systems that include mechanical equipment, waste management, cold storage, etc., that are not controlled by the Building Automation System.
Provide expertise and direction to technicians and contractors, execute activities as needed, and ensure successful completion of all electrical and control components.
Partner cross-functionally and work with various departments regarding the implementation and maintenance of electrical and automated equipment, systems and controllers.
Troubleshoot and repair electronic control system malfunctions, including both hardware and software.
Oversee the installation, setup, and commissioning of various third-party integration devices.
Integrate low-voltage sensors and building sub-systems using various industry protocols such as BACNet, N2, Modbus, etc.
Create and/or work with vendors to create graphics for Building Automation System interface.
Act as the project manager for assigned projects to ensure successful completion of all project activities.
Work cross-functionally with Charles River Information Technology teams and/or automation contractors to support the operations and maintenance of the Building Automation System and other network systems as required.
Oversee the installation, setup and commissioning building automation system controllers as required to support site growth, expansion, maintenance, and upgrades.
Ensure that project timelines and budgets are maintained.
Ensure clear communication among all groups involved in successful delivery of projects.
Interface with vendors relating to control systems, automation, and facilities/laboratory equipment.
Plan, coordinate, and supervise the work of Building Automation System service contractors to ensure satisfactory completion of work.
Ensuring compliance with national and local safety codes and regulations
Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:

Education: Bachelor’s degree in electrical engineering or controls system engineering
Experience: 3-5 years designing and implementing installations or improvements to HVAC building automated systems.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education listed above.
Certification/Licensure: Building Automation System certifications regarding programming and operation highly preferred.
Certified Energy Manager (CEM) or LEED certification preferred.
AutoCAD Certified Professional (ACP) or AutoCAD Certified User (ACU).
Other: Must have experience in writing computer programs and software applications related to the HVAC industry.
Experience with any of the following platforms preferred: Schneider EcoStruxure, Allen Bradley, Siemens, Johnson Controls, Tridium, Delta, Honeywell, Allerton, Automated Logic Controls, etc.
Experience in the integration of low voltage building sub-systems using various industry protocols, such as BACNet, N2, Modbus, etc. preferred.
Basic knowledge of Good Laboratory Practice (GLP) regulations preferred.

PHYSICAL DEMANDS:

Ability to work in a variety of circumstances, including climbing ladders, scaffolds, and high lift equipment, working in ducts, crawl spaces, roofs, basements, above ceilings, and in outside/inside/heat/cold/day/night conditions.
While performing the duties of this job, the employee is regularly required to talk, hear and work/type at a computer.
Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

The pay range for this position is $110k - 120k/year. Please note that salaries vary within the range based on experience and education.

WORK ENVIRONMENT:
General office working conditions; the noise level is usually quiet.

Comments:
This position may require occasional domestic travel.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Veterinary Pathologist II (Mattawan, MI, US, 49071)

Job Summary

We are seeking an Anatomic Veterinary Pathologist for our Safety Assessment Team at our Mattawan, Michigan facility.

Our Veterinary Pathologists are responsible for independently performing gross and microscopic evaluation of tissues, recording results, preparing reports delineating pathological findings, and assisting with necropsy supervision. With minimal supervision, work with customers as needed to market company services and to assure customer satisfaction.

Essential Duties and Responsibilities:

• With minimal supervision, interact with clients to assure satisfaction, provide scientific support and input, and to market services.

• Perform macroscopic and microscopic tissue evaluation and interpretation of assigned studies.

• Assist with necropsy supervision and may conduct necropsies, including gross pathology interpretation, sample collection and fixation.

• Enter pathology findings in data capturing system(s).

• Write comprehensive report narratives detailing all test article effects. As needed, work with study directors to ensure data is accurately integrated into study reports.

• Provide training, technical guidance and leadership to laboratory staff, pathology trainees, and less experienced pathologist.

• May provide scientific expertise for experimental design and other aspects of research studies as needed.

• May serve as a consultant in pathology-related issues.

• May serve as a study director or principal investigator.

• May function as a peer review pathologist or may participate in a pathology working group (PWG).

Job Qualifications

Qualifications:

Education: Doctoral degree (D.V.M./V.M.D.) from an accredited veterinary school, or acceptable international equivalent in veterinary medicine.
Experience: 3 or more years of pathology experience post-D.V.M.; specialized training and/or experience in toxicologic pathology preferred. Compensation commensurate with experience and qualifications.
Certification/Licensure: American College of Veterinary Pathologists (A.C.V.P.) board-eligibility required. ACVP board certification strongly preferred and required to enter the grade at the minimum experience level.
Other: Demonstrated success in technical proficiency, scientific creativity, collaboration with others and independent thought. Works on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Computer literacy in word processing, spreadsheet and database software.

Compensation Data

The salary for this position is $170,000 - $180,000 USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Documentation Data Reviewer 1 1 1 (Mattawan, MI, US, 49071)

Job Summary

HOURLY RATE: The pay for this position is $23.50/hr USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

SCHEDULE: Monday - Friday 8:00am - 4:30pm (must be onsite 5 days a week)

We are currently seeking a Data Analyst II for our Quality Control team located at our Mattawan, MI site.

Quality Control supports the review and archival of analysis performed and provides administrative support to the Project Scientists in Laboratory Science disciplines that may include dose formulations, large and small molecule analysis, molecular and cell-based assays, Biomarker, and flow cytometry-based lab work. Staff participate in the review of methods; equipment records and the creation of report tables. Staff participate in the tracking and managing study related materials, providing requested data/information to the Project Scientist or Sponsor as required. Staff are knowledgeable in the application of GxP’s and applicable SOPs, protocols and ensuring adherence to regulatory documents.

Essential Duties and Responsibilities

Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Accurately identify and effectively communicates any issues with data
Effectively support administrative tasks including but not limited to, filing, ordering, distribution of documents and study related materials as needed
Independently compile and archive data books and departmental records
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational area
Review and issue data sets in adherence to established timelines
Accurately review departmental and study specific data to ensure adherence to SOPs, methods/protocols, industry standards, and regulatory requirements as applicable in timely manner
Oversee and maintain responsibility for one operational area with minimal oversight
Identify data discrepancies involving collection and analyses compared to study plan by working with appropriate personnel with oversight
Ensure sample analysis data collected is accurate against study plans, methods/type of analysis conducted and subjects' collection time points with oversight
Create and compile report tables with oversight
Review methods for accuracy, consistency and formatting with oversight
Review and monitor study schedules to ensure timelines are met with oversight
Ensure documents align with requirements indicated in Client Information Database (CID)
Attend study and/or department related meetings to assure understanding of assigned projects
Attain CRL personnel and Sponsor signature/approval for study documents and distribute documents when necessary
Assist in preparation, review and/or processing of specialty data shared with Sponsors
Independently generate and maintain standard and complex draft study plans/protocols/amendments and reporting templates in accordance with CRL or Sponsor specific requirements within one operational area
Review laboratory study data to provide financial information for Unit Based Invoicing
Perform all other related duties as assigned

Job Qualifications

Bachelor’s degree (BA/BS) or equivalent in a relevant field with no previous work experience
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Ability to communicate verbally and in writing at all levels inside and outside the organization
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice
Ability to work under specific time constraints

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Senior Associate Scientist - Bioanalytical Method Development 1 1 (Mattawan, MI, US, 49071)

Job Summary

We are seeking an Senior Associate Scientist for our Bioanalytical Team site located in Mattawan, MI.

The following are responsibilities related to the Senior Associate Scientist:

An Senior Associate Scientist in Laboratory Sciences is responsible for developing and validating methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. The individual in this role is proficient in the use of instrumentation and laboratory techniques and in the execution of method development and validation procedures. An Senior Associate Scientist is expected to work independently, participate in process improvement initiatives, and may function as a Principal Investigator or Study Director.

Job Qualifications

The following are minimum qualifications related to the Senior Associate Scientist position:

Bachelors degree (BA/BS) with 5-7 years of relevant working experience. Master's degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with some relevant experience and CRO is preferred.
LCMS Experience Required
Proficient using laboratory software applications (i.e., LIMS and data acquisition software).
Working knowledge of GxPs and industry guidance documents.
Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts and/or extra shifts, sometimes on short notice.
Familiarity with Microsoft Office Suite.
Ability to work under specific time constraints.

The pay range for this position is $70 - 75,000 k/year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

For more information, please visit www.criver.com.

Senior Associate Scientist, Discovery Bioanalytical 1 (Mattawan, MI, US, 49071)

Job Summary

We are seeking a Senior Associate Scientist for our Discovery Bioanalytical team at our Mattawan, MI site.

The Senior Associate Scientist in Discovery Bioanalytical is responsible for quantitative analysis of drug in body fluids and tissue from non-regulated and regulated safety evaluation, pharmacokinetic/pharmacodynamic studies. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation & reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP's and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents.

The fundamental Competencies/Skills& Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Efficiently perform and document all procedures and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data.
Assist with laboratory investigations, assay troubleshooting, quality observations, and problem solving of technical and/or regulatory issues with minimal oversight.
Effectively develop and validate quantitative/qualitative LC/MS-MS methods/procedures with limited complexity/scope in one operational area with minimal oversight.
Independently perform data analysis in appropriate software for at least one analytical platform with minimal oversight.
Independently operate laboratory instruments including their respective software applications for 1-2 analytical platforms with minimal oversight.
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas.
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.
Able to recognize method and/or data issues and communicate them to management to minimize study impact with minimal oversight.
Independently prepare summary of method development data
Write both study and non-study deviations with minimal oversight.
Full understanding of regulatory and GXP requirements, industry standards and company SOPs within one operational area
Independently lead the lab staff in the completion of method validation studies
Provide support to staff members as required by operational area as needed.
Actively participate in internal process improvements, presentations, and harmonization efforts
Performs all other related duties as assigned.

The pay for this position is $75,000 annually USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

The following are the minimum requirements related to the Senior Associate Scientist position.

Bachelor's degree (BS) with 5-7 years of relevant working experience or Master's degree (MS) with 2-4 years of relevant work experience or Doctorate degree (PhD) with 1-2 year of relevant experience
An equivalent combination of relevant education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
LCMS Experience Required
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
This is an onsite position (no remote options) requires no travel.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Relief Veterinarian (Stilwell, KS, US, 66085)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

The Relief (Clinical) Veterinarian is a flexible schedule based on scope of work up to full-time. This role is meant to provide top notch and ethical veterinary health care for laboratory animals and ensure CRL’s mission of saving human and animal lives! A successful individual will also advise regarding the husbandry, care and maintenance of laboratory animals as well as facilitating training for technicians. This responsibility extends to promoting animal well-being during all phases of the animal's life as well as roles in compliance monitoring, quality management and safe work practices when working with animal models. Our goal is to save human and animal lives in the most ethical and humane way by not only adhering to regulations and guidance's such as the animal welfare act, the 3R's of ethical research, the AVMA guidance on human euthanasia, and “The Guide for the Care and Use of Lab Animals," but pursuing continuous improvement to approaches in research animal care.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Manage health care for the animals within the facility.
Perform veterinary rounds as scheduled and provide clinical care and preventive medicine support.
Perform surgical support and provide anesthesia, surgical and analgesic technical
Expertise/advice to facilitate protocol development.
Deliver training for staff. Training may include veterinary diagnostics, techniques, and minor surgical procedures.
Provide animal health care guidance for veterinary services personnel as required.
Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections.
Perform consultation and collaboration with Researchers regarding animal care, health, welfare and treatment.
May assist in sentinel animal monitoring and other monitoring programs.
Review veterinary care and/or necropsy SOPs as required.
Perform literature searches relating to veterinary subject matters.
Ensure facility is following all applicable regulations, guidelines and standards that relate to animal care and use (E.g., USDA, FDA, AAALAC).
Make recommendations and assist in establishing and enhancing veterinary and animal care standards.
May use controlled substances and be responsible for maintaining appropriate records.
May develop new or innovative procedural improvements appropriate to research studies.
Perform special projects and assist with administrative efforts as needed.

Job Qualifications

Education: Veterinary degree (D.V.M./V.M.D.) required.
Experience: Zero plus years related experience with animal care and surgical techniques. Strong preference for experience in a research/lab animal/GLP environment.
Certification/Licensure: Licensure to practice veterinary medicine in at least one U.S. state required. Ability to practice veterinary medicine in the work state highly desirable
Other: Computer literacy in word processing, spreadsheet and database software. Ability to organize, prioritize work and meet deadlines. Good communication skills.

Compensation Data

The pay range for this position is $120/hour - $150/hour. Please note that compensation varies based on factors including, but not limited to, experience, skills, education, and certifications.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Clinical Veterinarian II (Stilwell, KS, US, 66085)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

A Clinical Veterinarian II is responsible for providing consultation, oversight, and direct support of veterinary care activities for all animals used by Charles River Laboratories; supporting the IACUC to ensure compliance with animal welfare standards and regulations by AAALAC, Int., USDA, and PHS-OLAW; and supporting the evaluation of test article effects by performing examinations and making assessments to interpret study effects on animals.

Essential Duties and Responsibilities:

Oversee daily animal health assessment program including both routine stock and study examinations which support research.
Respond to requests for veterinary care, planned or emergency, by examining the animal, communicating with staff, and following the case until resolution, and address veterinary concerns.
May perform surgical support and provide anesthesia, surgical and analgesic technical expertise/advice.
Functions as departmental representative for interdepartmental communications and initiatives as required.
Supports and contributes to occupational health and safety program.
Support the overall training program for veterinary techniques/treatments performed by veterinary technicians/technical staff and ensure that training is properly documented and regularly updated. Contributes to training others in research animal techniques and other aspects of vivarium operations.
May assist in the development of operating objectives and Standard Operating Procedures (SOP's).
May serve as a full or ad-hoc member of the Institutional Animal Care and Use Committee (IACUC), assisting in protocol review and other efforts as identified.
Develop understanding of animal welfare regulations and standards and their application.
Development of understanding of the 3Rs and considers where refinements may be applied within the animal care program. Works with cross-site team members to implement refinements.
In consultation with the Study Director is a contact for Sponsor discussion on veterinary care and animal responses to the test article as well as review study plans as needed.
Actively engages with internal and external customers and demonstrates understanding of customers’ needs, requirements, and expectations.
Other duties as assigned

Job Qualifications

Education: DVM or equivalent degree required
Experience: 2+ years of experience in veterinary medicine required; experience in laboratory animal medicine or relevant area/education preferred
Licensure to practice veterinary medicine in at least 1 U.S. state required
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Must be able to obtain a veterinary license, controlled substances license, and USDA accreditation in state of employment.
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions and including ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended shifts and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.
Demonstrated ability to problem solve, make quick decisions, communicate decisions effectively, and lead/manage staff in a growing, changing environment

Compensation Data

The starting salary for this opportunity is $155,000 USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Note: Relocation assistance, sign-on bonus and a retention bonus will be part of the overall compensation package as well.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Vivarium Support Technician - Cagewash (Stilwell, KS, US, 66085)

Job Summary

We are seeking a Vivarium Support Technician at our Safety Assessment site located in Stilwell. The pay for this position is $19/hour plus benefits.

A Vivarium Support Technician is responsible for assisting in vivarium operations activities which facilitate clean housing and care for laboratory animals. Also responsible for helping assist in the preparation of materials which enable study activity completion.

Essential Duties and Responsibilities:

Clean and sanitize animal cages and related environmental items.
Perform daily routine maintenance checks on the automated cage wash machines.
Prepares appropriate housing for receipt of new animals; may assist with receiving animals.
Report the need for equipment repair (cages, racks, cagewash machines, etc.) to the appropriate personnel.
Sanitize floors, walls and other surfaces in the automatic cage wash area and in other areas of the lab.
Maintain a clean cage wash area.
Maintain storage area in an organized fashion.
Complete animal care technical duties such as changing liners and sanitizing animal room walls and floors.
Receive, store, and distribute animal husbandry supplies.
Perform limited troubleshooting and calibration of instruments as appropriate for assigned area.
Prepare environmental enrichment items (edible and durable).
Operate basic lab equipment and perform routine maintenance as needed.
Prepare study and colony supplies as needed.

Job Qualifications

Education: High School diploma or General Education Degree (G.E.D) preferred.
Experience: No experience necessary
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Demonstrated ability to problem solve, make quick decisions, communicate decisions effectively.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice
Ability to work under specific time constraints.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Animal Care Services, Technician I (Spencerville, OH, US, 45887)

Job Summary

We are seeking a Technician I for our Animal Care Services Team at our Safety Assessment site located in Spencerville, OH.

A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to support a study may include performing operational, administrative and technical tasks to provide comprehensive care for all species of laboratory animals at the site, including feeding/watering, sanitizing primary and secondary enclosures, environmental enrichment, handling and restraint and related tasks. Assist with the movement of animals and stocking of supplies. The technician is working under close supervision to gain proficiency.

Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which may include animal handling, sexing, restraint on multiple species as well as feeding, watering, and husbandry of multiple species.
Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

The pay for this position is $17/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.

Physical Demands:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Environment:

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

Comments:

This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site located in Hamilton, MT.

As the Animal Care Technician I, you will be working in ABSL 2-3 facility environments to perform a variety of duties, including cleaning, sanitizing, routine preventative maintenance, and repair of caging materials and autoclaves.

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position:

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD per hour.

For more information, please visit www.criver.com.

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site located in Hamilton, MT.

As the Animal Care Technician I, you will be working in ABSL 4 facility environments to perform a variety of duties, including cleaning, sanitizing, routine preventative maintenance, and repair of caging materials and autoclaves.

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position:

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD per hour.

For more information, please visit www.criver.com.

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site located in Hamilton, MT.

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position:

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD per hour.

For more information, please visit www.criver.com.

Animal Care Technician I (Hamilton, MT, US, 59840)

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site located in Hamilton, MT.

Additional responsibilities include:

Maintaining cagewash and animal holding facilities in a clean and organized manner
Operating equipment and performing general housekeeping
General animal care duties
Receipt, stocking, and maintenance of supply orders
Preparing and submitting all required written records, charts, logs, and inventories
Work actively with customers to address requests, inquiries, and complaints
Provide technical assistance

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position:

High school diploma/GED preferred
ALAT certification, or ability to obtain certification within one year of eligibility
Experience and/or training working with mechanical equipment preferred

The pay for this position is $22.00 USD per hour.

For more information, please visit www.criver.com.

饲养员-DIRECT LABOR 1 (Chengdu City, SC, CN, 610213)

工作总结

欲了解更多信息，请访问www.criver.com。

Cagewash Technician I (Chicago, IL, US, 60637)

Job Summary

We are seeking a Cagewash Attendant for our Insourcing Solutions site located in Chicago, IL.

As the Cagewash Technician, you will use existing SOPs and quality assurance standards to perform general housekeeping, as well as maintain facility equipment and perform routine preventative maintenance on cagewash and autoclaves.

Additional responsibilities include:

Sanitize, maintain, and repair animal caging materials
Ensure cagewash and animal holding facilities are kept in a clean and organized manner
Assist with the receipt, stocking, and maintenance of supply inventories
Prepare and submit required written records, charts, logs, and inventories
Actively interact with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Job Qualifications

The following are minimum requirements related to the Cagewash Technician position:

High school diploma, General Education Degree (G.E.D.) or equivalent

Experience and/or training working with mechanical equipment preferred

The pay for this position is $17.94 per hour.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

For more information, please visit www.criver.com.

Technician I-Histology-2nd shift (Ashland, OH, US, 44805)

Job Summary

We are seeking a Technician I for our 2nd shift Histology Team located in Ashland, OH. Candidate will transition to Mon-Thu 2pm-1230am after training.

A Histology Technician I is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, including various tasks within Pre-Trim with an introduction to Trimming. Technician is working under close supervision to gain proficiency.

Essential Duties and Responsibilities: (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which includes GLP Training, Animal Welfare Training and New Hire Orientation. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements. 
Use and maintain instrumentation and equipment.
Reading and understanding of protocols.
Excellent written and verbal communication skills. Knowledge of English.
Manage multiple tasks and priorities to achieve goals.
Ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Work under specific time constraints.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Perform all other related duties as assigned.

The pay rate for this position is $19/hour plus a 10% shift differential. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred. 
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.

Physical Demands:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

Work Environment:

Works in a research laboratory environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from quiet to moderately noisy.

Comments:

May occasionally work weekend/holidays and/or rotating on-call schedule.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Clinical Veterinarian I (Ashland, OH, US, 44805)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

Responsible for providing professional veterinary services and assisting with the management of all phases of health care for the animal colony.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Provide clinical care for the animal colony.
•   Perform veterinary rounds as scheduled, and provide clinical care and preventive medicine support.
•   Perform surgical support and provide anesthesia, surgical and analgesic technical expertise/advice to facilitate protocol development.
•   Assist in the development and deliver training for staff. Training may include veterinary diagnostics, techniques and minor surgical procedures.
•   Provide animal health care guidance for veterinary services personnel as required.
•   Ensure that reports and other materials are prepared and submitted as required.
•   May participate in the response to internal/external inspections and quality assurance audits of veterinary or animal welfare type content.
•   Provide support for activities of the Institutional Animal Care and Use Committee (IACUC), including protocol review, program review and facility inspections. May serve on the IACUC committee.
•   Write, review and update veterinary care and/or necropsy SOPs as required.
•   Perform literature searches relating to veterinary subject matters.
•   Ensure facility is in compliance with all applicable regulations, guidelines and standards that relate to animal care and use (e.g. USDA, FDA, AAALAC).
•   Make recommendations and assist in establishing and enhancing veterinary and animal care standards.
•   May use controlled substances and be responsible for maintaining appropriate records.
•   May develop new or innovative surgical techniques or other procedural improvements appropriate to research studies.
•   May assist in management of the activities of assigned section, including providing direction to junior employees, scheduling activities, and personnel development of veterinary technical team and husbandry staff.
•   Perform special projects and assist with administrative efforts as needed.
•   Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:
•   Education: Veterinary degree (D.V.M./V.M.D.).
•   Experience: Zero to two years related experience with animal care and surgical techniques. Strong preference for experience in a research/lab animal/GLP environment.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: Certification/Licensure: Licensure to practice veterinary medicine in at least one U.S. state required. Ability to practice veterinary medicine in the work state highly desirable. USDA accreditation or application submitted within 1 month of hire.
•   Other: Computer literacy in word processing, spreadsheet and database software. Ability to organize, prioritize work and meet deadlines. Good communication skills.

PHYSICAL DEMANDS:
•   While performing the duties of this job, the employee is regularly required to stand, crouch, bend, climb, reach overhead, kneel, push/pull and use hands to manipulate objects of varying size and with varying degrees of precision.
•   While performing the duties of this job, the employee is regularly required to discern animal health and well-being through visual and physical assessment.
•   Employees must be able to lift, move and/or hold up to 40 pounds; this includes equipment and animals.

Compensation Data

The pay range for this position starts at $120,000 annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Note: A sign-on bonus and a retention bonus will be part of the compensation package.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

Sample Manager - F/H - CDI (Saint-Nazaire, FR, 44600)

Depuis plus de 75 ans, les salariés de Charles River travaillent ensemble pour aider à la découverte, au développement et à la fabrication de nouvelles pharmacothérapies. Lorsque vous rejoignez notre famille, vous avez un impact significatif sur la santé et le bien-être des gens à travers le monde. Que vos antécédents soient en sciences de la vie, en finance, en informatique, en ventes ou dans un autre domaine, vos compétences jouent un rôle important dans le travail que nous effectuons. En retour, nous vous aidons à bâtir une carrière passionnante à nos côtés.

Le poste

Notre site de St Nazaire (44) est spécialisé dans la mise en place de tests de bioanalyses pour supporter le développement de nouveaux médicaments des phases précliniques aux essais cliniques de phase IV. Le site emploie environ 65 personnes et est doté d’équipements de dernière génération.

Intégré(e) au service Supply Chain, nous recrutons un Sample Manager - F/H en CDI afin de gérer l'intégralité des échantillons reçus et envoyés sur le site.

En partenariat avec le Sample Officier, les responsables d'études et sous la supervision du Supply Chain Manager, vous garantirez la bonne mise à disposition des échantillons pour le laboratoire.

Les missions

Participer à l’optimisation du process de gestion des échantillons
Assurer la préparation de la documentation relative à la gestion des échantillons (DDPP, CITES…)
Participer à la bonne réception des échantillons en termes de quantité, délais et documentation associée, si nécessaire
Participer à la création des design/import des listings d’échantillons dans les logiciels et outils utilisés par le site conformément aux plans d’étude ou protocoles et selon les procédures en vigueur
Participer à l’élaboration des DTA/DTS cliniques
Être le point de contact des clients et/ou sites d’expédition ainsi que des responsables d’études sur la gestion des échantillons de leurs études (réceptions, gestions des anomalies à réception, destruction, …)
Initier toutes déviations aux plans d’études ou protocoles concernant la gestion des échantillons et communique au responsable d’études
Participer aux réconciliations relatives à l’identification des échantillons dans le cas des études cliniques
Assurer le suivi des échantillons en fin d’étude ou de période d’archivage : transmission des formulaires de devenir des échantillons auprès des clients (demande de destruction/transfert, relance, attestation de destruction…)

Qualifications attendues

De formation Bac + 2 minimum, vous disposez d'une première expérience probante en gestion d'échantillons de bioanalyse dans un contexte BPL/BPC.

Vous avez de bonnes connaissances des normes BPL/BPC ou du travail en contexte qualité/réglementaire (suivi et respect de procédures et consignes).

Force de proposition et autonome, vous êtes reconnu(e) pour votre orientation solutions. Votre esprit d'analyse et votre capacité à gérer vos priorités vous permettent d'identifier et résoudre les problèmes rapidement.

Vous savez communiquer avec des acteurs internes comme externes (relation clients).

Enfin, notre environnement est international et un anglais professionnel (oral et écrit, B2 minimum) est attendu.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat : CDI cadre (forfaits jours, RTT)
Salaire : Environ 34 000 € bruts/an, sur 12 mois, selon expérience
Prise en charge de la mutuelle à 60% et tickets restaurants

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Technicien(ne) Support Informatique Biomédicale - CDI (Ecully, FR, 69130)

Qui sommes-nous ?

Aux portes de Lyon, le site Charles River d'Ecully offre à ses 90 collaborateurs un environnement dynamique et une cuture d'entreprise certifiés Great Place To Work®. Nos équipes, passionnées et impliquées, contribuent aux efforts que nous accomplissons chaque jour pour améliorer la santé et le bien-être du plus grand nombre possible de personnes.

Le poste

Le Nexus est le premier système de test d'endotoxines entièrement automatisé conçu spécifiquement pour les laboratoires de contrôle qualité. Dans un contexte de ventes croissantes de notre appareil, nous souhaitons renforcer notre équipe Customer Technical Support par l’ouverture d’un poste de Technicien(ne) Support Informatique Biomédicale en CDI.

Travaillant pour un périmètre européen depuis notre site d’Ecully, vous serez l’interlocuteur privilégié des clients externes et des équipes techniques itinérantes internes pour les assister techniquement dans la mise en service, le réglage et le dépannage des appareils Nexus de nos clients. Vous serez également impliqué(e) dans la formation des utilisateurs ainsi que dans la rédaction et la mise à jour de la documentation associée aux appareils.

Missions

Qualifier le support nécessaire et les améliorations logicielles pour toutes les demandes techniques de Nexus en utilisant le logiciel approprié (par exemple, service max/TSF/Knowledge Owl, etc.)
Fournir un support technique pour les produits Nexus aux équipes techniques itinérantes ou directement aux clients
Fournir un support de test pour les mises à jour effectuées avant le déploiement pour l'automatisation et les applications logicielles
Fournir une assistance technique pour les besoins d'installation de logiciels et de technologies de l'information à distance ou sur les sites des clients.
Résoudre les plaintes des clients concernant les logiciels
Tester les produits par des essais pratiques et automatisés, et identifier les défauts potentiels des produits/logiciels
Coordonner et travailler avec notre spécialiste global des applications logicielles et les ingénieurs des logiciels/produits pour rechercher et résoudre les problèmes liés aux logiciels/systèmes en vue d'une correction immédiate, ainsi que pour documenter les problèmes en vue d'une action corrective à long terme
Créer et maintenir des guides de dépannage pour aider les équipes techniques itinérantes à résoudre rapidement et efficacement les questions des clients
Contribuer à l'élaboration et à la révision de documents contrôlés tels que les procédures opérationnelles normalisées, les documents IQOQPQ et les spécification
Aider les clients à créer et à réviser les procédures pour la gamme Nexus
Former l'assistance technique à l'utilisation et au dépannage des demandes techniques concernant Nexus
Se rendre sur les sites des clients pour les former à l'utilisation des produits Nexus et aider le service extérieur à résoudre les problèmes et à prendre des mesures correctives ou préventives à long terme pour les produits Nexus

Qualifications souhaitées

Diplômé(e) d’une formation de niveau Bac+3 minimum en informatique, en mathématiques ou dans une discipline connexe d’ingénierie, vous disposez d’une solide expérience (5 ans minimum) dans le domaine du tests logiciels et de la robotique.
Vous connaissez le matériel informatique, les bases de données SQL, le développement de requêtes simples (Visual Basic) et des logiciels de base : produits basés sur Windows et Linux et systèmes robotiques de laboratoire.
La compréhension de la microbiologie dans le domaine pharmaceutique est un atout. A défaut, l’intérêt pour ce domaine est essentiel.
Au-delà de vos compétences techniques, vous disposez d’excellentes aptitudes à la communication orale et écrite, en français comme en anglais.
Vous savez gérer un dépannage de manière autonome et efficace, et savez être force de proposition face à des problèmes logiciels ou matériels.

Enfin, ce poste ayant un rayonnement européen, vous êtes enclin à vous déplacer ponctuellement sur nos différents sites clients ou internes.

À propos de Microbial Solutions

Notre groupe Microbial Solutions dispose d'un portefeuille très complet de services de test d'endotoxines, et de services et produits de détection et d'identification de microbes sans égal, qui a été spécialement conçu pour répondre aux besoins complexes et changeants de l'industrie. Nous aidons nos clients à garantir la qualité et l'innocuité de leurs produits grâce à des solutions de test faciles à utiliser et néanmoins extrêmement fiables qui sont conformes aux exigences réglementaires, qui sont axées sur le processus de prise de décisions critiques et qui visent à améliorer l'efficacité opérationnelle.

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Job Etudiant : Technicien Animalier - F/H - CDI Week-end Intermittent (Saint Germain Nuelles, FR, 69210)

Qui sommes-nous ?

Le site Charles River de Lyon est un site unique de 14 hectares, situé dans la vallée d'Azergues. Il offre un environnement scientifique innovant, dynamique et convivial où près de 1000 personnes travaillent chaque jour dans l'objectif commun de participer au développement de pharmacothérapies, dans le respect du bien-être animal.

Le poste

Pour travailler au sein de nos animaleries (rongeurs ou non-rongeurs) pendant les week-ends et vacances scolaires, nous recherchons plusieurs étudiants.
En contrat CDI Intermittent, vous interviendrez en tant que Technicien Animalier (F/H) après une formation initiale de 6 semaines, à temps complet, dispensée sur l'été 2025.

Les missions

Assurer le bien-être et les soins aux animaux dans les conditions optimales d’hébergement en étude : alimentation, abreuvement, change des animaux
Participer à l’entretien des installations : nettoyage et rangement du matériel
Observer l’état physiologique et sanitaire des animaux
Assurer les soins et traitements prescrits par les vétérinaires, les techniques de contention
Effectuer le relevé des observations cliniques et l’acquisition des données selon le plan d’étude et les protocoles

Qualifications souhaitées

Vous êtes reconnu(e) pour votre rigueur et votre adaptabilité. Vous savez travailler seul(e) comme en équipe.
A l'aise avec les outils informatiques, vous maitrisez les logiciels bureautiques (Word, Excel).
Notre environnement est propice aux étudiants de formations en biologie ou sciences.

Modalités contractuelles

Convention collective de l'industrie pharmaceutique, groupe : 2
Salaire de base : 11,65€ bruts/h + majoration forfaitaire de 45%
Contrat : CDI Intermittent (environ 200h par an, hors formation initiale)
Formation rémunérée à temps plein de 6 semaines minimum sur les mois de juin à août 2025 selon disponibilités
Planning annuel donné en août
Lieu de travail : St Germain Nuelles (69) - Permis B et véhicule obligatoire.

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Technicien Animalier Primates - F/H - CDI (Saint Germain Nuelles, FR, 69210)

Qui sommes-nous ?

Le poste

Afin de renforcer notre équipe de 4 personnes, nous recherchons un Technicien Animalier en CDI (F/H) pour travailler au sein de notre zone dédiée aux Primates.

Les missions

Participer au lancement des études en préparant les cahiers dont vous aurez la charge
Vérifier l'adéquation des conditions d'hébergement avec les procédures
Assurer l'ensemble des techniques de contentions, administrations, prélèvements et examens standards sur les animaux
Assurer tout ou partie des techniques spécifiques des études de reproduction et des études de perfusion
Contrôler l'état clinique (croissance, poids, comportement) des animaux en cours d'études et remonter les anomalies
Préparer quotidienne le matériel nécessaire à l'étude et assurer sa disponibilité
Acquérir les données selon nos plans d'études, assurer leur contrôle et leur enregistrement

Conditions spécifiques du poste

Amplitude horaire : 6h/18h
Permanences de weekend (1 week-end sur 3 environ, 3h d'intervention par jour )

Qualifications souhaitées

Vous êtes titulaire a minima d'un diplôme de niveau Bac et disposez d'une première expérience dans le domaine du soin animalier, idéalement auprès de primates.

En tant que technicien(ne), vous faites du bien-être animal votre priorité. Votre investissement, votre rigueur et votre relationnel seront également des atouts pour ce poste.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : CDI non-cadre (accord de modulation 35h)
Salaire : A compter de 25 800€ bruts / an sur 13 mois
Prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté, etc.
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Testreq - Training Req (Parma, IT, 43122)

Job Summary

test

Job Qualifications

test

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Vaccine Mandate
Charles River is a U.S. Federal Contractor. As a result, we must follow the Presidential Executive Order to mandate vaccinations, and ensure our employees are fully vaccinated against COVID-19. Our main priority is the wellbeing, health, and safety of our people. We require proof of vaccination from all employees.

For more information, please visit www.criver.com.

Senior BI & Data Analyst (Ahmedabad, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

Senior BI & Data Analyst

We are seeking an experienced Senior Business Intelligence (BI) & Data Analyst for our Enterprise Data Analytics Team.

There’s never been a more exciting time to be on the Enterprise Data Analytics team at Charles River Labs! We are on a mission to make the Enterprise Data Analytics team the backbone of today’s business, as data-driven decision-making enables business leaders to make informed choices quickly to boost revenue, improve productivity, and stay a step ahead of the market. We have already launched our own Enterprise Data Hub, the digital backbone of this company, and we need more experts and leaders in the data analytics discipline who are forward-thinking, self-guided, and innovative to continue to build out the hub across our lines of business, integrating all of our data, mastering data and focusing on data quality to fundamentally shift the way Charles River operates through data science and advanced analytics.

You will be joining a team with an unyielding dedication to the company's purpose; Together We Create Healthier Lives. This laser focus on the patient makes the broader Global Technology Team so exciting. We are taking Charles River to a place where the Enterprise Data Analytics team will be applying the techniques of AI, Generative BI, data management, data engineering, and strategy development, as well as the use of analytics techniques that range from forecasting and simulation to linear programming and optimization and we want you to join us.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

Responsibilities:

• Engage Business Stakeholders at all levels to identify requirements for current and future products through ongoing interaction
• Data Profiling, mining, and data validation to ensure data is fit for use by the business
• Ability to see the big picture and then identify key areas for deep analysis to support sound solutions
• Perform ad-hoc analysis and present results in a clear and user-friendly manner
• Perform testing, resolve issues, and work with developers to automate testing/data validation
• Design and create analytics solutions utilizing Power-BI and Copilot
• Lead requirements workshops and User Acceptance Testing for new data and analytics solutions
• Build strong business relationships that foster a collaborative and trusting approach and partnership
• Act as scrum master for the team and prepare detailed stories for developers.

Job Qualifications:

• Bachelor’s degree in Business Management, Computer Science (or related field), MBA Preferred
• 3+ years of experience with Data Visualizations tools such as Power BI, SSRS, or Tableau
• 1-2 years of experience with data analysis and profiling for Data Science Modelling
• 5+ years of experience in writing SQL queries, data mining, data profiling, and data validation/testing
• 5+ years of experience as a Business Systems Analyst / Data Analyst specializing in the Data & Analytics discipline
• Experienced in Microsoft Fabric and Copilot Power-BI components
• 5+ years of experience organizing and running User Acceptance Testing cycles and training with business users and stakeholders
• Strong business mindset with an ability to collaborate with business partners to identify needs and opportunities for improved data management and delivery

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Testreq - Italy Walkthrough (Ahmedabad, IN)

Job Summary

test test test test

Job Qualifications

test test test

Equal Employment Opportunity

For more information, please visit www.criver.com.

Recrutements de talents - Administratif (Ahmedabad, IN)

Job Summary

About RightSource (Biologics Testing)

The biopharmaceutical industry is growing at an unprecedented pace which is simultaneously changing current testing methodologies. To keep up with the demand, we offer a flexible testing platform which can be deployed on-site at the client site to their exact needs. Our biologics testing lab...in a box…at the client site. RightSource℠ is completely managed and operated using our quality management system, SOP’s, methods, and best practices. It’s as if you shipped your samples to an outsourced lab but walked down the hall instead.

Our Biologics Testing Solutions offers a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

For more information, please visit www.criver.com.

Senior Data Privacy Analyst (Bangalore, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

As a Senior Data Privacy Analyst, you have to be a subject matter expert across (Data Privacy) IT compliance areas, including privacy and compliance, to ensure appropriate processes, procedures, and controls are in place and adhered to. Collaborate with business groups and internal/external auditors to ensure that statutory and regulatory controls are adequately designed, implemented, and/or remediated to meet audit and compliance requirements. Steward improvement and/or remediation efforts associated with statutory and regulatory compliance.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Privacy & Data Protection experience is a mandatory experience for this role. e.g and not limited to India Digital Personal Data Protection Act, 2023 (DPDP Act) and GDPR

• Privacy Third-Party Risk Management: Conduct and manage end-to-end vendor privacy risk assessments

• Audit & Client Support: Coordinate with internal and external auditors during Privacy compliance reviews. Complete Privacy questionnaires for prospective and existing clients

• DSARs: Respond to data subject access requests (DSARs) and support ongoing data protection processes

• RoPA Management: Own and manage the Record of Processing Activities process, and continuous improvement of RoPA by leveraging the privacy management platform (TrustArc)

• Carrying out Data Privacy Impact Assessments

• Supporting, informing, and advising the business on the use of personal data (Privacy by Default and Design)

• Policy, Training & Awareness: Assist in developing and updating privacy and compliance policies, procedures, and training materials.

• Contribute to IT risk and controls program strategies, design, development, implementation, and communication.

• Ensure compliance with the CRL Global Privacy Framework by collecting and reviewing evidence

QUALIFICATIONS:

• Education: Bachelor's degree (B.A./B.S.) or equivalent in Computer Science, Information Systems Management, or related field.

• 5 plus years of related experience in a data privacy support and Compliance role.

• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Skills And Abilities:

Strong understanding of privacy laws e.g., DPDP Act, GDPR, CCPA, CPRA, UK-GDPR, China Data Privacy regulatory and internal control regulations and frameworks as they relate to IT processes. High desirable
Experience in Privacy Management Tools, such as TrustArc Desirable
Fluency in English

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

研究模型饲养- 支持类-DIRECT LABOR 1 1 (Changping District, BJ, CN, 100107)

工作总结

欲了解更多信息，请访问www.criver.com。

Production Supervisor (Small Animal) (Raleigh, NC, US, 27610)

JOB SUMMARY

We are seeking a Production Supervisor to support our Breed Operation in Raleigh, NC. As the Production Supervisor, you will provide daily supervision of personnel and operations to ensure achievement of departmental goals and levels. You will independently handle routine personnel-related issues; assist in the handling of complex personnel-related issues.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provide direct daily supervision and review work of assigned departmental employees to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, SOPs, safety procedures and biosafety protocols. Schedule and prioritize workload of group members.
Assist in the coordination and scheduling of activities of the department through hands-on technical support, delegation of responsibility and/or authority to departmental subordinates.
Oversee production and shipping activities of assigned group, including SOPs and OORs. Ensure proper record-keeping and report preparation.
Review safety issues and Workers’ Compensation claims.
Actively interact with and provide technical assistance to customers as required to resolve customer requests, inquiries, and complaints.
Review customer complaints and participate in the development and implementation of any resulting procedural changes. Create and maintain complaint chart.
Audit production rooms and/or isolators.
Review and ensure appropriate inventory levels of departmental supplies.
Interview and select qualified non-exempt personnel. Recom¬mend personnel actions, including hiring, promotions and raises. Partner with Human Resources and departmental management to assist in the handling of disciplinary issues. Draft appropriate personnel action paperwork.
Identify training and development needs of direct reports. Assist in the development, implementa¬tion and delivery of depart¬mental training programs; ensure that direct reports receive departmental orien¬tation and necessary on-the-job training. Oversee main¬tenance of group training manual and training records.
Monitor performance of direct reports. Provide regular coaching and counseling. Assist in preparation and delivery of salary and performance reviews of direct reports.
Schedule overtime as authorized. Review and approve timecards. Coordinate vacation/time off schedules.
Recommend short-range operating objectives, organizational structure of direct reports and staffing requirements. Assist in the development of a departmental plan for backup and succession of key technical personnel.
May assist in development of departmental budget.
Ensure optimum performance of group function. Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
Assist in the development, maintenance and communication of departmental systems and SOPs. Assist in the development and communication of job descriptions for subordinate positions.
Ensure that departmental equipment is maintained in good working condition and that departmental area(s) are maintained in a clean and orderly condition. Ensure proper recycling and setup of cages in assigned area(s).
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

Candidates must possess one of the following:

Bachelor’s degree in life sciences or related discipline and 4 years of supervisory experience of a high-performing team to deliver complex initiatives and/or support operations, and assistance in cross-functional collaboration to drive successful business outcomes.
Associates degree in life sciences or related discipline and 6 years of supervisory experience
High school diploma or GED and 8 years of supervisory experience

ADDITIONAL QUALIFICATIONS:

Effective communication and interpersonal skills required. Demonstrated computer skills (data input, word processing) required.

PREFERRED QUALIFICATIONS:

ALAT certification

Salary Range

The pay range for this position is $70,000 - $80,000 / annually. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

QA Specialist I - Quality Systems (Rockville, MD, US, 20850)

Job Summary

The QA Specialist I – Quality Systems is responsible for supporting Quality Systems, including investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control. This position will facilitate the compiling, trending (as required), and reporting key quality metrics for management, and other quality system functions, as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products.

Key Responsibilities and Duties:

Establishes and maintains Investigation, Deviation, CAPA, EV systems, and internal and external audit. This task includes collaborating with cross-functional departments to ensure timely implementation and closure of quality records
Provides guidance and advice on methods, procedures, standardization, and requirements associated with these systems
Responsible for tracking and trending (as required) aspects of the Quality System and provide reports to management identifying risks and trends on a routine basis
Performs CAPA effectiveness evaluation based on quantitative and qualitative measurements
Administers the Change Control process for the site and conduct effectiveness verification for changes implemented
Maintains tracking mechanisms to support various Quality Systems elements and ensures visibility throughout the organization
Continuously monitors and review systems and procedures for adherence to regulatory compliance, quality improvements, efficiency, and industry best practices. Provide compliance support and expertise for QA department
Compiles and reports site monthly corporate Quality metrics
Supports the Quarterly Management Review (QMR)
Supports Deviation system and ensure proper investigation and root cause analysis are performed
Supports CAPA/EV system to ensure proper corrective actions are implemented and effective
Supports Change Control system to ensure proper change and impact assessments are performed and tasks are implemented
Develops, implements, and delivers training content for Deviation, CAPA, EV and Change Control processes and procedures
Responsible for procedure reviews and facilitating procedure updates for the Deviation, CAPA, EV and Change Control systems
Assures that personnel are adequately trained in the principles, policies, and procedures of the Deviation, CAPA, EV and Change Control systems
Identifies and escalates compliance gaps across quality systems
Maintains customer complaint and suspect sample management system and ensure its implementation
Prepares the quarterly compliance report for management review
Actively participates in all recruiting efforts to secure, onboard, and develop new staff members
Additional duties as assigned

Job Qualifications

BS/ BA in life sciences or related fields.
Minimum 5 years of experience in GMP related experience in biopharmaceutical/ pharmaceutical
Strong knowledge of GMP, SOPs and quality system processes.
Excellent organizational skills and ability to review and update processes or procedures.
Proficient in MS Word, Excel, Power Point, Adobe Pro, and electronic quality management systems. Previous experience in TrackWise, Pilgrim is preferable
Strong written and verbal communication skills.
Experience in pharmaceutical or bio-pharmaceutical field.
Education or training in cell culture and gene therapy manufacturing environment is a plus.
Proficient in drafting and completing technical documents and presentations.
Expertise in document management processes.
Works on multiple assignments in collaboration with various department system owners.
Quality systems demonstrated knowledge in areas such as Deviation, CAPA, EV and Change Control system management practices/strategies.
Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211/600/820, ICH and EMA).
Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities.
Demonstrates basic understanding of training, instructional design, communication and/or education.
Demonstrates knowledge and understanding of pharmaceutical manufacturing and quality assurance, aseptic and packaging processes, and product transfer.
Demonstrates presentation skills with the ability to conduct training sessions.
Proven organizational skills, planning skills and ability to work effectively within teams.
Demonstrates ability to lead cross-functional project teams.

Compensation Data

The pay range for this position is $65,387-80,183. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Animal Care Technician I (San Diego, CA, US, 92121)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team, located in San Diego, CA.

As the Animal Care Technician I, you will provide the highest animal welfare standards and care, in addition to maintaining vivarium cleanliness.

Additional responsibilities include:

Ensure high standards of animal welfare are met.
Provide food, water and clean housing to animals according to applicable SOPs.
Perform routine animal health observations.
Monitor temperature and humidity, reporting any issues to supervisor or manager.
Receive, unpack, and house animals according to SOP and Animal Receiving Form
Understand proper room entry order and adhere to biosafety requirements.
Maintain accurate records organize supply areas.
Maintain vivarium cleanliness and waste removal in accordance with applicable SOPs.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position.

Required:
- Education: High school diploma, General Education Degree (G.E.D.)
Preferred:
- Education: Bachelor’s degree (B.A./B.S.) in animal or life sciences field preferred
- Experience: Directly related laboratory animal experience in a laboratory animal facility preferred.
- Certification/Licensure: Assistant Laboratory Animal Technician (ALAT) certification from AALAS preferred.

The pay range for this position is $20-22 USD per hour. Please note that salaries vary within the range based on factors including , skills, certifications, and location.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us and BE THE DIFFERENCE!

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Clinical Pathology Technician I (Reno, NV, US, 89511)

Job Summary

***Hours are from 9:30 a.m. To 6:00 p.m ***

BASIC SUMMARY:
Perform a wide variety of basic laboratory tasks. Maintain and perform record keeping. Review data recorded for others for quality control. Review, process, track, and store samples received into the laboratory.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Perform a wide variety of basic laboratory tasks.
•   Under supervision may act as lead/primary technician on routine studies.
•   Operate general laboratory equipment (i.e.: centrifuge, pipettes, water baths) used in the processing of b biological samples.
•   Perform all specialized processing under supervision
•   Read study protocols and extract pertinent information with guidance.
•   Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs) and Standard Operating Procedures (SOPs).
•   Monitor, and perform tasks, related to individual study assignments.
•   Receive, process, track and store all samples received into the laboratory.
•   Observe and assist with technical/study related duties with guidance.
•   File and maintain data for department activities.
•   Maintain and perform record keeping.
•   Review data recorded by others for quality control.
•   Assist with training for less experienced staff.
•   May perform phlebotomy when appropriately certified.
•   Perform all other related duties as assigned.

Job Qualifications

•   Education: High school diploma or General Education Degree (G.E.D.).
•   Experience: Experience in a laboratory setting preferred.
•   An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•   Certification/Licensure: None.
•   Other: Good keyboarding skills, proficient in utilizing personal computer, e-mail and standard office software packages (word processing, spreadsheet, presentation, database).

***The pay range for this position starts at $19.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Validation Engineer I (Rockville, MD, US, 20850)

Job Summary

The Validation Engineer I is responsible for supporting the execution of equipment, utilities, and facility validation activities in compliance with GMP regulations and company procedures. This role involves hands-on protocol development, execution, data analysis, and documentation under the guidance of senior validation personnel.

Key Responsibilities and Duties:

Preparation, execution, and documentation of validation protocols (IQ/OQ/PQ) for manufacturing equipment, analytical equipment, utilities, and facility systems.
Coordinate and schedule system vendors with respect to the execution of Installation, Operation, and Performance Qualification (IQ/OQ/PQ) protocols, and subsequent Re-qualification (RQ) protocols, if applicable, for new and in-use equipment to ensure compliance with site procedures, Validation Master Plan, and regulatory requirements.
Participate in change control and deviation investigations related to validated systems.
Collaborated cross-functionally with Quality Assurance, Engineering, Manufacturing, and IT.
Organize an efficient method to ensure all requirements of assigned validation deliverables are completed and that validation efforts are executed in a timely manner.
Maintain accurate and complete validation documentation in compliance with data integrity principles (ALCOA++)
Participate in the development of corrective actions, as needed, for deficiencies that may be uncovered/observed during validation efforts regarding equipment, processes, test methods, facilities, computer software/systems, SOPs, and other related issues to ensure compliance with applicable regulatory requirements/guidelines, procedures, and policies.
Participate in the development of CAPA’s and assess the effectiveness of corrective action.
Participate in validation project team meetings to ensure project milestone schedules are maintained and deliverables satisfy requirements.
Assist, as needed, during client and regulatory audits and help to resolve or mitigate audit findings related to system qualification/validation.
Validation contractor oversight, as needed.
Perform all other related duties, as assigned.

Job Qualifications

Bachelor’s degree or equivalent in a scientific, Engineering, IT discipline, or related field.
Experience: 0-3 years of experience in validation, quality, or engineering roles within a regulated (GMP) environment. Internship or co-op experience in pharmaceutical, biotech, or medical device industries is a plus.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Must have excellent oral and written communication skills. Strong documentation development and technical writing skills are critical to this position.
Understanding of validation principles and regulatory requirements, (e.g., FDA 21 CFR Part 11, EU Annex 15) is a plus.
Leadership ability, project management, and facilitation skills required. Must be proficient with Microsoft Office software (Word, Excel, PowerPoint). Must have good interpersonal, organizational, and analytical skills.

Compensation Data

The pay rate for this role is $67,000 - $78,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

研究模型饲养- 支持类 1 1 1 (Jiaxing, ZJ, CN)

工作总结

欲了解更多信息，请访问www.criver.com。

Senior Laboratory Analyst (Analytical Sciences) (Ballina, IE, F26D786)

Job Summary

We are seeking an experienced Senior Analytical Analyst for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Analytical Supervisor and the main duties & responsibilities shall be:

Carrying out analytical tests using different techniques like HPLC, Capillary Electrophoresis, UV-Vis spectroscopy, Ion Chromatography, GC, and wet chemistry.
Practical and theoretical knowledge on several analytical techniques, with capability of troubleshooting based on the specific request.
Strong knowledge of GMP regulation applied to a laboratory environment.
Assist in developing and/or verification/validation of analytical methods that use equipment like HPLC, Ion and Gas Chromatography, spectrophotometers as well as wet chemistry techniques and compendial methods.
Receipt and processing of test samples in LIMS.
Safe and compliant disposal of all laboratories generated waste.
Carry out data calculations and basic statistics.
Assist in internal, regulatory and client visits/audits and respond to findings.
Sourcing, purchasing and stocking consumables, standards and reagents required for testing.

Job Qualifications

The following are minimum requirements related to the Senior Analytical Analyst position:

BSc/MSc. in a relevant science discipline (e.g. chemistry, biochemistry, pharmacy, and biotechnology)
A minimum of 3 years relevant experience in Laboratory preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO, CMO, CDMO Industry.
Analytical techniques (HPLC, GC, MS and similar) experience essential.
Experience in development and validation of analytical methods according to ICH guideline required but not essential.
Experience in analytical techniques/immunoassays desirable but not essential.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Biologics Manufacturing Operator - Upstream / Downstream (Keele, GB, ST5 5SP)

Job Summary

Our manufacturing site in Keele, is offering an opportunity for an upstream Biologics Manufacturing Operator.

Responsible for the execution of assigned work of in house and contracted programmes of work for the development, transfer or cGMP Manufacture of processes as assigned to them.

What You'll Be Doing:

Responsibilities will include: participating in multidisciplinary teams for assigned work ensuring that all allocated activities are executed in a timely manner according to schedules set and ensuring that operational, quality and Health & Safety targets are met as required by the Company.

To execute and complete assigned programmes of work both in house and contractually in a timely manner.
To record data and communicate results through verbal and written work.
To ensure that all operations and procedures are performed after appropriate training; that training is maintained for performing all operations and procedures and regularly updated in job training manuals.
To actively maintain the execution of 5S system of facility management.
To ensure laboratory notebooks, Process Development and Production documentation is completed in a timely manner and maintained to high standards as per Company
To form part of multidisciplinary teams working within all areas of the Operations Group.
To perform manufacturing operations within the appropriate current Good Manufacturing Practice (cGMP) standards, ensuring compliance is maintained, as defined in the Company Quality system.
To ensure consideration for cGMP needs are met when developing processes.

Skills and Experience:

Minimum HNC/HND in a science subject or equivalent and / or Degree in Biochemistry, Biotechnology, Biochemical Engineering or equivalent qualification.
Previous practical laboratory experience is desirable.
Able to demonstrate strong written, verbal communication skills and practical skills.
A self-starter, who shows initiative and is a team player.
Able to work flexibly.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Cleaner (Edinburgh, GB, EH14 4AP)

Job Summary

We are looking to recruit a Cleaner for our site in Riccarton, Edinburgh. We are flexible in start and finishing times.

As a Cleaner you will have responsibility of cleaning services for office, laboratory and general areas within the Company including cleaning of surfaces, floors, benches and corridors as required.

The following is required for this role:

Previous cleaning experience would be a distinct advantage
Ability to work within a team
Good attention to detail
Flexible and hard-working attitude

The salary for the role is £23,842.35 per annum, which equates to £12.60 per hour.

Profile and Requirements

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Analist Ecotoxicologie en biodegradatie (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Al bijna 75 jaar werken de medewerkers van Charles River samen om te helpen bij het ontdekken, ontwikkelen en veilig maken van nieuwe geneesmiddelen. Wanneer u bij onze familie komt, heeft u een belangrijke impact op de gezondheid en het welzijn van mensen over de hele wereld. Of uw achtergrond in levenswetenschappen, financiën, IT, verkoop of een ander gebied is, uw vaardigheden spelen een belangrijke rol in het werk dat we uitvoeren. In ruil hiervoor helpen wij u een carrière op te bouwen waar u over gepassioneerd kunt voelen.

Ben jij op zoek naar een functie waarin je bij kunt dragen aan een betere leefomgeving voor mens en dier? Dan zal deze vacature op de afdeling ecotoxicologie jou zeker aanspreken!

Ben jij naast oplossingsgericht een echte proactieve teamspeler met een grote dosis enthousiasme? Dan komen wij graag met jou in contact.

Wegens uitbreiding van onze werkzaamheden zijn wij op zoek naar een:

ANALIST Ecotoxicologie en biodegradatie

Afdeling:

De afdeling Discovery & Environmental Sciences bestaat uit circa 90 medewerkers. Binnen deze afdeling wordt onderzoek uitgevoerd naar de veiligheid van bestaande en nieuwe stoffen. Kenmerkend voor het werk is de grote diversiteit aan testen, teststoffen, klanten en samenwerkingen.

Sectie Ecotox (Environmental Sciences): 

De Ecotox afdeling is een unieke groep binnen CRL waar effecten van producten vanuit  diverse industrieën op het milieu worden getest zowel voor de korte als de lange termijn.

Team:
Het team waarin je komt te werken, bestaat uit 14 collega analisten met daarnaast twee teamleiders en een Technisch Sectiehoofd (leidinggevenden). Daarnaast werk je nauw samen met een team van circa 7 studieleiders en draag  je zorg voor een goed verloop van de projecten van onze wereldwijde klantenkring. 

Over je rol:
Als analist werk je zelfstandig en in teamverband, onder leiding van de studieleider. Je onderzoekt hoe acuut toxisch de producten zijn voor bacteriën, algen, watervlooien en  vissen. Daarnaast onderzoek je lange termijn effecten door in chronische testen te kijken naar bijvoorbeeld groei van vissen, opname (accumulatie) in visweefsels of reproductie van watervlooien.  

Naast de toxiciteit testen werk je ook aan biodegradatie testen. Bij dit soort experimenten wordt onderzocht of bacteriën in staat zijn om de testmaterialen af te breken.

 Primaire verantwoordelijkheden: 

Werken volgens Good Laboratory Practice (GLP) of een vergelijkbaar kwaliteitssysteem; 
Uitvoeren van dagelijkse handelingen zoals; het controleren/kalibreren apparatuur, voeren van de dieren en onderhoud van kweken;
Contacten onderhouden met verschillende afdelingen binnen de organisatie;
Assisteren je bij de verwerking van de resultaten in de rapportage van de studies.

Wat is vereist?

Een achtergrond in:microbiologie, medische biologie; MBO/HBO
in het bezit van artikel 13F;
Bereidheid tot incidenteel weekendwerk;
32-40 uur beschikbaar;
Ervaring met laboratoriumwerkzaamheden: hierbij is zelfstandig en accuraat werken heel belangrijk;
Een goede beheersing van de Nederlandse taal;
Goede communicatieve en sociale vaardigheden;

Nice to Have:

Kennis van werken onder steriele omstandigheden;
Beheersing van de Engelse taal.

Ons aanbod:

Werken bij onze organisatie betekent werken in een dynamische internationale organisatie met een modern laboratorium en een grote diversiteit aan apparatuur en technieken tot je beschikking.

Daarnaast bieden wij uitstekende primaire en secundaire arbeidsvoorwaarden waaronder:

27,5 vakantiedagen en 2 collectieve dagen per jaar;
Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar;
Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris;
Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat;
Reiskostenvergoeding à € 0,23 cent per kilometer met een max. van € 250 netto per maand, of een NS-Businesscard;
Fiets(lease)plan;
Collectief pensioen met een eigen bijdrage van 2.9%;
Bedrijfsfitness
De mogelijkheid om samen met collega’s te sporten op ons eigen sportveld;
De mogelijkheid tot een consult van onze in house ergonoom;
Elke dag gratis vers fruit.

Heb je vragen over deze vacature?
Voor verdere informatie over de functie kun je contact opnemen met her-recruitment@crl.com. Heb je belangstelling voor deze functie, dan nodigen wij je uit te reageren via onze carreer site: Charles River Laboratories, Inc. Jobs (criver.com)

Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld

Over Safety Assessment

Charles River helpt zijn partners bij het versneld uitvoeren van preklinische geneesmiddelontwikkeling dankzij uitstekende programma's voor veiligheidsbeoordeling, de allernieuwste voorzieningen en deskundig advies op het gebied van wet- en regelgeving. Van individuele gespecialiseerde toxicologie- en “IND enabling”-onderzoeken tot pakketten op maat en complete laboratoriumondersteuning: ons ervaren team kan programma's ontwerpen en uitvoeren die anticiperen op problemen en obstakels uit de weg gaan, voor een probleemloze en efficiënte ontwikkelingsgang naar de markt. Bij onze Safety Assessment-vestigingen lopen jaarlijks zo'n 300 programma's voor experimentele nieuwe geneesmiddelen (investigational new drugs [IND's]).

Over Charles River

Charles River is een organisatie die op contract onderzoek naar vroege fasen verricht (CRO). Wij hebben op ons fundament van proefdieren, geneeskunde en wetenschap voortgebouwd om een brede portefeuille van discovery- en veiligheidsbeoordelingsdiensten te ontwikkelen (zowel Good Laboratory Practice (GLP) als non-GLP) en onze cliënten te helpen, van de inventarisatie van targets tot preklinische ontwikkeling. Charles River levert tevens een verzameling producten en diensten die tegemoetkomen aan de behoeften van onze cliënten op het gebied van klinisch laboratoriumonderzoek en productieactiviteiten. Dankzij deze brede portefeuille van producten en diensten kunnen onze cliënten een flexibeler model voor geneesmiddelontwikkeling creëren, wat de kosten verlaagt en de productiviteit en effectiviteit verhoogt zodat producten eerder op de markt gebracht kunnen worden.

Met meer dan 20.000 medewerkers bij 110 vestigingen in 20 landen wereldwijd zijn wij strategisch gepositioneerd voor het coördineren van wereldwijde middelen en kunnen wij multidisciplinaire inzichten inzetten om de unieke uitdagingen van onze cliënten op te lossen. Onze cliënten omvatten farmaceutische multinationals, biotechnologiebedrijven, overheidsinstellingen en medische en universitaire instellingen over de gehele wereld.

Bij Charles River zijn wij gepassioneerd over onze rol bij de verbetering van de levenskwaliteit van andere mensen. Onze missie, onze uitstekende wetenschap en onze doelgerichte instelling werken door in alles wat we doen, en we gaan elke dag opnieuw aan de slag met de kennis dat ons werk de gezondheid en het welzijn van vele mensen helpt te verbeteren. Wij zijn trots te kunnen zeggen dat wij een rol hebben gespeeld bij de ontwikkeling van circa 86% van de geneesmiddelen die in 2021 door de Amerikaanse FDA werden goedgekeurd.

Meer informatie vindt u op www.criver.com.

Animalier contrôle de production - F/H - CDI Week-end (Paris, FR)

Rejoignez une équipe passionnée par les animaux où chaque jour fait avancer la recherche scientifique !

L’activité Insourcing désigne la prestation de gestion d’animalerie, dans laquelle le client confie à Charles River le soin de réaliser les prestations définies dans un contrat au sein de ses installations adaptées à l’hébergement des animaux de laboratoire.

Nous recherchons un Animalier contrôle de production (F/H) pour un contrat en CDI week-end et jours fériés pour un contrat de 8h/semaine à raison de 4h par jour (samedi, dimanche et jours fériés) sur l'un de nos site client basé à Paris 13ème.
Vous contribuerez au respect du bien-être animal et au maintien des meilleures conditions d'hébergement pour les animaux (poissons).

Missions principales

Contrôle du bien-être des animaux selon les consignes préalablement transmises
Vérifier l'abreuvement, l'alimentation et l'enrichissement
Vérification et relevé des paramètres d'ambiance
Respect des consignes transmises
Garantir la mise à jour des registres de suivi.

Profil recherché

Vous êtes étudiant dans des études scientifiques, motivé, rigoureux, passionné par le travail des animaux et vous voulez acquérir une expérience en contact avec les animaux de laboratoire:

Formation initiale: étudiant en étude vétérinaire, biologie ou en cours d'obtention d'un diplôme dans un domaine scientifique ou animalier.
Expérience: une première expérience en contact avec les animaux et/ou en animalerie de laboratoire est un atout
Esprit d'équipe et capacité à collaborer avec les différents interlocuteurs
Organisation et rigueur au quotidien
Sens de l'observation et capacité à identifier des anomalies
Autonomie et proactivité

Modalités contractuelles

   • Convention collective de l’industrie pharmaceutique
   • Nous vous proposons un CDI avec le rythme de travail suivant : samedi, dimanche matin (4h/jour) et jours fériés
   • Prime de transport, 13e et 14e mois, Intéressement, participation, mutuelle et prévoyance, CE

À propos d'Insourcing Solutions
Insourcing Solutions℠ de Charles River peut rationaliser la recherche en favorisant l'efficacité opérationnelle et les économies de coût grâce à son processus stratégique de réalisation en interne pour les services de recherche GMP, GLP et hors GLP, depuis la découverte jusqu'à l'évaluation de l'innocuité. Insourcing Solutions℠ vous offre la possibilité de continuer à contrôler votre espace de travail et à rester maître de votre expertise tout en tirant le meilleur parti possible de l'espace disponible.

Pour plus d'information, consultez www.criver.com.

Plant Service Engineer (Tranent, GB, EH33 2NE)

Job Summary

A Plant Service Engineer vacancy now exists within the Building/Workshop department based in Tranent, East Lothian. This is a permanent full-time role.

Working as a Plant Service Engineer, you’ll join a team who carry out a range of maintenance, fault finding and repair duties in a large campus style estate and associated satellite sites.

Duties and responsibilities include:-

Carrying out maintenance and repairs
Ensuring the continuation of a fit for purpose working environment in accordance with company procedures

Applicants should have:-

A time-served mechanical engineer qualification
Experience of HVAC systems, air compressors and steam condensers
Competence in fabrication using a variety of materials
Experience in the use of basic machine tools would be an advantage
Welding experience and certification would be an advantage
A full driving licence

Working within a small maintenance team on a wide variety of plant there is an expectation that the successful applicant will be multi skilled and flexible. The post requires the ability to work at height as well as in enclosed spaces, and the post holder must also be able to negotiate crawl spaces. Practical experience of fault finding on a range of plant and equipment systems is desirable.

Due to the nature of this role, you must also be able to work outwith normal office hours, as required and as a member of a rotational on-call response team, for which an on-call allowance will be payable.

Closing date: 02 July 2025

The salary on offer for this role is up to £40,000 per annum, depending on skills and experience.

Profile and Requirements

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Environmental Health, Safety and Sustainability Manager (Hollister, CA, US, 95023)

JOB SUMMARY

We are seeking an experienced Environment, Health, Safety, and Sustainability (EHS&S) Manager to lead the integration of safety and sustainability practices across multiple operational sites. This role will be based at our Hollister, CA facility and will also support several CRADL locations in South San Francisco and San Diego. The position requires a minimum of 2.5 days per week on-site in Hollister, with the remaining 2.5 days dedicated to CRADL site support, either on-site or remote, as agreed upon with your manager and in alignment with each location’s needs. Time allocation may vary based on project priorities and operational requirements. In this role, you will be responsible for developing, implementing, and promoting EHS&S procedures and programs that align with our organizational framework, and embedding a culture of safety to ensure a safe and sustainable workplace.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Develop and implement policies and procedures targeted toward increasing the safety and protection of the environment for the businesses.
Ensure facility compliance with applicable environment health and safety regulations.
Implement site audit program of the EHS&S compliance of the site, track and report status of corrective actions, and alerting senior management to developing problems where intervention or oversight is required.
Participate in site leadership as a member of the site Leadership Team and conduct reviews at appropriate intervals with facility senior management.
Consult with site management and employees on Federal, State, and Local regulatory compliance related issues. Work with site facility management to ensure proper training programs are established with regards to environmental and health and safety compliance.
Responsible for timely submission of environmental reports and permits to local, state and federal regulatory agencies.
Work with site Leadership and Site/Global Procurement to develop cost savings initiatives to ensure business continuity and best in class service pricing.
Provide lead support and formal response to EHS agency inspections conducted by local, state and federal regulatory bodies.
Manage moderate size capital infrastructure projects from inception to completion including regulated areas.
Develop program budgets and schedules in support of EHS&S initiatives including platform tools (e.g. Enablon).
Monitor and drive progress of EHS&S projects and programs, maintaining budgets and schedules.
Lead the selection process for hiring third party service firms, evaluating proposals, conducting interviews and making recommendations to senior management, in partnership with site Procurement and Management
Provide supervision and development of EHS Site staff. Ensure appropriate communication takes place around EHS issues.
Consult with Corporate Engineering, Company management and workplace staff to identify and resolve potential EHS&S issues through engineering design changes or other means necessary, such as Facilities controls, risk assessments.
Clarify, define, and assist in enforcement and application of Agency and Company policies and practices.
Support and affirm the Company policy of Equal Opportunity through Affirmative Action.
Partner with site leadership to address audit findings from clients, regulatory agencies, or internal CRL audits.
Develop and provide EHS&S training to staff and contractors including SOP and EHS&S policy training.
Perform all other related duties as assigned.

MINIMUM QUALIFICATIONS

- Candidate will possess one of the following:
  - Master's degree (M.A. / M.S.) in life science (biology, chemistry), environmental engineering, or environmental health and safety with 5 years of related experience
  - Bachelor’s degree (B.A. / B.S.) in a life science (biology, chemistry), environmental engineering, or environmental health and safety with 7 years of related experience
  - Associate degree (A.A. / A.S.) in life science (biology, chemistry), environmental engineering, or environmental health and safety with 10 years of related experience
- Sound working knowledge of Good Laboratory Practices (GLPs), Good Manufacturing Practices (GMPs) and government regulatory requirements and guidelines, including California OSHA regulations. Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines. Proficiency in MS Office suite including Excel, Word, Power point and Project. In- depth knowledge of environment, health and safety regulations required.
- Ability to communicate and influence senior management on EHS compliance initiatives.

Compensation Data

The pay range for this position is $125,000 - $155,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (San Diego, CA, US, 92121)

Job Summary

We are seeking an Animal Care Technician I to join our Insourcing Solutions team, located in San Diego, CA.

As the Animal Care Technician I, you will provide the highest animal welfare standards and care, in addition to maintaining vivarium cleanliness.

Additional responsibilities include:

Ensure high standards of animal welfare are met.
Provide food, water and clean housing to animals according to applicable SOPs.
Perform routine animal health observations.
Monitor temperature and humidity, reporting any issues to supervisor or manager.
Receive, unpack, and house animals according to SOP and Animal Receiving Form
Understand proper room entry order and adhere to biosafety requirements.
Maintain accurate records organize supply areas.
Maintain vivarium cleanliness and waste removal in accordance with applicable SOPs.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position.

Required:
- Education: High school diploma, General Education Degree (G.E.D.)
Preferred:
- Education: Bachelor’s degree (B.A./B.S.) in animal or life sciences field preferred
- Experience: Directly related laboratory animal experience in a laboratory animal facility preferred.
- Certification/Licensure: Assistant Laboratory Animal Technician (ALAT) certification from AALAS preferred.

The pay range for this position is $20-22 USD per hour. Please note that salaries vary within the range based on factors including skills, certifications, and location.

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us and BE THE DIFFERENCE!

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Senior Associate Scientist- Manual Ion Channel Testing (Cleveland, OH, US, 44128)

Job Summary

We are seeking a Senior Associate Scientist for our Manual Ion Channel Testing team at our Safety Assessment site located in Cleveland, Ohio.

The Manual Ion Channel Testing group is responsible for evaluating test article effects on ion channels in vitro. Personnel are responsible for operating and maintaining manual patch clamp electrophysiology workstations. Validated hardware and software systems are used to collect and analyze data under regulated (GLP) or non-regulated conditions. The group prepares, collects and transfers test article formulation samples to the CLE analytical chemistry unit (or other appropriate laboratory) for concentration verification and homogeneity analyses, and is responsible for interpretation and reporting of data outcomes

Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with oversight
Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area
Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with oversight
Assist with oversight the completion of laboratory investigations, assay troubleshooting and quality observations
Assist in problem solving for technical and/or regulatory issues with oversight
Responsible for writing and preparing study plans/protocols/amendments with minimal oversight
Participate in Sponsor visits/tours with minimal oversight
Develop expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area with minimal oversight
Perform data analysis using appropriate software with minimal oversight
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Function as a liaison, maintaining timely and frequent communication between CRL and Sponsor/Client/SD with minimal oversight
Ensure scientific integrity of studies with minimal oversight
Function as a Principal Investigator, Individual Scientist and/or Study Director as assigned with minimal oversight
Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data
Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Write, review and approve deviations with oversight
Develop knowledge of regulatory and GXP requirements, industry standards and company SOPs within one operational area
Effectively manage a small portfolio of research projects including assay development and validation while ensuring timelines are met in a single operational area with oversight
Perform all other related duties as assigned

The pay range for this role is $75-78K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Bachelor’s degree (BA/BS) with 5-7 years of relevant working experience. Master’s degree (MS) with 1-2 years of relevant work experience. Doctorate degree (PhD) with no experience
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Ability to communicate verbally and in writing at all levels inside and outside the organization
Basic familiarity with Microsoft Office Suite
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice
Ability to work under specific time constraints

Equal Employment Opportunity

For more information, please visit www.criver.com.

QA Specialist II - Shift is 12pm - 10:30pm, Wed - Sat (Rockville, MD, US, 20850)

Job Summary

Key Responsibilities and Duties:

Job Qualifications

Compensation Data

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Senior Immunoassay Analyst (Ballina, IE, F26D786)

Job Summary

We are seeking an experienced Senior Immunoassay Analyst for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Immunoassay Supervisor and the main duties & responsibilities shall be:
• Project Management of routine batch release testing in the Analytical Services Department (client correspondence, /weekly calls, management of subcontractors, ensuring samples are released within the required timelines i.e. scheduling of tests, review of basic data, liaising with QA, generation of CoA etc.)
• Generation of GMP compliant SOPs, Protocols and reports.
• Sourcing, purchasing and stocking consumables, standards and reagents required for testing.
• Receipt and processing of test samples in LIMS
• Carry out data calculations, basic statistics and trending. Provide additional information at the clients request as required.
• Assist in internal, regulatory and client visits/audits and respond to findings.
• Assist in the development and validation of different immunoassays (ELISA, Western Blot, ELISPot, etc.) and activity based assays.
• Safe and compliant disposal of all laboratory generated waste.

Job Qualifications

The following are minimum requirements related to the Senior Immunoassay Analyst position:

• A minimum of 3-5 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry.
• Experience in project management essential.
• BSc/M.Sc. in a relevant science discipline
• Experience in analytical techniques/immunoassays desirable but not essential.

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Quality Control Associate I (Sun - Wed) (Rockville, MD, US, 20850)

Job Summary

The QC Associate I is responsible for performing in-process, release and stability testing in a GMP environment. The Associate may also contribute to testing as part of test method optimization, trouble shooting, and development/qualification studies.

Key Responsibilities and Duties:

Perform routine testing in a quality control laboratory to support in-process, lot release and stability testing
Experience performing some of the following in a QC laboratory setting: qPCR / ddPCR, cell-based assays, ELISA, other QC methods (pH, osmolality, endotoxin and appearance)
Perform sample receipt and log-in procedures as required
Contribute to generating SOP’s and qualification/validation/transfer protocols and reports
Responsible for cross training on multiple QC assays
Responsible for participation in method development/qualification studies
May train other associates on methods as appropriate
Perform general lab upkeep, order of lab supplies and maintenance of logbooks as required.
Other responsibilities as required

Job Qualifications

B.S. or M.S. and 1-2 years of experience in biology, virology, molecular biology, cell biology, biochemistry, or related field in a quality control testing laboratory
Team-player
Develop proficiency in compendial methods, molecular biology, cell culture, and ELISA techniques
Able to work in a GMP environment to execute testing
Able to support multiple projects and strong organizational skills
Able to learn data analysis and interpretation experimental data
Complete On-The-Job Training before executing the QC lab responsibilities
Develop communication skills with ability to present information to the internal QC team

Compensation Data

The pay range for this position is $22.24 - $28.17. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

QA Specialist II - Quality Systems and Compliance (Rockville, MD, US, 20850)

Job Summary

The QA Specialist II Quality Systems and Compliance is responsible for supporting Quality Systems, including investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control. This position will facilitate the compiling, trending (as required), and reporting key quality metrics for management, and other quality system functions, as needed. Continuously monitor systems and procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. This includes but is not limited to the following.

Key Responsibilities and Duties:

Establishes and maintains Investigation, Deviation, CAPA, EC systems, and internal and external audit. This task includes collaborating with cross-functional departments to ensure timely implementation and closure of quality records.
Provides guidance and advice on methods, procedures, standardization, and requirements associated with these systems.
Responsible for tracking and trending (as required) aspects of the Quality System and provide reports to management identifying risks and trends on a routine basis.
Performs CAPA effectiveness evaluation based on quantitative and qualitative measurements.
Administers the Change Control process for the site and conduct effectiveness verification for changes implemented.
Maintains tracking mechanisms to support various Quality Systems elements and ensures visibility throughout the organization.
Continuously monitors and review systems and procedures for adherence to regulatory compliance, quality improvements, efficiency, and industry best practices. Provide compliance support and expertise for QA department.
Compiles and reports site monthly corporate Quality metrics.
Supports the Quarterly Management Review (QMR).
Supports Deviation system and ensure proper investigation and root cause analysis are performed.
Supports CAPA/EC system to ensure proper corrective actions are implemented and effective.
Supports Change Control system to ensure proper change and impact assessments are performed and tasks are implemented.
Develops, implements, and delivers training content for Deviation, CAPA, EC and Change Control processes and procedures.
Responsible for procedure reviews and facilitating procedure updates for the Deviation, CAPA, EC and Change Control systems.
Assures that personnel are adequately trained in the principles, policies, and procedures of the Deviation, CAPA, EC and Change Control systems.
Identifies and escalates compliance gaps across quality systems.
Maintains customer complaint and suspect sample management system and ensure its implementation.
Prepares the quarterly compliance report for management review.
Actively participates in all recruiting efforts to secure, onboard, and develop new staff members.
Additional duties as assigned.

Job Qualifications

BS/ BA in life sciences or related fields.
Minimum 7 years of experience in GMP related experience in biopharmaceutical/ pharmaceutical
Strong knowledge of GMP, SOPs and quality system processes.
Excellent organizational skills and ability to review and update processes or procedures.
Proficient in MS Word, Excel, Power Point, Adobe Pro, and electronic quality management systems. Previous experience in Track Wise, Pilgrim is preferable.
Strong written and verbal communication skills.
Experience in pharmaceutical or bio-pharmaceutical field.
Education or training in cell culture and gene therapy manufacturing environment is a plus.
Proficient in drafting and completing technical documents and presentations.
Expertise in document management processes.
Works on multiple assignments in collaboration with various department system owners.
Quality systems demonstrated knowledge in areas such as Deviation, CAPA, EC and Change Control system management practices/strategies.
Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211/600/820, ICH and EMA).
Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities.
Demonstrates basic understanding of training, instructional design, communication and/or education.
Demonstrates knowledge and understanding of pharmaceutical manufacturing and quality assurance, aseptic and packaging processes, and product transfer.
Demonstrates presentation skills with the ability to conduct training sessions.
Proven organizational skills, planning skills and ability to work effectively within teams.
Demonstrates ability to lead cross-functional project teams.

Compensation Data

The pay range for this position is $76,250-90,400. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Quality Control Associate I (Wed - Sat) (Rockville, MD, US, 20850)

Job Summary

Key Responsibilities and Duties:

Perform routine testing in a quality control laboratory to support in-process, lot release and stability testing
Experience performing some of the following in a QC laboratory setting: qPCR / ddPCR, cell-based assays, ELISA, other QC methods (pH, osmolality, endotoxin and appearance)
Perform sample receipt and log-in procedures as required
Contribute to generating SOP’s and qualification/validation/transfer protocols and reports
Responsible for cross training on multiple QC assays
Responsible for participation in method development/qualification studies
May train other associates on methods as appropriate
Perform general lab upkeep, order of lab supplies and maintenance of logbooks as required.
Other responsibilities as required

Job Qualifications

B.S. or M.S. and 1-2 years of experience in biology, virology, molecular biology, cell biology, biochemistry, or related field in a quality control testing laboratory
Team-player
Develop proficiency in compendial methods, molecular biology, cell culture, and ELISA techniques
Able to work in a GMP environment to execute testing
Able to support multiple projects and strong organizational skills
Able to learn data analysis and interpretation experimental data
Complete On-The-Job Training before executing the QC lab responsibilities
Develop communication skills with ability to present information to the internal QC team

Compensation Data

The pay range for this position is $22.24 - $28.17. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Technician I (Stilwell, KS, US, 66085)

Job Summary

Charles River Laboratories (CRL) is seeking an Animal Technician to join our Integrated Toxicology (ITox) team at the Kansas City (CR-KAN) Site. This site is the first of its kind, bridging CRL’s Discovery and Safety Assessment business units, while bringing automation to standard lead optimization toxicology study models to deliver rapid study results to our clients. When you join, you will have a significant impact on the health and well-being of people across the globe. The technician is learning basic skills required to conduct a study, which include animal husbandry needs, animal handling/restraint, housing maintenance, feeding procedures; collecting data, observing the animals for health status, body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Ensure good welfare and humane care for all animals, using gentle and positive human-animal interactions.
Perform basic skills of the department including animal handling/restraint, housing maintenance, and feeding procedures; collecting data, observing the animals for health status, and body weight measurements; administering doses by various methods, conducting euthanasia, and/or biological specimen collections for analysis. Specific skills will be based on each area’s training plan and business needs
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

The pay range for this position is $20/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:

Education: High school diploma, General Education Degree (G.E.D.), preferred.
Experience: No previous experience required. Experience working with/around animals is preferred. Experience in a role requiring physical labor a plus.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform laboratory procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

COMMENTS:

This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Research Support Specialist I -Veterinary Technicians encouraged to apply (Poolesville) (Poolesville, MD, US, 20837)

Job Summary

We are seeking a Research Support Specialist I for our Insourcing Solutions site located in Poolesville, MD.

Prepare and administer research treatments; collect and record physiological data (weight, temperature, pulse, respiration)
Perform technical procedures as needed associated with the Animal Study Proposals in relation to NHP retroviral, human respiratory and flavivirus studies to include but not limited to blood collection, IV catheterization, intubation, broncho-alveolar lavage, tracheal and nasal lavages, documented research observations, and administration of research treatments
Must have a basic understanding of aseptic technique, anesthesia induction, monitoring, and recovery as well as drug dosage calculations and administration
Assist Veterinarian & Sr. RSS staff with surgeries and specialized procedures
Perform daily animal health observations and report any abnormal findings to veterinarian
Maintain electronic medical records, send daily emails regarding animal health information to vet staff
Collect, preserve, and prepare blood, urine, stool, and tissue samples
Participate in study related necropsies/tissue harvest
Set-up for procedures and prepare supplies and equipment
Ability to maintain freezer organization and sample inventory
Practice universal precautions appropriate to different levels of ABSL. Work safely with animal / human pathogen biohazards and help to maintain the research animal facility as a safe work environment / operation
Report any animal health, care, and / or wellbeing concerns to the appropriate facility management staff
Report any facility infrastructure issues, relative to the animal care and support areas to the appropriate facility management

Job Qualifications

The following are the minimum requirements related to Research Support Specialist I:

- High school diploma or general education degree (GED) required. BS degree in Animal Science, Biology, or similar discipline, or A.A. in Veterinary Technology is preferred.

- 2-3 years’ experience working with non-human primates in biomedical research or 2-3 years Veterinary Hospital technical experience preferred.

- Must have computer program proficiency such as MS Word / Access / Excel. Must have a proficient technical vocabulary.

- RVT/CVT/LVT or LAT certification preferred

The hourly range for this position is between $28/hour and $30/hour. Please note that salaries vary within the range based on factors including, but not limited to skills, certifications and locations.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

饲养员-DIRECT LABOR (Chengdu City, SC, CN, 610213)

近七十年来，查尔斯河员工一起努力协助新药治疗的发现，开发和安全生产。当您加入我们的家庭时，您将对全球人民的健康和福祉产生重大影响。无论您的背景是生命科学，金融， IT，销售还是其他领域，您的技能将在我们所执行的工作中发挥重要作用。作为回报，我们将帮助您建立一个您可以感受到激情的职业。

工作总结

欲了解更多信息，请访问www.criver.com。

Senior HVAC Technician (Wayne, PA, US, 19087)

Job Summary

The Senior HVAC Technician is responsible to perform a variety of master-level mechanical and pressure/temperature equipment repairs and maintenance requiring close interface with other trade/craft functions. Perform other semi-skilled tasks in the general maintenance of the physical plant and provide work direction to others performing HVAC projects.

This position will work on-site at the Wayne, PA Charles River site. Position will also be responsible to travel to additional CRL sites located in Malvern and Philadelphia.

Position is scheduled to work Monday - Friday, from 9am - 5pm.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Monitor and maintain HVAC systems including high/low temperature, water and electricity. Isolate and identify malfunctioning equipment for repair, adjustment, and replacement. Interpret instructions as required.
• Observe and interpret readings on gauges, meters, and charts to ensure correct functioning of systems. May calibrate equipment.
• Perform adjustments, repairs and replacement of parts and equipment following written specifications such as blueprints, drawings and schematics.
• Dismantle equipment/fixtures and plan systematic replacement or repair of accessories and parts and return equipment to operation.
• Oversee HVAC-related tasks being performed by other department personnel.
• Inspect completed work for quality, safety, and proper operation.
• Coordinate maintenance work with other departments and divisions; maintain accurate records of maintenance and repair work.
• Periodically perform preventative maintenance programs as required.
• Perform other semi-skilled tasks as assigned to assist in the general maintenance of the physical plant.
• Respond to emergencies as needed. Provide 24-hour on-call maintenance coverage, as scheduled in rotation.
• May perform waste vacuum maintenance.
• Take proper safety precautions and utilize appropriate safety gear/equipment in the performance of all duties.
• Perform all other related duties as assigned.

Job Qualifications

QUALIFICATIONS:
• Education: High school diploma or General Education Degree (G.E.D.) and trade school diploma.
• Experience: Four to six years related experience.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: Valid HVAC license (where required by state).
• Valid Driver's License.

PHYSICAL DEMANDS:
• While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel objects, tools, or controls; and reach with hands and arms. The employee is occasionally required to stoop, kneel, crouch, or crawl and talk or hear.
• The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move more than 100 pounds.
• Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, and depth perception.

WORK ENVIRONMENT:
• While performing the duties of this job, the employee frequently works near moving mechanical parts and in outside weather conditions.
• While performing the duties of this job, the employee occasionally works in high, precarious places and is occasionally exposed to wet and/or humid conditions, fumes or airborne particles, toxic or caustic chemicals, risk of electrical shock, risk of radiation, and vibration.
• The noise level in the work environment is usually moderate.

Compensation Data

The pay range for this position is $35.63/hr. USD. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Directeur des Productions - F/H - CDI (L'Arbresle, FR, 69592)

Qui sommes-nous ?

Le poste

Nous recherchons notre nouveau Directeur des productions F/H en CDI en charge de définir et piloter la stratégie pour l'ensemble des activités de production des modèles animaux, des services supports afférents (pré-zone, conditionnement et logistique) et des activités soumises au BPF et/ou cGMP sur les sites de l'Arbresle (69) et Châtillon sur Chalaronne (01) dans un contexte évolutif pour ces activités.

En tant que membre de Comité de direction, vous impulsez la définition d’actions garantissant l’intégration de votre département dans les objectifs et politiques générales de l’entreprise et du Groupe, en alignement avec la réglementation et nos standards exigeants.
Directement rattaché à notre Directeur Général, vous êtes responsable d’un département d'une centaine de personnes.

Vous jouez ainsi un rôle déterminant en assurant le bon déroulement, la conformité et la performance de l'ensemble des opérations de votre périmètre dans un environnement multisites, dans le respect des budgets, des procédures de l'entreprise et ce en vue d'obtenir le meilleur niveau de qualité possible.

Responsabilités principales

Garantir le développement de la culture, de la maturité et de la performance des activités de votre périmètre autour de 7 piliers majeurs : HSE, biosécurité, bien-être animal, sûreté, qualité, productivité et service client.

Sécuriser les activités en anticipant les risques, renforçant la culture sécurité et développant des actions de prévention en matière de sécurité, biosécurité et sûreté en lien avec les objectifs site
Assurer la productivité de votre département via le pilotage d’indicateurs clés de performance, en maîtrisant les coûts et garantissant l’efficacité de l’organisation
Être garant du respect des exigences réglementaires et de l’application des directives du groupe, proportionnellement aux réalités terrain et enjeux des activités.
Organiser et animer les équipes de votre département par un management structurant, engageant et orienté résultats. Assurer le développement des compétences et des talents en impulsant au quotidien une culture de transparence et de progrès.
Identifier et conduire des projets significatifs d'amélioration continue, de transformation ou d'investissement, dans un souci constant d'efficience.
Proposer aussi souvent que nécessaire les évolutions d'organisation permettant d'accomplir l'ensemble des missions ci-dessus de manière efficace
Tenir le rôle de représentant de l'entreprise auprès des clients, autorités, sociétés du groupe et autres partenaires extérieurs dans le périmètre de votre responsabilité.
Participer activement à la vie du Comité de direction, en apportant une vision opérationnelle, transverse et stratégique afin de faire progresser l’ensemble de l’organisation.

Profil recherché

Formation : Diplôme de niveau bac+5 minimum (Ingénieur, master ou équivalent)
Expérience d’au moins 7 ans dans des postes de management de production en environnement industriel structuré à forte exigence qualité et réglementaire
Appétence démontrée pour le pilotage en environnement multisites et la conduite de projets transverse
Leadership, capacité à fédérer vos équipes et à incarner au quotidien les valeurs fondamentales de l'entreprise.
Sens poussé de l'analyse et de la résolution de problèmes, avec une forte orientation résultat.
Capacités confirmées de communication, de présentation et de collaboration avec des publics très variés, en interne comme en externe.
Enfin, notre groupe international requiert un niveau d’anglais courant (lu, écrit et parlé).

Modalités

Convention collective de l’industrie pharmaceutique
Contrat : Poste cadre
Localisation : Basé à l'Arbresle (69) et déplacements réguliers à prévoir à Châtillon sur Chalaronne (01)
Salaire : A discuter selon profil, sur 14 mois + bonus + intéressement et participation
Indemnités de transport, accord de télétravail, prise en charge de la mutuelle à 60%, restaurant d’entreprise, CSE
Site non accessible en transport en commun : moyen de locomotion indispensable

Pour plus d'information, consultez www.criver.com.

Technicien.ne de Laboratoire Clinique (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Technicien.ne pour notre équipe de Laboratoire Clinique situé à notre site de Senneville, vous serez principalement responsable d’accomplir les tâches techniques et suivre les directives des plans d’étude/phase et les procédures. Votre réussite assurera le bon déroulement de nos recherches, ainsi que l’intégrité de nos études pré-clinique.

Dans ce rôle, les principales responsabilités incluront:

Effectuer les préparations ainsi que les analyses des échantillons.
Effectue le contrôle de qualité ainsi que les maintenances sur les différents instruments.
Accomplis les activités en temps opportun en suivant les horaires établis.
Utilise un système informatique pour effectuer la collecte des données précises et détaillées.
Participe à la formation.
Assure l’intégrité des études et satisfait les exigences des agences réglementaires en exécutant les activités et recueillant les données conformément aux Bonnes Pratiques de Laboratoires (BPL), aux Procédures Normalisées d’Opération (PNO) et aux règles de santé sécurité.
Effectue toutes autres tâches connexes, telle qu’assignée.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études collégiales en sciences;
Une expérience connexe est un atout;
Une combinaison équivalente d’éducation et d’expérience peut être considérée comme substitut acceptable pour l’éducation et l’expérience spécifique telle qu’énumérée ci-dessus;
Avoir la capacité de travailler sous la contrainte de temps et de s'adapter aux changements;
Lire et écrire en anglais est requis. Le bilinguisme est préférable;
Faire preuve de flexibilité et être capable de travailler de manière autonome.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 20$/hrs avec prime de fin de semaine et possibilité de commencer à un niveau supérieur avec un salaire plus élevé avec une expérience spécifique en recherche;
Bonus annuel basé sur la performance;
Horaire: Mardi au Samedi de 8h00 à 16h15 PM;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Clinical Laboratory Technician (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Technician for our Clinical Laboratory department located in Senneville, you will perform technical activities and follow directives from the study/phase plan and the procedures. Your success will ensure the smooth running of our research, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Perform the preparation and the analysis of samples with the use of Advia, Sysmex, Cobas, Novus, Blood smear, microscopy, STA compact;
Perform the quality control procedure and maintenances on different instruments;
Perform the activities in a timely fashion by adhering to preset schedules;
Use a computer system for accurate and detailed data collection;
Ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the GLP, SOP and health and safety rules;
Perform all other related duties as assigned.

Key Elements

We are looking for the following minimum qualifications for this role:

College diploma in science;
Relevant experience is an asset;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Reading and writing English is required. Bilingualism is preferred;
Ability to work under time constraint and adapt to change;
Demonstrate flexibility and ability to work independently.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: 20$/per hour, evening premiums and opportunity to start at higher level and higher salary with specific research experience;
Schedule: Tuesday to Saturday (8h00-16h15);
Annual bonus based on performance;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Opérateur.trice de lave-cage (poste de jour) (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire de l'emploi

Opérateur.trice de Lave-Cage – Horaire de jour – Aucune Expérience nécessaire

En tant qu’Opérateur.trice de Lave-Cage pour notre équipe de Toxicologie à notre site de Sherbrooke, vous aurez la charge d’assurer la propreté des équipements utilisés pour maintenir les conditions de vie des animaux selon les plus hauts standards de bien-être de l'industrie.

Dans ce rôle, les principales responsabilités incluront:

Faire fonctionner et effectuer les vérifications quotidiennes des laves-cages.
Surveiller l’utilisation des savons et les besoins divers des lave-cages.
Nettoyer tous types d’habitation d’animaux ainsi que leurs accessoires (jouet, bouteille, bols, etc…).
Effectuer l’entretien de base sur toutes les cages et accessoires afin de s’assurer que tout est sécuritaire pour les animaux.

Éléments Clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Organisé et Autonome.
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).
Bonne compréhension de l’anglais écrit.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose.

Informations spécifiques au poste :

Localisation: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5;
Transport: Facilement accessible avec le transport en commun. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire : 17.75$/HR.
Horaire : Poste temps plein et permanent (37.5HR/semaine), selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaire. Travail de fin de semaine par rotation et Prime de quart (2.75$/hr).

Pourquoi Charles River?

3 semaines de vacances et des congés personnels.
Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire).
Accès à un programme d’épargne et de retraite qui comprend une contribution de l’employeur.
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne.
Gym gratuit sur place.
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine).

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe! C’est Votre Moment!

Pour plus d'information, consultez www.criver.com.

Supervisor Quality Assurance (Wayne, PA, US, 19087)

Job Summary

Supervise and provide support in the management of daily work flow operations of Quality Assurance (QA) staff. Ensure staff assignments are in alignment with regulatory inspection and reporting requirements.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Oversee daily operational activities/schedules and ensure QA resources are properly assigned to manage regulatory oversight.
Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures.
Review, revise and approve (GMP QA) SOPs, protocols/batch records, reports, and other quality and regulated records involving technically complex issues and processes for accuracy and compliance with all applicable regulations and internal policies.
Participate in the preparation and review of study and QA files in preparation for sponsor site visits and regulatory inspections; assure that QA audit files are retained.
Participate in client site visits and regulatory inspections.
Participate in the development of recommendations for corrective and preventative actions to respond to client visit and regulatory inspection findings.
Routinely provide recommendations to Regulatory Affairs and Compliance management for improvements in auditing of Quality Systems based on extensive knowledge and understanding of regulations and quality principles.
Perform data audits to assess that records are attributable, legible, contemporaneous, original, accurate, and in compliance with regulations, international standards, SOPs, protocols/batch records, and corporate policies and procedures as needed to support departmental workload.
May participate in inspections and audits of subcontractors, vendors, and suppliers of products and services.
Assure the suitability of materials and supplies for compliance with specifications (GMP QA).
Review and approve all procedures related to production and maintenance, approving or rejecting incoming materials, in-process materials and finished product (GMP QA).
As required, oversee maintenance of group training manual and training records.
May assist in development of departmental budget.
Responsible for personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development.
Support the policy of equal employment opportunity through affirmative action in personnel actions.
Provide regular direction and feedback on performance, disciplinary actions and preparing and delivering annual performance and salary reviews.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent, preferably in a life science or related discipline.
Experience: Minimum 5 years experience in a Quality Assurance role or a GLP environment including 1 year supervisory experience.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Knowledge of Microsoft Office applications (e.g. Word, Access, Excel). Must be able to comprehend regulations and guidance documents and apply critical thinking skills to evaluate requirements. Excellent judgment, decision-making, training/mentoring skills and verbal/written communication skills. Strong leadership, organizational skills and detail oriented. Able to prioritize workload and manage multiple tasks.

Compensation Data

The pay rate for this role is $90,000 - $94,500 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Technician I Process Evaluation (Wayne, PA, US, 19087)

Job Summary

Under direct supervision, responsible for performing daily laboratory tasks as they relate to Process Evaluation Testing Services.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Perform daily laboratory operations.
• Prepare materials and buffers used in projects.
• Maintain inventories of all supplies/buffers used in projects.
• Perform routine experiments, tests and procedures following well-defined guidelines.
• Maintain a safe working environment by adhering to Company policies and procedures.
• Follow all protocols, S0Ps, and cGMPs/cGLPs as they relate to specific tasks.
• Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline.
Experience: 0-1 years related experience in biological lab.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None
Other: Knowledge of cGMPs or regulatory affairs pertaining to the pharmaceutical and biological industries is preferred. Must possess excellent interpersonal skills to maintain communication across biological functional groups. Able to communicate effectively in a group or one on one setting. Basic Microsoft Office skills are a plus.

The pay range for this position is $23.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Biotechnicus (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Baan Samenvatting

Voor de afdeling Toxicologie zoeken wij een enthousiaste

Biotechnicus/Proefdierverzorger in het bezit van artikel 13F.

Afdeling:
Met meer dan 200 medewerkers voert de afdeling Toxicologie onderzoek uit naar de veiligheid van bestaande en nieuwe medicijnen en chemische stoffen. Kenmerkend voor het werk is de grote diversiteit aan projecten, teststoffen en opdrachtgevers.

Team:
We bestaan uit 2 gezellige en hardwerkende afdelingen voor grote en kleine dieren, onderverdeeld in teams van 10-30 medewerkers per team onder leiding van een teamleider, in Den Bosch en Schaijk. Alle teams zijn dynamisch en betrokken bij de afdeling en elk lid draagt op zijn/haar manier een steentje bij aan de werkzaamheden en de goede sfeer op de afdeling.
Op de afdeling zijn er trainers die o.a. de voortgang van de opleiding voor nieuwe medewerkers en nieuwe technieken faciliteren. Ook heeft ieder teamlid het beheer over een aantal neventaken die zij min of meer zelfstandig uitvoert, onder leiding van de teamleiders/TSH.
Binnen de teams werken de teamleden intensief met elkaar samen en verzorgen gezamenlijk het diverse scala aan type studies, aanwezig in de faciliteit, van begin tot einde.

Over je rol:
Als beginnend biotechnicus bij Charles River verzorg je samen met je collega’s alle onderdelen die een dierstudie met zich meebrengt. Een belangrijk onderdeel hiervan is de dagelijkse verzorging en het verzorgen van het algemeen welzijn van alle dieren onder jouw verantwoordelijkheid. Daarnaast besteed je ook veel tijd en aandacht aan het aanleren van alle veel voorkomende handelingen, technieken en metingen die uitgevoerd worden binnen iedere studie. Hierbij sta je ook in nauw contact met studieleiders, dierenartsen en andere afdelingen.

Na een terdege, interne opleiding in alle basisvaardigheden, word je opgeleid tot coördinerend biotechnicus. Je bent medeverantwoordelijk voor meerdere, soms complexe studies die lopen op de afdeling en andere neventaken. Samen met je collega’s zorg je voor het dierwelzijn en een correcte uitvoer van alle werkzaamheden op de afdeling.

Weekenddiensten zijn een vast onderdeel van je werk en zal je elke paar weken ingedeeld worden hiervoor.

Primaire verantwoordelijkheden:
•   Je werkt op een prettige en constructieve manier samen met je directe collega’s, TSH, teamleiders en trainers. Je houdt je aan de gestelde regels.
•   Je werkt onder GLP (Good Laboratory Practice) en bewaakt de kwaliteit van je werk.
•   Je bewaakt de kwaliteit van dierwelzijn, en voldoet hiermee aan de AAALAC eisen en wet- en regelgeving rondom het gebruik van proefdieren.

Wat is vereist:

MBO of HBO werk- en denkniveau en een artikel 13F;
Beschikbaarheid van 32-40 uur per week, hiernaast werk je ook elke maand een aantal uren in weekenddienst en ben je ook bereid tot af en toe overwerk.
Je bent prettig in de omgang, durft je uit te spreken en bent een echte teamspeler.
Daarnaast kun je ook goed zelfstandig werken en je verantwoordelijkheden nemen voor je eigen werk.
Je zorgt dat alle processen soepel verlopen, je kan inspelen op veranderingen, vragen van collega's en andere afdelingen.
Je kunt snel schakelen tussen diverse werkzaamheden en prioriteiten stellen binnen het team en alle studies.
Je wil graag proactief meedenken in procedures en verbeteringen doorvoeren.
Flexibiliteit en stressbestendigheid is een pre.

Wat bieden we jou:
Wij bieden uitstekende primaire en secundaire arbeidsvoorwaarden waaronder:

27,5 vakantiedagen en 2 collectieve dagen per jaar;
Mogelijkheid tot de aankoop van 10 extra vakantiedagen per jaar;
Jaarlijks eenmalig 8% vakantiegeld van je bruto jaarsalaris;
Jaarlijks eenmalige uitkering op basis van het bedrijfsresultaat;
Reiskostenvergoeding á 0,23 cent per kilometer met een max. van 250 netto per maand, of een NS-Businesscard;
Fiets(lease)plan;
Collectief pensioen met een eigen bijdrage van 2.9%;
Bedrijfsfitness;
De mogelijkheid om samen met collega’s te sporten op ons eigen sportveld;
De mogelijkheid tot een consult van onze in house ergonoom;
Elke dag gratis vers fruit.

Heb je vragen over deze vacature?

Voor verdere informatie over de functie kun je contact opnemen met Maaike Verrijt via her-recruitment@crl.com of reageer direct via onze werken bij website: Charles River Laboratories, Inc. Jobs (criver.com)  

Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld  

Over Safety Assessment

Over Charles River

Meer informatie vindt u op www.criver.com.

Cage Wash Operator (Day Shift) (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Cage Washer Operator – Day shift – No experience necessary.

As a Cage Washer Operator for our Toxicology team in Sherbrooke, you will be responsible for ensuring the equipment used to maintain the animal’s living conditions is cleaned according to the highest wellbeing standards in the industry.

In this role, key responsibilities include:

Operating and performing daily checks on cage washer machines.
Monitor the use of soaps and various needs of the cage washers.
Clean all types of animal housing and accessories (cage, toys, bowl, waterbottle, etc…)
Perform basic maintenance on all cages and accessories to ensure that everything is safe for the animals.

Key Elements

If you possess the following qualifications, we will train you in the rest:

Organized and self-driven.
Being able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).
Understanding of written English.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role specific information:

Location: 1580 rue Ida-Métivier, Sherbrooke (Fleurimont), QC, J1E 0B5;
Transportation: Easily accessible using Sherbrooke’s public transit system. Free parking. Electric vehicle charging station;
Salary: 17.75$/hrs
Schedule: Full time, permanent position (37.5 hours/week), depending on the needs, you may have to do overtime. Weekend work (rotation) and bonus ($2.75/hour).

Why Charles River?

3 weeks’ vacation & Personal days.
Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage).
Access to a savings and retirement program that includes an employer contribution.
Excellent welcome program for new employees as well as in-house advancement and career development opportunities.
Access to a doctor and various health professionals (telemedicine).
Free gym on site.

If you want to contribute to the wellbeing of our communities across the country and around the world, join our team. This is Your Moment!

Equal Employment Opportunity

For more information, please visit www.criver.com.

Commis au lave-cage (Laval, Quebec, CA, H7V 4B3)

Sommaire de l’emploi

En tant que Commis au lave-cage pour notre équipe de Toxicologie à notre site de Laval, vous serez responsable du bien-être de tous nos animaux de recherche en gardant leur habitation propre. Votre réussite assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce poste, les principales responsabilités incluront:

Faire fonctionner et effectuer les vérifications quotidiennes des lave-cages;
Surveiller l’utilisation des savons et les différents besoins des lave-cages;
Nettoyer tous types d’habitation d’animaux ainsi que leurs accessoires;
Effectuer l’entretien de base et les réparations mineures sur toutes les cages et accessoires afin de s’assurer que tout est sécuritaire pour les animaux;
Au besoin, effectuer des tâches de manutention dans le vivarium.

Éléments clés

Si vous possédez les qualifications suivantes, nous vous formerons pour le reste:

Posséder un bon esprit d’équipe;
Polyvalence;
Bonnes aptitudes de communication et d’observation;
Apte à travailler physiquement (soulever jusqu’à 20kg, marcher, rester debout, s’accroupir, etc.).

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au rôle:

Localisation : 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transport : Stationnement gratuit. Près du métro Montmorency. Borne de recharge pour voiture électrique;
Salaire : 18$/hrs;
Primes : Soirée (2.50$), fin de semaine (2.75$), heure supplémentaire (temps et demi), fériés (temps double);
Bonus annuel basé sur la performance;
Horaire : Horaire flexible, vous devez être disponible de jour et de soir. Selon les besoins de l’entreprise vous pourriez avoir à effectuer du temps supplémentaires ainsi que des fins de semaine;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Formations de développement payées;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances & 5 jours de congé personnel/maladie par année;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Cage-Wash Clerk (Laval, Quebec, CA, H7V 4B3)

Job Summary

As a Cage-Wash Clerk for our Toxicology team located in Laval, you will be responsible for the well-being of our laboratory animals by keeping their living space clean. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Operate and perform daily checks on cage washer machines;
Monitor the use of soap and various needs of the cage washers;
Clean all type of animal housing and accessories;
Perform basic maintenance and minor repairs on cages and accessories;
Perform manutention tasks in the vivarium as required.

Key Elements

If you possess the following qualifications, we will train you in the rest:

Be a good team player;
Polyvalence;
Good observations and communications skills;
Able to work physically (lift up to 20 kg, walk, stand, stoop, etc.).

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 445 Boul. Armand-Frappier, Laval, QC, H7V 4B3;
Transportation: Free parking. Near the Montmorency Subway. Electric vehicle charging station;
Salary: $18/hrs;
Premiums: Evening ($2.50), Weekend ($2.75), Overtime (Time and a half), Holidays (Double time);
Annual bonus based on performance plan;
Schedule: Flexible schedule, you must be available days and evenings. Depending on the needs, you may have to do overtime and weekends;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Paid development training;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ vacation & 5 Personal/Sick day per year;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Automation Equipment Technician 1 (Charleston, SC, US, 29407)

Job Summary

Charles River Labs located in Charleston, SC is looking for a Automated Equipment Technician for our Microbial Solutions business.

The Automated Equipment Technician is responsible for the maintenance, upkeep, and proper functioning of all Production automation and associated equipment. This role ensures that production goals can be met by maintaining the automated production line in proper working condition through both preventative maintenance and repair / replacement of components.

Job Duties

Full knowledge of production lines as well as other production equipment.
Perform and document scheduled, routine maintenance on all production equipment.
Support Class 100 fill operations using automated and manual equipment.
Coordinate professionally with outside vendors that calibration/maintenance of equipment is performed on time and the impact to Production is minimal.
Troubleshoot, maintain and repair mechanical and electrical controls as well as pneumatic and hydraulic systems.
Responsible for proficiency with all SOP’s in areas of the department and documentation as required by FDA, company policy and cGMP.
Perform all other related duties as assigned.
After hours and weekend work may be required.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) in sciences or electronics or closely related technical field. Trade school graduate or equivalent.
Experience: 5 years or more experience working on Production automation and related systems, preferably in a pharmaceutical- type environment.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Other:

Laboratory experience, operation of production equipment, proficient with Microsoft Office products, and familiar with CAD tools a plus.
Must be capable of working from and understand equipment manuals, specifications, mechanical drawings, electrical schematic and ladder logic displays.
Advanced ability to troubleshoot equipment with but not limited to: Direct Logic PLC, Rockwell Automation, AC/DC Drive Systems, robotic programming and diagnostics (Robotic Systems).

Compensation Data

The pay range for this position is $28/hr - $29.25/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

For more information, please visit www.criver.com.

Customer Service Team Lead (Charleston, SC, US, 29407)

Job Summary

The Customer Service Team Leader oversees and provides direction to the Microbial Solutions, North American, Customer Service team.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Supervisory Duties
⦁ Oversee daily operational activities and training for a group of non-exempt employees. Ensure optimum group performance.
⦁ Coordinate activities of customer service department to ensure efficient and timely availability of product.
⦁ Resolve all customer disputes, including counseling Customer Service staff in dispute resolution, complaint memos, and Trackwise cases.
⦁ Establishes and maintains close working relationships with the customer, Account Managers, Key Account Managers, Customer Service Representatives, and other support resources
⦁ Supports management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing feedback and coaching on performance, preparing reports and KPIs for annual performance reviews.
⦁ May assist in development of departmental budget.
⦁ Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
⦁ Coordinate vacation/time off schedules.
⦁ Ensure optimum performance of group function. Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.

Functional SME Duties
⦁ Maintain records in SAP and generate reports. Work with Global Supply Chain team to provide sales forecast. Interact with accounting to provide sales reporting information required for SOX compliance.
⦁ Act as backup for sign off requirements
⦁ Work with Accounts Receivable to resolve discrepancies in billing and customer accounts
⦁ Perform UAT, Integration, and Regression testing prior to implementation of new processes within platforms
⦁ Provide post go-live production support in Salesforce and SAP
⦁ Assist with inter and intra-company orders

These responsibilities are in addition to the basic requirements of a Customer Service Representative.
⦁ Perform customer service functions, including processing orders, providing documentation (e.g., health certificates), and communicating availability of product to customers, telephoning/emailing/faxing quotes/delivery/product information, and order confirmations.
⦁ Ensure coordination between Customer Service, freight forwarders and domestic carries to ensure efficient and timely delivery of product.
⦁ Work closely with global distributers for accurate and timely allocation of products.
⦁ Perform all other related duties as assigned.

Job Qualifications

⦁ Education: Bachelor’s degree (B.A./B.S.) or equivalent in Business or related discipline.
⦁ Experience: 2-3 years related experience with a Bachelor’s degree or 4-6 years related experience in customer service or business.
⦁ Experience using SAP ECC Order Management and Salesforce Service Cloud and/or ServiceMax
⦁ An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
⦁ Certification/Licensure: None
⦁ Other: Supervisory and dispute resolution skills; excellent verbal and written communication skills; computer skills.

PHYSICAL DEMANDS:
⦁ Regularly operates a computer and other office productivity machinery, such as a calculator, copy machine, and computer printer.
⦁ Must occasionally move about inside the office to access file cabinets, office machinery, etc.
⦁ Regularly provides information to and receives information from/through various technologies, media, sources and contacts. Must be able to accurately exchange accurate information in these situations.

WORK ENVIRONMENT:
⦁ General office working conditions
⦁ The noise level in the work environment is usually quiet.

Comments:
⦁ This position requires occasional domestic travel.

Compensation Data

The pay range for this position is $55,000 to $58,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

For more information, please visit www.criver.com.

Alternance : Technicien de Toxicologie - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

Choisir Charles River Evreux, c’est intégrer un site unique de 500 personnes dans la province Normande, dans un environnement scientifique en constante évolution, ayant pour objectifs l'avancée de la recherche et le bien-être animal.

L’équipe

L’équipe de Toxicologie regroupe environ une vingtaine de personnes. Elle assure les techniques demandées dans le cadre des études scientifiques et est garante du bon report des tâches réalisées, dans le suivi des Bonnes Pratiques de Laboratoire (BPL).

Votre quotidien

•   Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsables, conformément aux bonnes pratiques de laboratoire, aux procédures standards, à la charte éthique, aux protocoles d’études et au règlement intérieur,
•   Réaliser les traitements, assurer le suivi de l’état clinique et l’évolution pondérale des animaux,
•   Procéder à des prélèvements sanguins, d’urine ou de fèces,
•   Saisir l’intégralité des actes réalisés sur informatique,
•   Assurer la qualité des données recueillies et de résultats,
•   Transmettre à votre supérieur hiérarchique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Pourquoi nous rejoindre ?

Vous êtes étudiant en Bac+2 dans le domaine de la biologie médicale (BTS BMB, Anabiotech...) et vous recherchez un contrat d’apprentissage avec des missions opérationnelles et polyvalentes.
Vous êtes dynamique, et êtes reconnu pour vos capacités d’organisation et votre proactivité.
Vous voulez obtenir une expérience enrichissante au sein d’un groupe International, leader dans le domaine de la santé.

Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Lab Technician Necropsy (Den Bosch (S-Hertogenbosch), NL, 5231 DD)

Al meer dan 75 jaar werken de medewerkers van Charles River samen om te helpen bij het ontdekken, ontwikkelen en veilig maken van nieuwe geneesmiddelen. Wanneer u bij onze familie komt, heeft u een belangrijke impact op de gezondheid en het welzijn van mensen over de hele wereld. Of uw achtergrond in levenswetenschappen, financiën, IT, verkoop of een ander gebied is, uw vaardigheden spelen een belangrijke rol in het werk dat we uitvoeren. In ruil hiervoor helpen wij u een carrière op te bouwen waar u over gepassioneerd kunt voelen.

Vacature: Medewerker Necropsy (mbo/hbo-niveau)
Locatie: Den Bosch of Schaijk
Uren: Fulltime

Vind jij het interessant hoe het lichaam van dieren in elkaar zit? Werk je graag met je handen in een team waar hard wordt gewerkt, maar ook ruimte is voor gezelligheid? Dan hebben wij een leuke baan voor jou!

Wat ga je doen?
Als medewerker op de sectiekamer start jouw werkdag om 07:30 uur. Je voert secties uit op verschillende diersoorten. Dit gebeurt volgens vaste richtlijnen (GLP) en altijd zorgvuldig, want kwaliteit is erg belangrijk. Je werkt vooral praktisch, maar ongeveer één keer per week heb je een administratieve dag waarbij je gegevens controleert en verwerkt. Je wordt ook opgeleid tot studieverantwoordelijke en zorgt hierbij voor een goed verloop van de studie en het naderhand nakijken van de data.

Je werkzaamheden bestaan onder andere uit:
Voorbereidende werkzaamheden voor de secties
Het uitvoeren van secties en het macroscopisch beoordelen van de organen
Het nakijken en controleren van ruwe data
Samenwerken met collega’s, trainers en je teamleider

Geen dag is hetzelfde en je krijgt volop de kans om te leren en jezelf te ontwikkelen!

Wie ben jij?

Je hebt een mbo of hbo-diploma richting biotechniek, paraveterinair of proefdierkunde (met mogelijkheid tot het behalen van artikel 13F)
Je werkt graag samen, maar ook zelfstandig
Je vindt het belangrijk om netjes en precies te werken
Je bent flexibel en leergierig
Je maakt makkelijk contact met collega’s

Wat bieden wij jou?

Een leuke en afwisselende baan in een enthousiast team van 22 collega’s
27,5 vakantiedagen + 2 collectieve vrije dagen
Mogelijkheid om 10 extra vakantiedagen per jaar bij te kopen
Vakantiegeld (8%) én een bonus afhankelijk van het bedrijfsresultaat
Reiskostenvergoeding (€0,23 per km tot max. €250 p/m), of een NS-Businesscard
Fiets(lease)regeling
Bedrijfsfitness
Pensioenregeling met lage eigen bijdrage
Gratis fruit op het werk
Sportmogelijkheden op ons eigen sportveld

Interesse?
Heb je vragen? Neem gerust contact op met Janneke Basten via 06-38857962.

Wil je direct solliciteren? Dat kan via onze website:
Charles River Laboratories Jobs: https://www.criver.com

Over Safety Assessment
Charles River helpt zijn partners bij het versneld uitvoeren van preklinische geneesmiddelontwikkeling dankzij uitstekende programma's voor veiligheidsbeoordeling, de allernieuwste voorzieningen en deskundig advies op het gebied van wet- en regelgeving. Van individuele gespecialiseerde toxicologie- en “IND enabling”-onderzoeken tot pakketten op maat en complete laboratoriumondersteuning: ons ervaren team kan programma's ontwerpen en uitvoeren die anticiperen op problemen en obstakels uit de weg gaan, voor een probleemloze en efficiënte ontwikkelingsgang naar de markt. Bij onze Safety Assessment-vestigingen lopen jaarlijks zo'n 120 programma's voor experimentele nieuwe geneesmiddelen (investigational new drugs [IND's]).

Over Charles River
Charles River is een organisatie die op contract onderzoek naar vroege fasen verricht (CRO). Wij hebben op ons fundament van proefdieren, geneeskunde en wetenschap voortgebouwd om een brede portefeuille van discovery- en veiligheidsbeoordelingsdiensten te ontwikkelen (zowel Good Laboratory Practice (GLP) als non-GLP) en onze cliënten te helpen, van de inventarisatie van targets tot preklinische ontwikkeling. Charles River levert tevens een verzameling producten en diensten die tegemoetkomen aan de behoeften van onze cliënten op het gebied van klinisch laboratoriumonderzoek en productieactiviteiten. Dankzij deze brede portefeuille van producten en diensten kunnen onze cliënten een flexibeler model voor geneesmiddelontwikkeling creëren, wat de kosten verlaagt en de productiviteit en effectiviteit verhoogd zodat producten eerder op de markt gebracht kunnen worden.

Met meer dan 20.000 medewerkers bij 90 vestigingen in 20 landen wereldwijd zijn wij strategisch gepositioneerd voor het coördineren van wereldwijde middelen en kunnen wij multidisciplinaire inzichten inzetten om de unieke uitdagingen van onze cliënten op te lossen. Onze cliënten omvatten farmaceutische multinationals, biotechnologiebedrijven, overheidsinstellingen en medische en universitaire instellingen over de gehele wereld.

Bij Charles River zijn wij gepassioneerd over onze rol bij de verbetering van de levenskwaliteit van andere mensen. Onze missie, onze uitstekende wetenschap en onze doelgerichte instelling werken door in alles wat we doen, en we gaan elke dag opnieuw aan de slag met de kennis dat ons werk de gezondheid en het welzijn van vele mensen helpt te verbeteren. Wij zijn trots te kunnen zeggen dat wij een rol hebben gespeeld bij de ontwikkeling van circa 85% van de geneesmiddelen die in 2021 door de Amerikaanse FDA werden goedgekeurd.

Bij Charles River Laboratories herkennen en werven wij talenten. Wij zijn een bedrijf dat zich inzet op het gebied van diversiteit en gelijkheid en we werken op inclusieve wijze.

Meer informatie vindt u op www.criver.com.

Operaio addetto gestione animali (PERUGIA) - ven/sab/dom (MILANO, Milano, IT, 20122)

Riepilogo del lavoro

Di cosa si occupa la Charles River

Alla Charles River, promuoviamo con convinzione il nostro ruolo nel miglioramento della qualità di vita delle persone. In tutto ciò che facciamo, siamo guidati dalla nostra missione, dalle nostre eccezionali competenze scientifiche e da una grande risolutezza e affrontiamo ogni giorno con la consapevolezza che il nostro lavoro contribuisce al benessere e al miglioramento della salute di molte persone in tutto il mondo. Abbiamo orgogliosi di aver collaborato allo sviluppo dell' 80% dei farmaci approvati dalla FDA negli ultimi cinque anni.

Per ulteriori informazioni, visita il sito www.criver.com.

Operaio addetto gestione animali (PERUGIA) - ven/sab/dom (MILANO, Milan, IT, 20122)

Job Summary

Per cliente sito in Perugia ricerchiamo un operaio stabularista

La risorsa sarà inserita all'interno del team operante nella struttura e si occuperà di svolgere le mansioni relative alla gestione dello stabulario

Effettuare la sostituzione degli alloggiamenti e garantire adeguato benessere;
Effettuare la pulizia dei locali ed il lavaggio delle attrezzature;
Fornire supporto nella preparazione delle attrezzature;
Fornire supporto nella gestione/movimentazione dei materiali;
Utilizzo di apparecchiature e carrelli

Job Qualifications

Buona capacità comunicativa e di lavoro in team
Disponibilità a lavoro part-time nelle giornate di venerdì - sabato e domenica

Di cosa si occupa la Charles River

In Charles River Laboratories, riconosciamo e reclutiamo tutti i talenti. Siamo un'azienda che favorisce la diversità e l'inclusione e lavoriamo quotidianamente in questa direzione.

Per ulteriori informazioni, visita il sito www.criver.com.

Scientific Support - Associate (Ashland, OH, US, 44805)

Job Summary

Perform QC review of study data and perform room inspections. Monitor and track common errors and assist with document medication to reduce error and deviations. Assist with implementing and monitoring quality control (QC) standards, methods, and procedures.

Essential Duties & Responsibilities:

Assist in monitoring quality control standards, methods, and procedures.
Monitor and track common deviations and problem documentation.
Perform general QC practices.
Assist in recommending form and SOP modifications, and changes to standard protocol wording to avoid deviations.
Assist in maintaining and revising QC documents, processes and manuals.
Assist in reviewing deviations.
Perform QC reviews of study data.
Perform room inspections.
Perform other duties as assigned.

Job Qualifications

Education:

High school diploma, or General Education Degree (GED) required.
Associate’s Degree in scientific discipline preferred.

Experience:

No previous experience required.
One- or two-years related experience in GLP environment preferred.
Previous and broad QC or QA experience preferred.
Knowledge and/or background in preclinical technical functions also preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None

Other:

Demonstrated leadership and word processing skills.
Effective written, verbal and communication skills.

Physical Demands:

While performing the duties of this job, the employee is regularly required to talk, hear and work/type at a computer.
Walking and standing for periods of up to 1 hour.
Specific vision abilities required by this job include close vision and the ability to adjust focus.
Must be able to communicate with other personnel regarding all aspects of a study.
Regularly provides information to and receives information from/through various technologies, media, sources and contracts.
Must be able to accurately exchange accurate information in these situations.

Work Environment:

General office working conditions.
The noise level in the work environment is usually low to moderate.
While performing the duties of this job, the employee occasionally is required to ear protective clothing (lab coat, shoe covers, safety glasses) when entering laboratory areas.

The pay range for this position is $19-22/hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Veterinary Technician Assistant I (Worcester, MA, US, 01608)

Job Summary

We are seeking a Veterinary Technician Assistant for our Discovery site located in Worcester.

The Veterinary Technician Assistant will assist veterinary staff in the documentation and triage of all laboratory animal health cases. Also responsible for daily health observations, preventative health care, environment enrichment and handling and restrain of laboratory animals. In addition, this individual will may also perform technical in-life procedures.

ESSENTIAL DUTIES:

Assist veterinary staff in the documentation and triage of all animal health cases noted by technical staff and/or Veterinarians.
Perform routine veterinary technical and husbandry skills including the following:
- Generate animal treatment records and perform treatment distribution
- Administration of various therapeutic measures by IM, SQ, topical, oral routes, etc. o Proficient animal restraint techniques.
- Observe basic care animals o Daily walk through of animal rooms
- Participate in colony management (new NHP processing, TB testing, collection of biological samples, routine health monitoring, etc.)
- Animal observations, reporting abnormalities
- Perform animal follow-ups as needed
Monitor animal heath, visually and by following detailed schedules.
Maintain accurate record keeping procedures for the veterinary department May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.
May assist in surgical pack preparation and cleaning of surgical instruments. Assistance in acclimation and behavior management of animals in our care.
Provide environmental enrichment for laboratory animals according to facility and Federal guidelines.
Assist in keeping inventory and stocking the vet rooms (i.e. drugs and supplies).
Assist in organizing and maintaining the vet exam rooms.
Record keeping of required logs.
Triage and recheck non-USDA covered species.

The pay range for this position starts at $22 to $24 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

MINIMUM QUALIFICATIONS:

Education: High School Diploma or G.E.D.
Experience: 1-2 years related experience in a laboratory animal facility. related experience working with animals in pre-clinical laboratory or clinical setting; experience working with a CRO with multi-species preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: ALAT preferred
Other: None.

PREFERRED QUALIFICATIONS:

LVT license or CVT/RVT certification.
AALAS certification.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Animal Care Technician I (Chicago, IL, US, 60637)

Job Summary

We are seeking an Animal Care Technician I for our Insourcing Solutions site in Chicago, IL

In the Animal Care Technician role, you will perform daily animal health observations, as well as animal husbandry duties to include water bottle/line and cage checks, provide food/water, and perform cage changes and/or clean cages all to maintain the quality and health of research animals.

Additional responsibilities include:

Maintain accurate records of things like animal breeding, as well as housing or support areas, and you may also be tasked with receiving, inspection, and housing of incoming animals.
Assist with restraint, handling, and manipulation of animal species, and you may become involved in the animal breeding and weaning procedures.
Other duties may include monitoring personnel and equipment entry into various rooms, operating required equipment and general housekeeping, when required.

Job Qualifications

The following are minimum requirements related to the Animal Care Technician I position:

Bachelor’s degree or high school diploma with 1 year of animal care/handling required. Interest in achieving ALAT certification upon eligibility.

The pay range for this position is $17.00 - $19.80 per hour. Please note that salaries vary within the range based on factors including experience, skills, education, certifications, and location.

For more information, please visit www.criver.com.

Facilities Technician I (Rockville, MD, US, 20850)

Job Summary

The Facilities Technician I is responsible for maintaining the facility in good operating and physical condition, as well as responding to normal and emergency service calls, and taking corrective action via diagnosis and repairs. As directed, conducts/oversees preventive maintenance. The Facilities Technician I will be required to perform a wide range of repair, maintenance, and escorting tasks.

Key Responsibilities and Duties:

· Perform routine GMP spaces cleaning

· Maintain stock of consumables (HVAC filters, cleaning supplies, etc)

· Perform routine simple maintenance and repair throughout the facilities, such as repairing cosmetic damage

· Oversee building utility systems equipment maintenance to ensure expected conditions in the facility. This may include HVAC, electrical, water (domestic and DI), compressed gasses, and controlled temperature storage systems.

· Recognize and correct potential safety hazards to avoid injuries

· Support building personnel by insuring the availability of water, gasses, and electrical, as well as furniture requests, office relocations, and general accommodations to assist employees with their work duties

· Paint & caulk small areas when paint or wall surface has become damaged

· Support general cleaning & housekeeping efforts as required. Pallet removal as needed from building

· Maintain relationship and coordination with janitorial contractor for non-lab domestic cleaning of facility

· Process/Manufacturing equipment support, ensuring written record keeping, and forms are completed as required

· Conduct systems rounds as required

· Check and confirm process gasses are at service pressure daily

· Move/relocate laboratory equipment as directed

· Work with the engineering personnel to handle process equipment needs

· Required to review relevant documentation for accuracy and completeness i.e., suite cleaning documentation

· Replace light bulbs as required

· Employ safe work practices

· Engage and inspire others

· Comprehends all duties assigned and performs responsibilities in absence of Manager when needed

· Other responsibilities as needed

Job Qualifications

· Associate degree in science preferred, or High School Diploma or GED with 0-3 years of prior work experience in the Biotechnology Industry in a GMP Facilities setting

· Proficiency with Microsoft Office including Word, Excel, PowerPoint, and Teams. Maintain Calendar(s)

· Possess the willingness to learn new concepts to fully understand aseptic techniques and demonstrate proper clean-room behavior

· Excellent interpersonal and communication skills

· Detail-oriented and demonstrate the ability to perform highly detailed work

· Excellent organizational, multitasking, and problem-solving skills

· Able to accurately perform basic math calculations, including time conversion, fractions, decimals, and percentages

· Availability - Overtime work and schedule changes are required to meet business needs. Holiday, weekend, and night work will also be required based on manufacturing schedule. On-call as business needs arise

· Reliable mode of transportation to travel between sites in the Rockville area

· Able to work standing, bending, stooping, pulling, pushing, sitting, and reaching overhead for long periods of time

· Able to work around various cleaning chemicals that produce non-hazardous odors like bleach and vinegar

· Able to wear appropriate gowning covering most parts of the body and face. (Gowning Qualification)

· Able to lift, push, and pull 50 lbs.

· Use of basic hand tools

· Use multimeter

· Work from height not to exceed 10’

· Confined spaces could be encountered

· Work in heat and cold as required

· Climb ladders

Compensation Data

The pay range for this position is $22.00 - $24.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Anesthésiste de recherche (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant qu’Anesthésiste de recherche pour notre équipe de Médecine & Chirurgie des Animaux de Laboratoire à notre site de Senneville, vous assurerez une anesthésie sécuritaire aux animaux pour un large éventail de chirurgie et de procédures. Votre contribution assurera la santé de nos animaux, ainsi que l’intégrité de nos études pré-clinique.

Dans ce rôle, les principales responsabilités incluront:

Effectuer diverses procédures et soins préopératoires et postopératoires comprenant la préparation des salles de chirurgie, les injections et la surveillance de l’anesthésie;
Assurer l’entraînement adéquat et approprié du personnel technique sur les sujets reliés à l’anesthésie;
Supporter les différents départements en offrant de la surveillance des procédures anesthésiques sur les études, des conseils et de l’expertise technique;
Fournir une excellente collaboration aux chirurgiens de recherche et au personnel soutenant la chirurgie.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes:

Diplôme collégial en Santé animale, en Bioécologie ou toutes autres disciplines en lien avec la Science animale;
Baccalauréat en Biologie ou autres disciplines reliées;
Bonnes aptitudes d’observation et de communication;
Capacité à travailler en équipe et à s’adapter aux changements.

Prendre note que dès votre embauche vous devrez vous soumettre annuellement à un test de tuberculose aux frais de l'entreprise.

Informations spécifiques au rôle:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 23$/hrs;
Bonus annuel basé sur la performance;
Horaire: 2 types d’horaire disponible après la formation.
- Du lundi au vendredi entre 7h00 et 15h15;
- Possibilité d’avoir un horaire condensé à temps plein à 4 jours par semaine entre 7h00 et 17h15;
- Vous devrez aussi faire une rotation de fin de semaine une fois par mois;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Research Anesthetist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Research Anesthetist for our Laboratory Animal Medicine & Surgery team in Senneville, you will provide safe anesthesia to animals for a wide range of surgeries and procedures. Your contribution will ensure the health of our animals, as well as the integrity of our pre-clinical studies.

In this role, primary responsibilities include:

Perform various preoperative and postoperative procedures and care including surgery room preparation, injections, and anesthesia monitoring;
Provide adequate and appropriate training of technical staff on anesthesia related topics;
Help support to different departments by providing anesthesia procedures oversight on study, technical advice, and expertise;
Provide excellent collaboration to research surgeons and staff supporting surgery.

Key Elements

We are looking for the following minimum qualifications for this role:

College Diploma in Animal Health, Bioecology or any related Animal Science discipline;
Bachelor’s degree in Biology or any related discipline;
Good observations and communication skills;
Able to work in a team environment;
Ability to adapt to changes.

Please note that upon being hired, you will have to undergo an annual tuberculosis test at the expense of the company.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: $23/hrs;
Annual bonus based on performance;
Schedule: 2 types of schedules available after the training
- Daytime Monday to Friday, 7:00 am to 3:15 pm;
- Possibility to have a condensed full-time schedule, 4 days per week between 7:00 am to 5:15 pm;
- You will also have to do a weekend rotation once a month;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Cuidador/a Animalario MAD (Madrid, M, ES, 28029)

Durante casi 75 años, los empleados de Charles River han trabajado juntos para ayudar en el descubrimiento, el desarrollo y la fabricación segura de nuevas terapias con fármacos. Cuando se une a nuestra familia, tendrá un impacto significativo en la salud y el bienestar de las personas en todo el mundo. Ya sea que su experiencia sea en ciencias de la vida, finanzas, TI, ventas u otra área, sus habilidades desempeñarán un papel importante en el trabajo que realizamos. A cambio, te ayudaremos a construir una carrera que puedas sentirte apasionada.

Charles River Laboratories España, S.A., empresa dedicada a la investigación y desarrollo experimental en biotecnología, necesita incorporar CUIDADORES/AS DE ANIMALARIO en Madrid.

• Jornada laboral de 40 h de lunes a viernes.

• Contrato laboral temporal por suplencia. Duración en función de la suplencia a cubrir.

• Incorporación inmediata.

• Formación remunerada a cargo de la empresa

Descripción de tareas

• Tareas de mantenimiento de animales con fines experimentales (cambio de jaula, rejilla y cobertor)

• Revisión de comida, agua y lecho

• Revisión del estado general de salud de los animales

• Desinfecciones de material de estabulación (racks ventilados, cabinas de cambio, jaulas, cobertores, etc.)

• Procesado de material de estabulación

• Mantenimiento de stocks de material en el área asignada

• Mantenimiento de registros ambientales (Tª, humedad, ciclos de luz, etc.)

• Mantenimiento de registros de tareas diarias según protocolos de trabajo

• Desinfección de salas de estabulación, pasillos, almacenes, zona de lavado, etc.

Requisitos

Experiencia 3 meses. Experiencia mínima de 3 meses, aunque formamos a nuestro propio personal.
Título CFGM
Técnico/a superior anatomía patológica y citodiagnóstico
Idioma español
Competencias / conocimientos: se valorará acreditación para funciones A y B o formación como ATV (asistente técnico veterinario)

Acerca de Charles River

Charles River es una organización de investigación por contrato (CRO) en fase temprana. Hemos ampliado nuestra oferta sobre la base de la medicina y ciencia con animales de laboratorio para desarrollar una cartera diversificada de servicios de descubrimiento y evaluación de la seguridad, tanto por medio de buenas prácticas de laboratorio (GLP) como sin ellas, para apoyar a los clientes desde la identificación de los objetivos hasta el desarrollo preclínico. Charles River también proporciona una serie de productos y servicios para apoyar las necesidades de pruebas de laboratorio clínico y actividades de fabricación de nuestros clientes. El uso de esta extensa cartera de productos y servicios permite a nuestros clientes para crear un modelo más flexible de desarrollo de fármacos, lo cual reduce sus costes y mejora su productividad y eficacia, logrando así incrementar la velocidad con la que llega al mercado.

Con más de 20,000 empleados en 90 centros de 20 países alrededor del mundo, nos encontramos posicionados estratégicamente para coordinar recursos internacionalmente y aplicar perspectivas multidisciplinarias de modo de resolver los desafíos únicos de nuestros clientes. Nuestra base de clientes incluye compañías farmacéuticas globales, compañías de biotecnología, agencias del gobierno, así como hospitales e instituciones académicas alrededor del mundo.

En Charles River, sentimos pasión con respecto al rol que cumplimos en mejorar la calidad de vida de las personas. Nuestra misión, nuestra ciencia de excelencia y nuestro fuerte sentido de propósito nos guía en todo lo que hacemos, y afrontamos cada día sabiendo que nuestro trabajo ayuda a mejorar la salud y el bienestar de muchas personas alrededor del mundo. Hemos apoyado con orgullo el desarrollo de ~85 % de los fármacos aprobados por la FDA en 2021.

En Charles River Laboratories, reconocemos y contratamos a todos los talentos. Somos una empresa comprometida con el principio de la diversidad y la inclusión y trabajamos diariamente en esta dirección.

Charles River España está comprometido con una política a favor de la integración y el empleo continuo de las personas con discapacidad. Todos nuestras vacantes están abiertas a trabajadores con discapacidad y se les dará especial consideración en los procesos de selección.

Para más información, visite www.criver.com.

Zootecnia de vivarios de investigación - Colaborador 1 1 (Madrid, M, ES, 28029)

Durante 75 años, los empleados de Charles River han trabajado juntos para ayudar en el descubrimiento, el desarrollo y la fabricación segura de nuevas terapias con fármacos. Cuando se une a nuestra familia, tendrá un impacto significativo en la salud y el bienestar de las personas en todo el mundo. Ya sea que su experiencia sea en ciencias de la vida, finanzas, TI, ventas u otra área, sus habilidades desempeñarán un papel importante en el trabajo que realizamos. A cambio, te ayudaremos a construir una carrera que puedas sentirte apasionada.

Resumen de trabajo

Acerca de Microbial Solutions

Nuestro grupo de negocios Microbial Solutions posee una exclusiva y completa cartera de productos y servicios de pruebas de endotoxinas, detección microbiana e identificación microbiana, que ha sido diseñada específicamente para cumplir con las necesidades complejas y siempre cambiantes de la industria. Ayudamos a los clientes a asegurar la seguridad y calidad del producto con soluciones de pruebas fáciles de usar pero robustas que satisfacen los requisitos regulatorios, apoyan el proceso de toma de decisiones críticas y mejoran las eficiencias operacionales.

Acerca de Charles River

Con más de 20,000 empleados en 110 centros de 20 países alrededor del mundo, nos encontramos posicionados estratégicamente para coordinar recursos internacionalmente y aplicar perspectivas multidisciplinarias de modo de resolver los desafíos únicos de nuestros clientes. Nuestra base de clientes incluye compañías farmacéuticas globales, compañías de biotecnología, agencias del gobierno, así como hospitales e instituciones académicas alrededor del mundo.

En Charles River, sentimos pasión con respecto al rol que cumplimos en mejorar la calidad de vida de las personas. Nuestra misión, nuestra ciencia de excelencia y nuestro fuerte sentido de propósito nos guía en todo lo que hacemos, y afrontamos cada día sabiendo que nuestro trabajo ayuda a mejorar la salud y el bienestar de muchas personas alrededor del mundo. Hemos apoyado con orgullo el desarrollo del 80% de los fármacos aprobados por la FDA en los últimos cinco años.

Para más información, visite www.criver.com.

Manager Virology Scientific Support (Wayne, PA, US, 19087)

Job Summary

Responsible for the management of a team dedicated to scientific development and assay optimization as it pertains to the Virology laboratory. Will provide operational supervision, technical support and professional and scientific expertise, as needed, to ensure operational excellence.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Planning and ensuring on-time delivery of client projects.
Lead the development, qualification and validation of new assays that meet industry expectations and current regulatory guidelines. As Virology Subject Matter Expert, provide guidance for resolution of technical problems affecting Virology assays.
Oversees the optimization of existing Virology assays and their life cycle management, which will include monitoring to assess the need for subsequent requalification.
Support and manage the technical transfer of in vitro Virology assays.
Work with Sales to identify and fill gaps in Virology testing.
Partner with Business Development in providing and reviewing pricing and proposals, and provide excellent service to clients.
Act as a liaison with other departments to ensure that any method development appropriately aligns with Virology processes and subsequent routine testing.
Supports other operational areas in relation to virus based work, as needed, by providing guidance for R&D.
Participate in client technical calls to assist with Virology assay development or trouble shooting.
Supervise technical staff and perform personnel management activities such as: scheduling, personnel actions (hiring, promotions, transfers, etc.), training and development, providing regular direction and feedback on performance, disciplinary actions, time and vacation approval and preparing and delivering annual performance and salary reviews.
Develop and maintain departmental systems and SOPs. Maintain compliance of operating documents through review and revision as required by SOPs. Assist in the development and communication of departmental policies and procedures.
Participate in and support cross-functional communication and laboratory activities, as necessary.
Assist in the development of the departmental budget, including resource allocations and needs, and authorize expenditures.
Ensure adherence to pertinent regulatory requirements and to departmental policies.
Perform all other related duties as assigned.
With respect to all Virology assays and tests, the manager assures that:
Study or assay protocols are approved as provided by applicable regulatory requirements and that the protocols are followed.
All experimental data, including unanticipated observations, are accurately recorded and verified.
Unforeseen circumstances that may affect the quality and integrity of the study are noted when they occur, and corrective action is taken and documented.
Test systems, including reagents, live cells, equipment or other materials are as specified in the protocol.
All applicable good laboratory or manufacturing practice regulations are followed, as applicable.
All raw data, documentation, protocols, specimens, and final reports are transferred for archiving during or at the close of the study.

Job Qualifications

Education: Bachelor's degree or equivalent in biology or a related discipline. Master's degree preferred.
Experience: Minimum of 4-5 years related laboratory experience in Virology or related field.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Demonstrated leadership skills required. Working knowledge of cGMPs or regulatory requirements pertaining to the pharmaceutical and biotechnology industries required.

PHYSICAL DEMANDS:

May have exposure to potential chemical, electrical, biological and waste-handling hazards.
Must regularly operate a computer and other office machinery (i.e., calculator, copy machine, and computer printer).
Regularly moves about to access file cabinets, equipment, and personnel.
Ability to observe laboratory test results using a microscope to differentiate shapes, colors and other qualitative properties.

WORKING ENVIRONMENT:

General office and laboratory working conditions.
Laboratory working conditions may occasionally require wearing personal protective equipment, including but not limited to: goggles, face shield, surgical mask, cap, gloves, scrubs and/or shoe covers.
Work with or near toxic or caustic chemicals and biological agents including potential biohazards. Possible exposure to fumes or airborne particles.

Compensation Data

The pay range for this position is $105,000-$110,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

Competencies

Lead - We lead when we advocate our purpose and model our values, when we deliver innovation, when we embrace change, and when we appreciate and celebrate the great work of others.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

Alternance : Technicien de Toxicologie Non-Rongeurs - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

L’équipe

Votre quotidien

Pourquoi nous rejoindre ?

Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Alternance : Technicien de Laboratoire en Immunologie - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

L’équipe

L’équipe d'Immunologie regroupe environ 15 personnes. Elle assure la réalisation des techniques d’Immunologie, dans le respect des normes des Bonnes Pratiques de Laboratoire (BPL).

Votre quotidien

•   Réaliser progressivement certaines techniques de laboratoire comme des dosages ELISA, des développements de méthode mais aussi des études de cultures cellulaires comme Elispot dans le cadre d’études dites de Cells based assays,
•   Assurer la saisie informatique des résultats et leurs conformités,
•   Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,
•   Lire les protocoles, avenants et notices en anglais.

Pourquoi nous rejoindre ?

Vous êtes étudiant en Bac+2/3 dans le domaine de la Biologie et vous recherchez un contrat d’apprentissage avec des missions opérationnelles et polyvalentes.
Vous êtes dynamique et proactif et recherchez une expérience avec beaucoup de technique.
Vous voulez obtenir une expérience enrichissante au sein d’un groupe International, leader dans le domaine de la santé.
Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

•   Rémunération : Selon convention
•   13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté,
•   Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
•   Accord de modulation 35h,
•   Convention collective de l’industrie pharmaceutique, groupe : 2
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Alternance : Technicien de Laboratoire en Analyses Physico-Chimiques - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

L’équipe

L’équipe d'Analyse Physico-Chimique regroupe environ 7 personnes. Elle assure la réalisation des techniques d’Analyses Physico-Chimiques, dans le respect des normes des Bonnes Pratiques de Laboratoire (BPL).

Votre quotidien

•   Recherches bibliographiques pour l'établissement du protocole d'étude,
•   Formations aux différentes techniques d'analyses (SEC-UV, UHPLC-UV, UV,etc....),
•   Développement et mise en place des méthodes génériques,
•   Réalisation d'une étude (test du protocole d'étude et des méthodes génériques).

Pourquoi nous rejoindre ?

Vous êtes étudiant en Bac+2/3 dans le domaine de la chimie Analytique et vous recherchez un contrat d’apprentissage avec des missions opérationnelles et polyvalentes.
Vous êtes dynamique, et êtes reconnu pour vos capacités d’organisation et votre proactivité.
Vous voulez obtenir une expérience enrichissante au sein d’un groupe International, leader dans le domaine de la santé.
Vous voulez bénéficier d'un véritable parcours d'intégration et formation dispensé par des experts techniques et scientifiques au sein de notre environnement BPL.

Les Modalités

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Scheduler I (Reno, NV, US, 89511)

Job Summary

The pay range for this position is $20.50 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

We are seeking an experienced Scheduler (Technical Operations) for our Safety Assessment site located in Reno, Nevada.

The Scheduler schedules all protocol-required tasks for in-life studies, ensuring proper placement of employees into specific study activities based on competency and responsibilities. Additionally, schedule employee department and global trainings, and manage the department level study schedule and resources.

The following are minimum requirements related to the Scheduler position.

Associate’s degree (A.A./A.S.) or equivalent in scientific support/administrative or related discipline.
2 years of related experience in a laboratory or research environment. Previous experience in a GLP environment preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Ability to interact with all levels of staff and sponsors. Strong communication and interpersonal skills and attention to detail. Proficient in the use of word processing, spreadsheet and database desktop applications.

About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet

Head of CSD (Sulzfeld, Bavaria (Bayern), DE, 97633)

Wir suchen ab sofort eine/n

Head of CSD (kaufmännische/r Angestelle/r) (m/w/d)

in Vollzeit

für unsere Niederlassung in 97633 Sulzfeld

DAS SIND IHRE AUFGABEN:

Planung und Koordination von Kundenprojekten
- - Leitung des Customer-Service-Department-Teams am Standort Sulzfeld
  - Spezialwissen zur Logistik in Deutschland und EU-weit
  - Aufbereitung, Informationssammlung und Analyse über europäische Logistik
  - Effiziente Fehlerbehebung und Optimierungen in SAP und anderen angewandten unterstützenden IT-Tools

DAS BRINGEN SIE MIT:

Abgeschlossene kaufmännische Ausbildung
Sie verfügen über mindestens 5 Jahre Berufserfahrung im Bereich Customer Service

Sie haben Spaß an der Kundenbetreuung
Sie bringen Erfahrung in SFDC und E-Commerce-Plattformen mit sowie im Bereich Zoll und Logistik
Sie sind offen für Arbeiten in großen Netzwerken auf internationaler Ebene
Sie sind zuverlässig, belastbar, flexibel, verantwortungsbewusst und teamfähig
Sie beherrschen die englische Sprache in Wort und Schrift
Der versierte Umgang mit Microsoft Office (Excel, PowerPoint, Word) sowie mit SAP und Inventarmanagementsystemen wird vorausgesetzt
Hohe Resilienz
Wünschenswert wären Personalführungserfahrung und Versiertheit bei Behördenkontakten

DAS BIETEN WIR:

eine ausführliche und betreute Einarbeitung
eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team mit Raum für Kreativität
ein internationales Arbeitsumfeld
attraktive Fort-/Weiterbildungsangebote
ein wettbewerbsfähiges Vergütungspaket
zahlreiche soziale Leistungen und Zuschüsse

Sie sind interessiert?

Dann freuen wir uns über die Zusendung Ihrer ausführlichen Bewerbungsunterlagen an:

Charles River Laboratories, Research Models and Services, Germany GmbH

Personalabteilung, Sandhofer Weg 7, 97633 Sulzfeld

Email: BewerbungenRMS@crl.com , www.criver.com

Vorabinfos unter: 09761-40611

Über Research Models & Services

Über Charles River

Weitere Informationen finden Sie unter www.criver.com.

In Vivo Technician I (Spencerville, OH, US, 45887)

Job Summary

We are seeking an In Vivo Technician I for our In Vivo Team at our Safety Assessment site located in Spencerville, OH.

A Technician I is in training to perform and become proficient in on-boarding tasks, procedures, and cooperating in a team environment. The technician is learning basic tasks required to conduct a study, which may include collecting and recording data in the performance of studies. Responsible for handling and restraining animals, clinical observations, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. The technician is working under close supervision to gain proficiency

Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed:

Ensure good welfare and humane care for all animals worked with through gentle, positive human-animal interactions.
Train in on-boarding tasks which may include animal handling, sexing, and restraint on multiple species as well as feeding, watering, husbandry of multiple species. Clinical observations, acclimation observations, and body weight determination on multiple species as well as qualitative and quantitative food consumption. Specific tasks will be based on each area’s training plan and business needs.
Collect, document, review, and verify data on forms, or in electronic data capture systems.
Review documentation of functions performed as part of quality control requirements.
Use and maintain instrumentation and equipment.
Perform all other related duties as assigned.

The pay for this position is $19/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High school diploma or General Education Degree (G.E.D.) preferred. Associate (A.A./A.S.) or Bachelor’s degree (B.A./B.S.) or equivalent in a biological science, desired.
Experience: No previous experience required.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None, unless required by local government.
Excellent written and verbal communication skills. Knowledge of English.
Ability to manage multiple tasks and priorities to achieve goals.
Computer skills (e.g., Microsoft Office Suite), commensurate with essential functions, including the ability to learn a validated system.
Ability to ensure that a safe working environment is maintained by observing all safety procedures and working methods by making proper use of protective clothing and equipment, and by reading, understanding, and following all safety documents issued or notified of.
Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory Practices (GLP), Standard Operating Procedures (SOP), Business Operating Procedures (BOP) and the Institutional Animal Care and Use Committee (IACUC) rules.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts, sometimes on short notice.
Ability to work under specific time constraints.

Physical Demands:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 50 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require, talking, hearing, standing or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus

WORK ENVIRONMENT:

Work in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Sample Management Technician 1 1 1 1 (Reno, NV, US, 89511)

Job Summary

Perform a wide variety of basic laboratory support tasks. Perform routine maintenance on basic laboratory equipment. Prepare all materials required for reagent receipt and storage. Compile required documentation and package reagents for shipping. Assist in the maintenance of general laboratory supply inventory and reagents within the Laboratory Sciences group.

Job Qualifications

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Perform all tasks in compliance with Good Laboratory Practice Regulations (GLPs), Good Clinical Practice Regulations (GCP), and Standard Operating Procedures (SOPs).
• Perform all other related duties as assigned.
• May generate reports, data, and forms.
• Maintain and perform record keeping.
• Review data recorded by others for quality control.
• May record observations and measurements for basic lab/research tasks
• Perform clerical duties (e.g.: filing, making copies, etc.).
Lab maintenance
• Perform routine laboratory maintenance of lab equipment.
• Remove biohazard and recycle waste from lab to appropriate locations for disposal.
• Wash and dry laboratory supplies and distribute to appropriate locations within the laboratory.
• Label tubes, devices and containers and perform laboratory set-up/clean-up
• Monitor and stock lab supplies in assigned areas.
Outgoing shipment preparations
• Help to prepare materials and data for shipment and archiving.
• Package biological reagents and ensure accurate completion of all required documentation for the shipment (i.e.: verify shipping lists).
• Prepare shipping documentation and assist in preparation of CITES permits as needed. Fax shipping documentation to sponsors as needed.
• Prepare domestic and international packages according to applicable guidelines.
• Deliver packages to a carrier/shipper as needed.
• Handle all details required for shipment of reagents (receiving, storage, inventory and verification) using Study protocol or Sponsor guidance documents

QUALIFICATIONS:
• Education: High school diploma or General Education Degree (G.E.D.) required.
• Experience: none
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: None.
• Other: Must be detail oriented and have general familiarity with lab procedures. Good verbal and written communication skills required. Basic computer skills; familiarity with Microsoft Office and Excel software. Ability to organize and prioritize work and meet timelines.

The pay range for this position is $19.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Supervisor, InVivo Operations (Stilwell, KS, US, 66085)

Job Summary

We are seeking an supervisor to join our Integrated Toxicology (ITox) team at the Kansas Site.  This site is the first of its kind, bridging CRL’s Discovery and Safety Assessment business units, while bringing automation to standard lead optimization toxicology study models to deliver rapid study results to our clients.  When you join our team, you will have a significant impact on the health and well-being of people across the globe. This role will be responsible for the oversight of in-vivo operations staff and all daily functions to support animal care and study execution. They will provide, coordinate, document, and schedule routine and highly complex training activities for In-Life, Animal Care, and Cage Wash personnel. This individual will also be responsible for defining a new technical training plan, in alignment with the global program, that includes developing, revising, and implementing the use of training documents and processes. They will also provide leadership and/or support of new hire orientation.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Provide guidance in the day-to-day activities of assigned departmental employees to ensure accurate, high-quality work, and adherence to pertinent departmental policies, practices, and procedures (SOPs, safety procedures and biosafety protocols). Ensure schedule is prepared daily, accurately reflecting required tasks and workload. Serve as a model as it relates to effective time management, communication, and utilization of resources.
Perform technical tasks to support completion of study tasks (as needed).
Lead and mentor less experienced training personnel.
Work with department management to coordinate and facilitate multi-species technical training at all levels of complexity for department personnel.
Maintain and update all documents and databases used for the support and conduct of training tasks, including but not limited to training standards, training records, training timelines, and proficiency standards.
Provide oversight, scheduling, and coordination of training animal use to enable optimal learning while prioritizing animal care and welfare.
Practice/maintain advanced technical skills and procedures, work independently, and follow operating procedures and processes.
May conduct sponsor/visitor tours and interact with clients.
Provide input/review of new, and/or revised processes, operating procedures, training standards, quizzes, proficiency standards, and other training documents.
Assist in facilitating, coordinating, and scheduling new hire orientation and on-the-job training for personnel.
Participate in recruiting efforts by assisting in interviews and selecting qualified non-exempt level departmental personnel.
Assist in the scheduling, coordination, and execution of study procedures.
24/7 emergency duty coverage as assigned.
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in scientific related discipline.
Experience: 4-6 years related experience in animal science, biology, chemistry/pharmacy, or similar lab environment.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: AALAS certification ALAT/LAT level strongly preferred; or other applicable certification/licensure.
Other: Demonstrated advanced technical and analytical skills. Effective communication and leadership skills. Ability to handle a variety of laboratory animals. Proficient in technical skills and the operation of data collection equipment. Knowledge of GLPs and other federal regulations and guidelines relating to the care of laboratory animals required. Understanding of basic, intermediate, and complex study design and protocols. Ability to organize and prioritize work to meet deadlines. Computer literacy including word processing, spreadsheet, and database programs.

PHYSICAL DEMANDS:

Employees must be able to lift, move, manipulate, and/or hold heavy objects up to and including 25 pounds; this includes work materials, equipment, and/or animals.
Must be able to perform procedures, which require, talking, hearing, standing, or sitting for long periods of time, entering data into a computer, using appropriate instruments, reaching with hands and arms, working in narrow spaces, and wearing safety equipment (PPE) according to OSHA regulations and company standards.
Must be able to frequently firmly hold species while utilizing fine motor skills.
Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

WORK ENVIRONMENT:

Works in a research environment, which requires use of sharp objects, working around mechanical parts, working with or near known or unknown toxic or caustic chemicals and/or biological hazards, exposure to fumes and airborne particles, working at noise levels ranging from moderate to loud.
The employee regularly works with live animals with risk of exposure to allergens, zoonotic disease, and biohazards.
The noise level in the work environment ranges from low to high depending upon the species housed.

Comments:
This position requires overtime, weekend, holiday, and/or after hours shift coverage, as needed.

The pay range for this position is $70-75k/year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Maintenance Electrician (Tranent, GB, EH33 2NE)

Job Summary

A Maintenance Electrician vacancy now exists within the Building/Workshop department based in Tranent. This is a permanent full-time role. This role is to carry out Electrical Maintenance, repairs and installation under the direction and supervision of the Electrical Supervisor or Senior Engineer.

Applicants Must Have:

Qualified Electrician which must include 18th Edition Wiring Regulations
You must have a full, clean drivers licence and your own transport
Previous experience working as a Maintenance Electrician
To be able to participate in overtime as is reasonably required to ensure the smooth running of the department.
To be available on a rota basis for emergency callouts out of hours
Ability to interact with peers effectively
Ability to adopt a methodical approach to work
Able to interact and communicate professionally with internal and external clients
Able to deal with people at all levels
Ability to work within a team
Great customer care skills
Ability to work to tight timescales
Adopt a can-do attitude

Key Responsibilities:

To carry out an electrical repair and maintenance service to Charles River Laboratories sites.
To carry out installation of electrical and computer wiring and systems to IEE regulations.
To carry out portable appliance testing and maintenance of records.
To maintain electrical equipment.
To advise scientific staff on use of electrical apparatus and systems.
To monitor room temperatures and conditions, calibration of temperature and humidity sensors/equipment.
To alter room controls.
To participate in Generator Testing and restart equipment.
To liaise and make themselves familiar with Plant Engineer duties.
To liaise with service engineers.
To maintain any necessary legible record of work carried out.
Fault finding and diagnostic testing.
Work on high voltage equipment (if qualified).

Please ensure that if you are successful for this position, you are fully able to make your own travel arrangements to and from work during normal working hours and for overtime hours at the weekend, evenings and early mornings.

Salary for this role £40,000 per annum. You will also be expected to participate in the on-call rota. You will receive an on-call allowance, and the details of this will be provided to you, once you commence in post. In the event that the call-out arrangement or your participation therein ceases for any reason, then the payment will be discontinued. The payment will not be included in your salary for pension purposes.

Profile and Requirements

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Technicien de laboratoire en Histologie - F/H - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Pathologie recrute un Technicien en Histologie pour intégrer son équipe composée de 33 techniciens.

Les missions 

Au sein du Département Pathologie, vous aurez pour principales missions sous la responsabilité du responsable d’équipe :

Réaliser les techniques de laboratoire en Histologie (colorations histologiques, techniques de fabrication de lames de routine ou d’immunohistochimie…),
Assurer la réalisation des autopsies pour toutes les espèces utilisées dans le cadre de nos études,
S’assurer de la conformité des résultats obtenus,
Assurer la saisie informatique des résultats,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 type DUT/BUT dans le domaine scientifique.

Vous maitrisez l’anglais scientifique (compréhension écrite)

Vous savez faire preuve d’autonomie mais vous appréciez également le travail en équipe

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.
Contact avec les animaux.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
CDD de 09 mois
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 400 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien de laboratoire en Immuno-Histo-Chimie - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le service d'Immunohistochimie recrute un Technicien pour intégrer son équipe composée de 10 techniciens.

Les missions 

Au sein du service d'Immunohistochimie, vous aurez pour principales missions sous la responsabilité de la responsable d’équipe :

Effectuer les opérations nécessaires à la conduite des tâches ou des études dont vous êtes responsable, conformément aux bonnes pratiques de laboratoire, aux procédures standards et aux protocoles d’études,
Réaliser progressivement certaines techniques de laboratoire en histologie (colorations histologiques, techniques de fabrication de lames de routine ou d’immunohistochimie…),
S’assurer de la conformité des résultats obtenus,
Lire les protocoles, avenants et notices en anglais,
Assurer la saisie informatique des résultats,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail,

En contact avec notre équipe de Vétérinaires Pathologistes :

Effectuer la digitalisation des lames : digitalisation, mise à disposition aux pathologistes et archivage,
Réaliser la digitalisation en fluorescence,
Préparer et envoyer des disques durs,
Réaliser de l’analyse d’images (développement & validation & application algorithmes, compilation des résultats, mise en forme et partage),
Construire des banques de lames pour de l'analyse d’images.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 dans le domaine scientifique (type BUT Génie Biologique).

Vous possédez idéalement une première expérience professionnelle dans le domaine.

Vous possédez une aisance relationnelle et un sens du contact et du service.

Vous êtes organisé(e) et vous appréciez le travail en équipe.

Votre anglais est opérationnel ; vous êtes à l’aise à l’écrit et à la compréhension scientifique.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 415 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté, accord de télétravail, ...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Technicien de Laboratoire en Génomique - H/F - CDD 9 mois (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Le département de Biologie Moléculaire recrute un Technicien de Laboratoire en Génomique pour intégrer son équipe composée de 17 techniciens.

Les missions 

Au sein du Département Biologie Moléculaire, vous aurez pour principales missions sous la responsabilité du responsable d’équipe :

Réaliser progressivement certaines techniques de laboratoire : extractions d’acides nucléiques, dosages quantitatifs et qualitatifs, réalisation de PCR,
Assurer la saisie informatique des résultats et leurs conformités,
Lire les protocoles, avenants et notices en anglais,
Transmettre au scientifique et/ou au directeur d’études les informations concernant tout événement survenant au cours du travail.

Qualifications souhaitées

Vous êtes titulaire d’un BAC+2/3 type DUT/BUT dans le domaine de la Biologie Moléculaire.

Vous maitrisez l’anglais scientifique (compréhension écrite).

Vous savez faire preuve d’autonomie mais vous appréciez également le travail en équipe.

Vous êtes rigoureux(se), vous respectez les délais, les procédures et les consignes.

Conditions spécifiques du poste

Annualisation des heures : plage horaire standard (35H00) avec possibilité d’horaires décalées en fonction des roulements et du service.

Les modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 24 000 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de l'évaluation de sécurité

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2019.

Alternance : Chargé de Missions RH - F/H (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Au sein du service RH, vous serez accompagné par l'équipe sur différentes missions, afin de découvrir et pratiquer plusieurs facettes de ce domaine de métier.

Les missions

Accompagner l'équipe sur différents pôles : Stratégie RH, Relations Sociales, GEPP, Recrutement, Formation, Administration du personnel,
Participer à la mise en place d'accords collectifs,
Alimenter la Base de Données Economiques et Sociales,
Mettre en place le Bilan Social,
GEPP : Mettre à jour la cartographie des métiers, les career ladders...,
Agir sur le pilotage de la mise en place de nouveaux process, et projets (logigrammes, etc),
Autres tâches diverses.

Qualifications souhaitées

Vous êtes en études de Master I ou II en Ressources Humaines et recherchez une alternance au sein d'un groupe international, reconnu mondialement.

Vous maitrisez l’anglais, à l’écrit comme à l’oral.

Vous êtes reconnu pour votre communication, votre goût du challenge et votre gestion des priorités.

Modalités

13ème mois, Indemnités de transport, intéressement/ participation, Accord d’ancienneté

Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE

Accord de modulation 35h

Convention collective de l’industrie pharmaceutique, groupe : 3

Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Electronic Technician - Hybrid (Charleston, SC, US, 29407)

Job Summary

We are seeking an experienced Electronic Technician, for our Microbial Solutions site located in Charleston, SC.

The Electronic Technician’s primary role is testing, troubleshooting, repairing, performing preventative maintenance, and calibrating Microbial Solutions instruments. The Electronic Technician must be able to troubleshoot to the component level. Support of our Field Technicians and production staff is included in this position. They must be able to operate test equipment including DVM’s, oscilloscopes, and soldering irons. All associated paperwork as required by cGMP and FDA, along with updates to our database are also part of the responsibilities. We are seeking a motivated individual with good communication skills and attention to detail. Your ability to handle these tasks in a timely manner will be a major part of meeting the service needs of our customers.

The following are the job duties & responsibilities related to the Electronic Technician:

Administer test, trouble shoot and repair electronics to the component level.
Understand and read schematics.
Mechanically assembly and disassemble new and existing equipment
Perform and operate on test equipment and solder equipment when needed.
Create, develop and continuously improve SOP’s pertaining to the PTS and MCS machines.
Able to analyze situations and apply own judgment when accessing mechanical problems, independently.
Coordinate scheduling and support department personnel in the absence of the PTS Engineer.
Responsible for proficiency in all SOPs in areas of responsibility.
Responsible for documentation as required by company policy, cGMP and FDA.
Support and serve as second back-up to Technical Services by loading software, calibration of new equipment and ensuring proper packaging of new equipment.
Perform and assess data entry in software program in order to track machine repairs.
Interpret past repairs on PTS and MCS machines, historically, in order to resolve and diagnosis new machine issues.
Perform all other related duties as assigned.

Job Qualifications

The following are minimum requirements related to the Electronic Technician position.

Education: Associates Degree(A.S) in Electronic Engineering Technology, or related discipline
Experience: 0-1 years related experience in a regulated environment.
Computer literacy with Windows Office Suite programs including data entry and tracking.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

The pay range for this position is $25.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Senior Project Manager CMC (Rockville, MD, US, 20850)

Job Summary

The Senior CMC Project Manager leads project execution after deal closure. Responsible for directing, leading, and motivating multi-disciplinary project teams, project managers, and hold team members accountable to deliver results within an agreed project governance structure to ensure customer satisfaction throughout the life of the projects. Holistically plans all projects at any stage through mapping resource across projects.

In this role, the Senior CMC Project Manager is the key interface between Business Development and Operations organizations and the customer. The Senior CMC Project Manager manages multiple projects, either within one technology or within multiple technologies, and oversees the complete life cycle of all the projects while managing a team of project managers.

Key Responsibilities and Duties:

Direct project manager and project's scope, timelines, budget, and Project profitability
Raise and prepare scope changes and communicate them to a customer in close collaboration with Business Development
In collaboration with Business Development, create mid-long-term Project strategies
Define, organize and be responsible for all customer communication (using an open communication model), agreeing on milestones and conducting "lessons learned" with the customer, as well as executing decommissioning at the end of contractual activities
Ensure the right and effective internal and external governance are in place and are effective. Also ensure very clear alignment of internal stakeholders
Responsible to ensure flawless and smooth execution of assigned contracted Projects according to defined timelines and cost, via leading multidisciplinary project teams
During execution, key focus is on the customer centricity and internally on quality, cost, profitability, timelines, and risk management
Manage Project budgets and material cost
Additional duties as requested

Job Qualifications

Bachelor's degree (B.A./B.S.) or equivalent in project management, business, biological sciences, or related discipline with Life Sciences technical background, or equivalent experience. Master's Degree preferred
Minimum of 5 years of experience in project management
Experience in biologics manufacturing, preferably in viral vector production
PMP Certification required and experience in a CRO/CMO preferred
Previous technical competency in the areas of the Biologics Industry e.g., process development, cGMP manufacturing, process registration, analytical science, Quality Assurance etc.
Strategic, operational, and technical project management experience
Proven business awareness and commercial acumen
Record of accomplishment of successfully managed projects and personnel
Leadership and motivational skills to maintain naturally high moral within the Project management team
Ability to communicate effectively at all levels across the organization. Has strength of character to have difficult conversations with senior stakeholders including customers, internal team members and senior management; excellent written, verbal, and presentation skills
Pragmatic, organized, and results-oriented and with ability to manage multiple priorities
Excellent planning, organizational, and controlling skills
Problem solving skills - ability to analyze using critical thinking and solve complex issues that do not have routine solutions
Skilled with Microsoft Project, Teams, and other automated presentations

Compensation Data

The pay rate for this role is $100,000 - $140,000 per year. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Data Coordinator - Reporting Services 1 (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a Data Coordinator for our Reporting Services team at the Senneville location, you will be responsible for providing the scientists with the information necessary for them to be able to write the summary and results sections of their reports, based on individual and summary data included in the appendices, tables and graphs customized to meet client specific reporting requirements.

In this role, primary responsibilities include:

Coordination of all pertinent data and scientific interpretation information in accordance with the Study Plan to enable the correct tabulation to be included in the report;
Transcribe data from hand-written data records and/or, process computer-generated data files, into formats suitable to meet sponsors’ needs;
Prepare finished reports, tables and/or graphs, that are clear and professionally presented as per Company requirements and guidelines;
Processing of reports or tabulated data, which are accessed either electronically or from hard copy sources following specific e-file management criteria involving the use of various software;
Ensure work is compliant with applicable guidelines and regulations.

Key Elements

We are looking for the following minimum qualifications for this role:

High School diploma;
Previous experience in Sciences or Information Technology;
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above;
Knowledge of computer skills including Microsoft Office applications (e.g. Word, Access, Excel);
Ability to work under time constraints, in order to respect deadlines;
Ability to work in a team environment.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging;
Salary: 18.50$/hrs;
Annual bonus based on performance;
Schedule: Day shift from Monday to Friday, flexible schedule with possibility to work remotely;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.

Coordonnateur.trice des données (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

En tant que Coordinateur.trice des données pour notre équipe de Services de rapport située au site de Senneville, vous serez responsable de fournir aux scientifiques l’information nécessaire pour qu’ils puissent écrire les sections de sommaire et résultats de leurs rapports basés sur les données individuelles et sommaires incluses dans les annexes, les tables et les graphiques adaptés afin de rencontrer les exigences spécifiques des clients.

Dans ce poste, les principales responsabilités incluront:

Coordination de toutes les données pertinentes et de l’interprétation scientifique des informations en fonction du plan d’étude pour permettre une tabulation adéquate pouvant être incluse dans un rapport;
Transcrire des données à partir d'enregistrements de données manuscrites et/ou traiter des fichiers de données générés par ordinateur dans des formats adaptés aux besoins des sponsors;
Préparer des rapports, des tableaux et/ou des graphiques finis, clairs et présentés de manière professionnelle conformément aux exigences et aux directives de l'entreprise;
Traitement des rapports ou de données tabulées, lesquels sont accessibles par sources électroniques ou par documents imprimés suivant les critères de gestion de l’e-file impliquant l’utilisation de divers logiciels;
S’assurer que le travail est conforme aux directives et réglementations applicables.

Éléments Clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

Diplôme d’études secondaire;
Expérience précédente en sciences ou en technologie de l’information;
Une combinaison équivalente d’éducation et d’expérience peut être considérée comme substitut acceptable pour l’éducation et l’expérience spécifique telle qu’énumérée ci-dessus;
Maîtrise des compétences informatiques notamment des logiciels de la suite Microsoft Office (par exemple Word, Access, Excel);
Être en mesure de gérer son temps efficacement, afin de respecter les échéanciers;
Capacité à travailler en équipe.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 18.50$/hrs;
Bonus annuel basé sur la performance;
Horaire: De jour du Lundi au Vendredi, horaire flexible et possibilité de télétravail;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Technicien de laboratoire en Pharmacie - F/H - CDD 9 mois (Evreux, FR, 27930)

Résumé du travail

Qui sommes-nous ?

Le poste

Au sein du département Pharmacie et dans une équipe composée de 22 collaborateurs, vous aurez pour objectif de vous assurer de la préparation des produits pour nos études.

Les missions

Etudes :

Réaliser tous les types de préparations galéniques (solutions, suspensions, remplissage de gélules, etc…) suivant les spécifications des dossiers d’études, des procédures et des BPL pour tous types d’études,
Réaliser les prélèvements d’échantillons de préparations galéniques et leur stockage, pour la réalisation d’analyses,
Mesurer les densités des substances d’essai, véhicule et formulation,
Livrer les substances d’essai ou les préparations galéniques aux services demandeurs sur notre site, selon le planning de livraison,
Assurer l’enregistrement des nouveaux lots de véhicules dans le système informatique,
Maintenir le matériel et les locaux propres à son poste de travail.

Documentation/Données :

Assurer l’acquisition des données d’études dans un environnement BPL,
Créer et /ou contrôler les conditions de préparations des études en cours dans le système informatique.

Conditions spécifiques du poste 

Prise de poste le matin (aux environ de 7h30)

Travail le week-end et jours fériés

Qualifications souhaitées

Vous êtes titulaire d’un Bac +2/Bac +3 idéalement spécialisé dans la formulation scientifique.

Vous maitrisez l’anglais, à l’écrit comme à l’oral.

Vous êtes rigoureux, ponctuel et assidu.

Vous possédez un bon esprit d’équipe.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 415 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté, accord de télétravail,...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Expert en Pharmacologie de Sécurité - F/H- CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Au sein du Département de Toxicologie, agir en tant qu’Expert de la pharmacologie de sécurité auprès de nos équipes et de nos clients, auprès du site d’Evreux et de Lyon.

Les missions

En tant qu’Expert Scientifique :

-   Agir comme un mentor auprès de l’équipe de Directeurs d’études, et assurer de la formation,
-   Participer à la rédaction d’articles, de posters, intervenir lors de congrès,
-   Conseiller nos clients sur les aspects scientifiques.

En tant que Directeur d’Etudes :

- Être responsable de la rédaction des plans d’études et modifications qui peuvent y être apportées,
-   Assurer le suivi, le respect du plan, en lien avec les services qui sont concernés. Apporter des corrections sur certaines procédures si besoin,
-   Veiller à la bonne réception et enregistrement des données d’études,
-   Réaliser l’interprétation des résultats et rédiger le rapport d’études,
-   Maintenir le lien avec le client pendant tout le suivi de l’étude,
-   Dans le cas d’études multisites, assurer le lien avec les différents services et responsables impactés (Pourra être nommé Responsable Principal d’Essai dans le cas d’études multisites).

Qualifications souhaitées

Vous êtes titulaire d’un Doctorat en Pharmacologie et avez idéalement 5 années d’expérience en pharmacologie de sécurité ou en toxicologie.
Avoir travaillé sur des études cardiovasculaires serait un atout pour ce poste.
Vous êtes bilingue en anglais, à l’écrit comme à l’oral.
Vous êtes reconnu pour votre relationnel, notamment clients ainsi que votre capacité de gestion de crises.

Modalités

•   Convention collective de l’industrie pharmaceutique, groupe : 7
•   Contrat : Cadre forfait jours
•   Salaire : A compter de 50 000 € bruts / an sur 13 mois
•   Prise en charge de la mutuelle à 100%, restaurant d’entreprise, CSE
•   Primes de transport, d’intéressement/participation, accord de télétravail,...
•   Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

Charles River est une organisation internationale de recherche de phase initiale sous contrat (ORC). Nous avons tiré parti de nos solides fondations dans le domaine de la médecine et de la science vétérinaire de laboratoire pour créer un portefeuille diversifié de services d'évaluation de découverte et de sécurité, conformes aux bonnes pratiques de laboratoire et autres, dans le but d'apporter à nos clients un soutien complet, de l'identification de cible au développement pré-clinique. Charles River propose également une gamme de produits et de services à l'appui des besoins en matière d'essais cliniques en laboratoire et des activités de fabrication de ses clients. Ce portefeuille considérable de produits et de services permet à nos clients de créer un modèle de développement de médicament plus flexible réduisant leurs coûts, accroissant leur productivité et améliorant leur efficacité, pour une mise sur le marché plus rapide.
Avec plus de 20 000 collaborateurs sur 90 sites dans 20 pays, nous sommes positionnés stratégiquement pour coordonner des ressources mondiales et appliquer des perspectives pluridisciplinaires à l'élaboration de solutions aux défis uniques de nos clients. Notre base de clientèle comprend des sociétés de biotechnologies et des laboratoires pharmaceutiques internationaux, des agences publiques, et des établissements hospitaliers, d'enseignement et de recherche partout dans le monde.
Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.
Au sein des laboratoires Charles River, nous reconnaissons et recrutons tous les talents. Nous sommes une entreprise attachée au principe de mixité, de diversité et d’inclusion et œuvrons quotidiennement en ce sens
Les Laboratoires Charles River France sont engagés dans une politique en faveur de l’intégration et du maintien dans l’emploi des personnes en situation de handicap. Tous nos postes sont ouverts aux travailleurs handicapés et une attention particulière sera portée aux candidats en situation de handicap qui postuleront auprès de Charles River.
Pour plus d'information, consultez www.criver.com.

Research Scientist LC-MS/MS - F/H - CDI (Saint-Nazaire, FR, 44600)

Le poste

Notre Laboratoire de chromatographie recrute un Research Scientist LC-MS/MS - H/F en CDI, basé sur le site de Saint-Nazaire (44).

Le site est spécialisé dans la mise en place de tests de bioanalyse pour supporter le développement de nouveaux médicaments des phases précliniques aux essais cliniques de phase IV. Le site emploie environ 65 personnes et est doté d’équipements de dernière génération (LC-MS/MS). Il est accrédité par les différentes autorités habilitées pour ce type d’établissement.

Vous ferez partie d’une équipe dans laquelle votre rôle sera la réalisation technique et la responsabilité de conduite d'études de développements de méthode de bioanalyse sur de nouveaux médicaments.

Les missions

Réaliser techniquement des développements de méthode de bioanalyse pour tout type de matrices biologiques (plasma, sang,tissus,…) de façon autonome et efficace
Assumer la responsabilité générale de la conduite d'étude de développement et y apporter son expertise technique et scientifique
S’assurer de la disponibilité du matériel et des réactifs pour respecter le planning établi
Interpréter les données avec précision et faire preuve de minutie dans la vérification et la validité des informations
Produire des documents analytiques précis et de haute qualité pour transférer efficacement les méthodes développées aux collègues chargés de la partie réglementaire (validation)
Travailler en étroite collaboration avec l’ensemble des personnes du laboratoire (techniciens de laboratoire, responsables d’études, responsables d’équipe) et des services supports (planification, Archiviste, Publisher et coordinateur scientifique, Magasin et achats, etc…)
Communiquer régulièrement avec les clients, fournisseurs, auditeurs, etc…

Qualifications recherchées

De formation Bac + 2 minimum, vous disposez idéalement d'une expérience technique d'au moins 5 ans en bioanalyse (préparation d’échantillons biologiques, LC-MS/MS).

Vous avez de bonnes connaissances des normes BPL/BPC ou du travail en contexte qualité/réglementaire (suivi et respect de procédures et consignes).

Rigoureux et autonome, vous êtes reconnu(e) pour votre bon sens du relationnel et êtes à l’aise avec les outils informatiques.

Enfin, notre environnement est international et un anglais professionnel (oral et écrit, B2 minimum) est attendu.

Modalités contractuelles

Convention collective de l’industrie pharmaceutique : groupe 6
Contrat : CDI cadre (forfait jours, RTT)
Salaire : Environ 34 000 € bruts/an, sur 12 mois, selon expérience
Prise en charge de la mutuelle à 60% et tickets restaurants

À propos de Safety Assessment

À propos de Charles River

Pour plus d'information, consultez www.criver.com.

Assistant vétérinaire - F/H - CDI (Evreux, FR, 27930)

Qui sommes-nous ?

Le poste

Au sein du département Vétérinaires, vous aurez pour objectif d'assurer le support aux Vétérinaires Cliniciens, dans le respect des réglementations.

Les missions

Agir en tant qu'accueil du service et hierarchiser les demandes pour optimiser les visites vétérinaires, en fonction des urgences,
Assurer les soins des animaux aux côtés du vétérinaire,
Réaliser les visites de suivis,
Participer à différents projets en soutien de l'équipe vétérinaire (amélioration des process, commandes, gestion des salles d'opérations),
Gérer la pharmacie des médicaments vétérinaires,
Maintenir le respect de la documentation et des données acquises, en appliquant rigouresement les procédures réglementaires.

Qualifications souhaitées

Vous êtes titulaire d’un Bac +2/Bac +3 dans le domaine des soins vétérinaires.

Vous possédez une première expérience sur ce type de poste, idéalement en CRO.

Vous êtes reconnu(e) pour votre organisation, votre assiduité et votre esprit d'équipe.

Modalités

Convention collective de l’industrie pharmaceutique, groupe : 3
Contrat : Non-cadre (accord de modulation 35h)
Salaire : A compter de 25 415 € bruts / an sur 13 mois
Prise en charge de la mutuelle à 90%, restaurant d’entreprise, CSE
Primes de transport, d’intéressement/participation, accord d’ancienneté, accord de télétravail,...
Site non-accessible en transport en commun – Moyen de locomotion indispensable

À propos de Safety Assessment

À propos de Charles River

Charles River prend très au sérieux sa contribution aux efforts accomplis pour améliorer la qualité de vie du plus grand nombre possible de personnes. Le sens de notre mission, notre excellence scientifique et notre détermination nous animent en permanence. Nous abordons chaque jour en sachant que notre travail contribue à améliorer la santé et le bien-être d'innombrables hommes, femmes et enfants de par le monde. Nous sommes fiers d'avoir contribué au développement de 85 % des médicaments approuvés par la FDA en 2021.

Pour plus d'information, consultez www.criver.com.

Cagewash Technician I (Bldg 35) 1 (Bethesda, MD, US, 20892)

Job Summary

We are looking for a Cagewash Technician I to join our Insourcing Solutions team, located in Bethesda, MD.

The duties of the Cagewash Technician I are to maintain facility equipment and perform routine preventative maintenance on cagewash and autoclaves.

You will also perform the following duties:

Sanitize, maintain, and repair animal caging materials as needed.
Ensure cagewash and animal holding facilities are kept in a clean and organized manner.
Assist with the receipt, stocking, and maintenance of supply inventories.
Prepare and submit required written records, charts, logs, and inventories.
Actively interact with customers to resolve requests, inquiries, and complaints, and to provide technical assistance.

Other duties will include general housekeeping, in addition to reviewing, comprehending and complying with all SOPs and quality assurance standards pertaining to specific areas.

Qualifications

Experience and/or training working with mechanical equipment preferred.

Obtain ALAT certification within 1 year of employment with HS Diploma/GED or within 2 years of employment if no HS Diploma/GED.

The pay for this position is $17.50-18.47 USD per hour.

For more information, please visit www.criver.com.

Technicien animalier - F/H - CDI (Paris, FR)

Rejoignez une équipe passionnée par les animaux où chaque jour fait avancer la recherche scientifique !

Dans le cadre de cette activité, nous recherchons un Technicien animalier F/H en CDI pour travailler au sein d'animaleries de recherche au sein de nos sites client basés à Paris.

A ce titre, vous intégrerez une équipe de zootechniciens engagés au cœur du bien-être animal et travaillerez en interface directe avec les équipes de recherche.

Missions principales

Gestion d'élevage (rongeurs)

Gestion les animaux selon les instructions données par équipes de recherche via un logiciel de gestion d'animalerie
- Contrôle de l'état de gestation, suivi des animaux, sexage et sevrage
- Réalisation des accouplements contrôlés
Identification des animaux
Réalisation de prélèvements à des fins de génotypage/phénotypage
Mise à jour et suivi des données d'élevages sur le logiciel d'animalerie
Travail en lien avec les équipes de recherche

Entretien, soin et surveillance des animaux

Assurer le bien-être des animaux au quotidien : observation, abreuvement, alimentation, enrichissement et la vérification des paramètres d'ambiance
Assurer l'hébergement des animaux: change des cages sous hotte de change
Nettoyage et désinfection des locaux en respectant les règles de prophylaxie et de biosécurité
Gestion des stocks de consommables, déclenchement des commandes et suivi des réceptions

Profil recherché

Idéalement niveau 2/Fonction A en Expérimentation animale
Expérience requises: expérience dans la gestion d'élevage de rongeurs
Savoir travailler en milieu confiné ou en zone protégée avec des équipements de protection individuelles (EPI)
Respect des procédures et de la réglementation en expérimentation animale
Esprit d'équipe et capacité à collaborer avec différents interlocuteurs
A l'aise avec les outils informatiques

Modalités

Convention collective pharmaceutique
Permanences ponctuelles les week-ends et/ou jours fériés
Rémunération à partir 30 K€ brut annuel sur 14 mois, selon profil.
Indemnité de transport, prime d’Intéressement et participation, accord d’ancienneté
Prise en charge de la mutuelle à 60%, tickets restaurants, comité d'entreprise

Pour plus d'information, consultez www.criver.com.

Medical Technologist I (Reno, NV, US, 89511)

Job Summary

BASIC SUMMARY:
Perform basic medical technology procedures according to protocol, SOP and GLP. Operate, maintain and perform basic troubleshooting procedures on analyzers. Process additional study samples. Perform and review study ordered parameters and computer input of raw data.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
•   Assist in the preparation of appropriate paperwork and materials prior to clinical pathology blood collection days. Assist with the computer protocol work schedule for each study, as needed.
•   Perform basic medical technology procedures such as record blood slide differentials, reticulocyte counts, and urinalysis with minimal supervision; prepare blood and cytology slide smears.
•   Inventory and package differential and reticulocyte blood slides for each study for shipment or storage.
•   Maintain proficient knowledge of hematology, clinical chemistry, coagulation, and urinalysis.
•   Analyze proficiency survey samples.
•   Review documentation of functions performed as part of quality requirements.
•   Input raw data into the computer system and review data.
•   Operate, maintain, and troubleshoot clinical pathology analyzers.
•   Perform daily maintenance and quality control of instruments.
•   Perform all other related duties as assigned.

Job Qualifications

Education: Associate’s degree (A.A./A.S.) or equivalent in medical laboratory technology (MLT) or related field required. Bachelor’s degree (B.A./B.S.) or equivalent in medical technology (MT) desired.
Experience: 2-3 years of experience in a clinical pathology laboratory.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: MT or MLT with certification or certification-eligible (ASCP or HEW) preferred.
Other: Experience with computer software programs is desirable. Effective organizational and leadership skills desired.

The pay range for this position is $30.00-32.00 an hour.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Environmental Health and Safety Specialist (Cambridge, MA, US, 02142)

Job Summary

Responsible for implementing/maintaining the Environmental, Health, Safety & Sustainability (EHS&S) Program(s) for adherence to local, state, and federal regulations. Identify and mitigate potential hazards to reduce/eliminate risk exposure.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Establish, administer, and update specific EHS&S programs for compliance with state and federal Occupational Safety and Health Administration (OSHA), Environmental Protection Agency (EPA), Department of Transportation (DOT) and other regulations as necessary.
Manage OSHA and EPA records and maintain reporting and documentation standards.
Provide initial and periodic safety and environmental training to all employees as required and advise management on safety and environmental issues.
Review new regulatory standards and make compliance recommendations.
Inspect the facility for compliance with OSHA and EPA regulations as applicable. Recommend solutions to management that address deficiencies in EHS&S compliance. Submit work orders for facility corrective action on EHS&S concerns.
Assist in the development of EHS&S programs and metrics.
Manage the hazardous waste (RCRA) and medical waste disposal function including waste profiling, permitting, manifesting, and record keeping and reporting.
Assist management team in emergency response and function as EHS&S Emergency Coordinator for 24-hour incident response.
Serve or Co-chair as a member of the Safety Committee(s)
Assist in the investigation of injuries resulting in lost time claims and/or safety violations and property damage. Make recommendations for corrective action.
Provide regulatory guidance on EHS&S issues to all staff.
Available to clients and federal and state investigators to explain procedures and produce written documentation as proof of compliance.
Request and maintain necessary facility permits, licenses and compliance reports to federal, local and state regulatory authorities.
Obtain necessary licenses to function as wastewater and underground storage tank operator.
Coordinate communications to regulatory agencies and client inspections on EHS&S related matters.
Provide initial and periodic safety and environmental training to all employees as required by regulation and as needed for ‘best practice’.
Liaise with Document Control team to ensure SOPs and BOPs are properly formatted, updated, and entered.
Recommend and implement changes to facility SOPs, Global Operating Framework (GOFs) and Business Operating Procedures (BOPs) relating to EHS&S.
Ensure adherence to pertinent regulatory requirements and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].
Perform all other related duties as assigned.

Job Qualifications

Education: Bachelor’s degree (B.A./B.S.) or equivalent in Environmental Science, Occupational Health and Safety, Environmental Engineering or related discipline.
Experience: 3 – 5 years related experience in Environmental Health, Safety.& Sustainability.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: None.
Other: Ability to interpret federal and state regulation and apply them to address compliance solutions as required. Effective writing, organizational and time management skills. Computer skills including MS Office and database management. Ability to speak Spanish is a plus.

Compensation Data

The pay range for this position is $95,000 - $105,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

For more information, please visit www.criver.com.

QC Officer (Ballina, IE, F26D786)

We are seeking an experienced QC Officer for our Biologics Division located in Ballina, Co. Mayo, Ireland.

This role shall report to the Biosafety and Cell Based Assay Department Manager and the main duties & responsibilities shall be:

Project Management of routine batch release testing in the Biosafety and Cell Based Assay Department (client correspondence,/weekly calls, management of subcontractors, ensuring samples are released within the required timelines i.e. scheduling of tests, review of basic data, liaising with QA, generation of CoA etc.)
Generation and updating of GMP compliant SOPs, Protocols and reports.
Sourcing, purchasing and stocking consumables, standards and reagents required for testing.
Receipt and processing of test samples in LIMS
Carry out data calculations ,basic statistics and trending. Provide additional information at the clients request as required.
Assist in internal, regulatory and client visits/audits and respond to findings.

The following are minimum requirements related to this Position;

A minimum of 2 years relevant experience in Scientific Research preferably within a GMP regulated environment (EMEA/FDA) within the Pharmaceutical, Medical Device, CRO Industry.
Experience in project management essential.
BSc/M.Sc. in a relevant science discipline (e.g. cell biology / Molecular Biology / Biomedical Science)
Experience in cell-based assays / molecular techniques desirable but not essential.

Job Summary

Job Qualifications

About Biologics Testing Solutions
With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterzation, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.

At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.

Veterinary Technician I (Horsham, PA, US, 19044)

Job Summary

Assist veterinary staff in the documentation and triage of all laboratory animal health cases. May also perform technical in-life procedures.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Assist veterinary staff in the documentation and triage of all animal health cases noted by technical staff and/or Attending Veterinarian.
Perform routine veterinary technical and husbandry skills which may include administration of various therapeutic measures by IV, IM, SQ, topical, oral routes, etc., bandage/wrapping techniques, venipuncture techniques and other techniques.
Perform animal follow-up observations or new findings as required.
Monitor animal health, visually, and by following detailed schedules.
Generate animal treatment records and perform, track and schedule follow-ups.
Maintain appropriate medical records for each animal in accordance with study and regulatory requirements. Assist in maintaining accurate record keeping procedures for the veterinary department.
Maintain and follow complex procedures to ensure appropriate animal health and treatment.
Assist in providing leadership, animal health training, and guidance to other laboratory personnel.
May be responsible for tissue sampling, routine animal manipulations and administration of fluids or other treatments as required.
May perform routine technical and husbandry functions (general housekeeping) on studies and must adhere to safety procedures.

The pay for this position is between $26.00 and $28.00 an hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

Job Qualifications

QUALIFICATIONS:
Education: Graduate of a collegiate veterinary technology program accredited by the American Veterinary Medical Association Committee on Veterinary Technician Education and Training Activities or equivalent program in veterinary technology.
Experience: 0-2 years related experience working with animals in a pre-clinical laboratory or clinical setting; experience working in a CRO with multi-species preferred.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above if the individual is credentialed as a Certified Veterinary Technician
Certification/Licensure: LVT license or CVT/RVT certification preferred.. AALAS certification desired.
Other: Demonstrate understanding of Standard Operating Procedures. Excellent organizational, time management and recordkeeping skills. Basic word processing skills required. Excellent communication skills both written and verbal. Must be proficient in routine veterinary technical and husbandry techniques.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Assembler - Associate (Charleston, SC, US, 29407)

Job Summary

An essential member of the larger production team, responsible for mechanical assembly, rework, documentation and installation of software. Reports to the production manager, receives direction from the production manager, production engineer, and general production coordination direction from the Instrument Release and Production Coordinator.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
The following statements are intended to describe the general nature and level of work being performed by individuals assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified.

Mechanically assemble and disassemble new and existing equipment
Receive, sort, inspect and stock components in a warehouse area
Identify and report defects, including potential defects to aid in product improvement
Operate hand and power tools such as torque drivers, screw drivers, wire cutters and other tools for instrument assembly
Perform rework including but not limited to soldering, crimping, separating, cutting etc.
Read and understand CAD drawings, BOM etc.
Assist in:
- Perform general housekeeping and adhere to safety procedures.
- Production process development
- Continuous improvement
  - Product improvements
  - Manufacturing processes
  - Testing processes
Perform SAP operations to facilitate the processing of components and instruments
Work with PLM system and work instructions
Perform general housekeeping and adhere to safety procedures.
Proficient in all SOPs in areas of responsibility
Perform all other related duties as assigned.
Responsible for adhering to all documentation as required by company policy, cGMP and FDA.
Cross train as required for all other roles within the department
Periodically assist in those roles with direction as needed

Job Qualifications

Education: High school diploma or General Education Degree (G.E.D.)
Experience: Experience working in ESD and production of electronic assemblies is preferred

PHYSICAL DEMANDS:

Specific vision abilities required by this job include close vision and the ability to adjust focus..
Sitting and standing for periods of time.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

WORK ENVIRONMENT:

General production working conditions, the noise level in the work environment is usually quiet.

COMMENTS:

Employee is responsible to verify and validate his or her job output as specified through verbal and/or written instructions. Verbal and written instructions may include training, policy statements, work instructions, Standard Operating Procedures, or workmanship standards.

Compensation Data

The pay range for this position is $19.00 to $20.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.

For more information, please visit www.criver.com.

Data Engineer (Ahmedabad, IN)

At Charles River, we are passionate about improving the quality of people’s lives. When you join our global family, you will help create healthier lives for millions of patients and their families.

Charles River employees are innovative thinkers, who are dedicated to continuous learning and improvement. We will empower you with the resources you need to grow and develop in your career.

Job Summary

There has never been a more exciting time to be part of the Enterprise Data Analytics team at Charles River Labs. We are on a mission to position data as the core driver of our business, empowering leaders to make informed, data-driven decisions that accelerate revenue, enhance productivity, and keep us ahead of the competition. Our recently launched Enterprise Data Hub serves as the company's digital backbone, and we are looking for visionary people in data analytics to help us further expand and refine this hub.

Your role will be key in integrating, mastering, and ensuring the quality of our data across all business functions, ultimately transforming how Charles River operates through data science and advanced analytics. You will be joining a team that is deeply committed to our purpose: Together We Create Healthier Lives. This unwavering focus on patients makes our global technology team uniquely inspiring. As we look to the future, we reimagine how we do business through our Digital Journey.

Note: It’s a fully remote home-based role for professionally qualified and experienced candidates based in India, who are willing and open to work UK shifts.

Essential Qualifications:

•    Bachelor’s degree in computer engineering, Computer Science, or a related discipline (Master’s degree preferred)
•    3+ years of experience in ETL design, development, and performance tuning using the Microsoft BI Stack in a multi-dimensional data warehousing environment.
•    3+ years of advanced SQL programming expertise (PL/SQL, T-SQL)
•    1+ years of experience in Enterprise Data & Analytics solution architecture
•    1+ years of experience in Python Programming
•    1+ years of hands-on experience with Azure, especially for data-heavy/analytics applications leveraging relational and NoSQL databases, Data Warehousing, and Big Data solutions.
•    1+ years of experience with key Azure services: Azure Data Factory, Data Lake Gen2, Analysis Services, Databricks, Blob Storage, SQL Database, Cosmos DB, App Service, Logic Apps, and Functions.

Preferred Skills:

•    Experience with Big Data technologies, such as Hadoop, Sqoop, Hive, Kafka, Spark, Pyspark, Python, Scala, or Pig
•    Experience managing both relational and non-relational data using Big Data Management (BDM) techniques (formats like JSON, XML, Avro, Parquet, etc.)
•    Experience setting up and operating data pipelines using Python or SQL
•    Familiarity with DevOps processes (CI/CD) and infrastructure as code
•    Knowledge of Master Data Management (MDM) and Data Quality tools
•    Experience developing REST APIs using Java Spring Boot
•    Familiarity with stream-processing systems (e.g., Event Hubs, Storm, Spark-Streaming)
•    Experience in data and analytics within the Life Sciences industry is a plus.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River Laboratories is an Equal Opportunity Employer - M/F/Disabled/Vet.

For more information, please visit www.criver.com.

Laboratory cook (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

As a laboratory cook for our formulation team located at the Senneville site, you will be responsible of preparing different formulations required for dosing, in solution, suspension or powder mix , for our research teams.

In this role, primary responsibilities include:

Prepare formulations for dosing, in solution, suspension or powder mix using various techniques while adhering to GLP regulations;
Operate various computer programs and equipment such as PH meter, homogenizer, balance, osmometer, densimeter and glove box;
Handle samples in a fume hood using aseptic method;
Prepare study materials according to protocol.

Key Elements

We are looking for the following minimum qualifications for this role:

AEC/DEC in Laboratory Sciences;
Comfortable following strict procedures;
Motivated, autonomous, and meticulous person;
Positive attitude and good team spirit.

Role Specific Information:

Location: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transportation: We offer a free shuttle service from the Sainte-Anne-de-Bellevue train station and John Abbott College to the Senneville site. Free parking. Electric vehicle charging station;
Salary: 23$/hour;
Annual bonus based on performance;
Schedule:
- Monday to Friday & 1 weekend out of 2 in rotation;
- Start time between 6AM and 9AM;
- Holidays;
Permanent position as of the hiring, full-time 37.5hrs per week.

Why Charles River ?

Competitive benefits as of the hiring. We pay up to 85% of premiums (health & dental coverage);
Free gym on site;
Employee and family assistance program;
Excellent welcome program for new employees as well as in-house advancement and career development opportunities;
Access to a doctor and various health professionals (telemedicine);
3 weeks’ Vacation & 5 Personal day policy;
Many social activities!

If you are interested in contributing to the well-being of our communities, not only across the country but around the world, please join us. This is Your Moment.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex (including sexual orientation, gender identity, and expression), religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.

For more information, please visit www.criver.com.

Cuisinier.ère de laboratoire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l’emploi

En tant que Cuisinier.ère de laboratoire pour notre équipe de Formulation située au site de Senneville, serez responsable de préparer les différentes formulations requises pour le dosage, en solution, suspension ou mélange de poudre, pour nos équipes de recherche.

Dans ce poste, les principales responsabilités incluront:

Préparer des formulations pour le dosage, en solution, suspension ou mélange de poudre en utilisant différentes techniques tout en respectant les règles des BPL;
Utiliser différents programmes informatiques et équipements tels que PH mètre, appareil d’homogénéisation, balance, osmomètre, densimètre et boîte à gants;
Manipuler des échantillons sous la hotte en utilisant une méthode aseptique;
Préparer le matériel de l’étude selon le protocole.

Éléments clés

Les qualifications minimales recherchées pour ce poste sont les suivantes :

AEC/DEC en sciences de laboratoire;
À l’aise de suivre des procédures strictes ;
Personne motivée, autonome et minutieuse ;
Attitude positive et un bon esprit d’équipe.

Informations spécifiques au poste:

Localisation: 22022 route Transcanadienne, Senneville, QC, H9X 1C1;
Transport: Nous offrons un service de navette depuis la gare de Sainte-Anne-de-Bellevue et le collège John Abbott vers le site de Senneville. Stationnement gratuit. Borne de recharge pour voiture électrique;
Salaire: 23$ de l’heure;
Bonus annuel basé sur la performance;
Horaire:
- Lundi au vendredi avec 1 fin de semaine sur 2 en rotation;
- Heure de début entre 6 et 9 heures du matin;
- Journées fériées;
Poste permanent dès l’embauche, temps plein à 37.5hrs par semaine.

Pourquoi Charles River?

Avantages concurrentiels dès l’embauche. Nous payons jusqu’à 85% des primes (couverture médicale & dentaire);
Gym gratuit sur place;
Programme d'aide aux employés et à leur famille;
Excellent programme d’intégration à nos nouveaux employés ainsi que des possibilités de croissance et de perfectionnement professionnel à l’interne;
Accès à un médecin et différents professionnels de la santé en tout temps (télémédecine);
3 semaines de vacances et 5 jours de congé personnel;
Nombreuses activités sociales organisées!

Si vous souhaitez contribuer au bien-être de nos communautés, non seulement à travers le pays, mais dans le monde entier, joignez-vous à l’équipe. C’est Votre Moment.

Pour plus d'information, consultez www.criver.com.

Research Scientist I - Method Development, Bioanalytical Chemistry (Cleveland, OH, US, 44128)

Job Summary

We are seeking a Research Scientist I - Method Development for our Bioanalytical Chemistry team for our Safety Assessment site located in Cleveland, Ohio.

Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents.

Effectively manage a portfolio of sample analysis projects while ensuring timelines are met in a single operational area with minimal oversight
Execute review and approval of data with minimal oversight for final scientific/technical decisions within a single operational area
Develop understanding of compliance expectations to respond to quality assurance audit observations in appropriate software with minimal oversight
Assist with minimal oversight the completion of laboratory investigations, assay troubleshooting and quality observations
Independently assist in problem solving for technical and/or regulatory issues
Responsible for review of study plans/protocols/amendments
Participate in Sponsor visits/tours with minimal oversight
Provide expertise in developing and validating quantitative/qualitative methods/procedures with limited complexity/scope in one operational area
Independently perform data analysis using appropriate software
Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas
Demonstrate effective communication skills through informal discussions with peers, supervisor, and team
Independently function as a liaison, maintaining timely and frequent communication between CRL and Sponsor/Client/SD
Independently ensure scientific integrity of studies
Independently function as a Principal Investigator, Individual Scientist and/or Study Director

Essential Duties and Responsibilities: continued

Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data
Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Write, review and approve deviations with minimal oversight
Full understanding of regulatory and GXP requirements, industry standards and company SOPs within one operational area
Effectively manage a small portfolio of research projects including method development and validation while ensuring timelines are met in a single operational area with minimal oversight
Able to recognize method and/or data issues and communicate them to management to minimize study impact with minimal oversight
Provide support to staff members as required by operational area as needed
Actively participate in internal process improvements, presentations and harmonization efforts
Performs all other related duties as assigned

The pay range for this position is $85-90K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Bachelor’s degree (BA/BS) with 7-9 years of relevant working experience. Master’s degree (MS) with 3-4 years of relevant working experience. Doctorate degree (PhD) with 1-2 years of experience.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Ability to communicate verbally and in writing at all levels inside and outside the organization.
Basic familiarity with Microsoft Office Suite.
Computer skills, commensurate with Essential Functions, including the ability to learn a validated system.
Ability to work extended hours beyond normal work schedule to include, but not limited to evenings, weekends, extended shifts, and/or extra shifts; sometimes on short notice.
Ability to work under specific time constraints.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Scientific Associate, Clinical Pathology (Ashland, OH, US, 44805)

Job Summary

We are seeking a Scientific Associate for our Clinical Pathology Team at our Safety Assessment site located in Ashland, OH.

Basic Summary:

Provide scientific support for nonclinical research or laboratory-based studies; perform basic study management tasks and interpretation and reporting of study data/conclusions.

Efficiently perform and document all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)
Assist with the completion of laboratory investigations, assay troubleshooting, SOP revisions, quality observations, and problem solving of technical and/or regulatory issues, with oversight.
Develop critical thinking, troubleshooting, and time management skills aligned with needs of laboratory.
Develop ability to recognize method and/or data issues and communicate them to management to minimize study impact, with oversight.
Execute review and approval of data for final scientific/technical decisions, with oversight.
Develop understanding of compliance expectations to respond to quality assurance audit observations with oversight.
Write, review, and approve deviations, with oversight.
Ensure scientific integrity of studies, with oversight.
Function as a Principal Investigator, Individual Scientist, and/or Project Scientist as assigned, with oversight.
Assist in generating study protocols/plans for regulated and non-regulated studies and assist in obtaining sponsor approval.
Actively communicate and collaborate within the lab (peers, supervisor, and team) and across departments and CRL sites in order to adhere to timelines and produce quality data.
Function as liaison, maintaining timely and frequent communication between CRL and sponsor/client/SD, with oversight.
With close guidance from senior scientific staff participate in method development and validation activities.
Shadow the study director or project scientist of laboratory method developments to further develop research and validation skills and techniques.
Perform basic system qualifications and decommissions, with oversight.
Provide leadership and technical guidance and serve as a mentor to less experienced staff.
Attend scientific meetings, conferences, and training courses to enhance job and professional skills.
Perform all other related duties as assigned.

The pay range for this position is $68-72K. Please note that starting salaries vary based on factors including, but not limited to experience, skills, education, certifications, and locations.

Job Qualifications

(Knowledge, Experience, Skills and Abilities required to accomplish the essential functions) include but are not limited to:

Education: High School diploma or General Education Degree (G.E.D.) preferred. Associate’s degree (A.A./A.S.) or equivalent from a two year college recommended. Bachelor's degree (B.S./B.A.) or equivalent in a scientific related discipline strongly recommended.
Experience: 3 to 5 years related experience in animal science, biology, chemistry/pharmacy, or similar laboratory environment, including 1 year related experience in the contract research or pharmaceutical industry.
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Certification/Licensure: Medical Laboratory Technician (MLT), Medical Technologist (MT), or Medical Laboratory Scientist (MLS), preferred.
Other: Effective written and verbal communication skills. Ability to handle multiple projects, prioritize work and meet deadlines.
Proficiency in the use of standard software including Microsoft® Excel, Word, PowerPoint, etc. and with standard laboratory calculations.

Physical Demands:

While performing the duties of this job, the employee is regularly required to talk, hear and work/ type at a computer.
Specific vision abilities required by this job include close vision and the ability to adjust focus.

Work Environment:

General office working conditions, the noise level in the work environment is usually quiet.
While performing the duties of this job the employee may occasionally be required to wear protective clothing (goggles, face shield, surgical mask, cap, gloves, scrubs, boots), work near toxic or caustic chemicals, work with biohazards, and/or work with live animals with risk of exposure to allergens and/or zoonotic diseases.
The employee may occasionally be exposed to fumes or airborne particles, unpleasant odors, and/or wet, humid and/or extreme temperature conditions.

Comments:

This position may require occasional travel.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.

Equal Employment Opportunity

For more information, please visit www.criver.com.

Mitarbeiter*in Personalwesen*, Teilzeit 50 % (20 Std/Wo) (Freiburg, DE, 79108)

Tierpfleger*in in der Krebsforschung (Freiburg, DE, 79108)

.

Befristeter Vertrag: 18 Monate -Human Resources Business Partner (m/w/d) (Sulzfeld, Bavaria (Bayern), DE, 97633)

Job Summary

Mitarbeiter für den internen Produktions- und Logistikbereich (Sulzfeld, Bavaria (Bayern), DE, 97633)

Mitarbeiter/in in der Tierpflege (m/w/d) (Sulzfeld, Bavaria (Bayern), DE, 97633)

· eine interessante und verantwortungsvolle Tätigkeit in einem zukunftsorientierten Team

Veterinary Technician Assistant I (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Group Housing Technician I (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Group Housing Technician I (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Veterinary Technician I - $5,000 Sign On Bonus! (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Research Analyst I -Bioanalytical Sciences (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Clinical Pathology Team Lead (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Senior HVAC Technician (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Security Officer - Part Time (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Animal Care Technician I (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Animal Care Technician - Group Housing (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Surgical Laboratory Technician I (Reno, NV, US, 89511)

Job Summary

Job Qualifications

Account Development Representative - Initial 6 Month FTC (Cambridge, GB, CB23 6DP)

Job Summary

Commis aux soins des animaux (St. Constant, Quebec, CA, J5A 2E7)

Sommaire de l'emploi

Éléments clés

Animal Care Clerk (St. Constant, Quebec, CA, J5A 2E7)

Job Summary

Job Qualifications

Étudiant.e - Commis aux soins des animaux (St. Constant, Quebec, CA, J5A 2E7)

Sommaire de l'emploi

Éléments clés

Student - Animal Care Clerk (St. Constant, Quebec, CA, J5A 2E7)

Job Summary

Key Elements

Animalier.ière (Fleurimont, Quebec, CA, J1E 0B5)

Sommaire du poste

Éléments Clés

Animal Care Technician (Fleurimont, Quebec, CA, J1E 0B5)

Job Summary

Key Elements

Mechanical Engineer (Margate, GB, CT9 4LT)

Mechanical Engineer

Clinical Veterinary Surgeon (Tranent, GB, EH33 2NE)

Job Summary

Job Qualifications

Senior Data Scientist (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Key Elements

Scientifique de données sénior (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Éléments clés

Veterinary Technician (Montreal (Senneville), Quebec, CA, H9X 3R3)

Job Summary

Key Elements

Technicien.ne vétérinaire (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Éléments clés

Animalier.ière (Montreal (Senneville), Quebec, CA, H9X 3R3)

Sommaire de l'emploi

Mitarbeiterin Personalwesen, Teilzeit 50 % (20 Std/Wo) (Freiburg, DE, 79108)