Sen.Lab Technician I

Req ID #:  233332
Location: 

Erkrath, NW, DE, 40699

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.

Du arbeitest gern präzise, verantwortungsvoll und mit modernen bioanalytischen Methoden? Du bringst Erfahrung in Zellkultur, Bioassays oder regulierten Laborprozessen mit und möchtest in einem GMP-Umfeld den nächsten Schritt machen? Dann werde Teil unseres Teams im Bereich Bioassays an unserem Standort in Erkrath - für die Dauer von 2 Jahren

In dieser Position übernimmst Du eine wichtige Rolle in der Durchführung und Sicherstellung von zellbasierten Bioassays im GMP-Umfeld.

Zu Deinen Aufgaben zählen:

  • Durchführung von zellbasierten Bioassays im Rahmen von Routineprüfungen unter GMP-Bedingungen
  • Unterstützung von Scientists bei der Planung, Vorbereitung und dem Abschließen von Prüfungen
  • Mitwirkung bei der Bearbeitung interner GMP-Dokumente (z.B. SOPs und Abweichungen)
  • Eigenständige Prüfung der Labordokumentation
  • Auswertung, Zusammenfassung und Dokumentation von Analyseergebnissen
  • Fachliche Unterstützung des technischen Personals bei der Durchführung von GMP-Prüfungen
  • die Pflege und Aufrechterhaltung des GMP-Systems im Laboralltag
  • Verantwortung für Geräte und Infrastruktur im LAborbereich
  • Mitarbeit bei GerätequalifikationenValidierungen und weiteren qualitätssichernden Maßnahmen
  • Laborarbeiten mit Zellkulturen und Viren der Risikogruppe S1 und S2

Das bringst Du mit:

  • abgeschlossene Ausbildung als BTA / Biologielaborant (m/w/d) o.ä. oder
  • ein naturwissenschaftliches Studium (B.Sc. oder M.Sc) in Biologie, Biochemie ö.ä. 
  • praktische Laborerfahrung in mindestens einem der folgenden Bereiche: Zellbiologie / Zellkultur, Bioassays, Immunologie, regulierte Laborprozesse
  • sorgfältige, strukturierte und zuverlässige Arbeitsweise
  • sehr gute Deutsch- und gute Englischkenntnisse
  • Erfahrung im GMP-regulierten Umfeld

Auch wenn du nicht alle Punkte erfüllst: Bewirb dich gerne, wenn du praktische Laborerfahrung in Zellkultur, Bioassays oder qualitätsgesicherten Prozessen mitbringst.

Das erwartet Dich

  • Befristete Festanstellung für 2 Jahre
  • Strukturierte Einarbeitung in ein spannendes Laborumfeld
  • Verantwortungsvolle Aufgaben im Bereich Bioassays & Zellkultur
  • Kollegiales Team mit enger Zusammenarbeit zwischen Labor und Wissenschaft
  • Möglichkeit zur fachlichen Weiterentwicklung im Bereich Bioassays, GMP und Qualitätsprozesse

Haben wir Dein Interesse geweckt?

Wenn ja, bewirb dich bitte unter der Job-ID 233332 über unser Karriereportal https://jobs.criver.com/ mit deinem Lebenslauf und Motivationsschreiben.

Wir freuen uns auf deine Bewerbung!

 

Charles River Laboratories Germany GmbH
Human Resources
Max-Planck-Str. 15a-b
40699 Erkrath
Email: RecruitBPS@crl.com

 

Job Description

Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Executes scientific testing strategies and studies. May participate in development as part of team. May lead assay research, assay validation or study conduct, or is involved in preparation of material (e.g. protein, nucleic acid, cells, etc.). Reviews and interprets study data, communicates results to clients and writes final reports. Ensures compliance with protocols and all applicable SOPs. Troubleshoots and resolves assay or technical issues in the laboratory when scientific expertise is needed. Contributes to specific dataset interpretation, or when appropriate answering questions from regulatory authorities. For singular focus of Chemistry or Biology disciplines, refer to specified role on job architecture.

Education

No degree required

Physical Requirements

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.

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 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 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 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.

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.


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