Supervisor, Clinical Pathology

Req ID #:  227956
Location: 

Spencerville, OH, US, 45887

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 Supervisor for our Clinical Pathology team at our Safety Assessment site located in Spencerville, OH.

 

Responsible for performing and reviewing all ordered parameters.  Proficient in all areas of Clinical Pathology Department.  Train clinical pathology technicians and coordinate clinical pathology studies.  Initiate, test, and validate new standard operation procedures and equipment.  

 

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:

 

  • Maintain proficient knowledge of hematology including blood slide differential and reticulocyte counts, clinical chemistry, coagulation, urinalysis and fecal analysis.
  • Coordinate operation, maintenance, and troubleshooting of all clinical pathology analyzers.
  • Maintain proficient knowledge on testing new procedures and standard operation procedures; establish new methods and procedures.
  • Oversee training of clinical pathology technicians.
  • Review documentation of functions performed as part of quality control requirements.
  • Provide direct daily supervision and review work of assigned departmental employees to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, and procedures [SOPs, safety procedures and biosafety protocols.]  Schedule and prioritize workload of group members.
  • Assist in the interview and selection of qualified non-exempt personnel.  Recommend 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, implementation and delivery of departmental training programs; ensure that direct reports receive departmental orientation and necessary on-the-job training.  Oversee maintenance 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.  
  • Perform all other related duties as assigned.

 

The starting pay for this position is 70k.  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:  Associate’s degree (A.A./A.S.) or equivalent desired.  Bachelor’s degree (B.A./B.S.) or equivalent desired with a Medical Technology discipline preferred.
  • Experience:  3-5 years of experience in a clinical pathology laboratory desired.
  • 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 preferred (ASCP or HEW).
  • Other:  Demonstrated leadership and word processing skills.  Effective organizational and verbal skills. 

 

Physical Demands:

  • While performing the duties of this job, the employee is regularly required to talk, hear, use hands to handle glassware, tools, or controls; reach with hands and arms; and type at a computer.
  • Occasionally stoops and bends.
  • Frequently lifts and moves up to 40 pounds.
  • Frequently uses a microscope.
  • Stands/walks for up to 90% of the workday (varies).
  • Specific vision abilities required by this job include close vision, color vision, depth perception, and the ability to adjust focus.

 

Work Environment: 

  • While performing the duties of this job, the employee regularly wears protective clothing (scrubs, lab coats, safety glasses, and gloves).
  • Regularly works with biohazards.
  • Occasionally works with sharp objects (e.g., needles).
  • Occasionally works with known and unknown toxins and chemicals
  • The noise level in the work environment is moderate.
     

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.


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 (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.

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.


Nearest Major Market: Lima
Nearest Secondary Market: Findlay

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