Quality Control Supervisor Job at Charles River Laboratories, Ashland, OH 44805

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Job Description

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

BASIC SUMMARY:
Perform QC review of study data and perform inspections. Monitor and track common errors and assist with document modification to reduce error and deviations. Assist with implementing and monitoring quality control (QC) standards, methods, and procedures.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Efficiently review 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.
  • Assist with maintenance/review of equipment.
  • Actively participate in process improvement initiatives with oversight.
  • Assist with training, as applicable.
  • Perform general QC practices as well as perform QC reviews of daily study data in one QC discipline.
  • Perform lab walk inspections.
  • Participate in Liaison Meetings.
  • Assist in recommending form and SOP modifications, and changes to standard protocol wording to avoid deviations.
  • Actively participate in logbook review and other projects as assigned.
  • Assist in maintaining and revising QC documents, processes, and manuals.
  • Actively participate in 1:1 meetings.
  • Performs all other related duties and functions as assigned.

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

Job Qualifications

  • Education: HS/GED/Associate degree or equivalent with 1 year of relevant experience preferred. Bachelor’s degree (BA/BS) in a relevant field with no work experience recommended.
  • Experience: Previous 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.

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.

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