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QC Manager

Job in Camarillo, Ventura County, California, 93010, USA
Listing for: Hired by Matrix
Full Time position
Listed on 2026-06-14
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
Job Description & How to Apply Below
At-a-Glance:
Are you ready to build your career by joining a certified technology solutions and compliance consulting services company? If so, our client is hiring a QC Manager.

Position Type:
  • Contract
  • On-Site
Required:
  • 5 to 10 years of experience in Quality Control within pharmaceutical, biotech, or CDMO environments.
  • Previous experience as QC Manager, QC Supervisor, QC Lead, or senior QC professional.
  • Experience with GMP laboratory operations, documentation review, sample management, and product release support.
  • Background in sterile drug product, biologics, aseptic manufacturing, or formulation development would be preferred.
  • Good understanding of analytical testing and/or microbiology testing.
  • Strong knowledge of GMP, FDA expectations, laboratory controls, and data integrity principles.
  • Ability to work independently and manage priorities in a fast-paced environment.
  • Strong communication and cross-functional collaboration skills.
  • Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, or related field.
Responsibilities:
  • Supporting and managing daily QC laboratory operations, ensuring testing activities are completed on time and in compliance with internal procedures, client requirements, and applicable GMP regulations.
Key Responsibilities:
  • Manage daily QC laboratory operations and support testing priorities.
  • Oversee analytical and/or microbiology testing activities, depending on site needs.
  • Support raw material, in-process, finished product, and stability testing processes.
  • Review and approve QC documentation, test results, protocols, reports, and SOPs.
  • Ensure compliance with cGMP, FDA requirements, internal procedures, and client expectations.
  • Coordinate QC activities with Manufacturing, QA, Validation, Supply Chain, and Project teams.
  • Support product release timelines from a QC perspective.
  • Maintain inspection readiness within the QC area.
  • Identify operational gaps and support process improvements within the laboratory.
  • Provide guidance to QC team members and support workload prioritization.
Get in Touch:
We want to hear from you! If you think you'd be a good match, submit your resume and reach out to Vaibhav at  to learn more.

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