QC Manager

QC Manager Hired by Matrix - 3.6 Camarillo, CA Job Details Contract $65 - $70 an hour 6 days ago Qualifications Data integrity assurance Biological sample management Pharmaceutical regulatory compliance GMP Data integrity and documentation Bachelor's degree Pharmaceutical company experience Compliance documentation Quality control within pharmaceutical industry Cross-functional communication FDA regulations Pharmaceutical manufacturing facility experience Laboratory compliance and regulatory documentation

Full Job Description 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 c

GMP, 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 551-227-9117 to learn more. #LI-VK1 #HbM6349