QC Manager

Hired by Matrix

Camarillo, CA

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JOB DETAILS

SALARY

$65–$70 Per Hour

SKILLS

Analysis Skills, Asepsis, Biology, Biotech and Pharmaceutical, Chemistry, Communication Skills, Consulting, Corporate Compliance, Cross-Functional, Current Good Manufacturing Practice (cGMP), Data Quality, Documentation, Documentation Review, Drug Products, Establish Priorities, FDA (Food and Drug Administration), FDA Requirements, GMP (Good Manufacturing Practices), Laboratory, Laboratory Management, Laboratory Operations, Maintain Compliance, Manufacturing, Microbiology, Operational Support, Operations, People Management, Process Improvement, Product Support, Product Testing, Quality Assurance, Quality Assurance Methodology, Quality Control, Regulations, Specimens/Samples, Standard Operating Procedures (SOP), Supply Chain, Team Player, Testing, Time Management

LOCATION

Camarillo, CA

POSTED

29 days ago

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 551-227-9117 to learn more.

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About the Company

Hired by Matrix

We believe in putting people together for the right reasons. Getting you a great job that makes you feel fulfilled in your career. Finding the perfect candidate to help you achieve business success. Whether you are looking for the best candidate for your company or searching for your next career move, we are dedicated to making sure you thrive. We take your needs personally and have a variety of services to ensure you reach your goals. We listen to the needs of our clients and candidates and then thoughtfully match the right person with the right job. When people come together doing what they love success is guaranteed and partnerships last.

COMPANY SIZE

100 to 499 employees

INDUSTRY

Staffing/Employment Agencies

WEBSITE

http://www.hiredbymatrix.com

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