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Hub Group

Hub Group

62 jobs near Columbus, OH

Hired by Matrix

QC Manager

Camarillo, CA · On-site

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.

ATMI Indy, LLC

Quality Control Manager

Greenfield, IN · On-site

As Quality Control Manager, you'll lead the QC team at our Greenfield facility and oversee the inspections, testing, documentation, and quality processes that support production. This is a strong fit ...

ECC

Quality Control Manager

Honolulu, HI

$96K - $135K/yr

The Quality Control Manager must manage the Contractor Quality Control program and organization for the assigned project to assure compliance with the site-specific Quality Control Plan and contract ...

Mai Placement

Quality Control manager

Lebanon, NJ · On-site

Quality Control Manager - Food Manufacturing Lebanon, NJ 110 - 120K Overview A growing dairy manufacturing operation is seeking a Quality Control Manager to take ownership of food safety and quality ...

SPECTRA TECH, Inc.

Quality Control Manager

Memphis, TN · On-site

Spectra Tech, Inc. is hiring for a Quality Control Manager in Olive Branch, MS. Position Overview Spectra Tech, Inc. is seeking a Quality Control Manager to oversee Quality Control operations within ...

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Quality Control Manager

Fort Dix, NJ · On-site

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McGough

Quality Control Manager

Wichita Falls, TX · On-site

QUALITY CONTROL MANAGER Quality Control Manager will manage the Quality Assurance and Quality Control requirements for the project. The role will provide management and oversight with the authority ...

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Showing results 41-60

QC Manager

Hired by Matrix

Camarillo, CA • On-site

Full-time

Re-posted 22 days ago

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 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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