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Quality Control Supervisor

Santa Clara, CA, USA

Job ID

7553

Job Type

Full Time

Workspace

On-Site

Industry

Life Sciences

Date Posted

November 4, 2024

Date of Expiry

November 25, 2024

About the Role

The Quality Control Supervisor will be responsible for the QC Department and ensuring that all company products meet quality standards.

Key Activities

  • Oversees general QC approval of company products (Enzyme Immunoassay (EIA) Bulks, EIA kits, Work in Progress Raw Materials). Responsible for inspection of final product specifications and approving or rejecting finished products.

  • Manages QC retains, testing schedule, data and reports, and related Standard Operating Procedures (SOP) documents. Review and make decisions regarding retaining testing and final QC long-term results.

  • Oversees raw material qualification/re-qualification and disposal.

  • Coordination and oversight of instrument and equipment validation and equipment maintenance.

  • Responsible for QC Team project rotation scheduling and assignments.

  • Process improvement, procedure, and protocol development. Revise, write up, and implement updated Standard Operating Procedures.

  • Coordination of QC and Quality Assurance (QA) meetings and documentation of meeting minutes.

  • Communicate QC-related troubleshooting issues to the VP of Operations for discussion at Research & Development Meetings.

  • Communication and coordination with other departments (including but not limited to Production, Packaging, Regulatory, Shipping, Customer Service/Technical Support, etc.) and participation in management-related meetings.

  • Coordinate and communicate with Customer Service/Technical Support Associate regarding product and customer issues.

  • Propose corrective actions to improve compliance with quality standards and interface with the Regulatory Department regarding corrective action follow-up and audits.

  • Prepare reports for post-launch, specification change risk, and stability meetings.

  • Responsible for the investigation and troubleshooting of product issues. 

  • Manage raw material secondary vendor studies and stability studies.

  • Hiring, including candidate selection and interviewing and creating relevant job descriptions.

Preferred Skills

  • Knowledge and experience with Quality Control Management preferred.

Education and Experience

  • M.S. in Biology (or related) with 5+ years of QC experience or equivalent.

  • 1-3 years of supervisory experience required.

About Us

Finding a great opportunity that fosters growth, a great culture, and leadership opportunities can be difficult. Top Quality Recruitment (TQR) connects professionals with leadership opportunities across the Packaging, Food and Beverage, Medical Devices, and Biotechnology industries. With 50+ years of experience, we believe in one-to-one communication and finding the best candidate/employer match possible.    


TQR is an equal-opportunity employer that encourages diversity. We will consider all applications.    
   
Accommodation for applicants with disabilities is available upon request.    

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