QC Team Lead Finished Products - Torrance
Quick Summary
QC Team Lead Finished Products Location: Torrance, CA | Employment Type: Full-Time Lead quality where it matters most. PolyPeptide is seeking a Quality Control Team Lead – Finished Products to oversee critical testing activities that ensure the safety, quality, and release of pharmaceutical…
Lead and coordinate finished product QC testing activities Review and approve analytical data and documentation for compliance and accuracy Ensure on-time testing and product release aligned with production schedules Troubleshoot analytical methods…
Bachelor’s degree in Chemistry, Biochemistry, or related field (advanced degree preferred) 5+ years of QC experience in pharma or biotech, including 2+ years in a lead or supervisory role Strong knowledge of cGMP, ICH guidelines, and analytical…
QC Team Lead Finished Products
PolyPeptide is seeking a Quality Control Team Lead – Finished Products to oversee critical testing activities that ensure the safety, quality, and release of pharmaceutical products. This is a hands-on leadership role for someone who thrives in a GMP environment and is passionate about developing teams while driving operational excellence.
The QC Team Lead is responsible for leading finished product testing operations, ensuring compliance with cGMP and regulatory requirements, and delivering results aligned with production timelines. You will serve as both a technical expert and people leader, supporting your team while partnering cross-functionally to ensure high-quality, on-time product release.
Responsibilities
~1 min read- →
Lead and coordinate finished product QC testing activities
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Review and approve analytical data and documentation for compliance and accuracy
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Ensure on-time testing and product release aligned with production schedules
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Troubleshoot analytical methods and instrumentation issues
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Train, mentor, and develop QC analysts
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Partner with QA, Manufacturing, and Regulatory teams on investigations and batch release
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Support method and equipment validation activities
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Serve as a SME during audits and inspections
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Drive continuous improvement in QC processes and lab operations
Requirements
~1 min readBachelor’s degree in Chemistry, Biochemistry, or related field (advanced degree preferred)
5+ years of QC experience in pharma or biotech, including 2+ years in a lead or supervisory role
Strong knowledge of cGMP, ICH guidelines, and analytical techniques (HPLC, UV-Vis, KF, MS)
Experience with data review, investigations, and LIMS systems
Strong leadership and team development skills
High attention to detail with a focus on compliance and data integrity
Ability to troubleshoot and make decisions in a fast-paced environment
Effective communicator across cross-functional teams
What We Offer
~1 min readLocation & Eligibility
Listing Details
- Posted
- May 1, 2026
- First seen
- May 6, 2026
- Last seen
- May 10, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 42%
- Scored at
- May 6, 2026
Signal breakdown
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