BioTalent Ltd
Senior Incoming QC Lab Supervisor
San Diego, CA (On-site) Full-time | QA & RA | 1st Shift $100,000 – $125,000 annually (depending on experience) The Role As the
Senior Incoming QC Lab Supervisor , you’ll oversee all incoming QC lab activities, ensuring compliance with GMP, ISO 13485, and company standards. You’ll manage and train the QC team, develop inspection methods, and ensure quality verification of incoming, in-process, and finished goods. This role requires advanced knowledge of mechanical inspections, GD&T, and blueprint reading. What You’ll Do Lead QC inspections of incoming materials, in-process, and finished goods
Supervise and train QC staff, ensuring technical competence
Develop and implement advanced QC inspection methods
Oversee use of measuring tools (calipers, micrometers, gauges) and vision systems (Micro-VU, Keyence)
Support CAPAs, NCRs, MRB activities, and SOP updates
Collaborate with cross-functional teams (Operations, QA, Materials, R&D, Engineering)
Ensure compliance with GMP, ISO 13485, and 21 CFR Part 820 standards
What You’ll Bring Bachelor’s degree (or equivalent experience)
12+ years of progressive Quality experience in a GMP QC lab
2+ years of supervisory experience
Strong background in regulated medical device or IVD manufacturing
Hands-on experience with GD&T, blueprint reading, and inspection tools
Knowledge of ERP systems (SAP preferred)
Strong organizational, problem-solving, and leadership skills
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San Diego, CA (On-site) Full-time | QA & RA | 1st Shift $100,000 – $125,000 annually (depending on experience) The Role As the
Senior Incoming QC Lab Supervisor , you’ll oversee all incoming QC lab activities, ensuring compliance with GMP, ISO 13485, and company standards. You’ll manage and train the QC team, develop inspection methods, and ensure quality verification of incoming, in-process, and finished goods. This role requires advanced knowledge of mechanical inspections, GD&T, and blueprint reading. What You’ll Do Lead QC inspections of incoming materials, in-process, and finished goods
Supervise and train QC staff, ensuring technical competence
Develop and implement advanced QC inspection methods
Oversee use of measuring tools (calipers, micrometers, gauges) and vision systems (Micro-VU, Keyence)
Support CAPAs, NCRs, MRB activities, and SOP updates
Collaborate with cross-functional teams (Operations, QA, Materials, R&D, Engineering)
Ensure compliance with GMP, ISO 13485, and 21 CFR Part 820 standards
What You’ll Bring Bachelor’s degree (or equivalent experience)
12+ years of progressive Quality experience in a GMP QC lab
2+ years of supervisory experience
Strong background in regulated medical device or IVD manufacturing
Hands-on experience with GD&T, blueprint reading, and inspection tools
Knowledge of ERP systems (SAP preferred)
Strong organizational, problem-solving, and leadership skills
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