Supervisor II, Quality Assurance (OSD) (3rd shift)
Core
Oversee Quality Assurance operations and supervise staff in a manufacturing environment, ensuring GMP compliance, product quality, and regulatory adherence.
Role type
Senior IC Quality Assurance Supervisor
Builds
Manufacturing quality controls, batch records, and compliance documentation for pharmaceutical products
Domain
Pharmaceutical manufacturing / Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work -> physical/clinical work (manufacturing quality control)
Required skills
GMP compliance, FDA regulations, team supervision, batch record review, corrective action planning, procedure development, manufacturing operations knowledge
Preferred skills
Direct manufacturing interface, change request management, continuous improvement initiatives
Technologies
None explicitly stated
Responsibilities
Lead QA team in hiring, performance management, and development; Provide quality support on the manufacturing shop floor; Investigate QC holds, quarantines, and rejects; Review and approve procedures and change requests; Release batch records
Seniority
Senior, hands-on IC with mentorship duties