Description
The QC Laboratory Manager is responsible for GMP-compliant evaluation of analytical raw data and starting-material results, issuance of analysis certificates, timely release of starting materials, analytical problem-solving, and handling deviations, complaints, notifications, investigations, audits, CAPAs, and SOPs. The role also leads or supports cross-functional quality-control improvement projects and provides technical and disciplinary leadership to laboratory process-group managers. Candidates need a natural-sciences degree, several years of pharmaceutical quality-control or GMP-regulated experience, analytical-data and GMP expertise, and leadership experience.
