Description
The role is responsible for GMP-compliant evaluation of analytical raw data and finished-product results, issuance of analytical certificates, complex analytical problem-solving, timely release of analytical work, handling deviations, complaints, notifications, investigations, SOPs, audits, CAPAs, and continuous QC-process improvement. It also leads or supports cross-functional improvement projects and provides technical and disciplinary leadership of laboratory process groups. The profile requires a natural-sciences degree, several years of pharmaceutical quality-control or GMP-regulated experience, analytical-data evaluation expertise, GMP and CAPA knowledge, and leadership experience.
