Candidate should have the working exposure in regulatory environment (USFDA & MHRA). Candidates from OSD Manufacturing will only be considered for interview.
Responsible for managing QMS activities including deviations, change control, CAPA, and OOS/OOT, ensuring timely closure and compliance with GMP and data integrity standards.
Experience in analysis of Solid Oral - FP, RM, In-process or Stability. Experience of Analytical Method Validation. Experience of PMQC and Dissolution.