
Detail-oriented M.Sc. Pharm with five years of experience in GMP-regulated environments. Expertise in GMP documentation, data integrity, and inspection readiness. Collaborates effectively across QA, production, and engineering teams to ensure compliance and support sterile production processes.
Sterile production
GMP compliance
Validation readiness
Environmental monitoring
Batch record management
Root-cause analysis
Clinical documentation
SAP and KEEPit
Cross-functional collaboration
Title: M.Sc. Pharm | GMP & Drug Product Support | Sterile Production | Aseptic Operations