6-8 years hands on experience in Sterile Process Department.
Exposure to USFDA/MHRA Inspection
Experience in Finished Pharmaceuticals QA
M. Pharma ( Pharmaceutics, QA)/ MSc (Microbiology) preferable
Involved in Media fill Validation Study, Internal Audit , Validations and CAPA
Handled regulatory compliance, experience on handling data integrity Issues etc.
Good communication skills
Candidate must have good communication and analytical skills.