Shall be responsible for Quality Assurance support for USFDA approved formulations plants for Oral dosage form and adherence of cGMP as per international guidelines. Internal audits, selection and suppliers validations.
Monitoring the Transfer of Technology
Liaison with Export Department
Training and Development of subordinates and SOPS training.
M.Pharm with relevant experience in 100% export oriented ODF manufacturing plant catering to regulated market. Currently holding senior position in a reputed pharmaceutical company.