Responsible and Accountable for all Quality Management Systems in the department.
SOP management and implementation of the corporate quality guidelines in the department.
Ensure that all departmental documentation is updated daily and all regulatory and statutory requirements are complied with.
Ensure optimum usage of manpower resources and train and develop them to achieve their deliverables.
Periodic Audits and self inspection of the department to ensure that all the requirements of cGMP are maintained and that the plant is always 100% audit ready.
Operational matters such as BMR and Batch release, OOS and product complaints/ Recalls.
Generate relevant and accurate MIS.
Preferred candidate profile
Qualification: B.Pharm / M.Pharm
Experience: 3-4 years of relevant experience in Pharmaceutical