Over all responsible for the activities of Quality Control section (RM/PM/IP/FP/ Stability & Micro) and ensure the GMP compliance in plant.
Planning for daily analysis of in process, Finished Products, Raw Material Finished, Packaging Materials, and Stability Samples with respective intervals.
Reviewing the Quality control analytical documents of IP (Inprocess)/FP (finished product), Stability samples, Raw material Packaging material samples
Responsible for ensuring correctness of Quality control Analytical the documents as the sample testing and approvals.
Preparation of Instrument related and General SOPs.
Monitoring of Quality Control daily activities, Stability chamber and activities monitoring.
Monitoring and planning of the Quality control daily activities
Organizing and follow ups, internal audits and reviews.
Candidate should have experience in pharma industry (Formulation)