Day-to-Day Responsibilities
Reviews batch manufacturing and packing records to confirm each batch followed approved procedures.
Audits production areas, equipment and documents against GMP requirements.
Investigates deviations, out-of-specification results and complaints, and tracks corrective and preventive actions (CAPA).
Maintains and updates standard operating procedures (SOPs) and other controlled documents.
Reviews and approves batches for release, working with production, quality control and regulatory teams.
Prepares for and supports internal audits, customer audits and regulatory inspections.
Trains production and lab staff on GMP, documentation and hygiene practices.


