Effectively manage the site Quality Control activities .
Manage to run the QC operation including release of incoming materials, drug products and stability studies as per cGMP requirement and regulatory commitments.
Review, and approve specifications, testing procedure, SOPs and validation protocols and reports .
Monitor and review investigations and QMS (Change controls, Deviations, OOS, OOT) with adequate CAPA to minimize errors.
Responsible for ensuring compliance to regulatory requirements on product, process and release procedures.
Provide strong leadership and expertise to ensure achievement of all Quality Control accountabilities at site.
Monitor the performance of resources includes instruments and ensure required services are effective at all times
Coach and develop the team through performance feedback, annual performance reviews and the provision of training and development opportunities.