M. Pharm Pharmaceutical Quality Assurance

Develop, apply, revise, and maintain quality standards for processing materials into partially finished or finished products.

Perform project documentation audits and conduct supervisory review and approval and issue audit reports.

Review SOPs (standard operating procedures), forms and formats applicable/originated at USP-India.

Implement and follow Quality Management systems and document control.

Conduct internal audits independently / with a team of auditors, prepare reports and assess adequacy of CAPA.

Conduct cGMP site audits at of dietary supplements, active pharmaceutical ingredient (API), excipient, and dietary ingredient manufacturing sites, according to the appropriate cGMP guidelines and USP program requirements.

Coordinate and monitor the tasks in the laboratories and consults in the design and development of clinical trials.

Take up opportunities in fields like environment, biomedicine, computer and software testing, etc.