Job Overview
-
Date PostedNovember 25, 2022
-
Location (State / UT)
-
Expiration date--
-
Experience8 Years, 13 Years
-
GenderAny
-
Desired QualificationBachelor Degree, Master’s Degree
Job Description
Roles and Responsibilities
- Supervise compliance with all cGMP, GxP, and other regulatory requirements
- Preparation of Quality procedures and upgradation of systems at sites
- Execute and supervise all tasks/activities as per applicable SOPs
- To conduct Corporate Quality audits at all manufacturing sites
- Support to site QA for handling QMS documents
- To prepare/review audit reports
- Ensuring compliance of all applicable GSOPs at Manufacturing sites
- Review and aware of Stability studies data compilation
- Effectiveness monitoring of implemented systems and corrective and preventive actions
Required Qualification & Experience
Qualification: B Pharma/M Sc
Experience: 8 to 12yrs of experience in Quality Assurance