Job Description
- Handling and initiation of QMS elements like change control, deviation, CAPA, Market complaint, Investigation etc.
- Preparation and review of APQR of manufactured products.
- Preparation and review the Risk Assessment and Mitigation Plan.
- Ensure that process and cleaning validation activities are being carried out by following approved protocols.
Work Experience
Approx 7 to 9 years
Education
Masters in Biotechnology or Biotechnology
B.Tech in Biotechnology or Biotechnology
Competencies
- Innovation & Creativity
- Developing Talent
- Result Orientation
