Role & responsibilities
- Review of BMR, ECR and Analytical Raw Data.
- Review of QC Analytical data.
- Preparation and Review of BMR, ECR, MMF.
- Preparation and review of Process validation protocol and Report.
- Monitoring of process validation.
- Preparation of Annual Product Review.
- Preparation and review of SOPs of Cross Functional Department.
- Handling Cleaning Validation.
- Handling Dispatch and line clearance activity.
- Initiation of QMS related activities like Change Control, Event and related CAPA.
- To ensure the EHS (Environmental Health and Safety) related activities to be completed on time and to support EHS activity as per requirement.
- To report near miss and incidences as observed as per EHS requirement.

Preferred candidate profile
- Valuable knowledge of cGMP, GDP, and pharmaceutical quality systems.
- Experience in BMR, ECR, MMF, and analytical data review.
- Understanding of Quality Control analytical documentation and data integrity requirements.
- Familiarity with Annual Product Review (APR/PQR) preparation and documentation.

📌 Executive QA (Navi Mumbai)
🏢 Piramal Pharma
📍 Navi Mumbai