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