Role & responsibilities

- Issuance, archival and retrieval of documents

- Issuance of control copies to respective dept.

- Tracking of all QA documents

- Maintaining of backup of QA soft copies.

- Maintaining SOPs with proper indexing

- Preparation and review of SOPS

- Perform qualifications for new equipment's /existing equipment's.

- Ensure coordination of Area Validations

- Reviewing of Calibration/PM Schedules.

- Preparation of VMP and Validation documents

- Handling of Vendor Qualifications activities

- Handling of Contract testing laboratory

- Handling of External Service Provider.

- Handling of Deviations, Change Controls, OOS, OOT, CAPA, compliants, return goods, risk assessment and product recall (QMS related activities)

Preferred candidate profile

- Basic understanding of GMP, documentation, and quality systems

- Strong attention to detail and compliance orientation

- Good coordination and communication skills

- Ability to manage and organize QA documents and records

- Willingness to learn and adapt in a regulated pharmaceutical setting

📌 Trainee - QA (Navi Mumbai)
🏢 PIRAMAL PHARMA
📍 Navi Mumbai