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 current 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
Robust attention to detail and compliance orientation
Valuable coordination and communication skills
Ability to manage and organize QA documents and records
Willingness to learn and adapt in a regulated pharmaceutical environment

📌 Trainee Qa Navi Mumbai
🏢 Piramal Pharma
📍 Navi Mumbai