Apprentice QA
Piramal Pharma Ltd
Ahmedabad, Gujarat, IndiaFresher2h agovia LinkedIn
This job at a glance
- Who can apply
- Freshers
- Must know
- Auditing
- Work
- On-site in Ahmedabad
- Pay
- Not stated by the employer.
- Listed
- 28 Oct 2026 · still open
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About the Role
Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle.
Key Responsibilities
- Responsible for document control and records management, including issuance, archival, retrieval, and maintenance of GMP documents.
- Oversees retention sample storage monitoring.
- Maintains and takes regular follow-up for QMS records related to change controls, deviations, OOS, and other quality events.
- Issuance and control of documents (e.g. SOPs, BMR, BPR, Formats, Logbooks and LNBs).
- Management of archival and retrieval of documents.
- Updating of logbooks related to QMS documents (i.e. change control, deviation, OOS etc).
- Monitoring of temperature for retention sample storage.
- Participation in audit for arrangement of documents pre-audit and timely document availability during audits.