Apprentice QA

Piramal Pharma Ltd; Ahmedabad District; On-site; INR 201,000 - 268,000; Full time

Job summary

Piramal Pharma Solutions, a division of Piramal Pharma Ltd, seeks an Apprentice QA to manage GMP documents, archival, and records. You will ensure timely document issuance, control, and retrieval, maintaining QMS-related records and supporting audit readiness.

Responsibilities include updating logs for change controls, deviations, and OOS events, plus monitoring retention sample storage temperatures and ensuring proper document availability during audits.

Qualifications

• Document control and records management routines.
• GMP document handling and archival processes.
• Logbook updates for QMS documents (change control, deviations).

Responsibilities

• Issuance and control of GMP documents (SOPs, BMR, BPR, formats).
• Management of archival and retrieval of documents.
• Updating of logbooks and related QMS records.
• Monitor retention sample storage temperature and condition.
• Support pre-audit document availability and audit readiness.

Job description

Job Description

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Apprentice QA

Job Description

Responsible for document control and records management, including issuance, archival, retrieval, and maintenance of GMP documents. Oversees retention sample storage monitoring. Maintains and take 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.