Senior Executive-QA

Piramal Pharma Ltd; Ahmedabad District; On-site; INR 800,000 - 1,100,000; Full time

Job summary

Piramal Pharma Solutions in Ahmedabad is seeking a Senior Executive-QA to manage document control and archival activities, ensuring GMP documents are issued, retrieved, and maintained, and overseeing retention samples, in-process and verification sampling in the Pilot Plant.

You will support the QMS through SOP preparation, training delivery, logbook maintenance, and management of quality events, while promoting data integrity awareness across site operations.

Responsibilities

• Responsible for document control and archival management, including issuance, retrieval, and maintenance of GMP documents.
• Reviews batch manufacturing and packaging records to ensure GMP compliance in the Pilot Plant.

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

Senior Executive-QA

Job Description

• Responsible for document control and archival management, including issuance, retrieval, and maintenance of GMP documents. Oversees retention sample storage monitoring, in-process and verification sampling activities, line clearance, and control sample management. Reviews batch manufacturing and packaging records and ensures compliance with quality systems and GMP requirements in the Pilot Plant. Supports the Quality Management System (QMS) through SOP preparation, training delivery, logbook maintenance, and management of quality events. Promotes and ensures data integrity compliance and awareness across site operations.
• Issuance and control of documents. (e.g. SOPs, BMR, BPR, Formats, Logbooks and LNBs).
• Management of Archival and Retrieval of documents.
• Monitoring of temperature for retention sample storage
• In process sampling of Clinical batches, Sampling of Swab during cleaning verification, Line clearance in pilot plant, water sampling, management of control samples.
• To review master and executed Batch Manufacturing Record, Batch Packaging Record and other documents related to manufacturing/packaging activity.
• To ensure practices being followed in Pilot Plant are in compliance with the quality procedures of the site.
• Prepare SOPs related to QA Department.
• Impart Induction Training on topics and on which training has been taken.
• Updating of Logbooks related to QMS documents (change control, deviation, OOS).
• Ensure compliance and awareness of data integrity at site.