Role & responsibilities Preferred candidate profile

- Conduct in-process quality assurance (IPQA) checks across various areas of the facility to ensure compliance with quality standards.
- Ensure effective implementation of systems and procedures in accordance with current Good Manufacturing Practices (cGMP) across the site, along with proper documentation.
- Ensure line clearance during product changeovers to prevent mix-ups and contamination.
- Verify Standard Operating Procedures (SOPs) and ensure procedural compliance on the shop floor
- Verify Batch Manufacturing Records (BMR), Batch Equipment Cleaning Records (BECR), logbooks, and other documentation for completeness and contemporaneous entries.
- Identify and report potential risks of contamination or cross-contamination within the facility.
- Ensure compliance with data integrity principles during all site activities.
- Monitor and verify that materials are stored under defined conditions and appropriately labeled.
- Ensure that deviations are reported in real-time and documented as per procedure.
- Conduct periodic reviews of quality records to ensure accuracy and completeness.
- Train shop floor personnel on SOPs, protocols, and quality standards.




- Review and trend alarm data as required to support quality and compliance.
- Manage Quality Management System (QMS) activities including documentation and follow-up.
- Review schedules and records related to validation, qualification, calibration, and preventive maintenance (PM).
- Conduct internal audits (self-inspections) to assess compliance and identify areas for improvement.
- Prepare and review SOPs to ensure clarity, accuracy, and regulatory compliance.
- Review Annual Product Reports (APR) to assess product performance and compliance.
- Support Environment, Health, and Safety (EHS) activities, ensure timely completion of EHS tasks, and report near misses and incidents as per EHS guidelines.
- Perform any other responsibilities assigned by the Head of Department (HOD).
- Follow Valuable Manufacturing Practices (GMP) and safety guidelines.

Preferred candidate profile

- Quick learner with excellent communication skills
- Punctual with proven track record of dedication & reliability
- A team player who is equally capable of working alone
- Fluent in both written and spoken English
- Knowledge /Experience in peptides

📌 Senior Executive - Quality Assurance (Navi Mumbai)
🏢 Piramal Pharma
📍 Navi Mumbai