Executive – Quality Assurance at Piramal Group, Mahad – Apply Now!
Are you ready to shape the future of pharmaceutical quality standards? Piramal Group is hiring a Quality Assurance Executive in Mahad, Maharashtra. This role offers hands-on involvement in validation processes, compliance auditing, and regulatory documentation. With responsibilities ranging from SOP preparation to change control management, this opportunity is ideal for B. Pharm or M. Pharm professionals looking to grow with an industry leader. Join Piramal and play a vital role in ensuring excellence in every batch.
About the Company
Piramal Group, with a legacy of over three decades, is one of India’s most respected business conglomerates. Operating in diverse sectors such as pharmaceuticals, financial services, and real estate, the group is known for its strong ethical values and sustainable growth strategies. Piramal Group is committed to innovation, inclusion, and excellence, empowering professionals to make a meaningful impact in global healthcare.
Job Details:
Job Posting: Executive – Quality Assurance
Location: Mahad, Maharashtra, India
Qualification: B. Pharm or M. Pharm
Experience: Preferred experience in pharmaceutical QA processes.
Executive – Quality Assurance Job Description
- Preparation and updation of Validation Master Plan (VMP)
- Preparation of Process validation, Computer system validation protocol, and report.
- Preparation of product matrix, cleaning, Validation/verification protocol, and Report.
- Preparation of qualification and requalification protocol and report for processing equipment/instrument, utilities, and facility.
- Preparation of the area validation protocol and reports.
- Preparation and review of quality risk assessments.
- Review of calibration certificate (External/internal).
- Preparation, issuance, review & archival of BMR/BPR.
- Batch Record storage, retrieval & destruction.
- Preparation of APQR.
- Line Clearance for Manufacturing, Packing & Dispensing activity.
- Sampling of Bulk and Finished Goods.
- Review of production records and Finished Goods verification.
- Online observation of process deviation and effective implementation of CAPA.
- Management of Change Control / CAPA / Incidents.
- Handling of Change Control and follow-up for the implementation of Changes.
- To coordinate & maintain change control, deviation records.
- Complaint handling.
- Preparation and updation of Q.A departmental SOPs and loading it in DCS (Document Control System) ENSUR 4.2
- To give training as per the Training schedule.
- Coordinate the company’s training program along with HR, including on-the-job training.
- Documentation Management as per SOP.
- To provide the necessary documents/data required by CQA and as per the customer’s requirement.
- Conduct, monitor, and review the compliance of the Self-Inspection Program.
- Audit compliance coordination: Compile the CAPA and prepare a response to the Audit report in coordination with the QA Head and the technical team.
- Execution of requirements for food / Dietary supplements regulations for export market (US)-21 CFR Part 111
- Ensuring the avoidance of breach of data integrity in the area.
- Implementation of an effective sanitation programme in the area.
- Adherence to the requirements of EHS norms.
- Execution of various initiatives as suggested by corporate functions.
- To determine internal and external QEHS issues, as well as the needs and expectations of relevant interested parties, and monitor them.
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