Pharma Jobs at Piramal Group | BSc Graduates Apply Now for the Senior Executive RoleÂ
Piramal Group is seeking a Senior Executive – IPQA to ensure compliance and quality assurance across production processes. The role involves line clearance for production operations, review of BMR/BFR/BPR, in-process QA activities, control sample management, GMP verification, and coordination for batch release and process validations. Additional responsibilities include APQR data compilation with trend analysis, vendor management documentation, document archival management, and issuance/control of SOPs and specifications.
About The Company
Piramal Pharma Limited is a global pharmaceutical company based in India, known for providing end-to-end solutions across the pharmaceutical value chain. The company operates in diverse segments, including contract development and manufacturing (CDMO), complex hospital generics, and over-the-counter consumer healthcare products. With a strong focus on innovation, quality, and patient-centric solutions, Piramal Pharma serves customers in more than 100 countries. Leveraging its world-class manufacturing facilities, research capabilities, and regulatory expertise, the company is committed to improving access to affordable, high-quality medicines and advancing global healthcare.
Job Posting: Senior Executive – IPQA
Location: Medak, Telangana, India
Qualifications:
- B.Sc./M.Sc/B.Pharm/M.Pharm (Science/Pharma background)
- Strong knowledge of GMP, APQR, documentation, and quality standards
Key Skills:
BMR/BFR/BPR review, SOP management, GMP compliance, vendor management, and documentation control.
Why Join?
- Be part of a global critical care solutions provider
- Exposure to regulatory-compliant manufacturing facilities
- Opportunities for career growth in quality assurance
Why This Role?
This role is ideal for professionals passionate about ensuring the highest standards of quality and compliance in pharmaceutical manufacturing. As a Senior Executive – IPQA at Piramal, you will play a key role in maintaining GMP excellence, supporting regulatory audits, and driving continuous improvements in production quality. The position offers hands-on experience with critical care products, collaboration with cross-functional teams, and opportunities to contribute to a company recognized globally for its ethical practices and innovation. It’s a chance to build a rewarding career while making a tangible impact on patient safety and product quality worldwide.
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