Chemical Engineering Job at Lupin | GMP Compliance Officer
Looking for a rewarding Chemical Engineering Job in the pharmaceutical and biotechnology industry? Lupin has announced an exciting Officer – GMP Compliance opening at its Pune Biotech facility. This excellent Lupin Career opportunity is ideal for professionals with experience in cGMP compliance, biotechnology manufacturing, documentation systems, and equipment qualification. Candidates can gain valuable exposure to pharmaceutical operations, quality systems, and regulatory compliance while building a strong long-term career profile.
About Lupin
Lupin is one of India’s leading pharmaceutical and biotechnology companies with a strong global presence in healthcare innovation and manufacturing excellence. The company focuses on advanced pharmaceutical products, biotechnology solutions, and quality-driven operations while maintaining world-class compliance standards. Through its growing Lupin Career opportunities, the organization provides professionals with excellent exposure to pharmaceutical manufacturing, quality assurance, biotechnology research, and Chemical Engineering Job roles across multiple healthcare sectors.
Job Overview
The Officer – GMP Compliance role focuses on ensuring compliance with cGMP standards during manufacturing operations across mammalian and microbial facilities. Selected candidates will prepare and review GMP documentation, handle change controls, deviations, CAPA reports, and equipment qualification documentation such as IQ, OQ, PQ, and RQ. This Chemical Engineering Job is
highly suitable for candidates interested in biotechnology manufacturing, pharmaceutical quality systems, compliance operations, and industrial documentation management within a leading Lupin Career environment.- Job Post: Officer – GMP Compliance
- Location: Pune Biotech, MH, IN
Responsibilities:
- Responsible for compliance with cGMP and related elements like facilities, documentation, training, reports, and records during manufacturing operations. Preparation and Review of GMP documents related to all mammalian manufacturing facilities, microbial manufacturing facility, and drug product manufacturing department.
- To raise and handle the documents like Change controls, deviations, CAPA, and Investigation reports for all mammalian and microbial manufacturing facilities.
- To prepare and review IQ, OQ, PQ, and RQ documents for equipment qualification in all mammalian and microbial manufacturing departments.
Requirements:
- Work Experience: 2-3 years
- Education: Post-Graduation in Biotechnology, B.Tech in Chemical Engineering
The Officer – GMP Compliance position is an excellent opportunity for professionals seeking a stable and growth-oriented Chemical Engineering Job in the pharmaceutical sector. With hands-on exposure to cGMP systems, biotechnology manufacturing, equipment qualification, and quality compliance operations, candidates can significantly strengthen their technical and regulatory expertise. Professionals interested in pharmaceutical manufacturing and biotechnology operations should consider applying for this valuable Lupin Career opportunity.
