MSc Chemistry Job at Enzene Biosciences Ltd | Executive - IPQA Role

MSc Chemistry Job at Enzene Biosciences Ltd | Executive – IPQA Role

Are you looking for an Executive IPQA job in Pune? This pharma QA job is a great opportunity for candidates seeking an M.Pharm job or MSc chemistry job in the biopharmaceutical industry. With experience in IPQA job roles, GMP, and data integrity, this Pune job offers strong career growth in quality assurance, validation, and manufacturing oversight.

About Enzene Biosciences Ltd

This biopharmaceutical company is a leading organization offering excellent Executive IPQA job opportunities in Pune for candidates seeking a pharma QA job in the biotechnology and life sciences sector. Known for its strong GMP compliance, advanced quality systems, and focus on data integrity, the company provides ideal M.Pharm job and MSc chemistry job roles. With a commitment to innovation, validation, and regulatory excellence, it supports professionals in IPQA job functions, batch documentation, and quality assurance. This Pune job environment promotes continuous improvement, making it a preferred choice for candidates looking to grow in pharma QA job and biotechnology job careers.

  • Job Post:Ā Executive – IPQA
  • Location:Ā Pune, Maharashtra, India
  • Job ID:169

Job Overview

This Executive IPQA job in Pune is a strong pharma QA job opportunity for professionals with 3–5 years of experience in the biopharmaceutical industry. The IPQA job involves manufacturing oversight, batch documentation review, validation, and compliance with GMP standards. This Pune job is ideal for candidates seeking an M.Pharm job or MSc chemistry job in quality assurance and process validation.

Key Responsibilities

  • Perform IPQA job activities, including line clearance and batch oversight
  • Provide manufacturing QA support in the pharma QA job role
  • Review batch manufacturing records and documentation
  • Ensure GMP compliance and data integrity (ALCOA+)
  • Conduct audit trail review and analytical QA checks
  • Handle deviations, complaints, and quality events
  • Support validation, CPV, and cleaning validation processes
  • Manage SOPs and QMS documentation

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