Lupin

Officer - GMP Compliance

Lupin  •  Pune, IN (Onsite)  •  3 days ago
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Job Description

  • Responsible for compliance with cGMP and related elements like facilities, documentation, trainings, reports, 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, 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.

Work Experience

2-3 years

Education


Post Graduation in BiotechnologyB.Tech in Chemical Engineering

Competencies

Lupin

About Lupin

Lupin Limited is a global pharmaceutical leader headquartered in Mumbai, India, with products distributed in over 100 markets. Lupin specializes in pharmaceutical products, including branded and generic formulations, complex generics, biotechnology products, and active pharmaceutical ingredients. Trusted by healthcare professionals and consumers globally, the company enjoys a strong position in India and the U.S. across multiple therapy areas, including respiratory, cardiovascular, anti-diabetic, anti-infective, gastrointestinal, central nervous system, and women’s health. Lupin has 15 state-of-the-art manufacturing sites and 7 research centers globally, along with a dedicated workforce of over 23,000 professionals. Lupin is committed to improving patient health outcomes through its subsidiaries – Lupin Diagnostics, Lupin Digital Health, and Lupin Manufacturing Solutions.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Mumbai, IN
Year Founded
1968
Website
lupin.com
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