Prepare, review, and maintain Artwork-related activities for India Region Formulations in compliance with regulatory and corporate requirements.
Prepare and review of specification and STP of Raw material, Packing Material and Drug Product.
Update and manage all required QMS and documentation activities in Veeva Vault, ensuring data integrity and timely compliance.
Perform audits as and when required and provide support in the preparation and finalization of audit reports (US and IR Formulation).
Review raw data and analytical reports of contract manufacturing products to ensure accuracy, compliance, and adherence to approved specifications.
8-12 years in relevant area as mentioned in the Job description
GraduationPost Graduation in Pharmacy or Science
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.
