1. Manage the Quality Systems of Grin Laboratories.
2. Manage the Documentation System and Qdoc System.
3. Ensure that all GMP-related documents at Grin Laboratories are created, reviewed, updated, and stored in accordance with applicable regulations.
4. Ensure that each generated document complies with the coding system for each document type.
5. Ensure the efficient use of the area's material resources.
6. Ensure that all documents are reviewed periodically and kept up to date.
7. Send the validity status of all documents to the responsible parties in each area.
8. Manage the logbook lifecycle.
Bachelor's degree in Chemical Engineering, Pharmaceutical Chemistry, Pharmaceutical Engineering, or equivalent. Skills: Initiative, Teamwork, Adaptability, Integrity, Planning, and Goal-oriented.
2 years of experience in Quality Assurance or Quality Systems.
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.
