1. Comply with all cGMP, GDP, Data integrity and EHS requirement.
2. Conduct all activities as per the applicable SOPs.
3. Report any quality concern or suggestion for improvement to supervisors/ managers.
4. Manufacturing / processing of batches of assigned products under supervision as per instructions given in the BMR.
5. Operation and cleaning of equipment’s and accessories used in related production activities as per respective SOPs.
6. Up-keeping area and machines as per GMP requirements.
7. Performing in-process checks as per respective BMR and recording of results in respective documents as applicable.
8. Ensure calibration and preventive maintenance of manufacturing equipment and instruments as per approved schedule and the results of same meeting the standards.
9. To perform line clearance activity during batch-to-batch and product to product change over and ensure the compliance as per SOP.
10. To handle the Granulation related equipment such Sifter, RMG, FBD and Co mill.
11. Trouble-shooting of Granulation related problem of machine and process as and when necessary.
2-5 years
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.
