5+

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies.

To propose and fix the batch size i.e. of the Demo, Scale up, Exhibit and Commercial based on Equipment Capacity/Qualification, Scale Up factor calculations & annual requirements.

Ensure assigned products remain in a validated and compliant state as per MS&T and regulatory expectations. Contribute to investigations and prepare OPV reports, PPQ documentation, regulatory responses, and scale up proposals.

Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff.

Bachelor degree in Medical, Life Science or other healthcare related majors. Good understanding for regulations and policies issued by India, US FDA and EU, and ability to interpret international regulatory requirements. Medtronic

B. Pharm / M. Pharm, or M.Sc. in Life Sciences. Advanced proficiency in regulatory portals (SUGAM, NSWS) and expert-level understanding of the Drugs & Cosmetics Act and CDSCO guidelines. Elanco Animal Health

M.Pharm as Executive Pharmacokinetics. Literature search and study designing of Bioavailability and Bioequivalence studies of oral & non-oral products towards different regulatory submission. Sun Pharma

Zydus Life sciences, we nurture a culture of innovation, excellence, and inclusivity, driving meaningful advancement in the pharmaceutical and healthcare industries.

Post-graduation in Life sciences or any other applicable qualification and experience. Standard office or home working equipment required.