Ensure compliance with cGMP, GLP and regulatory requirements for in-process and finished products. Review and approve batch records, deviations, investigations and CAPA.
Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world. Today, Intas is present in more than 85 countries worldwide and is growing at 20% CAGR. Around 70% of its revenues come from the international markets, particularly the highly regulated markets of EU and US. At Intas, every day and everyone works to create a world of good health, happiness and hope.
B.Pharma having 3-6 years of experience in Production/Packing Department (Area: Granulation/ /Compression/ Coating/ Inspection/ QMS/ Primary Packing/Secondary Packing)
Part of multi-disciplined team of healthcare professionals who support Apotex products by coordination of the development of medical documents such as Risk Management & Risk Evaluation Mitigation Plans.
Lead cross-functional regulatory discussions, align stakeholders on submission strategy, and communicate regulatory implications to support business and product development decisions.
M.Sc / M.Tech / M.Pharm / M.S. or equivalent degree in Life Sciences, Biotechnology, Biochemistry, Neuroscience, Pharmacology or allied biomedical sciences. Fellowship 2026 at NIPER Ahmedabad