Regulatory Affairs Specialist is responsible for ensuring that medical devices comply with all applicable regulations in India and international markets
First Class M.Pharm, MS (Pharm) Masters in Pharmacognosy or Bachelor of Ayurvedic Medicine and Surgery. PhD in Natural Product Chemistry, Life Sciences, Pharmaceutical Sciences or related disciplines.
knowledge of various sophisticated instrumental methods for qualitative and quantitative analysis of tissue engineered constructs and regenerative technology development for clinical translation.
Clinical batch data review, method validation, and stability study evaluations as per cGMP & regulatory norms. Routine analysis of clinical samples and stability samples.