Novartis is hiring an International Program Regulatory Director IPRD in Hyderabad. Apply if you have exp in global/regional regulatory roles and expertise in drug registration strategies.
Ph.D. in Chemistry, Chemical Sciences, Material Sciences, Electrochemistry or equivalent. Experience in the field of design, development, and fabrication of electrolyser, fuel cell, energy devices and characterization techniques.
A PhD in Biological or Chemical Sciences, Life Sciences is essential. postdoctoral experience in the relevant field with at least one research paper in a SCI journal and laboratory experience is desirable.
Ph.D. or equivalent degree OR three years of research, teaching, design and development after MVSc, M.Pharm, M.E, M.Tech with at least one research paper in Science Citation Index Journal.
An ability to read and understand diverse literature across the many disciplines relevant to drugs, nucleic acid delivery to distill the best new ideas in the field and apply them to your work. An ability to identify the challenges associated, bottle necks in development and suggest mitigation proposals during development at various stages.
Knowledge and experience in the international regulatory environment of clinical trial applications, non-clinical and/or clinical variations to marketing authorizations and product labelling relevant for biotechnology and/or oncology products