Post Graduate Degree, including the integrated PG degrees, with five years post qualification experience or PhD plus two years post qualification experience.
Masters in Chemistry, Organic Chemistry, Medicinal Chemistry from a recognized University OR Any equivalent qualifications duly recognized by the concerned authority as per the functional requirement
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
Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations, guidances and defined regulatory strategies.