Responsible for discussion and planning strategies for product development, executing them and recording them in E-Lab notebook. Identify and proactively discuss potential challenges along with possible way forward.
The role is responsible to asses / audit Sun manufacturing sites against current regulatory expectations / standards to ensure regulatory compliance. It includes adhering to applicable regulations, as well as Sun Pharma's policies and procedures.
Analytical Method Transfer of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray. Analytical method development and validation for pharmaceutical dosage forms.
M.Pharm./MS.Pharm. Pharmaceutical Analysis / Quality Assurance / Natural Products/ Medicinal Chemistry or Post graduation in M.Sc. Analytical Chemistry/ Organic Chemistry, National Institute of Pharmaceutical Education and Research.
For Senior Research Assistant the candidates should have an of M. Sc., M. Sc. (Ag.), M. Pharm., M.V.Sc. or equivalent degree with high academic attainment and at least two years of research experience
Review documents required for regulatory submissions across global markets, including product development reports and scientific justifications for responding to regulatory queries.