Sun Pharma

M.Sc / B.Pharm. Assess regulatory inspection citations from internal sites to identify and implement global corrective and preventive actions.

Review of R&D documents such as stability data, Analytical reports, Method verification reports, Method validation protocols & reports, analytical data of pilot bio batches / DQ batches and Product development data for its adequacy.

Quality Control Analyst will play a critical role in ensuring the integrity and safety of our pharmaceutical products. Youll conduct analytical testing on raw materials, in-process samples, and finished goods, adhering to Standard Operating Procedures and current Good Manufacturing Practices

Life Cycle management of branded portfolio from IP perspective including competition tracking. IP support for out-licensing projects.

To handle process like manufacturing of liquid product including media, complex injectable and suspension manufacturing.

Preparation & review of New and Existing Products artwork. Responsible to maintained artworks track records in excel.

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.

Bachelors or Masters degree in a field related to Science, Healthcare, Clinical Research or Life Sciences like Biology, Pharmacology, Nursing, or a related discipline.

To design and conduct experiments for preformulation, formulation optimization of Microsphere and long acting complex non oral dosage form based on QbD approach. To execute the experiments as per Design of experiments