Sun Pharma

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.

Review documents required for regulatory submissions across global markets, including product development reports and scientific justifications for responding to regulatory queries.

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

Granulation, Compression, Tablet Coating, OSD Bottle Packing activities in OSD Manufacturing Plant

Review of Product Quality Complaint Investigation Reports Drug Products.Coordinate with other stakeholders involved in the complaint handling process.

B.Pharm / M.Pharm, Skid, Filling & Manufacturing, General Parenteral