Sun Pharma

To support for commercial troubleshooting/remediation/Market complaints for Non-Oral manufacturing sites. To support for timely investigation/execution and to resume commercial manufacturing and to meet market/ sales requirement.

Master of Pharmacy Participation in Investigations, Root cause analysis and proposing relevant CAPAs against OOS: OOT: incident, and change control complaints and audit observations to QMS team.

Preparation of registration strategy for Brazil submission. Prepare response to deficiency letter received from Anvisa, Brazil. Sun Pharma, Executive Regulatory and Business Continuity

Responsible for executing technology transfer activities for injectable dosage forms, including planning and performing Scale-up, Exhibit and Process Validation batches with optimal utilization of manpower, materials, and equipment.

Granulation / Compressior / Coating / Packing OSD formulation. Sun Pharma is the fourth largest specialty generic pharmaceutical company in the world

Good Communication Skills. Good Subject Knowledge.

To manage and strengthen relationships with regulatory and government bodies, ensure compliance with licensing and regulatory requirements, WHO-GMP standards for plants and warehouses in the assigned region, and lead Corporate Social Responsibility

B.Pharm / M.Pharm and MBA. The Product Manager is essential in assisting with the creation, execution, and optimization of strategic and operational initiatives

Knowledge of Manufacturing process and must have handled QMS activities independently, knowledge of EDMS &Track wise shall be preferred