Halol

Responsible for monitoring of cGMP activities at site and to have the oversight, monitoring and compliance with quality system.

Handling of Contract Service Provider. Facilitate for timely preparation, review and adequate response to the Observation and monitor CAPA planner for it timely closures. 

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.

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.

B.Pharma / M.Pharma ; Sun Pharmaceutical Industries Limited is taking this opportunity to balance employment and the medications for the world.

Review of all the documents received from stake holder for dossier compilation , Query response and Life cycle management

Monitoring for Documents compilation activities for New product filing , Re-Registration, renewals from plant dossier filing , sample requirements etc. Participation in Action plan discussion for queries from different Regulatory agencies and monitoring for submission of data/documents from plant.

B.Pharm, M.Pharm ; Granulation, Compression, Coating, FBE, Capsule Hard Gelatin and Soft Gelatin, Blister Packing Primary and secondary for Cytotoxic, Sex Hormones

To monitor & prior checkup of equipment planned for usage in Scale up, Exhibit, Process validation batches i.e. Equipment preparation, vial washing and dehydrogenation, CIP, SIP System, PLCs, instruments etc.