Create Alert
Apply Now »

Title:  Executive - Analytical Development

Date:  Oct 17, 2024
Location:  Tandalja - R&D
Company:  Sun Pharmaceutical Industries Ltd
  • Responsible for review of raw data, preparation of CoA of Peptide related Reference standards.
  • Coordination with plant location regarding the supply of Peptide RS/GRS/PRS and ensure the business continuity with uninterrupted supply to all locations
  • Responsible to investigation of any noncompliance/event occur during execution of GMP activities for Peptide related activities.
  • Review and approval of Quality Management System documents related to Peptide projects through Track wise (CCR/PD/UPD/INVESTIGATION/OOS/OOC, Lab event and related documents).
  • Responsible to escalate any issue/incidence to superior for prompt corrective action.
  • To work as per cGMP and ensure its compliance and responsible for review of raw data of GMP document of peptide projects.
  • Responsible for training related activities for team members.
  • Other job responsibility assigned by reporting authority.

Apply Now »