Syngene International Ltd is hiring B. Pharma/ M. Pharma as a QMS Coordinator – Apply Now

Exciting news for B. Pharma/M. Pharma professionals! Syngene International Ltd is seeking talented individuals to join our team as QMS Coordinator. Join a dynamic and innovative environment where you can utilize your skills to ensure top-quality standards. Take the next step in your career with a leading global contract research organization. Don’t miss this opportunity to be part of groundbreaking projects and contribute to scientific advancements. Apply now and unleash your potential with Syngene International Ltd!

About Syngene

Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.

Job Description:
Key Responsibilities:

• Create/ revise procedures and other related documents as applicable.
• Review of SOPs, IOPs, EOPs, Protocol and Reports for Formulation Facilities.
• Handling of Change Controls, Deviations, CAPA, Customer complaints, Self-Inspection and Internal Quality Audit.
• Perform Trending of Change Controls, Deviations, CAPA, LIR and Customer complaints.
• Ensure compliance with observations of Self Inspection, Internal Quality Audit and client or regulatory audit.
• Perform activities related to SAP.
• Vendor qualification of raw material, packing material, consumables, contractors engaged in manufacturing pertaining to GMP manufacturing with respect to vendor questionnaire verification, vendor audit and compliance report verification for approval.
• Approval of vendors by desktop and site audits. (As required)
• Review of Risk assessment document from the vendor.
• Verification of vendor rating documents from the purchase.
• Inspection of RM, PM and consumables for any damage and discrepancy possible during receipt, storage dispensing and handling of these materials in warehouse.
• Review of vendor Quality Agreement.
• Preparation and updation of requalification schedule for Manufacturers.
• Archival of documents.
• Issuance of annexures and logbooks.
• Provide data for QMR and QGF meeting.
• Provide line clearance to Dispensing, Manufacturing and Packaging area.
• Provide dispatch clearance for Shipment.
• Preparation & Review of RSG report.
• Review and Approval of Calibration Certificate.
• Review of executed BMR and BPR.
• Responsible for review and release of Batches.

Behavioural Skills:

• Should have good communication skill and should be a good team player.
• Ability to work successfully in a dynamic, ambiguous environment.
• Ability to meet tight deadlines and prioritize workloads.
• Ability to develop new ideas and creative solutions.
• Should be a focused employee.

MORE JOBS: Walk-In Interview for B. Pharma/ M. Pharma/ M. Sc for Quality Control at Intas Pharmaceutical Ltd – 4th May 2024

<<<<<<<<<<<<JOIN US>>>>>>>>>>>>>>>>