Executive QC Posts for M.Pharma @ Syngene | Apply Online

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Syngene International Limited
Incorporated in the year 1994
, Syngene International is one of India premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

Job Title:  Executive Quality Control

No. of Posts:  5

Job Description:  

1. Responsible to manage all activities in IP/FP team like preparation and review of Protocols, method of analysis and documents like validation study Protocols, observation data sheet, analysis report, summary and trend sheets.
2. Assisting in the technical aspects of the Change Control, CAPAs, and Test Methods Reviews and Revisions and assisting to resolve Laboratory incidents, Out of Specification (OOS), complaints, discrepancies and CAPA (corrective actions preventive actions).
3. Responsible to interface with customers/Clients to understand and establish requirements to meet and deliver their needs.
4. Responsible to check, update and review all the compliance documents on time for Equipments and Instruments documents like calibration records/reports, Log books, Stability chamber temperature/Humidity log sheets, etc.,
5. Review of daily laboratory monitoring, daily/monthly Verification, calibration records and reports for Equipments and Instruments.
6. Co-coordinating and supporting to the team for the preparation and review of QMS documentation such as SOPs, IOPs and EOPs.
7. Co-coordinating and supporting to the team for the preparation, review and approval of batch release documents, Protocols and Ext.,
8. Responsible to troubleshoot the problems, provide technical guidance, and mentor junior staff.
9. To participate in investigations, audits and inventory management, continuous improvement initiatives for each project.
10. Responsible to complete all planned Quality & Compliance training as and when required by the department/section or asked by the HOD/designee

Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: R&D
Role: Chemical Research Associate/Scientist
Employment Type: Permanent Job, Full Time

Qualifications:   PG – M.Pharma – Pharmacy, MS/M.Sc(Science) – Biotechnology

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