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
