Opportunity to work as AGM/DGM - QA in Cadila Pharma

Cadila Pharmaceuticals Ltd., one of the largest Indian pharmaceutical companies has presence in 90 countries across the globe catering to over 45 therapeutic areas. The company has one of the best R&D setup in India which forms the backbone of our state-of-the-art manufacturing facilities in India and abroad, approved by various regulatory authorities including USFDA, MHRA (UK).
We have been making rapid strides and as part of our expansion plans, we are looking to acquire talent on an Pan India basis.

Post: AGM/DGM - QA

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Job Description:
1.Overall responsibility for Quality Assurance functions for Injectable facility.
2.Responsible for compliance to various cGMP guidelines including national and international guidelines for Injectable facility .
3.Ensure adequate implementation of corporate policies / guideline across the department.
4.Overall responsible for manpower planning and performance appraisal for Injectable facility.
5.Responsible for handling and compliance of any of the audits (regulatory / customer) performed by national and international agencies for Injectable facility.
6.To conduct cGMP and / or cGLP audits of entire facility on periodic basis.
7.To review and ensure the updation of Quality System and procedures of Warehouse , Manufacturing , Maintenance , Quality Assurance , Quality Control etc. as per the latest updation of national and International cGMP requirement.
8.To review and give authorization of Sops , MMD – I , MMD – II , validation and qualification protocol and reports, Deviations , Change control , CAPA , Market complaints , PQR (Product Quality Review) , Vendor documents , Batch documents.
9.To conduct investigation of any market complaint and sending replies to the complaints within stipulated time frame.
10. To highlights and resolve any Quality related issues pertaining to the Injectable facility.
11. To ensure cGMP related training programme for manpower associated with warehouse, Manufacturing, Maintenance, Quality Assurance and Quality Control etc.
12. To ensure smooth transfer of new products to plant level pertaining to the Injectable facility.
13. To provide necessary help to finance department in preparation of departmental budget pertaining to the Injectable facility
14. To conduct technical training to the respective staff members periodically for the updation and enhancement of the personnel

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Additional Information:
Experience: 15-25 Years
Location: Ahmedabad
Education: B.Pharm, M.Pharm, B.Sc, M.Sc-Biochem, Chemistry
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D, IPR