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Opportunity for Graduate / Postgraduate in Pharmacy as Executive/Asst. Manager QA Documentation in GlaxoSmithKline

 

 

academics

 

Clinical research courses

GlaxoSmithKline Pharmaceuticals Ltd. (GSK Rx India) is one of the oldest pharmaceuticals company and employs over 5000+ people. Globally, we are a £ 27.4 billion, leading, research-based healthcare and pharmaceutical company. In India, we are one of the market leaders. At GSK, our mission is to improve the quality of life by enabling people to do more, feel better and live longer. This mission drives us to make a real difference to the lives of millions of people with our commitment to effective healthcare solutions.

Post: Executive/Asst. Manager QA Documentation

Job Description
- To liase with manufacturing, planning and operational quality for issuance of documents like BMR, BPR, logbooks, registers, recording forms etc. Ensure all GMP documents are issued and archived in controlled manner & record of the same is maintained. Management of documentation control room
- To coordination with production, planning, engineering, quality control, operational quality, validation, warehouse (RM, PM & FP) & other support functions for document controls
- Coordination with planning for production plans.
- Plan and issue batch manufacturing and packing records to production.
- Issuance of log books, registers, recording forms etc. to all concerned departments.
- Maintain document masters for all critical documents.
- Maintain issuance record for all the documents.
- Proper storage of batch mfg. and packing records along with analytical records to ensure timely and effective retrieval.
- Tracking of documents for retention period as per QMS & regulatory requirements.
- Timely destruction of documents as per SOP after completion of retention period.
- Management of documentation control room and ensure proper labeling and segregation of documents for easy retrieval.

Candidate Profile
- Graduate / Postgraduate in Pharmacy / Life-sciences preferably with specialization in Quality Assurance documentation
- Minimum 3-5 years experience in handling quality system documents for regulated markets.
- 1 Full-Time position(s) available.


Additional Information:
Experience: 3-5 years
Location: Nashik
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QA
End Date: 30th October, 2014

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