Job Description:
* Laboratory Upgradation: Up-gradation of current laboratory.
* Documentation: Responsible for the review and approval of key Documents like Standard Operating Procedure, Specifications, method of analysis, General Analytical method and Formats.
* Laboratory planning: Day-Today planning of testing, execution of plan, approval and release of raw material, intermediate and finish products with effective communication with stores and Production.
* Validation plan: Key member for planning of validation activity, execution and finalisation of protocol and report.
* Regulatory submission : Provide all QC related documents for regulatory submission of DMFs
* Audit faced during above period: USFDA, GMP, WHO and customer audits

Additional Information:
Experience: Above 3 Years
Qualification: M.Sc
Location: Ambernath
Functional Area: QC
Industry Type: Pharma
Last Date: 30th November, 2016

If you are interested then send your updated CV on hr4.nurture@hotmail.com

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