* 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
Experience: Above 3 Years
Functional Area: QC
Industry Type: Pharma
Last Date: 30th November, 2016
If you are interested then send your updated CV on firstname.lastname@example.org
Please mention following details: