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Friday, 14 October 2016

Job Description
- Responsible to guide in preparation / update of Quality Management System Documents Responsible to prepare / review / update Design Master File, Technical Master File Responsible to prepare / review / update Technical documentation for the international registration of products.
- Responsible to prepare / review / update to get clinical trial approval from Drug Controller General India.

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Please mail your cv at  hr@espl.net.in
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