Stelis Biopharma is hiring!!
Location: Bangalore
Experience: 2-8 years in Quality Assurance Validation
Please find JD below:
1. To carry out the qualification/ validation activities such as preparation, execution and review of qualification/ validation documents for validating/ Qualifying GMP equipment at all sites of Stelis Biopharma.
2. Preparation, review and implementation of Standard operating procedures, Protocols, etc., pertaining to Quality Assurance Validation in line with standard guidelines, Global GMP compliance regulations and industry practices related to the Biopharma industry.
3. Preparation support for Qualification/ Validation policies and Validation Master Plan.
4. To ensure compliance in qualification/ Validation activities in accordance with standard guidelines and site SOP.
Interested Candidates can share resumes to
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