Stelis Biopharma Recruitment Notification for Quality Assurance Validation Department working personals
Vacancy Information :
Quality Assurance Validation jobs
Experience: 2-8 years in Quality Assurance Validation
Job Description :
1. To carry out the qualification/ validation activities such as preparation, execution and review of qualification/ validation documents for validating/ Qualifying GMP equipment’s at all sites of Stelis Bio Pharma.
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 Biopharma industry.
3. Preparation support for Qualification/ Validation policies and Validation Master Plan.
4. To ensure compliance in qualification/ Validation activities in accordance to standard guidelines and site SOP.
Application Process :
Interested Candidates can share resume to email@example.com