Vacancy Description
JOB DESCRIPTION 5+ years of experience in Computer System Validation (CSV). 3 to 5 years of experience in pharmaceutical, biotech, life sciences, or regulated manufacturing environments. 3+ years of hands-on experience with MES validation and GxP validation lifecycle. Good understanding of 21 CFR Part 11, EU Annex 11, ALCOA+, and data integrity expectations. Experience in validation document preparation, review, execution, and approval workflows. Ability to coordinate with QA, Manufacturing, IT, Automation, and vendor teams. Strong documentation discipline and attention to detail.
We are currently seeking a CSV Specialist / CSV Consultant - MES Validation to join our team in Hyderabad, Telangana (IN-TG), India (IN).
Role: CSV Specialist / CSV Consultant - MES Validation
Location: Hyderabad (5 days a week)
30 Days’ Notice period
Required Experience and Skills
Preferred...
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