Job Description
Skills:
Computerized System Validation, GxP Compliance, 21 CFR Part 11, IQ, OQ, PQ,
Were Hiring! CSV Validation Engineer - Pharma Project | Multiple Locations
Position: CSV Validation Engineer
Company: INSTRUMENTATION AND CONTROL SOLUTIONS (ICS)
Location: Hyderabad
Experience: 1 to 7 Years
Notice Period: Immediate to 30 Days preferred
Key Responsibilities & Skills
Preparation and execution of Validation Deliverables in accordance with GAMP5 and 21 CFR Part 11 guidelines.
Hands-on experience with GAMP, 21 CFR Part 11, GxP, IQ/OQ/PQ, and validation of manufacturing systems (SCADA, HMI, PLC).
Conduct and document Computer System Validation (CSV) activities for pharmaceutical/life sciences environments.
Prior Experience With Regulated GxP Systems Is Essential.
Ability to collaborate across cross-functional teams in a regulated environment.
Interested candidates are invited to share their updated CV at:
Email: [Confidential Information]
Whats App/Call: +91 91091 88709
