- Must have experience in Computer System Validation / Computer Software Assurance / Quality Compliance within the life sciences industry.
- Strong experience working in GxP-regulated manufacturing environments, preferably pharmaceutical, biotechnology, medical devices, or other regulated manufacturing sectors.
- Must have Hands-on experience with validation of infrastructure, IT/OT platforms, shopfloor systems, manufacturing applications, or related technology programs.
- Solid understanding of CSV lifecycle deliverables including URS/FRS, risk assessment, validation plan, IQ/OQ/PQ, test scripts, traceability matrix, deviation management, and validation summary report.




- Good to have Experience supporting technology changes in live manufacturing or production environments where downtime, compliance, and product quality are critical considerations.
- Familiarity with change control, incident management, problem management, SOP governance, and audit readiness in regulated environments.
- Experience working with global delivery teams, site teams, Quality organizations, and technical SMEs across multiple geographies.

Location - Pune,Bengaluru,Chennai,Hyderabad,Gurugram,Kochi,Indore

Contact Person - Mithra Dayalan

Email - [email protected]

📌 Computer System Validation ( CSV ) Professional (Pune)
🏢 Golden Opportunities
📍 Pune