Engineering CSV & QMS Manger

About the role

Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

What you'll do

• Lead Computer System Validation (CSV) and Engineering Quality Management Systems (QMS) activities across the site, ensuring compliance with regulatory requirements
• The role is responsible for maintaining inspection readiness and supporting business continuity through robust validation and quality systems
• Computer System Validation (CSV)
• Lead validation activities for GxP computerized systems, including equipment, automation systems, laboratory instruments, utilities, and software applications
• Ensure compliance with regulatory requirements including 21 CFR Part 11, EU Annex 11, GAMP 5, Data Integrity, and company procedures

What you need

• 12–15 years in pharma & medical sales
• ISO 9001
• Documentation
• Instrumentation
• SOP writing
• B.Tech or B.E.

Good to have

• SCADA
• PLC
• SAP