Sun Pharmaceutical Industries Ltd
Company: Sun Pharmaceutical Industries Ltd
Location: Ahilyanagar (Ahmednagar – Information Technology)
Employment Type: Full-Time
Experience Required: 8–10 Years
Industry: Pharmaceutical Manufacturing
Department: Information Technology
Posted On: 22 Feb 2026
🌞 About Sun Pharma
At Sun Pharmaceutical Industries Ltd, employees are empowered to “Create your own sunshine” by growing continuously, taking charge of their journey, and thriving in a collaborative and supportive environment.
Sun Pharma encourages self-drive, leadership, and teamwork—helping professionals become better every day.
💼 Job Summary
The Validation Lead – API will be responsible for managing the Plant GxP Application Inventory and acting as the Technical Owner for Computer System Validation (CSV) documentation related to GxP applications.
The role includes overseeing periodic CSV and QMS activities across the system lifecycle—from implementation through retirement—and supporting audit readiness and remediation activities.
🎯 Key Responsibilities
📋 GxP & CSV Management
- Manage inventory of GxP Applications for Manufacturing & Quality IT
- Plan and review validation deliverables for CSV projects
- Prepare, review, and approve CSV documents as Technical Owner
- Ensure compliance with GSOPs/SOPs and regulatory requirements
🖥 Systems & Compliance
- Understand and support systems such as Trackwise, Validator, and EDMS
- Ensure compliance with IT policies, procedures, and regulatory requirements
- Support internal and external audits and remediation activities
🏗 Qualification & Vendor Coordination
- Coordinate with vendors for IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification)
- Identify continuous improvement opportunities for CSV projects
- Manage documentation control for IT-related CSV records
⏱ Delivery & Audit Readiness
- Ensure timely completion of validation activities with zero timeline extensions
- Maintain full audit readiness with complete, compliant documentation
- Ensure timely closure of QMS records (deviations, CAPA, change controls, etc.)
🤝 Stakeholder Interactions
Internal
- System Owners (Quality & Manufacturing)
- CQIT and Corporate IT teams
External
- Business Users
- External Vendors
🌍 Travel & Scope
- Travel to other sites may be required based on business needs
- Provide onsite and remote support to other sites as necessary
🎓 Educational Qualification
- BE / B.Tech
- MCA / BCA
- MSc IT / BSc IT
- Graduation + PGDCA
🛠 Required Skills
- Computer System Validation (CSV)
- Understanding of IT regulatory requirements in pharma
- Execution of validation & qualification activities
- Strong documentation and compliance expertise
💼 Experience
- 8–10 years of IT experience
- Preferably in pharmaceutical manufacturing environments
📩 Apply for This Job
Interested candidates can apply through the official Sun Pharma careers portal.
👉 Apply Now – https://careers.sunpharma.com/job/Ahilyanagar-Validation-Lead-API%28Ahmednagar%29/47479544/
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To apply for this job please visit careers.sunpharma.com.
