Validation Lead API(Ahmednagar)

SUN PHARMA; Ahmednagar; Hybrid; MXN 900,000 - 1,200,000; Full time

Job summary

Sun Pharma is seeking an experienced IT professional to manage the Plant GxP Application Inventory and serve as the Technical Owner for CSV documentation. You will oversee CSV and QMS activities from implementation to retirement, ensuring audit readiness and regulatory compliance across the system lifecycle.

You will collaborate with System Owners in Quality & Manufacturing and IT teams, coordinate IQ/OQ/PQ activities, and support internal and external audits by explaining processes and

Qualifications

• BE/B.Tech, MCA, BCA, MSc IT, BSc IT, Graduation + PGDCA.
• Experience of 8-10 years in IT activities in pharma manufacturing.
• Knowledge of CSV/QA processes and regulatory requirements.

Responsibilities

• 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 during CSV execution.
• Support audits by explaining CSV processes and remediation.

Skills

Computer System Validation

IT regulatory requirements

Validation & Qualification execution

Education

BE/B.Tech

MCA

BCA

MSc IT

BSc IT

Graduation + PGDCA

Tools

Trackwise

Validator

EDMS

Job description

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

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.”

Job Summary

The job holder will be responsible for managing the Plant GxP Application Inventory and serving as the Technical Owner for Computer System Validation (CSV) documentation related to GxP applications. They will oversee periodic CSV and QMS activities throughout the system lifecycle, from implementation to retirement. Additionally, they will support the business during internal and external audits by explaining processes and documentation related to CSV and remediation.

Responsibilities

• To manage Inventory of GxP Applications for Manufacturing & Quality IT .
• Planning and review of validation deliverables for CSV Projects.
• Preparation, reviews and Approval of CSV documents as Technical Owner.
• Ensuring the compliance of GSOP’s /SOP’s related to Computer System Validation documentation and regulatory requirements during execution of CSV Project.
• Understanding the working and usage of Systems such as Trackwise, Validator and EDMS.
• Compliances to IT policies and procedures & regulatory requirements and support for the internal and external audits and remediation.
• Vendor coordination and support during Installation qualification (IQ), Operational qualification & Performance qualification (PQ).
• Identify the continuous improvement opportunities for CSV projects.
• Documentation and control for management of CSV documents w.r.t. IT.
• Timely completion of validation activities with zero timeline extensions
• Full audit readiness with complete and compliant documentation
• Effective and timely closure of all related QMS records (deviations, CAPA, change controls, etc.)

Travel Estimate

Based on the need job holder can travel to other sites.

Job Scope

Internal Interactions (within the organization)

System Owners from site Quality & Manufacturing and CQIT, Corporate IT.

External Interactions (outside the organization)

Business Users, External Vendors

Geographical Scope

Provide onsite support to the site & other site whenever needed Remotely.

Financial Accountability (cost/revenue with exclusive authority)

NA

Job Requirements

Educational Qualification

BE/B. Tech, MCA, BCA, MSc IT, BSc. IT, Graduation + PGDCA.

Specific Certification

NA

Skills

Computer System Validation, Understanding of IT regulatory requirements, Execution of Validation & Qualification activities.

Experience

8-10 Years in IT activities preferably in Pharma Manufacturing.

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!