Live opening · Posted 6 hours ago

CSV Engineer (Lifesciences & Medical Devices)

Capgemini India
Successfactors
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At a glance

The key details from the original listing.

Posted 6 hours ago
CompanyCapgemini India
SkillsDocumentation
SourceSuccessfactors
ListedPosted 6 hours ago

About the role

Description supplied by the original job listing.

CSV ENGINEER
At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as they provide unique R&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same.
WHAT YOU´LL LOVE ABOUT WORKING HERE
Join a multicultural and inclusive team environment.
Enjoy a supportive atmosphere promoting work life balance.
Hybrid work.
Your career growth is central to our mission. Our array of career growth programs and diverse professionals are crafted to support you in exploring a world of opportunities.
Access valuable training and certifications in cutting edge technologies.
Engage in exciting national and international projects.
Health and life insurance.
Referral program with bonuses for talent recommendations.
Great office locations.
YOUR ROLE
Plan, define, and execute Computer System Validation (CSV) activities in compliance with GxP guidelines (e.g., GAMP5, FDA, EMA)Develop and maintain validation documentation, including:
Validation Plans (VP)
User Requirement Specifications (URS)
Functional and Design Specifications (FS/DS)
IQ/OQ/PQ protocols and reports
YOUR PROFILE
Academic background in Pharmaceutical Sciences, Life Sciences, Engineering, or a related field, ensuring understanding of regulated environments and industry practices
Strong experience in Computer System Validation (CSV) within regulated environments (pharmaceutical, biotech), with solid knowledge of GxP, GAMP5, and compliance standards
Proven ability to translate business and regulatory requirements into validation deliverables, ensuring full traceability and high-quality documentation
Hands-on expertise in validation lifecycle activities (URS, FS/DS, IQ/OQ/PQ) combined with a structured and detail-oriented approach
Comfortable working in international, multicultural teams, with strong communication skills and fluency in English
ABOUT CAPGEMINI
Capgemini is the business transformation partner for enterprises in the age of AI. We help organizations imagine and build an intelligent, sustainable future, combining AI, technology and human ingenuity to transform how they operate, innovate and grow. With unique end-to-end capabilities spanning strategy, technology, engineering and intelligent operations, we bring together deep industry expertise and market-leading capabilities in AI, cloud and data to turn ambition into measurable business outcomes at scale. Supported by a robust ecosystem of partners and nearly 60 years of expertise, Capgemini is a responsible and diverse global organization of over 410,000 team members in more than 50 countries.

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