Computer System Validation Specialist at Merck Group
Livingston, Scotland, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

08 Oct, 25

Salary

0.0

Posted On

08 Jul, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Information Technology/IT

Description

Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Responsibilities

We have an exciting opportunity for a Computer Systems Validation (CSV) Specialist at our Livingston site. In this role, you will lead Computer Systems Validation across the site and support the execution of the Validation Master Plan. You will ensure compliance with regulatory requirements (21 CFR Parts 11, 211, 600, ISO 9001, ISO 13485) and provide guidance on validation issues. Your responsibilities will include participating in investigations for failures, managing CAPA, and driving continuous improvement initiatives while maintaining and updating validation procedures.
You will stay informed on the latest regulatory requirements and support the IT department in Software and Hardware Validation compliance. As a subject matter expert (SME) for GxP systems, you will drive compliance strategies and manage GxP system life cycle activities, including change management and system integration projects.

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