Csv Senior Compliance Advisor - Labs & Test Equipment

ConvaTec Group

Deeside, Wales, United Kingdom
Hybrid (on-site presence required as needed)
Gxp and medical device regulations
Validate laboratory systems
Validate test equipment
ConvaTec Group is seeking a Senior Compliance Advisor specializing in Computer Systems Validation (CSV) for laboratory systems and test equipment. The role focuses on ensuring compliance with regulatory standards in a medical device manufacturing environment and requires collaboration across multiple teams

Job Summary

  • The CSV Senior Compliance Advisor will play a critical role in ensuring that laboratory systems and computer‑controlled test equipment supporting GxP activities are validated and maintained in a compliant state.
  • This role is heavily focused on laboratory and test equipment in manufacturing environments within a medical device manufacturing organization, including systems and equipment used for product testing, verification, and quality assurance.
  • The CSV Senior Compliance Advisor will support and oversee CSV activities for laboratory systems and test equipment, ensuring systems are inspection‑ready, data integrity principles are applied, and validated systems remain fit for intended use throughout their lifecycle.

Matching Summary

Match Score: 85

ConvaTec Group is seeking a Senior Compliance Advisor specializing in Computer Systems Validation (CSV) for laboratory systems and test equipment. The role focuses on ensuring compliance with regulatory standards in a medical device manufacturing environment and requires collaboration across multiple teams.

Skills & Requirements

Must-have

  • GxP and medical device regulations
  • validate laboratory systems
  • validate test equipment
  • data integrity principles
  • cross-functional collaboration

Nice-to-have

  • experience in Saas based applications
  • experience validating enterprise IT applications
  • experience in migration of data

Key Requirements

  • 5+ years’ experience in CSV
  • Bachelor’s degree in Life Sciences, Engineering, Computer Science or related field
  • Experience in CSV, QA, validation or compliance roles within the medical device industry

Work Rights

Not specified

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