QA Systems Specialist

JR United Kingdom; Chester; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading company is seeking an experienced QA Systems Specialist responsible for implementing and maintaining electronic Quality Management Systems in the pharmaceutical industry. The role involves leading validation activities, managing system documentation, and ensuring compliance with regulatory standards. Candidates will benefit from mentorship and have the opportunity to tackle real-world scientific challenges with cutting-edge technologies.

Qualifications

• Experience with MasterControl or similar QMS platforms is preferred.
• Strong knowledge of CSV and pharmaceutical regulatory standards.
• Excellent communication and project coordination skills.

Responsibilities

• Lead and support eQMS implementation, migration, and validation activities.
• Provide training and ongoing support to system users and stakeholders.
• Ensure systems remain audit-ready and compliant with GxP, GLP, and CSV requirements.

Skills

Communication

Project Coordination

Validation Documentation

Education

Degree in Life Sciences, Engineering, Computer Science

Tools

MasterControl

ETQ

Job description

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Are you an QA Systems Specialist seeking their next exciting opportunity?

We’re helping our client seek an experienced QA Systems Specialist to support the implementation, validation, and maintenance of electronic Quality Management Systems and pharmaceutical computerised systems.

Responsibilities

• Lead and support eQMS implementation, migration, and validation activities
• Maintain and manage system lifecycle documentation (URS, IQ/OQ/PQ, SOPs, etc.)
• Provide training and ongoing support to system users and stakeholders
• Ensure systems remain audit-ready and compliant with GxP, GLP, and CSV requirements
• Act as SME for validated systems and support continuous improvement
• Manage archiving processes and act as GLP archivist
• Communicate project progress and risks

Requirements

• Degree in Life Sciences, Engineering, Computer Science, or related field preferred
• Experience with MasterControl, ETQ, or similar QMS platforms
• Strong knowledge of CSV and pharmaceutical regulatory standards
• Experience with Empower CDS validation and data integrity
• Skilled in validation documentation and system configuration
• Excellent communication and project coordination skills
• Contribute to impactful, global drug development initiatives
• Benefit from mentorship and guidance from experienced industry leaders
• Thrive in a culture rooted in integrity, innovation, and lifelong learning
• Collaborate across functions to tackle real-world scientific challenges
• Work with advanced technologies and proprietary research platforms