QA Systems Specialist

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

Job summary

A leading company is looking for a QA Systems Specialist to enhance their Quality Management Systems and support compliance activities. In this role, you will lead eQMS implementations, mentor users, and ensure systems remain audit-ready, contributing to impactful drug development initiatives. Ideal candidates will possess a degree in Life Sciences and substantial experience with validation documentation and project coordination.

Benefits

Mentorship from industry leaders

Culture of integrity and innovation

Lifelong learning opportunities

Qualifications

• Experience with QMS platforms like MasterControl, ETQ.
• Strong knowledge of pharmaceutical regulatory standards.
• Skilled in validation documentation and system configuration.

Responsibilities

• Lead and support eQMS implementation, migration, and validation activities.
• Maintain system lifecycle documentation, ensuring compliance with GxP, GLP standards.
• Provide training and support to stakeholders.

Skills

CSV knowledge

Project coordination

Communication

Validation documentation

System configuration

Education

Degree in Life Sciences

Degree in Engineering

Degree in Computer Science

Tools

MasterControl

ETQ

Empower CDS

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