QA Systems Specialist

JR United Kingdom; Basildon; On-site; GBP 40,000 - 65,000; Full time

Job summary

A leading company in the pharmaceutical sector seeks an experienced QA Systems Specialist in Basildon. You will support the implementation and validation of electronic Quality Management Systems, ensuring compliance with GxP standards. Ideal candidates hold a degree in a related field and have experience with QMS platforms. Join a team dedicated to impactful global drug development initiatives and thrive in a culture rooted in integrity and innovation.

Qualifications

• Degree in Life Sciences, Engineering, or related field preferred.
• Strong knowledge of CSV and pharmaceutical regulations.
• Experience with MasterControl, ETQ, or similar QMS platforms.

Responsibilities

• Lead eQMS implementation and validation activities.
• Manage system lifecycle documentation and ensure audit readiness.
• Provide training and support for system users.

Skills

Communication

Project Coordination

Validation Documentation

System Configuration

Education

Degree in Life Sciences

Engineering

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