QA Systems Specialist

JR United Kingdom; Preston; On-site; GBP 35,000 - 55,000; Full time

Job summary

A prominent UK client seeks a QA Systems Specialist to oversee the implementation, validation, and maintenance of Quality Management Systems within the pharmaceutical sector. Candidates should possess a degree in a relevant field and experience with QMS platforms, ensuring all systems meet compliance standards while supporting global drug development. The role offers opportunities for mentorship and collaboration in a culture of innovation and integrity.

Qualifications

• Degree in Life Sciences, Engineering, or Computer Science preferred.
• Experience with MasterControl, ETQ, or similar QMS platforms.
• Strong CSV knowledge and regulatory standards familiarity.

Responsibilities

• Lead eQMS implementation and validation activities.
• Maintain system lifecycle documentation and user training.
• Ensure compliance with GxP and GLP standards.

Skills

Knowledge of pharmaceutical regulatory standards

Validation documentation skills

Communication skills

Project coordination skills

Education

Degree in Life Sciences, Engineering, Computer Science

Tools

MasterControl

ETQ

Job description

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QA Systems Specialist, preston, lancashire

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Client:

Blackfield Associates

Location:

preston, lancashire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

07.06.2025

Expiry Date:

22.07.2025

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Job Description:

QA Systems Specialist

Location: South East

Job Type: Permanent

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