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QA Technician (Contract)

Hays Specialist Recruitment Limited·Birmingham (West Midlands (Region))On-site6-month contractSenior
£13 – £15 / hour
Vox Summary
  • Role Responsibilities: Supporting batch review and release activities, reviewing Device History Records, ensuring documentation compliance, supporting CAPA and non-conformance activities, and assisting with audits and quality projects.
  • Key Requirements: Experience in a QA role within a GMP environment, understanding of GxP principles, reviewing batch documentation, knowledge of quality systems, and familiarity with medical devices, pharmaceuticals, or diagnostics.
  • Conditions & Benefits: 6-month contract, Monday to Friday schedule, immediate start, working in a regulated manufacturing environment, and full right to work in the UK required.
Apply on sourceYou are leaving VoxJobs for reed.co.uk — the application is handled directly by the company. reed.co.uk

Job description

Your new company Your new company will be a globally recognised life sciences organisation operating within the speciality diagnostics sector. Supporting the development and manufacture of products that help improve patient outcomes worldwide, the business maintains a strong focus on quality, compliance and continuous improvement within a highly regulated environment. Your new role You will join the Quality team on an initial 6-month contract as a Senior QA Technician, supporting batch review and release activities within a GMP-regulated environment. Responsibilities will include reviewing Device History Records, ensuring documentation compliance, supporting CAPA and non-conformance activities, maintaining quality documentation, assisting with audits and quality projects, and working closely with cross-functional teams to ensure products are released in line with quality and regulatory requirements. What you'll need to succeed • Previous experience working within a QA position in a regulated GMP environment. • Strong understanding of GxP principles, particularly GMP. • Experience reviewing batch documentation and quality records. • Knowledge of CAPAs, deviations and quality systems. • Excellent attention to detail and document control skills. • Strong communication and organisational abilities. • Experience with medical devices, pharmaceuticals or diagnostics would be advantageous. • Familiarity with Microsoft Office and quality management systems Applicants must have full right to work in the UK for the duration of this 6-month contract. Visa sponsorship is not available for this position. What you'll get in return • Initial 6-month contract opportunity. • Monday to Friday working pattern. • Opportunity to join a global leader in the life sciences and diagnostics sector. • Exposure to a highly regulated manufacturing environment. • Collaborative and supportive quality team. • Immediate start available. Applicants must have full right to work in the UK for the duration of this 6-month contract. Visa sponsorship is not available for this position. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

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Original source
reed.co.uk
Posted
Jul 21, 2026 · true date
Last verified
3 hours ago
Quality score
65/100
Salary stated30
Company identified0
applyUrl0
postedAt15
Complete description20

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