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 ...
QA Technician (Contract) • Birmingham, West Midlands (County), UK
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