Your new company

You will be joining a leading global organisation within the life sciences sector, recognised for its commitment to quality, innovation, and improving global health outcomes. The company operates within a highly regulated environment and fosters a collaborative, high-performing culture focused on continuous improvement and operational excellence.

Your new role

• Supporting compliance with GMP/GxP and ISO standards
• Leading and contributing to deviation investigations and root cause analysis
• Managing change control and CAPA processes
• Authoring and reviewing quality documentation (SOPs, reports, etc.)
• Supporting internal and external audits and regulatory inspections
• Analysing quality data and reporting on trends and metrics
• Collaborating with manufacturing, QA, and engineering teams to drive improvements

What you'll need to succeed

• A degree in Life Sciences, Engineering, or a related discipline
• Experience within a regulated industry (pharmaceutical, biotech, or medical devices)
• Strong knowledge of GMP/GxP and ISO standards
• Experience with quality systems, including deviations, CAPA, and change control
• Familiarity with QMS platforms (e.g. MasterControl or similar)
• Strong investigation and root cause analysis skills
• Excellent technical writing and documentation skills
• Strong communication skills and ability to work cross-functionally
• The ability to work both independently and collaboratively

What you'll get in return

• Competitive hourly rate
• Flexible, primarily remote working arrangement
• Opportunity to work within a well-established and reputable organisation
• Exposure to a fast-paced, quality-driven environment
• Potential for contract extension

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.