Your new company
An innovative biotech start-up is pushing the boundaries of immune profiling and precision diagnostics using AI and machine learning. Backed by cutting-edge research and a collaborative, cross-functional team, this company is dedicated to transforming the way immune-related diseases are understood and treated. They're growing fast and looking for mission-driven individuals ready to make an impact.
Your new role
As Quality Manager, you'll take ownership of the Quality Management System (QMS), ensuring full compliance with ISO 13485 and associated regulatory standards. You'll lead internal and external audits, drive CAPA implementation, manage documentation and validation processes, and promote continuous improvement across quality systems. This is a full-time, office-based role (minimum 3 days per week on site) with occasional international travel.
What you'll need to succeed
Hands-on experience managing ISO 13485:2016 compliant QMS
Strong knowledge of risk management (ISO 14971), GCLP, CAPA, and validation (IQ/OQ/PQ)
Background in biotech, biomedical science, immunology, or similar
Solid understanding of regulatory submissions and eQMS platforms
Confident communicator and proactive team player with excellent problem-solving skills
Experience training others on quality procedures and compliance
Desirable: M.Sc./PhD, flow cytometry knowledge, quality certifications, previous start-up experience.
What you'll get in return
Competitive salary based on experience
Bonus scheme eligibility
Career progression in a fast-paced, high-growth biotech environment
Opportunity to shape and scale the QMS from within
Exposure to groundbreaking science and multidisciplinary collaboration
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.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
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