Specialist recruitment for Regulatory Affairs and Quality Assurance professionals in the In Vitro Diagnostics and Medical Technology sector. We understand your world.
We don't just fill roles — we understand the regulatory landscape, the technical demands, and the compliance requirements of the IVD and broader medical device sector.
CE marking, UKCA, EU MDR / IVDR submissions, technical files, notified body interactions, and regulatory strategy across UK and European markets.
QMS design and implementation, ISO 13485 compliance, CAPA management, internal auditing, and supplier quality roles across the full product lifecycle.
Specialist knowledge of IVD Regulation (EU 2017/746), performance evaluation, clinical evidence, and the unique demands of diagnostic device development.
Broader MedTech placements spanning Class I–III devices, combination products, software as a medical device (SaMD), and digital health platforms.
Post-market surveillance, vigilance, PMCF study design, clinical evaluation reports, and complaint handling specialists.
Flexible engagement models from day-rate contractors and interim consultants to permanent placements at every level of seniority.
Register your profile with us and be considered for both live and upcoming roles across the IVD and MedTech space. We work with manufacturers, CROs, and consultancies of all sizes.
Thank you — we'll be in touch shortly.
Whether you're a hiring manager with a role to fill or a candidate exploring options, we'd love to hear from you.
Vesper Reach, 124 City Road
London, EC1V 2NX
We'll get back to you within one business day.