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Blackbull International
MDR, clinical trials, GxP compliance – in healthcare, regulatory details determine market access and patient safety. We source interim managers who can lead in this environment.
Quality management, regulatory affairs, study management, medtech production management, Head of QA and MDR transition project leads. Profiles in our network bring experience from medtech manufacturers, pharma companies and hospital groups.
The Medical Device Regulation has reshaped the entire market. We source interim managers who have led MDR transition projects, created technical documentation and guided organisations through notified body audits.
Study management, CRO oversight, regulatory submissions – clinical development is time-critical and heavily regulated. Through our network, we find interim managers with Phase I-IV experience at pharma and medtech companies.
GMP, GDP, GCP, ISO 13485 – in healthcare, there is no such thing as "roughly compliant". Our network includes interim managers who have built quality systems, prepared audits and systematically resolved deviations.

Whether a vacancy, project or transformation – tell us what you need and we will find the right solution. Fast, confidential and free of charge.