Connecting MedTech organisations with the regulatory and quality professionals who bring medical devices to market and ensure ongoing compliance throughout the product lifecycle.
Bringing a medical device to market requires more than technical innovation — it demands rigorous regulatory expertise and robust quality systems. From product development and regulatory approval through to post-market surveillance, organisations rely on specialist professionals to ensure compliance, maintain product quality and navigate an evolving global regulatory landscape.
At SciPro, we partner with MedTech organisations to connect them with the regulatory and quality talent needed to successfully develop, launch and support innovative medical technologies. Our consultants understand the complexities of global regulatory frameworks and quality standards, enabling us to identify professionals who can help organisations achieve compliance while accelerating product development.
Whether you're preparing a regulatory submission, strengthening your Quality Management System or expanding your post-market surveillance capabilities, we provide tailored recruitment solutions designed around your business objectives.
Our specialist consultants recruit across the full Regulatory Affairs & Quality landscape, including:
Our consultants support permanent, contract and executive appointments across the full regulatory, quality and compliance lifecycle.
Regulatory Affairs Associate · Regulatory Affairs Specialist · Regulatory Affairs Manager · Senior Regulatory Affairs Manager · Director of Regulatory Affairs
Quality Assurance Specialist · Quality Engineer · Quality Manager · Compliance Manager · Head of Quality
QMS Specialist · Design Assurance Engineer · Validation Engineer · CAPA Specialist · Quality Systems Manager
Post-Market Surveillance Specialist · Vigilance Specialist · Risk Management Engineer · Complaint Handling Manager · Post-Market Surveillance Manager
Director of Quality · Vice President, Quality · Vice President, Regulatory Affairs · Global Head of Regulatory Affairs · Chief Quality Officer (CQO)
We partner with organisations developing, manufacturing and commercialising medical devices across global markets.
Whether you're making a strategic regulatory leadership appointment or strengthening your quality function ahead of product launch, our specialist consultants understand the expertise required to navigate today's regulatory landscape.
Every regulatory and quality hiring challenge is different. That's why we offer a range of specialist recruitment solutions designed to support organisations at every stage of growth.
Whether you need to appoint a Director of Regulatory Affairs, build a Quality Assurance team, recruit specialist contractors for a remediation project or strengthen your post-market surveillance capability, our consultants will recommend the solution best suited to your objectives.
Discover how we've helped MedTech organisations build regulatory and quality teams that accelerate approvals, strengthen compliance and support successful product launches.
Whether you're preparing for regulatory approval, strengthening your Quality Management System or making a strategic quality leadership appointment, our specialist consultants are ready to help.
Explore the latest Regulatory Affairs & Quality vacancies or speak to one of our specialist consultants about your next career move.
Regulatory Affairs & Quality is one part of our wider MedTech & Medical Devices offering. Explore our other specialist recruitment areas.
Clinical Affairs, Clinical Research, Clinical Evaluation and Evidence Generation.
