Achieve global medical device brand recognition - Enter the 2026 EMAs Now:
Enter 2026 EMAs

Regulatory Affairs Recruitment

Specifically looking to hire an ISO 13485 Lead? Visit our dedicated service page:
ISO 13485 Recruitment
Regulatory Recruitment Excellence in Life Sciences
At Adaptive Life Science, we've established ourselves as the definitive authority in regulatory recruitment for the Medical Device, IVD, Biotech, and Pharmaceutical industries. What sets us apart isn't just our extensive network, it's our recruiters' unparalleled expertise in navigating the complex regulatory landscape that defines these critical sectors.

Deep Regulatory Knowledge That Makes the Difference
Our regulatory recruitment specialists undergo intensive training to understand the nuances that matter most. They're well-versed in ISO 13485 for medical devices, ISO 15189 for medical laboratories, and ISO 14155 for clinical investigations. Beyond the foundational standards, our team recognizes the significance of niche requirements like ICH guidelines, 21 CFR Part 820 quality system regulations, MDR compliance frameworks, and IVDR transition complexities.

This specialized knowledge means we don't just match resumes, we identify candidates who truly understand regulatory submission pathways, post-market surveillance requirements, and the intricate dance between innovation and compliance that drives successful product launches.

Connecting Experience with Opportunity
Our regulatory recruitment process focuses exclusively on seasoned professionals with a minimum of three years' experience, extending to industry veterans with over four decades of regulatory expertise. This approach ensures our clients access candidates who've navigated real-world challenges, from FDA 510(k) submissions to CE marking processes and beyond.

We attract top-tier regulatory talent by offering our services to candidates completely free of charge, building a robust community of professionals who trust us to advance their careers. Meanwhile, our fee-based client services deliver the dedicated, tailored regulatory recruitment experience that complex hiring decisions demand.

Your Regulatory Recruitment Partner
When regulatory compliance can make or break a product launch, you need recruitment partners who understand the stakes. Our deep industry expertise, combined with meticulous candidate evaluation, ensures every regulatory recruitment placement meets the exacting standards your organization requires.

Trust Adaptive Life Science to deliver regulatory recruitment solutions that don't just fill positions—they strengthen your entire regulatory framework with proven expertise.
Contact Us
Digital Health 
The Digital Health Sector is one of the fastest growing sectors within Healthcare, if not the fastest, and the global pandemic has only helped accelerate it.

Whether it’s a DiGA, new product coming to market, device utilizing AI or VR, we know them all and the companies offering innovation and creative freedom.

From VC backed start-ups to global players entering the digital health space, we have options to suit your style and product interests.

For our clients in digital health, we’re in contact with professionals across the wide spectrum of product management, from technical (with a track record of managing product development and design, including the planning process) to UX/UI, product growth and owners responsible for an entire app.
Traditional Medical Devices
Adaptive’s highly experienced consultants have grown an extensive network of top professionals and medical device manufacturers. We support product professionals with experience in all areas of the Medial Device space including Class I – III products, IVDs, Software, Invasive and Non-Invasive Devices, as well as Prosthetics and Implants.
Contact Us

Read Our Blogs

May 1, 2025
What is ISO 9100: A Crucial Guide for Medical Device Industry Leaders in Germany and Europe

In today's highly regulated medical device industry, ensuring quality management and compliance is paramount. As CEOs, COOs, VPs, Presidents, and leaders in Germany and across Europe, understanding and adhering to ISO 9100 standards is not just a regulatory requirement but a strategic imperative. What is ISO 9100? ISO 9100 is an internationally recognized standard for […]

April 16, 2025
Understanding ISO 27001 Standards: A Crucial Guide for Medical Device Industry Leaders

In today's digital age, safeguarding sensitive information is paramount, especially in the medical device, IVD, and biotech industries. As CEOs, COOs, VPs, and Presidents, understanding and adhering to ISO 27001 standards is not just a regulatory requirement but a strategic imperative. What is ISO 27001? ISO 27001 is an internationally recognized standard for information security […]

March 17, 2025
Emerging Technologies in the Medical Device Industry

The medical device industry stands at the intersection of healthcare and technology, continually evolving to improve patient outcomes and streamline medical processes. As we navigate the 21st century, several emerging technologies are set to revolutionize this sector. Let's explore these innovations and their potential impact. From smartwatches that monitor heart rates to wearable ECG monitors, […]

March 17, 2025
Understanding Wearable Medical Device Regulations

The rapid growth of wearable medical devices has revolutionized healthcare by enabling continuous monitoring and real-time data collection. From heart rate monitors to glucose sensors, these devices provide invaluable insights that can improve patient outcomes. However, as with any medical product, wearable devices must meet strict regulatory standards before they can be marketed and used. Understanding these […]

1 4 5 6 7 8 17

Submit Vacancy

    linkedin facebook pinterest youtube rss twitter instagram facebook-blank rss-blank linkedin-blank pinterest youtube twitter instagram