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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.
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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.
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Read Our Blogs

June 5, 2025
Navigating IVDR Regulation (EU) 2017/746: What Medical Device and IVD Companies Need to Know

By Adaptive Life Science The European Union’s In Vitro Diagnostic Medical Devices Regulation (IVDR) — Regulation (EU) 2017/746 — represents one of the most significant regulatory overhauls in the diagnostics sector in decades. Officially applicable since 26 May 2022, the IVDR replaces the previous Directive 98/79/EC, introducing a more robust, transparent, and risk-based framework for […]

June 4, 2025
Cultural Fit Matters in Medical Devices

Why Cultural Fit Matters in the Medical Device Industry: Beyond Experience and QualificationsThe medical device industry operates at the intersection of precision, innovation, and compliance. Given the critical nature of its work, designing and manufacturing devices that directly impact patient care, it’s no surprise that experience and qualifications are often the top priorities when hiring. […]

May 22, 2025
ISO 13485:2016 Internal Audit Checklist – What Quality Professionals Need to Know

Published by Adaptive Life ScienceSpecialists in Medical Device, IVD, and Biotech Recruitment Why Internal Audits Matter in ISO 13485:2016 Internal audits are a cornerstone of any compliant Quality Management System (QMS) under ISO 13485:2016. For Quality Engineers, Regulatory Affairs professionals, and QMS leaders, these audits are not just about ticking boxes—they’re about ensuring product safety, regulatory readiness, […]

May 1, 2025
Are ISO Standards Mandatory for MDR Compliance?

In the medical device industry, compliance with regulations is crucial to ensure the safety and efficacy of products. For companies operating in Germany and across Europe, understanding the relationship between ISO standards and the Medical Device Regulation (MDR) is essential. Understanding MDR Compliance The European Union Medical Device Regulation (EU MDR 2017/745) sets out the […]

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