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Regulatory Affairs

At Adaptive Life Science, we pride ourselves on being the premier choice for recruiting support in regulatory affairs roles within the Medical Device, IVD, and Biotech industries. Our deep industry expertise, combined with a meticulous selection process, ensures that we connect our clients with highly qualified candidates who possess a minimum of three years to over forty years of relevant experience. By offering our services to candidates free of charge, we attract a diverse and talented pool of professionals, while our fee-based services for clients guarantee a tailored and dedicated recruitment experience. Trust Adaptive Life Science to provide authoritative and expert recruitment solutions that meet the stringent regulatory demands of your industry.
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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

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 […]

March 15, 2025
Global Trends in BioTech

Imagine a world where diseases are not just treated but predicted, where food scarcity is a thing of the past, and where the environment heals with the help of microscopic allies. Sounds like science fiction? Welcome to the future of BioTech! Let's embark on a journey through the global trends shaping the BioTech industry and […]

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