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Operations Recruitment

Adaptive Life Science support medical device companies with hiring across four key operations functions; Marketing, Project Management Office, Supply Chain Management and Technical Service.

So whether you’re looking for a UX/UI Designer, a specialist in Channel Marketing, a Product Marketing Manager, a Technical PM, a Procurement Director or Field Service Engineer, we have the talent, all bringing a wealth of experience with medical devices.

Looking for an opportunity in the space yourself, get in touch!
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Marketing
Adaptive can present Marketing Operations candidates from Mid-Leadership level including C-Suite, that bring relevant market experience across UX/UI, Digital Marketing, Product Marketing, Channel Marketing and CRM to name but a few.

Our candidates bring experience collaborating with the other departments from product to engineering, analytics/BI and sales, creating effective marketing campaigns and materials that help showcase your products and solutions.
Project Management
Having a well run PMO is crucial to ensuring and maintain high standards for project management across an organization. Adaptive can help your business to find fitting and experienced project managers from either an operational or technical perspective.

A good project manager is like the glue that holds and brings the team together, ensuring issues are forecast, change requests are handled, risk management is followed and that processes are efficient and streamlined to hit specific objectives.
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Supply Chain Management
Adaptive can support hires across the supply chain in the medical device industry, from procurement to supplier management and logistics.
We match not only on the role, but also on the industry focus. Our candidate network is comfortable working in a highly regulated sector and the compliance topics that come with it.

Our team of specialist consultants screen not only for technical ability and experience, but soft skills vital for success like stakeholder management, hands-on ability vs strategic mindset, project leading ability and much more.
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Technical Service
Adaptive recruit for start-up and well-established medical device companies, supporting hires across their technical service team from Biomedical Engineers, to Field Service Engineers, Installation Engineers, Training Specialists and Application Engineers.

Whether it’s an IVD product, digital solution or software/hardware combination product – our candidate network of engineers and service professionals all come with the same customer facing skill set and problem-solving attitude to support local and international customers in multiple languages.

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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