Connecting World Class Talent With The Most Innovative Medical Companies

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Years Experience

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Specialist Candidates

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Placements

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CV to Interview Ratio

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Clients We Work With

Here at Adaptive Life Science we provide specialised recruitment services to the Life Science sector, covering the Medical Device, Diagnostic and BioTech industries globally.

Are you looking to move on to new professional challenges?

You can rely on our specialized consulting experience, market knowledge and strong network: all completely free for candidates. We support you every step of the way in finding your dream job, including CV application advice, consultation on salaries, personalised interview preparation, introduction to positions, and negotiating the optimum package. The key element is consultation, and being a secure partner and source of advice during the recruitment process, taking the stress out of the process for you, and working to your time-frame and around your schedule.

Who do we work with?

From MedTech start-ups with multi-millions in investment to the top 10 global players with 10,000+ employees.
We partner with companies and candidates from early-stage start-ups planning for CE-marking to the Top 10 global manufacturers distributing globally, offering you versatility and an open view of the German market in all therapeutic areas.

Why should we be chosen as your recruitment partner?

We understand our clients from a 360 perspective and offer full visibility of the company and share this with our candidate partners. We have close contact not only with the HR department to understand the benefits, working culture and development, but also with the senior decision makers and hiring managers to appreciate the position, team structure and tasks.

Our Areas Of Expertise

Our Areas Of Expertise

Latest Vacancies

Nuremberg
Germany
€60,000 - €80,000 DOE
Join a world-leading company in MedTech, who are working in the field of cancer detection & treatment, as they search for a new team member to support the Risk & Requirements activities. You will join a strong team, have a great deal of visibility, and work on varied and interesting projects. Your role supports the following tasks: Responsibilities:   Help to ensure that the safety, usability, and cybersecurity requirements are accurately defined and documented. Oversee that the software and hardware projects follow the ISO 14971 risk management process. Contribute to the maintenance and updating of the risk management file. Ensure that cybersecurity requirements are addressed as part of the risk management activities. Work closely with cross-functional teams, contribute to training and advising team members on Risk Management and Requirements topics. Experience required: A degree in the medical or scientific field (or equivalent). 3-5 years of experience in Requirements and/or Risk Management in the medical technology field. Experience with agile software development.   Knowledge in the field of cybersecurity is desirable. Fluency in English (German is desirable). Knowledge of regulatory requirements and medical device relevant standards (e.g. ISO 13485, EU-MDR, ISO 14971). If you're interested in this position, please apply here and/or contact Hollie Dear. #LI-HB1  #LI-Hybrid  
Remote
Germany
70,000EUR - 90,000EUR
Medical Affairs Director/Senior Manager Are you an expert in Medical/Clinical Affairs in Class III Implantable Devices? Are you looking to take your next step into a leadership role? Do you want to work with a global technology leader in regenerative medicine? We are currently supporting our client headquartered in Germany to strengthen their clinical/medical affairs function. This is a remote role, so you can be based anywhere in Germany but must be willing to travel from time to time. Does this sound like your next career step? Tasks Management of a small team (2-5 employees) Ensure regulatory compliance for clinical trials and medical products on the market in accordance to MDR, TGA and FDA Pre-market and post-market clinical projects, including medical writing, CERs, PMS, and PMCFs Clinical trial project management (documentation, budget planning, collaboration with stakeholders on an international level as well as CROs) Reimbursement and compliance (Europe, especially Germany) Your profile Degree in a scientific field such as biomedical, biology, medicine, medical engineering or a comparable field of study Experience in clinical (e.g. CER), regulatory affairs, bio-medical publication or medical writing, especially for class III implants Strong communication skills and project management experience Team player who can also work independently Knowledgeable in MS Office Fluency in English, German is a bonus Please apply with your CV or contact May-Lynn Capocciama-Knecht for further details on this opportunity and additional vacancies in R&D, Regulatory Affairs and Quality Management. may-lynn.ck@adaptivelifescience.com +49 30 1663 7750 #LI-MC2  
Remote
Germany
Flexible, depending on experience
Are you a specialist in the cardiovascular field? Would you like to join a dynamic healthcare company who are innovating in the field to help transform treatment options for patients? Currently, our long-standing client are searching for a Clinical Application Specialist to join them and support their mission! *Can be based in Germany, or France with 50-60% travel expected. Focuses: Act as the designated expert on the device and educate hospital workers by imparting your knowledge. Train medical professionals in the handling, insertion, and troubleshooting of the device. Oversee in-service education initiatives and one-on-one training sessions in a hospital setting. Find prospects for the adoption of therapies in conjunction with other internal teams in Clinical Affairs and R&D. Work together with R&D to offer input on new device development and feature enhancements. Arrange and participate in patient screening meetings and offer assistance with device suitability and patient selection. Requirements: 5+ years of experience in Clinical Support/Clinical Application/Field Clinical activities within the cardiovascular field OR clinical experience as a Cardiovascular Technician, Physician Assistant or CV Sonographer. Strong customer-facing experience and great communication skills. Experience in clinical engineering from roles connected to the industry that aid in clinical case assistance and development. Experience in presenting clinical and medical information. Willingness to travel (50-60%). Fluency in English is required. If you're interested in this position, please apply here and/or contact Hollie Dear at Adaptive Life Science for more information. #LI-HB1  #LI-Remot
Dresden
Germany
70,000EUR - 90,000EUR
Production & Supply Chain Manager (m/w/d) Salary: €70,000 - €90,000 DOE Location: Dresden, Saxony, Germany (Hybrid) Our client is an innovative MedTech startup. They are setting new standards in this field with their products, which are characterized by unique technology, electronics, software, and artificial intelligence. Their products are used directly by end customers/patients and they realize production and logistics through a partner network. For their team in Dresden, they are looking for a Production & Supply Chain Manager Tasks: Support in the transfer of development results to production Participation in the selection of our manufacturing and logistics partners Independent support of the manufacturing partners Optimizing manufacturing and logistics processes with manufacturing partners in terms of quality and costs Ensuring delivery capability in accordance with sales planning Participating in the definition of service processes and returns processing with the partners involved Your Profile: Sound technical training and practical experience in the field of electrical engineering/electronics/mechatronics and/or corresponding technical or industrial engineering studies Approx. 5 years of professional experience in the production area with independent implementation of production control in compliance with cost and quality specifications Strong teamwork and communication skills Willingness and ability to create (in the start-up sector) Open to new approaches Knowledge of the medical technology sector is an advantage Sound knowledge of English. Benefits: An exciting and varied working environment in a dynamic and agile team Creative freedom in an agile start-up environment with a pioneering high-tech medical product Flexible trust-based working hours and the option to work remotely A permanent full-time contract with remuneration in line with the market Professional and personal development opportunities For more information or to apply, please reach out to luke.fines@adaptivelifescience.com with a copy of your CV or alternatively call +49 30 1663 4514  
Bausch
Freseus
Getinge
KaiaHealth
Karl
Systemex
ThermoF
Vyaire