Active Medical Devices Expert
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices organization, based in Gelderland Netherlands.
Medical Devices company in Gelderland.
ROLE DESCRIPTION
- You are responsible for the assessment of technical files and the auditing of the quality system of your customers (from high innovative start-ups to large
multinationals, both national and international)
- You act as a linchpin and maintain frequent contact with your customers, colleagues, external experts like physicians, contractors and authorities
- You will have the opportunity to represent the company at conferences
- The position entails travelling within and outside Europe, approximately 20-30% of the time.
RESPONSIBILITIES
- Higher vocational or university level education, in life and/or engineering sciences
- A minimum of 4 years of full time work experiences in medical device related industry, including at least 2 years in R&D, QA/RA
- Experienced in at least one of the following devices categories and areas of expertise: Active medical devices, Active implantable medical devices
- Experience with quality management systems and relevant laws and regulations, at least CE
- Project management and auditing experience is considered an advantage.
REQUIREMENTS
- You need to have a degree in Electrical Engineering or something related
- Deep knowledge on ISO 13485
- Deep knowledge on MDD 93/42/EEC
- Deep knowledge on Technical Files
- R&D background
- At least 5 years experience
- Willing to travel
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.
