In this new position it is your job to collect all necessary information about country-specific regulations and procedures which need to be met in order to get new components certified and admitted.
• You will be in close contact to certification authorities and regulatory bodies (e.g. the FDA in the US).
• You will be doing research which compulsory test protocols need to be implemented and you will seek and contract test houses.
• You will inform the Group Management about initiatives, budgets and time schedules, which are required for realizing market admittance.
• It will be your responsibility to create an organization-wide accessible knowledge system, take care of all necessary documentation and secure that people in the organization comply with the latest regulations and work processes.
• You will report to the CTO.
For you it is a challenge to build a sound knowledge base by thorough investigation, accurate and systematic recording and organization-wide implementation.
• You feel rewarded when your efforts result in faster market introductions.
• Your independent approach and convincing communication skills support your professional, advisory role towards Group Management and your expertise role towards technical professionals.
• At least a Bachelor degree (technical studies).
• At least five years of professional experience in an independent, international compliance position.
• It is a plus if you are familiar with the medical equipment market and/or X-ray technologies.
• You are fluent in English.
Please apply by sending you CV to [email protected]
Education Backgrounds: |
Biomedical Science Electrical Engineering Mechatronics |
Specialties: |
Analog Power Supply Mechatronics Power Electronics Process Management Product Development |
Education Level: |
Undergraduate (Bachelors) Postgraduate (Masters) |
Experience: |
10 - 15 years 2 - 5 years 5 - 10 Years |
Languages spoken: |
English |
Job Location: | Almelo, Netherlands |
Type: Job
Deadline: 16th March 2012
Job reference (ID): 3967
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