Your new company
nternational service corporation focusing on testing, inspection and certification for the safety of the world.

Your new role
Clinical expert with following duties:
• Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR)
• Preparing deficiency reports in case of non-conformities according to the requirements of the Medical Device Regulation (MDR)
• Delivering high-quality, reliable, and predictable services within defined timeframes
• Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support of and close exchange with colleagues
• Independent supervision of certification projects for our international customers as a project manager
• Optionally providing support during
o clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)
• Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within the company
• Possibility of attending medical conferences
• Optionally continuing to practice medicine part-time
RESPONSIBILITIES
• Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR)
• Preparing deficiency reports in case of non-conformities according to the requirements of the Medical Device Regulation (MDR)
• Delivering high-quality, reliable, and predictable services within defined timeframes
• Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support of and close exchange with colleagues
• Independent supervision of certification projects for our international customers as a project manager
• Optionally providing support during
o clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)
• Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within the company
• Possibility of attending medical conferences
• Optionally continuing to practice medicine part-time

RESPONSIBILITIES
• Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR)
• Preparing deficiency reports in case of non-conformities according to the requirements of the Medical Device Regulation (MDR)
• Delivering high-quality, reliable, and predictable services within defined timeframes
• Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support of and close exchange with colleagues
• Independent supervision of certification projects for our international customers as a project manager
• Optionally providing support during
o clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)
• Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within the company
• Possibility of attending medical conferences
• Optionally continuing to practice medicine part-timeRESPONSIBILITIES
• Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid down in the European Medical Device Regulation (MDR)
• Preparing deficiency reports in case of non-conformities according to the requirements of the Medical Device Regulation (MDR)
• Delivering high-quality, reliable, and predictable services within defined timeframes
• Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support of and close exchange with colleagues
• Independent supervision of certification projects for our international customers as a project manager
• Optionally providing support during
o clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)
• Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within the company
• Possibility of attending medical conferences
• Optionally continuing to practice medicine part-time

What you'll need to succeed
• Physician with completed medical degree
• Fluency in written and spoken English
• Ability to create qualified deficiency reports
• Experience working with MS Office applications and programs
• Excellent organizational and professional communication skills
• Ability to work in a team, pronounced customer orientation and good self-organization
• Curiosity and willingness to learn
• A total of at least four years of professional experience in the field of
o clinical practice in health care services or related sectors including two years in usage, development or testing/evaluation of medical devices or clinical studies/investigations or clinical evaluation of medical devices
• Experience with scientific literature searches in the medical context

What you'll get in return
• Full home-office
• Opportunity to work for global leader in audits
• Atractive salary
• International environment

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. #1172018