
Senior Medical Device Professional
3 days ago
About This Opportunity
This role involves working on early-stage product development and testing stages of product validation. It requires collaboration between engineering teams and external key opinion leaders.
- Understanding clinical needs from end-users and translating them into technical requirements.
- Providing feedback from end-users and offering insights on the clinical workflow use of products.
- Designing and running benchtop ex vivo and preclinical feasibility studies.
- Analyzing feasibility study findings and writing reports for regulatory documentation filing.
- Assisting in drafting risk management documents such as Design FMEA and Assembly FMEA.
- Participating in project design review meetings.
- Liaising with CROs and hospital partners to plan and perform product clinical studies.
- Assisting in drafting contractual agreements with partners.
- Staying up-to-date with medical device trends, clinical trials, and publications to provide clear-sighted improvements and inputs to our product portfolio.
Your Qualifications and Experience
To be successful in this role, you should have:
- A Master's degree in Engineering or Science.
- At least 3 years' experience in a clinical or human factor engineering role in the medical device industry.
- Familiarity with the medical device design control process.
- Understanding of IEC 62366, IEC , and USFDA human factor and usability engineering guidance documents.
- Excellent communication and interpersonal skills.
Benefits and Opportunities
This is an excellent opportunity to work in a leading medical device developer and manufacturer. You will have the chance to contribute to the development of innovative medical devices and work with a talented team of engineers and clinicians.
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
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