Cure Talent
Medical Device Product Review Specialists
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Medical Device Product Review Specialists | Ad Hoc Contractor | UK Based
Cure Talent are delighted to be partnered with a growing medical device certification organisation that is expanding its scope into additional medical device technologies.
As part of this expansion, we are looking to speak with experienced Medical Device professionals who could join an ad hoc contractor Talent Pool, providing specialist product and technical review expertise.
The organisation is currently building and evidencing its technical capability as part of its designation process, so these are specialist requirements rather than developmental positions.
Current Product Review Requirements Include:
MDN 1210 | Contraception & STI Prevention Devices Non-active, non-implantable devices used for contraception or prevention of sexually transmitted diseases.
MDS 1007 | Nanomaterial Medical Devices Medical devices incorporating or consisting of nanomaterial.
The Role
Depending on your area of expertise, assignments may include:
- Reviewing product and technical evidence within your specialist device category.
- Assessing technical documentation and supporting evidence.
- Evaluating whether applicable regulatory and technical requirements have been adequately demonstrated.
- Identifying gaps or areas requiring additional evidence.
- Reaching clear, evidence-based product assessment conclusions.
- Producing structured and technically robust review reports.
- Working alongside regulatory, technical and clinical specialists as required.
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Who We Are Looking For
You will need:
- A relevant degree in a scientific, engineering, technical, medical or related discipline.
- Significant direct experience within MDN 1210 or MDS 1007.
- Demonstrable depth of product and technical knowledge within the relevant category.
- Experience reviewing, assessing, developing or taking regulatory responsibility for relevant products.
- The ability to evidence your competence through previous products, projects, qualifications and professional experience.
- The ability to independently assess technical evidence and reach clear, defensible conclusions.
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Previous Notified Body, Approved Body, technical assessment or product review experience would be particularly relevant.
Strong manufacturer-side or pharmaceutical experience will also be considered where your experience directly aligns with the relevant product category and you can demonstrate sufficient technical depth.
Contract Arrangement
This is an ad hoc contractor opportunity rather than a full-time assignment.
Successful specialists will complete the organisation's competence and evidence-onboarding process now so they can form part of the relevant specialist pool for its designation process.
There is no guaranteed volume of work and it may be six months or more before paid assignments become available. Future assignments will depend on successful designation, customer demand, your specialist area and your availability.
The arrangement is designed to sit alongside your existing employment, consultancy or other professional commitments.
Rates are flexible and will depend on experience and specialist expertise.
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