At a Glance
- Tasks: Lead regulatory projects and manage 510k submissions for medical devices.
- Company: Join a UK-based medical device company with a focus on innovation.
- Benefits: Remote work, competitive pay, and the chance to make a real impact.
- Other info: Immediate start available for the right candidate.
- Why this job: Be a key player in shaping regulatory compliance in the medical field.
- Qualifications: Expertise in regulatory affairs and experience with international standards.
The predicted salary is between 50000 - 60000 £ per year.
LennTech are supporting a medical device UK based client who is seeking to hire a Regulatory Affairs Consultant for an initial 6 month contract. This role is classed as Inside IR35 and will be remote based. UK candidates are preferred for possible ad hoc onsite visits. Needs to be someone immediately available to start within the next week.
KEY REQUIREMENTS
- Field expert in the areas below.
- Someone who can hit the ground running and take on the project and accountability as the group lead.
- 510k submissions experience.
- Lead or support key regulatory projects, including EUDAMED implementation, QSMR, UKCA compliance, and development devices.
- Experience of working with regulatory bodies.
- MDSAP - Preferential.
- Previous country experience working with US, Canada, Australia.
- MDR experience.
Regulatory Affairs Manager in Nottingham employer: LennTech Search
LennTech is an exceptional employer that values expertise and innovation in the medical device sector. With a remote working model, we offer flexibility and a supportive work culture that fosters professional growth through challenging projects and collaboration with regulatory bodies. Join us to make a meaningful impact while enjoying the benefits of a dynamic and forward-thinking team.
