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 with excellent growth potential.
- Why this job: Be a key player in shaping regulatory compliance in the medical field.
- Qualifications: Expertise in regulatory affairs and experience with global regulatory bodies.
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 employer: LennTech Search
LennTech is an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the medical device sector. With a strong focus on employee growth, we provide opportunities for professional development and the chance to lead impactful regulatory projects from the comfort of your home. Our remote-first culture ensures flexibility while maintaining a commitment to excellence, making us an ideal choice for those seeking meaningful and rewarding employment.
