Job Ref: 212457449

Date: 2020-09-17 15:19:16

Apply Now

Regulatory Supervisor (Medical Device)
The company
I am delighted to work with a successful and growing medical device company. Providing a diverse range of capital equipment and consumable devices, my client offer a busy and dynamic environment in which to gain new skills and progress your career.
About the role
The role is ideal for someone who has strong demonstrable experience in a supervisory regulatory affairs role. Applicants must have strong experience with MDD technical file writing and approval for classes I, IIa and IIb. Candidates with 5 years+ relevant work experience will be considered.
Ongoing training will be provided where necessary.
Key responsibilities
* Line management of a team of 4 regulatory staff
* Training and progression of staff
* Ownership of regulatory output for the company
* Technical writing and review
Required experience;
* Circa 5 years+ experience in a supervisory regulatory affairs role
* Experience with medical device regulations is essential
* Class IIa and IIb experience is preferred but not essential
* Line management experience is essential
* Strong leadership skills
* Excellent communication skills and a good sense of humour
Keywords:
Medical device, class, anaesthesia, critical care, surgery, regulatory affairs, RA manager, supervisor, senior, associate, lead, MDD, technical, Snr, advisor, clinical evaluation, file, implementation, team.
Harris Lord is acting as a recruitment agency for this role

Apply Now