Overview

Reference Number: JO-2105-467588_2
Senior / Principal Regulatory Consultant
Rate: Negotiable
Job Type: Permanent
Location: Letchworth Garden City

Senior / Principal Regulatory Medical Device Consultant

Permanent positions

Location: Hertfordshire (Home working and flexible working hours on offer)

Salary: Dependant on level of experience

Job reference:JO-2010-455978

We’re collaborating with a specialist consultancy who is looking to build a medical device unit to support ongoing and developing project requirements. The correct applicant should have experience working with medical devices from a consulting perspective and have strong business acumen. This is a high profile hire for the business , and could in time become a senior management role. Responsibilities include;

  • Building and developing a Medical device team of consultants
  • Prepare and manage responses for regulatory submissions
  • Managing a portfolio of projects for a number of clients, including projects in development, at regulatory filing stage and post-approval lifecycle management
  • Leading / supporting regulatory projects, including supervised liaison and negotiation with regulatory authorities
  • Providing regulatory strategic advice on guidelines, legislation, and procedures to clients on assigned projects

Requirements

  • 10 years+ experience working across a range of Medical Device products
  • Experience developing and executing regulatory strategies for IVD medical device products.
  • European market experience is essential, US would be advantageous.
  • Must have a relevant life sciences degree
  • Must have leadership skills aligned to business and team development

If you would like to apply for this position or discuss our other active positions, please contact Charlie on 01189 522 797 orCharlie.Harris@cpl.com