Regulatory Affairs Specialist

Job Ref: J24515
Sector: Clinical
Sub-sector: Pharmaceuticals
Date Added: 27 November 2017
  • Scotland, UK
  • Competitive
  • Natasha Rollason

Quick Apply

Request a callback

Send To A Friend

The Role:

This role will support the RA Project Leads for new blood glucose monitoring system development projects.

Key Responsibilities:

  • Supporting the project RA Lead during characterization, verification & validation, labelling & claims development.
  • Assisting in preparation of pre-market applications to regulatory agencies.
  • Researching, consolidating and communicating global regulatory requirements to enable development of global regulatory strategies.
  • Partnering with global regulatory affiliates and providing documentation to support international applications for new products/maintenance of existing product licenses.
  • Assisting in the development of best practices for Regulatory Affairs processes

Skills required:

  • Demonstrated experience working in a Regulatory Affairs role within the medical device industry
  • Degree qualified, preferably in a scientific or technical field
  • Familiarity with medical device regulations in US and/or EU
  • Excellent verbal and written communication skills
  • Strong organizational, interpersonal, and problem solving skills; detail oriented
  • Ability to work independently and collaboratively with minimal supervision
  • Working knowledge of MS Office programs (Word, Excel, PowerPoint, Outlook) and electronic document management systems

If you are interested in this role or would like to have a confidential discussion regarding other Regulatory Opportunities. Please contact me: or 01753 589673

The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU/UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.