Regulatory Affairs Specialist

England Permanent
  • Fantastic opportunity to be apart of a global Medical Device Business
  • Excellent opportunity to be apart of a globally growing business

About Our Client

My client is a leading Medical Devices manufacturer, for a range of procedures in critical care and surgery.

Job Description

  • Apply technical solutions to problem solving
  • Apply technical solutions to quality improvement projects
  • Use technical writing skills to clearly describe technical information
  • Analyse customer complaints, identify trends and execute corrective actions
  • Review and assess of change control activities for potential impact on current regulatory filings.
  • Maintenance of Regulatory procedures to ensure continued compliance.

The Successful Applicant

  • Engineering/Science qualification with 2/3 years of working within R&D/QA/RA in a medical device environment.
  • 2/3 years experience in R&D, QA/RA, Validations - essential
  • 2/3 years experience in Risk, Clinical and Biocompatibility - an advantage
  • Excellent technical writing experience within a medical device environment - essential
  • Attention to detail and accuracy - essential
  • Fluent English, both written and oral - essential
  • Ability to work well under deadlines and pressure
  • Problem solving skills for developing creative solutions and meeting objectives are required.
  • Skills that enable coordination of data, including MS-Office (primarily PowerPoint, Word, MD Project, Outlook and Excel);
  • Excellent analytical ability
  • The ability to prioritize tasks and be able to manage several projects and tasks simultaneously; and the ability to interface with all levels of management.
  • Travel up to 10%

What's on Offer

Competitive Package Available

Kelly Percival
Quote job ref
Phone number
+44 1727 730 143

Job summary

Life Sciences
Regulatory Affairs
Healthcare / Pharmaceutical
Contract type
Consultant name
Kelly Percival
Consultant phone
+44 1727 730 143
Job reference