Senior Regulatory Affairs Specialist

Reading Permanent
  • Fantastic opportunity to be apart of a global Medical Device Business
  • Great opportunity to be apart of a dynamic team working on exciting projects

About Our Client

My client is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care.

Job Description

  • Lead RA representative for design change assessment projects for active medical devices (PEMS), responsible for assessing regulatory impact of the change - determining testing needs/ documentation needs/ registration needs. Close liaison with supply chain/ regional regulatory folks etc. to ultimately implement the change in production.
  • Lead and execute international product registrations attending to individual country specific requirements; monitor and report progress
  • Participate to the review of process/product changes, labelling, claims, product complaints, A&Ps (Advertising & Promotional materials), etc., to determine the need for any regulatory activities and to ensure compliance to International requirements;
  • Prepare and maintain regulatory files such as STED and MDD/MDR Technical Files;
  • May participate in cross-functional product development teams as the regulatory representative; development of regulatory strategies
  • May attend to audits performed by internal and external authorities to represent RA positions and processes;
  • Assesses changes in regulations and helps to determine their impact;
  • Prepare regulatory dossiers for submission to Health Authorities and maintains them along the whole product life-cycle.
  • Handle CAPAs to implement corrective and preventive actions
  • Drive regulatory affairs procedural updates, as needed, in collaboration with cross functional inputs.

The Successful Applicant

  • Sound knowledge of the regulatory framework pertaining to Medical Devices such as the MDD/MDR CE Marking;
  • Good working knowledge of Design Control, Software Life Cycle, Risk Management, V&V processes;
  • Solid knowledge and material experience in international registrations/approval process for medical devices
  • Degree or equivalent in engineering or scientific discipline, or equivalent proven experience.

What's on Offer

Competitive package available

Contact
Kelly Percival
Quote job ref
JN-062022-5638273
Phone number
+44 1727 730 143

Job summary

Sector
Life Sciences
Subsector
Regulatory Affairs
Industry
Healthcare / Pharmaceutical
Location
Reading
Contract type
Permanent
Consultant name
Kelly Percival
Consultant phone
+44 1727 730 143
Job reference
JN-062022-5638273