Regulatory Affairs Executive

Job details

Regulatory Affairs Executive - This exceptional medical devices company is looking for a highly professional Regulatory Affairs Executive to join their Gloucestershire based team. The Regulatory Affairs Executive will be looking for an opportunity to support a growing business with an expanding portfolio of medical products which are sold worldwide. Ideally the new Regulatory Affairs Executive will be able to commence the role as soon as possible and quickly become an integral part of the future success of this business.

Regulatory Affairs Executive - key responsibilities and duties:

• Administration and management of the company's Quality Management System (QMS)
• Work closely with colleagues to promote continuous improvement and the importance of the Quality Management System
• Planning and conducting internal quality audits
• Advising departmental managers in procedure preparation and implementation
• Interpreting standard and regulatory requirements for the implantation of Quality Documentation

Regulatory Affairs Executive - quality, skills and experience:

• Exceptional interpersonal skills
• The Regulatory Affairs Executive will need to have an understanding of, or a willingness to learn about the Medical Devices Directive, ISO13485 and FDA Quality System requirements
• Flawless communication skills
• Ability to assess and implement solutions to problems
• Able to work under pressure and work effectively as part of a team

An excellent opportunity for a Regulatory professional to join a forward thinking and rapidly growing medical devices organisation in Gloucestershire.

Apply now, send a full CV to m.norris@x4group.co.uk or call Michael on 020 7812 7700 for more information.