RA Specialist - Med Device - Spain

£35000.00 - £45000 per annum
  1. Permanent
  2. Consultant / Specialist
  3. Spain
Madrid
Posting date: 15 May 2019
RA.VP.23345_1557918531

An international staffing and recruiting company is currently recruiting an Regulatory Affairs (RA) Specialist - Med Device to join their office in Spain. This organisation is one of the largest workforce management solutions companies in the world who specialise in multiple scientific and engineering sectors. This is an exciting opportunity to work with a firm dedicated to innovative and dynamic approaches to the changing workforce landscape.

The Regulatory Specialist will provide direct regulatory support to various projects and products, both new and existing.

Job Responsibilities:

  • Preparing regulatory registration, notification, and pre-market submission requirements, including the necessary regulatory documents.
  • Providing regulatory support for product changes/modifications, labeling, and promotional material review and approval.
  • Supporting strategic planning and product development efforts.
  • Managing product lifecycle from pre-market to post-marking phase, including reviewing and approving promotional material in compliance with corporate and government requirements.
  • Providing regulatory guidance to local business partners and liaising with RA teams.
  • Preparing regulatory registration, notification, and pre-market submission requirements, including the necessary regulatory documents.
  • Providing regulatory support for product changes/modifications, labeling, and promotional material review and approval.
  • Supporting strategic planning and product development efforts.
  • Managing product lifecycle from pre-market to post-marking phase, including reviewing and approving promotional material in compliance with corporate and government requirements.
  • Providing regulatory guidance to local business partners and liaising with RA teams.

Skills and Requirements:

  • Minimum of a B.A. /B.S. within a technical related discipline is required.
  • Minimum of 2-5 years of experience in Regulatory Affairs or Master's degree with equivalent experience.
  • Knowledge of FDA Regulations and CE Marking Requirements.
  • Proficiency in Spanish.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Valaince Penteng at +44 203 846 0643 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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