Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms RSS Feed RSS Feeds

Job Details

Regulatory Affairs Specialist - Medical Device

Company: Barrington James Clinical
Reference: RASPEC - CRBG
Closing Date: 03 Feb 19
Type: Permanent
Salary (£): Competitive

Job Summary:

This position is responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level for the EMEA region. Primary responsibilities are to ensure regulatory compliance for assigned product lines as the company evolves.


Main Duties/Responsibilities:

  • Assist with determination of EMEA regulatory pathways for various projects including product classification and type of regulatory submission or rationale required.
  • Participates on various teams to define regulatory requirements for EU international submissions within the EMEA region.
  • Identifies guidance documents, international standards, consensus standards and assists teams with their interpretation.
  • Prepares regulatory submissions to regulatory authorities.
  • Interacts with various levels of management, external agencies and companies.
  • Assists with analysis and making recommendations regarding complaints received by the company and whether they are MDR, MPR or Vigilance reportable; participates in complaint related meetings.
  • Assist with developing, maintaining and analyzing department systems and provides training when needed.
  • Remains current on developing regulations and revises systems as necessary.
  • Participates in and assists with FDA facility inspections, Notified Body Audits and other governmental inspections as directed.
  • Performs other related duties and tasks, as required.

Minimum Qualifications/Competencies:

  • Education and experience equivalent to a Bachelor's Degree in the biological, physical, engineering or material science disciplines and four years of related experience.
  • Knowledge of U.S. FDA regulations, the Medical Devices Directive (93/42/EEC, as amended), and ISO 13485 Quality System Standards.
  • Knowledge of the international regulatory environment and their regulations within the EMEA region
  • Self-motivated, self-directing, strong attention to detail and excellent time management skills.
  • Strong interpersonal skills and the ability to communicate well - verbally and in writing - with others.
  • Demonstrated computer skills preferably spreadsheets, word processing, database, internet research and other applicable software programs.

Apply for this job: Regulatory Affairs Specialist - Medical Device

Contact Information:

Address:  Head Office
Victoria House Consort Way Horley Surrey
Tel:  01293 776644
Fax:  01293 822333
Website:  Visit Our Web Site

Site Map | Privacy & Security | Cookies | Terms and Conditions is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.