• 10 juli 2018
  • Vacaturennummer lv-64963
Requisition Number: 573-15453
Working Hours:See Job Posting for Work Hours
Job Title:Senior Regulatory Affairs Specialist
Location: Maastricht

Job Description
Responsible for coordinating, preparing, and maintaining regulatory submissions and documents on a global level for Europe, and EMEA region. Primary responsibilities are to ensure regulatory compliance for assigned product lines and countries. Other responsibilities include coordinating recalls, identifying relevant standards and guidance documents that affect Merit's business and products, assisting with Competent Authorities inspections, Notified Body audits, and other internal audits. Performs duties with limited input from management and/or senior members of the department.

1.Determines regional regulatory pathways for various projects including product classification and type of regulatory submission or rationale required.
2.Participates on various teams to define regulatory requirements of international submissions, Technical Files or regulatory rationales.
3.Identifies guidance documents, international standards, Consensus Standards and assists teams with their interpretation.
4.Prepares regulatory submissions to the Notified Body and other regulatory authorities and /or Distributors.
5.Interacts with various levels of management, external agencies, and companies.
6.Analyzes and makes recommendations regarding field complaints.
7.Develops, maintains and analyzes department systems and provides training when needed.
8.Remains current on developing regulations and revises systems as necessary.
9.Participates in and assists with Competent Authorities inspections, Notified Body Audits and other inspections and audits as directed.
10.Assists with supervision of department staff, as directed.
11.Performs other related duties and tasks, as required.

  • As recommended by Occupational Physician at pre-employment medical.
  • Education and experience of at least a Bachelor's Degree in a technical field such as the biological, physical, engineering or material science disciplines and six years of related industry experience.
  • Demonstrated knowledge of EMEA country regulations, U.S. FDA regulations, the Medical Devices Directive (93/42/EEC, as amended), and various Quality System Standards/Regulations/Laws, including but not limited to ISO 13485, etc.
  • Demonstrated and verifiable experience with authoring regulatory submissions and interacting with reviewers.
  • 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.
  • Regulatory submission/rationale preparation/publishing
  • Global Regulatory paths/strategies
  • Computer skills/internet research
  • Interpersonal/communication skills
  • Regulatory system development/training
  • Field Action coordination and reporting
  • Product development and change qualification processes
We are offering
Merit Medical is an innovative company and fast-growing company. You will be working in a creative and positive environment with lots of opportunities. Salary and employment terms are negotiated based on experience.

If you are interested in this position, please send in your application ASAP in English, 1-page letter + CV. We will evaluate incoming CVs continuously.