Regulatory Affairs Specialist

Company Details

LeMaitre

Overview: The Regulatory Affairs Specialist will be responsible for supporting International Registrations and other regulatory activities.
Responsibilities:

  • Responsible for supporting International Registrations
  • Working with development teams on projects
  • Other responsibilities assigned by the management

Qualifications:

  • Bachelor’s degree from four-year college or university
  • At least one year regulatory experience in industry (including internship)
  • Achieved a degree in Regulatory Affairs in medical device is a plus
  • Ability to read, analyze, and interpret technical procedures, and regulations.
  • Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the regulators.
  • Fluent in English
  • Ability/experience to understand scientific/technic aspects of the medical devices, preferentially for vascular devices.
  • RAC certified is a plus.

EEO Statement: In order to provide equal employment and advancement opportunities to all individuals, employment decisions at LeMaitre Vascular will be based on merit, qualifications, and abilities. LeMaitre Vascular does not discriminate in employment opportunities or practices on the basis of race, color, religion, sex, national origin, age, disability, sexual orientation, gender identity, breastfeeding or related medical conditions, religious dress, military or veteran status or any other characteristic protected by law.

This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination, and access to benefits and training.

Location: 32 Third Avenue, Burlington, MA 01803

Job Type: Full-time

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