Senior Regulatory Affairs Specialist

3 weeks ago

Portsmouth, United States Laborie Full time

We believe that great healthcare is an essential safeguard of human dignity.

At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you.

We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

Who We’re Looking For:

Laborie Medical Technologies is currently searching for a Senior Regulatory Affairs Specialist to join our team in the Portsmouth, NH office. The Senior Regulatory Affairs Specialist provides hands-on regulatory affairs support for new product marketing approvals and renewals for existing products, including development of regulatory requirements and preparation of submissions. The Senior Regulatory Affairs Specialist performs regulatory submission/approval activities for Laborie Medical products and will represent Laborie Medical with Regulatory Bodies during external audits as a subject matter expert. The position must ensure compliance with required regulations and established corporate standards and is responsible for ensuring that product approvals are properly maintained, and product re-registrations are properly managed.

How you contribute:

  • Preparing documentation for international regulatory registrations
  • Preparing technical documentation compliant to MDD and EU MDR
  • Defining worldwide regulatory requirements necessary for regulatory approval of products
  • Participating on cross functional teams as regulatory lead
  • Maintaining regulatory documentation to ensure availability for external audits and preparation of submission packages
  • Authoring submissions, researching requirements, setting priorities and maintaining project schedules
  • Providing guidance and oversight to team members related to regulatory compliance
  • Reviewing marketing literature for compliance to applicable regulations
  • Executing on additional responsibilities as defined by management
  • Act as a Subject Matter Expert (SME) to support internal and external audits

Minimum Qualifications:

  • Bachelor’s Degree in Science, Engineering, or other relevant discipline
  • Minimum 5-8 years’ experience in Regulatory Affairs in the medical device industry
  • FDA, EU, Health Canada, and international registrations experience
  • Working knowledge with quality system regulations and guidelines
  • Ability to develop clear, concise, and timely oral and written reports
  • Great communication skills with all levels of personnel
  • High level of organization and planning skills
  • Working knowledge of medical devices, procedures, and terminology
  • Drug-combination experience a plus


Laborie is a specialty manufacturer and supplier of medical technologies and devices, committed to excellence in diagnostics and therapeutics for Urological, Gastrointestinal, Obstetric, Gynecological, and Neonatal healthcare and committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education and employment for individuals with disabilities.

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