Senior Regulatory Manager - Regulatory Affairs Medtech

Senior Regulatory Manager - Regulatory Affairs Medtech

Alira Health

Barcelona or Remote, Spain

The Senior Regulatory Manager, Regulatory Affairs Medtech is a critical member of the Alira Health project team. The Sr Reg Manager will work closely with Directors and VP and work with clients to guide, write and streamline regulatory projects. The Director will help to set direction for clients in the coordination, execution, guidance and implementation of regulatory programs, requirements and compliance activities. The individual will be a key resource for all regulatory activities.


  • Be hands-on on planning, organizing, executing, writing and delivering projects;
  • Monitor and analyze the impact of emerging or revised laws, regulations, enforcement actions and other changes that impact the manner by which the clients' products are regulated around the world;
  • Plan, manage, prepare and submit EU/NB-related submissions: Roadmaps, Gap Analysis, Product categorization, Technical Documentation compilation, Response to non-conformities, etc.;
  • Plan, manage, prepare and submit FDA-related submissions: RFD, Pre-Submissions, 510(k), De Novo, PMA, IDE, BDD, etc.;
  • Provide, as needed, regulatory strategic support and direction to client programs and initiatives;
  • Design and implement regulatory strategies to obtain, maintain and extend product registrations for new device/combination product/companion diagnostic portfolios;
  • Oversee the development and submission of regulatory filings to FDA and EU;
  • Serve as liaison with regulatory agencies;
  • Lead core regulatory activities to ensure effective agency interactions that are consistent with clients’ regulatory strategies;
  • Provide regulatory guidance and input to clients;
  • Provide regulatory operations and electronic submissions support;
  • Performs additional duties as assigned.


  • BS/BA from a top undergraduate program in a scientific discipline;
  • 10+ years’ experience in a regulatory role within medical device sector;
  • Knowledge of appropriate regulations within the specific sector;
  • Previous experience in consulting will be favorably valued;
  • Knowledge of FDA procedures;
  • Knowledge of MDR and IVDR;
  • Strong analytical skills and ability to problem-solve unstructured or ambiguous challenges;
  • Demonstrated ability to communicate complex information and analyses to a variety of audiences;
  • The role for Director requires ability to work hands-on on the execution and delivery of the projects;
  • Strong command of English, both written and verbal;
  • Excellent communication and interpersonal skills with client service orientation;
  • Advanced skills in MS Office Suite, particularly Word;
  • Thrives in collaborative, yet less structured team environment;
  • We will not sponsor work visas.

Apply Now

Don't forget to mention EuroPharmaJobs when applying.

Share this Job

More Job Searches

Spain      Clinical Research      Medical Devices      Regulatory Affairs      Alira Health     

© EuroJobsites 2024