Regulatory Affairs Co-op
Date de publication :
26 septembre 2024Taux d'activité :
100%Type de contrat :
Durée indéterminée- Lieu de travail :Danvers
Abiomed is a pioneer and global leader in healthcare technology and innovation, with a mission of Recovering Hearts & Saving Lives. With corporate headquarters in Danvers, Massachusetts, and offices in Baltimore, MD, Woburn, MA, Aachen & Berlin, Germany and Tokyo, Japan, Abiomed’s 2,000 employees form one of the fastest growing medical device companies in the world. We attract and retain exceptional talent with our collaborative culture, passion for our work, and a strong commitment to employee professional development.
Patients First | Innovation | Winning Culture | Heart Recovery
POSITION SUMMARY
Our Regulatory Affairs team supports Abiomed in navigating complex regulatory landscapes to bring the latest innovations in heart recovery to our patients. We are looking for a co-op who will be fully integrated as a member of our team, achieving global regulatory approvals, registrations, and licenses for our products and services while ensuring compliance with global regulations and internal procedures.
KEY RESPONSIBILITIES:
The co-op will:
- Assist in completing/documenting global regulatory assessments for changes to medical devices
- Attend project team meetings with Regulatory Affairs lead
- Prepare and maintain Regulatory Affairs data and metrics
- Evaluate current processes and propose opportunities for internal efficiencies
- Compile and/or write regulatory dossiers for global submissions