Job Summary
A pharmaceutical company needs applicants for an opening for a Remote Senior Pharmaceutical Regulatory Affairs Specialist.
Candidates will be responsible for the following:
- Working to provide regulatory input to product lifecycle planning
- Acquiring specific documentation to regional regulatory personnel to support global regulatory submissions
- Assisting business regulatory managers with documentation
Must meet the following requirements for consideration:
- Bachelor’s degree in a related medical, science, engineering services, quality or regulatory discipline or equivalent experience
- 2-4 years experience in the medical device field
- Experience with international regulatory submissions for Medical Devices
- Experience working with multi-cultural business partners
- Experience with submission of product dossiers to global regulatory authorities
- Proficiency with Microsoft systems
