• Communicate technical file status and location to regional RA.
  

• Work with regional RA to meet registration timing to prevent gaps in supply.
  

• Maintain registration schedule tracker and update status as submissions are approved.
  

• Familiarity with Quality Management experience
  

• Provide Regulatory Documentation Support to Global Regulatory Affairs team members for Product Registrations, Renewals, Launches, etc. Provide support and needed information to all global regions on all US products across the product portfolio so that regions can file products with the needed documentation and information for their submissions.

Qualifications 

• BS in Biological Sciences or Engineering preferred.
  

• 2-5 years of Experience in Regulatory Affairs preferably Medical Devices, preferably on Global programs
  

• Preferred Skills: Organization, Communication, Attention to detail, Self-motivated, Experience using Microsoft Project to manage multi-year projects,
  

• Proficient in Microsoft Excel
  

• Strong Microsoft Office skills

What happens next
Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.
Helping you discover what’s next in your career is what we’re all about,
#P1