Job Abstract

Regulatory Affairs Specialist (Hybrid) 
Kelly® Science & Clinical is seeking a Regulatory Affairs Specialist for our client in Bridgewater, New Jersey.  If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
This client is a company that’s leading the way in pharma/med device industry.

Schedule: HYBRID Monday through Friday 8am to 5pm
Length of assignment: Until the end of 2023 likely to extend into 2024
Pay: $43.00-45.00 an hour

• Responsibilities: Provide Regulatory Documentation Support to Global RA team members for Product Registrations, Renewals, etc.
  

• Provide support and needed information to all global regions on products across the company and subsidiaries product portfolio utilizing external manufacturing organizations EMO so that regions can file products with the needed documentation and information for their submissions.
  

• Communicate with Global RA Team members regarding required RA documentation for their submissions.
  

• Track RA requests from Global RA team.
  

• Communicate RA requests to partners at external manufacturing organizations EMO and partners.
  

• Communicate with External Quality partners.

Qualifications: BS in Biological Sciences preferred.

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

• Organization, Communication, Attention to detail, Self-motivated

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,
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