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Sr. Specialist, Regulatory Affairs

Job Attributes

Job Id:

33126

Job Category:

Clinical & Life Sciences

Job Location:

Sommerville, NJ  

Security Clearance:

None

Business Unit:

Piper Companies

Division:

Piper Clinical Solutions

JOB DESCRIPTION

Piper Companies is looking for a Sr. Specialist, Regulatory Affairs to lead the US/EU submissions and provide guidance to project teams for a Medical Device company in Sommerville, NJ.  

Responsibilities for the Sr. Specialist, Regulatory Affairs include:

  • Ensure compliance with regulatory agencies
  • Represents RA on project teams
  • Gathers necessary information for submissions
  • Responds to Regulatory agency requests and prepare/submit documentation
  • Prepare regulatory labeling requirements
  • Provide RA support during internal/external audits

Qualifications for the Sr. Specialist, Regulatory Affairs include:

  • BS required
  • 2-4 years experience in Regulatory Affairs/Labeling
  • Medical Device experience preferred
  • RAC (Regulatory Affairs Certification) is a plus

 

Compensation for the Sr. Specialist, Regulatory Affairs include:

  • Yearlong consulting assignment
  • Hourly Rate is commensurate with experience¬†

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New Search

Job Id:

33126

Job Category:

Clinical & Life Sciences

Job Location:

Sommerville, NJ  

Security Clearance:

None

Business Unit:

Piper Companies

Division:

Piper Clinical Solutions