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Regulatory Affairs Project Lead

Location: Princeton, New Jersey Salary: competitive
Sector: Medical Devices, Regulatory Affairs (RA) Type: Contract

I am partnering with a globally leading Medical Device & IVD Organisation to secure them a Regulatory Affairs Project Lead for a 6 month contract to be based in Princeton, New Jersey.

The successful Regulatory Affairs Project Lead will need at least 3 years of experience in the Medical Device industry and have excellent communication skills to be able to effectively work closely with internal customer groups.

Key Responsibilities:

  • Assists in definition/implementation of regulatory strategy and priorities in conjunction with management, peers, commercial, and affiliate personnel
  • Tracking and timely completion of regulatory strategies and issues, scientific substantiation for product claims, and label/promotional material activities
  • Communicates issues to management through project management tracking and issue briefings
  • Effective communication of regulatory requirements to project teams and internal customers
  • Manage and track broad and strategic projects
  • Communicate effectively in writing crisp briefings and issue analysis

Key Skills & Experience:

  • Bachelor's degree in relevant field
  • 3+ years of Regulatory Affairs experience in the Medical Device industry
  • Knowledge of US and/or Canadian Medical Device regulations

If this is of interest, apply now!

Sthree US is acting as an Employment Business in relation to this vacancy.