Regulatory Affairs Specialist

Beckettcottingham

Tempe, AZ, USA
Fully remote
Regulatory submissions preparation
Compliance process support
Medical device regulatory knowledge
The Regulatory Affairs Specialist provides primary regulatory support for product lines and participates independently on new product development teams

Job Summary

  • The Regulatory Affairs Specialist provides primary regulatory support for product lines and participates independently on new product development teams.
  • BD is a global medical technology company that fosters a culture of learning, growth, and innovation to advance health worldwide.
  • The role requires up to 25% travel and supports a fast-paced, team-oriented environment with a focus on collaboration and regulatory compliance.

Matching Summary

The Regulatory Affairs Specialist provides primary regulatory support for product lines and participates independently on new product development teams.

Skills & Requirements

Must-have

  • Regulatory submissions preparation
  • Compliance process support
  • Medical device regulatory knowledge
  • Regulatory strategy development
  • Regulatory databases management
  • Interpretation of regulatory requirements

Nice-to-have

  • Experience with regulatory audits
  • Strong organizational skills
  • Excellent written communication
  • Ability to work independently
  • Problem solving and analytical skills

Key Requirements

  • Bachelor’s degree in technical or medical-related field
  • Minimum one year experience or equivalent
  • Preferred two to four years medical device experience
  • Preferred two years regulatory role experience
  • Ability to travel up to 25%

Work Rights

Not specified

Tailored Resume

Cover Letter