Specialist, Medical Affairs

Becton, Dickinson, and Company (BD)

Franklin Lakes, NJ, USA
Base: $106,600.00 - $175,900.00 usd annual; bonus:...
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Bachelor's degree in biomedical or life sciences
1+ year experience in quality or medical affairs
Knowledge of fda regulations and iso standards
** Becton, Dickinson, and Company (BD) is seeking a Specialist in Medical Affairs for Post-Market Surveillance in Franklin Lakes, NJ, with a focus on compliance and report generation related to in vitro diagnostics. The role requires a Bachelor's degree in a relevant field and at least one year of related experience, with excellent writing and coordination skills being essential. **

Job Summary

  • This role is responsible for coordinating post-market surveillance reports and ensuring alignment with US, EU, Canada, and other regional regulations.
  • The position requires managing proactive customer quality response activities and supporting safety risk assessments for Specimen Management products.
  • BD offers a competitive compensation package including annual bonus potential, comprehensive health benefits, and a performance-based culture focused on collaboration.

Matching Summary

Match Score: 75

** Becton, Dickinson, and Company (BD) is seeking a Specialist in Medical Affairs for Post-Market Surveillance in Franklin Lakes, NJ, with a focus on compliance and report generation related to in vitro diagnostics. The role requires a Bachelor's degree in a relevant field and at least one year of related experience, with excellent writing and coordination skills being essential. **

Salary

Base: $106,600.00 - $175,900.00 USD Annual; Bonus: Annual Bonus Potential and Discretionary LTI Bonus; Benefits: Comprehensive health, dental, vision, 401(k), and wellness programs

Skills & Requirements

Must-have

  • Bachelor's degree in biomedical or life sciences
  • 1+ year experience in Quality or Medical Affairs
  • Knowledge of FDA regulations and ISO standards
  • Strong technical writing and documentation skills
  • Understanding of IVD and post-market surveillance

Nice-to-have

  • PhD in relevant scientific discipline
  • Publication history in technical writing
  • Experience with CyberGrants portal management
  • Familiarity with BD products and processes
  • Professional certification in medical affairs

Key Requirements

  • Bachelor's degree required
  • Minimum 1 year experience in Quality/Medical Affairs
  • Knowledge of FDA/ISO/IVDR regulations

Work Rights

Not specified

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