Associate Specialist, Regulatory Affairs

Becton, Dickinson, and Company

Irvine, CA, US
Hourly: $33.80 - $55.80 usd; bonus/equity: not spe...
**
Strong attention to detail
Proficiency in excel and data manipulation
Ability to manage multiple priorities
** Becton, Dickinson, and Company is seeking an Associate Specialist in Regulatory Affairs to support global product distribution and ensure compliance with regulatory requirements. This fully remote position requires attention to detail, strong analytical skills, and collaboration with cross-functional teams. **

Job Summary

  • This role is responsible for managing product data attributes, certificates, and country-specific compliance requirements within internal regulatory systems.
  • The position requires close collaboration with cross-functional teams including Master Data Management, Supply Chain, and Quality to ensure timely and compliant product release.
  • BD prioritizes on-site collaboration with a minimum of 4 days per week to foster creativity and innovation in the fast-paced healthcare industry.

Matching Summary

Match Score: 75

** Becton, Dickinson, and Company is seeking an Associate Specialist in Regulatory Affairs to support global product distribution and ensure compliance with regulatory requirements. This fully remote position requires attention to detail, strong analytical skills, and collaboration with cross-functional teams. **

Salary

Hourly: $33.80 - $55.80 USD; Bonus/Equity: Not specified; Benefits: Comprehensive Total Rewards program including performance-based culture

Skills & Requirements

Must-have

  • Strong attention to detail
  • Proficiency in Excel and data manipulation
  • Ability to manage multiple priorities
  • Cross-functional collaboration skills

Nice-to-have

  • Self-motivated with proactive mindset
  • Results-driven and diligent
  • Comfortable multitasking in dynamic environment
  • Quick learner adapting to new systems

Key Requirements

  • Bachelor's degree in scientific or engineering field preferred
  • Experience with EU MDR/MDD and FDA regulations
  • Knowledge of UDI requirements and CE marking processes
  • Familiarity with ERP systems like SAP

Work Rights

Not specified

Tailored Resume

Cover Letter