Regulatory Affairs Project Manager - Vascular (on-site)

Abbott

Westford, Massachusetts, United States
Base: $99,300.00 – $198,700.00; bonus/equity: not ...
Regulatory input to product lifecycle
Develop multi-country regulatory strategy
Assess documentation for submission
Abbott is a global healthcare leader with a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines

Job Summary

  • Abbott is a global healthcare leader with a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines.
  • The Regulatory Affairs Project Manager will provide regulatory input to product lifecycle planning, assist in developing multi-country regulatory strategy, and assess documentation for submission filing.
  • Abbott offers career development, competitive benefits including medical coverage and retirement savings, and tuition reimbursement programs.

Matching Summary

Abbott is a global healthcare leader with a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines.

Salary

Base: $99,300.00 – $198,700.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Regulatory input to product lifecycle
  • Develop multi-country regulatory strategy
  • Assess documentation for submission
  • Interact with regulatory authorities
  • Ensure compliance with post-marketing requirements
  • Capital equipment and software regulatory input

Nice-to-have

  • Work effectively on cross-functional teams
  • Exercise good and ethical judgment
  • Follow scientific arguments
  • Mentor less-experienced staff

Key Requirements

  • Bachelor's Degree
  • 4-5 years of experience in a regulated industry
  • 2-5 years of experience in regulatory affairs
  • Effectively communicate verbally and in writing
  • Ability to work effectively on cross-functional teams
  • Pay strong attention to detail
  • Organize and track complex information

Work Rights

Not specified

Tailored Resume

Cover Letter