Regulatory Program Director

Abbott

St. Paul, Minnesota, United States
Base: $149,300.00 – $298,700.00; bonus/equity: not...
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Project leadership in regulated industry
Strategic analytical thinking skills
Ability to negotiate consensus among diverse groups
** Abbott is seeking a Regulatory Program Director to lead regulatory program management within its Global Regulatory Operations team, focusing on medical devices. The ideal candidate will have extensive experience in project leadership within regulated industries, coupled with strong strategic and analytical skills. **

Job Summary

  • The Director will join the Global Regulatory Operations team to lead portfolio management of regulatory programs across medical device business units.
  • Abbott offers excellent benefits including free medical coverage options, a high employer contribution retirement plan, and tuition reimbursement.
  • This role requires a candidate with 10+ years of relevant experience and a Bachelor's degree in science, math, engineering, or a medical field.

Matching Summary

Match Score: 75

** Abbott is seeking a Regulatory Program Director to lead regulatory program management within its Global Regulatory Operations team, focusing on medical devices. The ideal candidate will have extensive experience in project leadership within regulated industries, coupled with strong strategic and analytical skills. **

Salary

Base: $149,300.00 – $298,700.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • Project leadership in regulated industry
  • Strategic analytical thinking skills
  • Ability to negotiate consensus among diverse groups
  • Strong written and presentation skills
  • Managing expectations on program deliverables

Nice-to-have

  • Personal integrity and courage to escalate issues
  • Adaptability to manage deadline pressure
  • Organizational savvy and strategic context understanding

Key Requirements

  • Bachelor's degree in science, math, engineering, or medical field
  • 10+ years relevant experience in regulatory, quality assurance, or R&D
  • Experience in project leadership roles within medical device or biomedical industries

Work Rights

Not specified

Tailored Resume

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