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Senior Manager of Global Regulatory Affairs

United States, Deerfield Employment contract 136000.00 - 187000.00 USD / Year · Job Posted March 05, 2026
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Job Description

A Senior Manager of Global Regulatory Affairs leads the development and execution of regulatory strategies to support product approvals, lifecycle management, and compliance across international markets, with deep expertise in US FDA requirements. This role coordinates cross‑functional teams to prepare, review, and submit high‑quality regulatory filings, ensuring alignment with evolving global and US regulations. They serve as a strategic advisor to leadership, providing risk‑based guidance and driving regulatory excellence to enable timely market access and sustained product compliance.

Job Responsibility

  • Serves as the Global Regulatory Lead for Baxter’s hemostat and sealant product(s) registered as biologic/combination products
  • Provide technical and strategic input for regulatory decisions aligned with business strategy
  • Identify & prioritize key areas of risk and probability of occurrence as well as ensure implementation of mitigation plans and follow ups
  • Monitor, evaluate, and interpret all applicable regulatory requirements, assure compliance with Baxter and external standards
  • Assess impact of new regulations and provide feedback
  • Evaluate technical and scientific information, identify deficiencies, implement and execute strategies to remediate risks
  • Act as primary contact for meetings with regulatory authorities including planning and leadership
  • Maintain appropriate communication within the RA function, with Global Marketing, and with other functions primarily at the project team level
  • Plan and manage complex projects and prioritize workload
  • Initiate, manage and maintain operational activities in support of new and existing marketing authorizations
  • Set team, group, or service objectives to assure they align with the regulatory strategy
  • Represent Baxter interests in industry and working groups
  • Mentor junior colleagues on US regulatory requirements and submission strategies

Requirements

  • Bachelor’s degree or country equivalent in a scientific discipline
  • Minimum of 7-year experience in RA
  • Expert Regulatory knowledge
  • Sound basis of Scientific (Training/ Communications) knowledge
  • Management skills
  • Ability to oversee multiple projects in a matrix team environment
  • Excellent oral and written communication and presentation skills
  • Demonstrated excellent interpersonal and collaboration skills, including diplomacy to negotiate conflicting priorities
  • Technical and management skills
  • Ability to lead, coach, and motivate others
  • Ability to accomplish results through others
  • Ability to work effectively in multinational/multicultural environment

Nice to have

Master’s and/or PhD

What we offer

  • Medical and dental coverage that start on day one
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
  • 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
  • Flexible Spending Accounts
  • Educational assistance programs
  • Paid holidays
  • Paid time off ranging from 20 to 35 days based on length of service
  • Family and medical leaves of absence
  • Paid parental leave
  • Commuting benefits
  • Employee Discount Program
  • Employee Assistance Program (EAP)
  • Childcare benefits

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