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Research Scientist II - Toxicologist

https://www.baxter.com/ Logo

Baxter

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Location:
United States , Round Lake, Illinois

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Category:
Research and Development

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Contract Type:
Not provided

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Salary:

120000.00 - 165000.00 USD / Year
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Job Description:

Lead in ensuring product compliance and patient safety through cutting-edge toxicology strategies. Define, create, and execute non-clinical safety and efficacy assessments essential for the development of groundbreaking medical devices as per ISO 10993 series of standards and pharmaceutical packaging systems as per US pharmacopeia and other ministries of health as required. Apply expertise in pre-clinical science and toxicological principles to support new product development (NPD), sustain product organization (SPO), and drive manufacturing improvement projects (MIP). Serve as the primary point of contact for Pre-Clinical Toxicology within the assigned Business Segment or Division.

Job Responsibility:

  • Provide technical and strategic input to project teams
  • Lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments
  • Plan and manage complex projects
  • Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
  • Support innovation initiatives by providing technical direction
  • Participate in standards organizations and regulatory committees
  • Work closely with R&D, Clinical, Medical Affairs, Regulatory Affairs, Quality, Manufacturing, and Environmental Health and Safety teams
  • Articulate the Pre-Clinical Toxicology vision, goals, and performance to project teams
  • Establish and nurture professional networks both internally and externally

Requirements:

  • BS with 8+ years, MS with 6+ years, or PhD with 2+ years of relevant experience in R&D and/or GLP environments
  • Medical Device experience strongly preferred
  • Solid understanding of national and international non-clinical safety and biological evaluation regulations, including Good Laboratory Practices (GLP)
  • Direct experience working with regulatory bodies such as the US-FDA, EU Notified Bodies, and other national or international reviewers
  • A strong track record of presenting at scientific conferences and authoring/co-authoring published articles in peer-reviewed journals
  • Demonstrated ability to advance new product development projects and provide innovative non-clinical solutions for pharmaceutical and medical device challenges
  • Experience in a GLP and/or R&D environment, with a solid understanding of project management principles
What we offer:
  • Medical and dental coverage
  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
  • Employee Stock Purchase Plan (ESPP)
  • 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

Additional Information:

Job Posted:
March 13, 2026

Employment Type:
Fulltime
Work Type:
Remote work
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