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Baxter Logo Baxter · Research and Development

Senior Research Scientist - Toxicologist

United States, Round Lake 144000.00 - 198000.00 USD / Year · Job Posted February 16, 2026
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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 that are 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 your assigned Business Segment or Division.

Job Responsibility

  • Provide technical and strategic input to project teams, ensuring compliance with Baxter and external standards while driving business objectives
  • Take the lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments, to support global programs
  • Plan and manage complex projects, prioritizing workloads and meeting major organizational objectives in collaboration with senior management
  • Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
  • Support innovation initiatives by providing technical direction and ensuring the quality of deliverables that integrate state-of-the-science theory with practical approaches
  • Participate in standards organizations and regulatory committees to influence emerging regulations based on sound scientific principles
  • Work closely with R&D, Clinical, Medical Affairs, Regulatory Affairs, Quality, Manufacturing, and Environmental Health and Safety teams to support various projects and initiatives
  • Articulate the Pre-Clinical Toxicology vision, goals, and performance to project teams, fostering a culture of high standards and stretch goals
  • Establish and nurture professional networks both internally and externally, participating in global task forces and committees to exchange technical information

Requirements

  • BS with 12+ years, MS with 10+ years, or PhD with 4+ 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

  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • 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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  • BS with 12+ years, MS with 10+ years, or PhD with 4+ years of relevant experience in R&D and/or GLP environments
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  • 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
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  • Provide technical and strategic input to project teams, ensuring compliance with Baxter and external standards while driving business objectives
  • Take the lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments, to support global programs
  • Plan and manage complex projects, prioritizing workloads and meeting major organizational objectives in collaboration with senior management
  • Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
  • Support innovation initiatives by providing technical direction and ensuring the quality of deliverables that integrate state-of-the-science theory with practical approaches
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  • Work closely with R&D, Clinical, Medical Affairs, Regulatory Affairs, Quality, Manufacturing, and Environmental Health and Safety teams to support various projects and initiatives
  • Articulate the Pre-Clinical Toxicology vision, goals, and performance to project teams, fostering a culture of high standards and stretch goals
  • Establish and nurture professional networks both internally and externally, participating in global task forces and committees to exchange technical information
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  • Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
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Senior Research Scientist - Toxicologist

Lead in ensuring product compliance and patient safety through cutting-edge toxi...
Location
Location
United States , Round Lake
Salary
Salary:
144000.00 - 198000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BS with 12+ years, MS with 10+ years, or PhD with 4+ 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
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  • Provide technical and strategic input to project teams, ensuring compliance with Baxter and external standards while driving business objectives
  • Take the lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments, to support global programs
  • Plan and manage complex projects, prioritizing workloads and meeting major organizational objectives in collaboration with senior management
  • Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
  • Support innovation initiatives by providing technical direction and ensuring the quality of deliverables that integrate state-of-the-science theory with practical approaches
  • Participate in standards organizations and regulatory committees to influence emerging regulations based on sound scientific principles
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  • Articulate the Pre-Clinical Toxicology vision, goals, and performance to project teams, fostering a culture of high standards and stretch goals
  • Establish and nurture professional networks both internally and externally, participating in global task forces and committees to exchange technical information
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Lead in ensuring product compliance and patient safety through cutting-edge toxi...
Location
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United States , Round Lake
Salary
Salary:
144000.00 - 198000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
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  • BS with 12+ years, MS with 10+ years, or PhD with 4+ 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
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  • Take the lead in authoring pre-clinical sciences and toxicology deliverables, including non-clinical testing plans and toxicological risk assessments, to support global programs
  • Plan and manage complex projects, prioritizing workloads and meeting major organizational objectives in collaboration with senior management
  • Assess technical and scientific information, identify deficiencies, and design innovative solutions to mitigate risks
  • Support innovation initiatives by providing technical direction and ensuring the quality of deliverables that integrate state-of-the-science theory with practical approaches
  • Participate in standards organizations and regulatory committees to influence emerging regulations based on sound scientific principles
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  • Establish and nurture professional networks both internally and externally, participating in global task forces and committees to exchange technical information
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