Senior Research Scientist - Toxicologist Job at Baxter (Round Lake)

New

Senior Research Scientist - Toxicologist

Lead in ensuring product compliance and patient safety through cutting-edge toxi...

Location

United States , Round Lake

Salary:

144000.00 - 198000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Fulltime

New

Senior Research Scientist - Toxicologist

Lead in ensuring product compliance and patient safety through cutting-edge toxi...

Location

United States , Round Lake

Salary:

144000.00 - 198000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Fulltime

New

Senior Research Scientist - Toxicologist

Lead in ensuring product compliance and patient safety through cutting-edge toxi...

Location

United States , Round Lake

Salary:

144000.00 - 198000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Fulltime

New

Administrator

We have an exciting opportunity for skilled and motivated Administrator to join ...

Location

United Kingdom , Colchester

Salary:

27976.00 GBP / Year

Alliance Medical Ltd

Expiration Date

Until further notice

Requirements

experience using Microsoft office
skills of organising filing systems and computer files
good customer service skills
excellent communication skills
IT literacy
excellent organisational skills
the ability to work well under pressure
the ability to multi task
experience in a Healthcare environment
able to work in the UK without the requirement of sponsorship

Job Responsibility

make telephone bookings for patients attending our services
meet and greet patients

Fulltime

New

Commis Chef

We’re on the lookout for a Commis Chef to join our team! Prep, create and bring ...

Location

United Kingdom , Swarkestone

Salary:

14.25 GBP / Hour

Marston's Pubs

Expiration Date

Until further notice

Requirements

Experience in a similar Chef role or an experienced KP
Know or be willing to learn about the kitchen areas and procedures
Work within a team in a fast-paced environment
Help to support the kitchen team with the day to day running of the kitchen
Have a passion to deliver great, hot food to spec each and every time

Job Responsibility

Prep, create and bring our pub menu to life
Learning new prepping skills
Bringing a meal to life for the first time
Owning a section of the kitchen

What we offer

30% off at all our pubs, restaurants, and hotels
A reliable hours contract
£4.50 meal deal option whilst on shift
Flexible and part time hours offered
High street, online discounts and cashback offers
Apprenticeship programmes
A friendly and lively atmosphere
Access to Licensed Trade Charity for financial, mental, and emotional well-being support
Privilege card discount
Marston’s Rewards

New

Pet-ct Radiographer/technologist

We have an exciting opportunity for a skilled and motivated PET CT Radiographer/...

Location

United Kingdom , Southampton

Salary:

31500.00 - 41000.00 GBP / Year

Alliance Medical Ltd

Expiration Date

Until further notice

Requirements

HCPC or equivalent voluntary registration
Background in Nuclear Medicine
Experience in handling and dispensing radiopharmaceuticals
High level of competency in cannulation preferable
Significant experience working as a Radiographer considered
Patient-focused attitude
Flexible, adaptable team player
Excellent communication skills, both verbal and written
Patient care experience/skills
Excellent interpersonal and organisation skills including time management

Job Responsibility

Undertake a competency programme in PET-CT to develop knowledge and gain a full understanding of PET-CT
IV cannulate patients as part of the role
Work across 2 sites, supporting the staffing of the Salisbury mobile service 1-2 days per week

What we offer

Training will be delivered “On the Job” and in collaboration with the Christie School of Oncology via the PET-CT training academy
Full training provided for IV cannulation if no prior experience

Fulltime

New

Quality Support Manager

This is an opportunity to join a well-established, quality-focused elderly care ...

Location

United Kingdom , Chesterfield, Nottingham & South Yorkshire Region

Salary:

50000.00 - 52000.00 GBP / Year

Compass Associates

Expiration Date

Until further notice

Requirements

Active NMC PIN (RGN)
Strong elderly care clinical background
Experience as a peripatetic or regional support manager
Experience operating within a wider quality/governance team
Strong understanding of CQC regulations and inspection frameworks
Ability to quickly assess and prioritise across multiple services
Confident communicator with inspectors and external professionals
Coaching-led leadership style
Ability to manage pace, complexity, and significant travel

Job Responsibility

Conducting in-depth clinical audits and quality assessments
Providing clinical supervision and strengthening nurse competency
Preparing homes for CQC inspections and liaising confidently with inspectors
Identifying gaps across clinical practice, leadership, and culture
Supporting infection control, housekeeping, and nutrition standards
Analysing data to track trends and monitor improvement
Coaching Home Managers to drive ownership of quality standards
Contributing to the development of quality tools and a wider nursing strategy
Supporting services requiring improvement while maintaining regional oversight

What we offer

£600 per month car allowance
Significant autonomy within a supportive governance structure
Direct influence on inspection readiness and quality ratings
Exposure to services with varied needs — from high-performing to improvement-focused homes
Involvement in wider nursing strategy and organisational development projects

Fulltime

New

Software Engineer II

The Azure PostgreSQL team is building advanced, cloud-native capabilities that e...

Location

United States , Redmond

Salary:

100600.00 - 199000.00 USD / Year

Microsoft Corporation

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Computer Science or related technical field AND 2+ years technical engineering experience with coding in languages including, but not limited to, C, C++, C#, Java, JavaScript, or Python
OR equivalent experience.
Ability to meet Microsoft, customer and/or government security screening requirements are required for this role. These requirements include, but are not limited to the following specialized security screenings: Microsoft Cloud Background Check: This position will be required to pass the Microsoft Cloud background check upon hire/transfer and every two years thereafter.

Job Responsibility

Design and implement AI-native capabilities in PostgreSQL including vector indexing, semantic search operators, and graph query features
Build high-performance extensions and core engine integrations in C, C++, or Rust
Collaborate with senior engineers, product teams, and AI researchers to deliver scalable and intuitive capabilities
Contribute to end-to-end development, including performance tuning, operability, and service integration
Participate in code reviews, technical design discussions, and the evolution of engineering standards
Help shape developer experience through APIs, control plane integration, and extensibility
Stay informed on research and industry trends in AI indexing, graph systems, and database-AI convergence
Embody our culture and values

Fulltime

Senior Research Scientist - Toxicologist

Baxter

Location:
United States , Round Lake

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 16, 2026

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Senior Research Scientist - Toxicologist

Baxter

Location:United States , Round Lake

Category:Research and Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 16, 2026

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Job Posted:
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