Research Scientist II Job at Baxter (Round Lake)

Research Scientist II

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

United States , Round Lake

Salary:

128000.00 - 176000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's degree in a scientific discipline with 10 years' experience, MS with at least 5-7 years, or PhD with 2 + years in relevant discipline required
Research lab experience includes research in GMP/QSR environment and cross-functional teamwork within the area of pharmaceuticals
Formulation experience desired
Must possess working knowledge of specific scientific discipline governing day-to-day activities
Must be able to able to carry out strategy and vision set by upper management and be able to communicate the vision to more junior associates
Can effectively communicate with internal and external customers
Ability to break down technical processes and effectively delegate to junior team members
Demonstrates flexibility and the ability to shift gears between projects comfortably

Job Responsibility

Under direction of senior scientific staff, create innovative pharmaceutical products through novel combinations of expertise within the organization
Reach conclusions based on research analysis and incorporate recommendations into larger projects
Apply advanced techniques to solving difficult problems
Approve technical feasibility of complex design concepts within area of expertise
advise management regarding appropriate action as pertains to the development and registration of pharmaceutical products
Independently plan, execute and manage projects/programs that both span multiple disciplines and utilize established methods, techniques or approaches for the purpose of creating new pharmaceutical products
Shares research outcomes, methodology and product development cycle-time reduction methods with team members and other divisional personnel
Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development (pharmaceutical product development,) to ensure compliance in all research, data collection and reporting activities
May supervise and direct Associate and Research Scientists

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

Research Scientist II

Microsoft is a company where passionate innovators come to collaborate, envision...

Location

India , Hyderabad

Salary:

Not provided

Microsoft Corporation

Expiration Date

Until further notice

Requirements

Master's Degree in relevant field AND 1+ year(s) related research experience
Bachelor's Degree in relevant field AND 2+ years related research experience
OR equivalent experience
Proven ability to communicate complex technical concepts to diverse stakeholders
Ability to meet Microsoft, customer and/or government security screening requirements
Microsoft Cloud Background Check
Doctorate in relevant field OR Master's Degree in relevant field AND 3+ years related research experience OR Bachelor's Degree in relevant field AND 5+ years related research experience OR equivalent experience
Experience publishing academic papers as a lead author or essential contributor
Experience participating in a top conference in relevant research domain
Strong track record in cross-functional product development and delivering measurable impact through data-driven iteration

Job Responsibility

Build and expand collaborative partnerships across product, engineering, and research groups inside and outside Microsoft
Provide growing expertise that accelerates technology transfer, strengthens data security practices, and advances internal tools, benchmarking efforts, patent filings, and whitepaper development
Contribute to cutting-edge research by collaborating with peers and engineering teams to advance existing projects, develop new ideas, and publish high-quality papers
Coauthor or lead publications for top-tier conferences and journals with impact on par with postdoctoral research output
Drive research projects to completion, delivering novel algorithms, prototypes, theories, datasets, tools, or insights that meaningfully advance one or more open research problems
Uphold Microsoft’s commitments to security, ethics, and privacy by incorporating responsible research practices into data collection, experimentation, and system design
Support the development of trustworthy, robust, privacy-preserving, and ethically aligned technologies
Help define clear research problems and goals, contributing to the formulation of compelling problem statements and feasible research plans with measurable impact
Develop deep understanding of the state of the art, tracking new methods, tools, and breakthroughs in the research community
Contribute domain expertise in multiple specialized techniques to guide project planning, scoping, and execution

Fulltime

New

Research Scientist II - Toxicology

We are looking for a dynamic and detail-oriented Research Scientist II to join o...

Location

Canada , Vancouver

Salary:

100000.00 - 125000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

PhD in Toxicology or related biological science field and a minimum of 2-5 years of related experience in an academic or industry environment
candidates with a MSc and 7+ years of relevant experience will also be considered
hands-on experience with in vitro and/or in vivo toxicology studies
strong desire to learn and develop proficiency with nonclinical safety assessment of large molecules/biologics
strong analytical and problem-solving skills
excellent communication and collaboration skills

Job Responsibility

Designing, planning, and supporting the execution of in vitro and/or in vivo toxicology studies as needed, adhering to the appropriate regulatory guidelines and communicating toxicology study results internally
Updating and maintaining proper recording of nonclinical safety study data, as required by Good Laboratory Practice (GLP)
Assisting with the authoring of toxicology sections of Regulatory documentation
Collaborating with scientists across various teams at AbCellera to ensure high data quality and that studies meet the company’s objectives
Contributing to the development of our toxicology programs and participating as a nonclinical safety/toxicology representative as needed
Maintaining an active scan of published toxicology data relevant to AbCellera’s product portfolio, and continuously expanding your knowledge base

What we offer

Equity
annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
annual vacation
professional development opportunities
comprehensive health benefits
scientific and technical mentorship

Fulltime

Research Scientist II - Toxicologist

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

Location

United States , Round Lake, Illinois

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Fulltime

Research Scientist II - Toxicologist

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

Location

United States , Round Lake

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

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

Fulltime

Research Scientist II - Toxicologist

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

Location

United States , Round Lake

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

Job Responsibility

Provide technical and strategic input to project teams
Take the 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

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)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Research Scientist II - Toxicologist

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

Location

United States , Round Lake; Milwaukee; Chicago

Salary:

120000.00 - 165000.00 USD / Year

Baxter

Expiration Date

Until further notice

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

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

Applied Scientist II / Senior Applied Scientist

The CoreAI Platform and Tools organization is building transformative experience...

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, Computational Linguistics, or related field AND 2+ years related experience (e.g., statistics, predictive analytics, research)
OR Master's Degree in Computer Science, Computational Linguistics, or related field AND 1+ year(s) related experience
OR Doctorate in Computer Science, Computational Linguistics, or related field
OR equivalent experience
Ability to meet Microsoft, customer and/or government security screening requirements
Microsoft Cloud Background Check

Job Responsibility

Conduct supervised fine-tuning of LLMs, applying Reinforcement Learning from Human Feedback in the process, and conducting thorough evaluation of those
Work with tech lead on the design and implementation of Agent adversarial evaluations and safety mitigations, enabling agent creators to identify potential risks and apply appropriate safeguards to ensure the safety and security of Agents
Collaborate closely with the Responsible AI engineering team to deliver these mitigations at scale for Responsible AI customers, refine existing implementations based on operational performance, and troubleshoot and resolve end-to-end issues

Fulltime

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Research Scientist II

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