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Associate Scientist II

United States, Round Lake 80000.00 - 120000.00 USD / Year · Job Posted January 06, 2026
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Job Description

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.

Job Responsibility

  • Conduct critical chemical and physical analyses on finished product R&D stability samples, and support testing of raw materials and other R&D initiatives
  • Act as a study director for studies, independently evaluating results and determining their impact
  • Provide training and supervision to junior members within the laboratory
  • Review test data meticulously, perform documentation reviews in LIMS and other computerized systems
  • Apply sophisticated laboratory instrumentation and computer systems for data collection and recording
  • Participate in validations and transfers, ensuring compliance with regulatory standards
  • Perform detailed chemical assays
  • Complete all testing, including special project/protocol testing, in a timely manner
  • Maintain data integrity and ensure compliance with company SOPs, FDA regulations, and other quality standards
  • Collaborate with various departments to solve problems, boost efficiency, improve quality, and provide outstanding product support
  • Support project teams, leading initiatives and making critical decisions
  • Influence program, project, and functional leadership, proposing and driving solutions to complex technical challenges
  • Maintain laboratory safety standards, perform equipment maintenance/calibration, and troubleshoot sophisticated instrumentation

Requirements

  • Bachelor’s degree or equivalent experience in a relevant scientific field (e.g., chemistry, pharmaceutical sciences) with at least 2+ years of proven experience
  • Experience working with analytical chemistry instruments such as HPLC, pH meters, UV spectroscopy, titrations, particle analysis, TOC, flame photometry, and sample extraction techniques
  • Proficiency in a regulated environment and strong technical problem-solving skills
  • Excellent oral and written communication skills, strong analytical abilities, and keen attention to detail
  • Experience with Electronic Lab Notebooks and pharmaceutical GMP laboratories is preferred
  • Experience with Empower software is advantageous
  • Ability to manage multiple tasks concurrently and efficiently
  • Strong laboratory/technical, writing, and computer skills
  • Ability to effectively coordinate and communicate complex information with managers and peers

Nice to have

Familiarity with GC and LC-MS is an advantage

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
  • 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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Associate Scientist II

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  • Bachelors degree in Chemistry or related with 3+ years of related experience
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Job Responsibility
  • Effectively contribute solid technical knowledge and possess relevant laboratory skills (HPLC/UPLC, GC, KF Titration, UV-Vis spec, Osmometer, PH, ect..) to a variety of projects within the relevant discipline with minimal assistance
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  • Maintain knowledge of relevant QSR and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities
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What we offer
  • Support for Parents
  • Continuing Education/Professional Development
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  • 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
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Associate Scientist II

This is where your work saves lives. The research we do and the products we deve...
Location
Location
United States , Round Lake
Salary
Salary:
88000.00 - 121000.00 USD / Year
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelors degree in Chemistry or related with 3+ years of related experience
  • Possess relevant laboratory/technical and writing skills
  • Experience in HPLC/UPLC
  • Effectively able to contribute on a project team
  • Demonstrates flexibility and can shift gears comfortably
  • Ability to objectively assess, organize, and clearly communicate complex information
  • Interpret available information and make recommendations to resolve technical challenges
  • Appropriately prioritize assignments to meet project schedules
Job Responsibility
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  • Effectively contribute solid technical knowledge and possess relevant laboratory skills (HPLC/UPLC, GC, KF Titration, UV-Vis spec, Osmometer, PH, ect..) to a variety of projects within the relevant discipline with minimal assistance
  • Conduct routine/non-routine research and design experiments with minimal assistance
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  • Maintain knowledge of relevant QSR and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities
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  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
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Associate Scientist II, R&D, Complex Product Development

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  • Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family
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  • Formulate new, innovative approaches to solve technical problems on a consistent basis
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  • Ensure response to customer queries, agencies query, market compliance
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Associate Scientist - II, R&D - SPO

This is where new knowledge is discovered. Baxter’s Research and Development tea...
Location
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India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
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Requirements
Requirements
  • Master's in Pharmaceutics or equivalent
  • Hands on experience in laboratory batch execution and drive the towards the expected result
  • Good communication skills for effective liaison and teamwork
  • Problem-solving skills, analytical skills and attention to detail
  • Excellent organizational skills and the ability to work on several tasks or projects concurrently
  • Presentation skills - for presenting ideas and findings to colleagues and customers
  • Ability to work well independently, with minimum supervision
  • Drive, enthusiasm and self-motivation
  • An aptitude for mathematics and statistics and highly developed IT and technical skill
  • Postgraduate with minimum 07 years of experience in pharmaceutical industry preferably in formulation development
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Job Responsibility
  • Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems
  • Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family
  • Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements. Formulate new, innovative approaches to solve technical problems on a consistent basis
  • Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation
  • Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety. Provide support to analytical team by providing the required product solution/placebo solution samples. Execute batches in laboratory, assess the study outcome to support the compendial product change requirement
  • Ensure response to customer queries, agencies query, market compliance. Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance
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  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
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Arrow Right

Associate Scientist - II, R&D - SPO

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master's in Pharmaceutics or equivalent
  • Postgraduate with minimum 07 years of experience in pharmaceutical industry preferably in formulation development
  • Hands on experience in laboratory batch execution and drive the towards the expected result
  • Good communication skills for effective liaison and teamwork
  • Problem-solving skills, analytical skills and attention to detail
  • Excellent organizational skills and the ability to work on several tasks or projects concurrently
  • Presentation skills - for presenting ideas and findings to colleagues and customers
  • Ability to work well independently, with minimum supervision
  • Drive, enthusiasm and self-motivation
  • An aptitude for mathematics and statistics and highly developed IT and technical skill
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  • Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems
  • Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family
  • Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements
  • Formulate new, innovative approaches to solve technical problems on a consistent basis
  • Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation
  • Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety
  • Provide support to analytical team by providing the required product solution/placebo solution samples
  • Execute batches in laboratory, assess the study outcome to support the compendial product change requirement
  • Ensure response to customer queries, agencies query, market compliance
  • Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance
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  • Continuing Education/ Professional Development
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  • Fulltime
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Associate Scientist - II, R&D - SPO

Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master's in Pharmaceutics or equivalent
  • Hands on experience in laboratory batch execution and drive the towards the expected result
  • Good communication skills for effective liaison and teamwork
  • Problem-solving skills, analytical skills and attention to detail
  • Excellent organizational skills and the ability to work on several tasks or projects concurrently
  • Presentation skills - for presenting ideas and findings to colleagues and customers
  • Ability to work well independently, with minimum supervision
  • Drive, enthusiasm and self-motivation
  • An aptitude for mathematics and statistics and highly developed IT and technical skill
  • Postgraduate with minimum 07 years of experience in pharmaceutical industry preferably in formulation development
Job Responsibility
Job Responsibility
  • Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems
  • Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family
  • Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements
  • Formulate new, innovative approaches to solve technical problems on a consistent basis
  • Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation
  • Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety
  • Provide support to analytical team by providing the required product solution/placebo solution samples
  • Execute batches in laboratory, assess the study outcome to support the compendial product change requirement
  • Ensure response to customer queries, agencies query, market compliance
  • Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance
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Arrow Right

Associate Scientist II, R&D, Complex Product Development

This is where new knowledge is discovered. Baxter's Research and Development tea...
Location
Location
India , Ahmedabad
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master's in science with 8 to 12 years of Experience
  • Good experience in the execution of analytical method development, validation and technology transfer and routine analysis for peptides and iron colloidal drug products for regulatory submission
  • Competency with method relevant to iron DS/DP analysis, including particle size distribution by gel filtration chromatography, light scattering/diffraction/obscuration methods, assay of various iron forms, e.g. ferrous, ferric, labile iron, chelation assays, reduction potential and kinetics, etc, is strongly desired
  • Basic Knowledge and execution of Chemical Analysis using techniques relevant to complex injectables
  • Knowledge of pharmacopoeia, ICH Guidelines
  • Execution of Operational and Calibration of Instrument on periodic basis
  • Trouble shooting of various problems obtain during the during analysis
  • Knowledge of Transfer of Technology
  • Knowledge of Good Laboratory Practice and Good Documentation Practices
  • Communication skills
Job Responsibility
Job Responsibility
  • To plan and perform sample analysis (analytical method development, validation, technology transfer, etc) activity following GxP & GDP practices for regulatory submissions for complex injectables like peptides, iron formulations, etc
  • Assist in regulatory query responses for Complex Products
  • To perform testing of Complex Injectable samples, including, API, development, validation, stability, bulk hold, RLD, PDR and any other samples as required, according to appropriate method of analysis
  • To be competent in analytical problem-solving, focus on innovation, process improvement and operational excellence
  • To keep track of all activities related to product analysis, ensure completion in the stipulated time, and inform the Sub-department manager if any deviation or issues observed
  • Preparation and review of analytical reports, SOPs and MOAs by referring to GQP & current pharmacopoeia as per requirement
  • To carry out all testing and data recording according to the approved SOPs following GDP & ALCOA++ principles and current pharmacopoeia
  • To use appropriate reference and working standards for analysis and maintain their records
  • To complete all training as per the quality matrix targets
  • To perform or review the calibration records of instruments as per approved SOPs
What we offer
What we offer
  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
Read More
Arrow Right