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Associate Scientist II

India, Bengaluru · Job Posted June 28, 2026
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Job Description

This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives. 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.

Job Responsibility

  • Effectively contributing solid technical knowledge to a variety Stability projects (NPD or SPO) with minimal assistance
  • Ensuring stability study initiation, study protocol and reports writing, results review and evaluation
  • Displaying basic technical understanding of theories & practices related to solutions stability
  • Participate in the development of stability programs: establish routine stability strategies in agreement with the technical leader, analytical leader and regulatory affairs
  • Accurately assess results for validity and conformance to specifications
  • Support lab sample preparations by participating in lab related investigations that correspond to atypical or out-of-specifications / out-of-trend test results
  • Without assistance, make sound technical recommendations regarding project thar are more routine than not
  • Maintain knowledge of relevant Quality System requirements 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
  • Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines
  • Have a working knowledge and understanding of GxP and related regulations and guidance
  • Demonstrate ability to anticipate risks, issues and opportunities, work independently to make sound technical recommendations regarding projects, and collaborate with team to devise mitigations and solutions
  • Contribute to technical feasibility analysis of complex research and design concepts
  • Coordinate and manage interactions with Contract Research Organizations (CROs) to ensure timely, high-quality delivery of outsourced activities aligned with project objectives

Requirements

  • Fluent in English (read, write, speak)
  • Possess relevant laboratory/technical/analytical, writing, and computer skills
  • 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
  • Master’s in science: for instance, Analytical, Organic chemistry, Biochemistry, Bio-engineering, Pharma Science
  • 6-10 years of experience in pharmaceutical industry, R&D, manufacturing…
  • Demonstrate Quality and compliance-oriented accomplishments
  • Possess basic understanding of analytical chemistry including theoretical knowledge and practical experience
  • Knowledge of GLP and GMP is a must
  • Fluent spoken, read, and written English is a must
  • Trackwise knowledge is an asset

Nice to have

Trackwise knowledge is an asset

What we offer

  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer

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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
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Salary:
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https://www.baxter.com/ Logo
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Expiration Date
Until further notice
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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
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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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  • Master's in Pharmaceutics or equivalent
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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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  • Paid Time Off
  • 2 Days a Year to Volunteer
  • Fulltime
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Associate Scientist II, R&D, Complex Product Development

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  • 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
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  • 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
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  • 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
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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
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  • 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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Arrow Right

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
What we offer
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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
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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
Read More
Arrow Right