Job Description

This is where you save and sustain lives


At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.


Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.


Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.


Join us at the intersection of saving and sustaining lives--where your purpose accelerates our mission.

About Us: Baxter's Mission
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At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.


Baxter's products and therapies are found in almost every hospital worldwide, in clinics, and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.


Together, we create a place where we are happy, and successful and inspire each other. This is where you can do your best work.


Join us at the intersection of saving and sustaining lives--where your purpose accelerates our mission.

Your Role at Baxter
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This is where your work saves lives


The research we do and the products we develop improve outcomes for patients around the world. As a Research Assoc I, R&D - ADL at Baxter, your work contributes directly to making a significant impact on others. It's challenging work--and you're not on your own. Our teams collaborate cross-functionally and lead by influence. Whether guiding a team through a project or managing direct reports, our research and development team is responsible for influencing others to achieve results.


Our colleagues within our R&D organization desire to work on products that make a meaningful difference in others' lives. We are motivated by the power of teamwork and are natural leaders who are skilled at influencing others.


When you join Baxter as a Research Assoc I, R&D - ADL, you'll use your analytical approach to identify risks and opportunities for innovation quickly. Agile and willing to take action, you stay calm under pressure.

Your Team
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While everyone at Baxter has a shared passion for our mission, the R&D teams play a critical role in our ability to save and sustain lives. Scientists and engineers in R&D work together to develop, test, and launch products that enhance patient care.


We encourage teamwork and collaboration and prioritize building relationships with each other. It's easy to do because we all share common traits of reliability, ethics, and caring. We lean on our colleagues for their expertise and hold each other accountable.


Baxter understands that learning and development are important. Whether it's training, striving toward a promotion, or gaining experience with other portfolios or business units, Baxter leaders frequently speak with their teams about how employees are trying to grow and how they can support those efforts. With the ability to chart your own path, the development opportunities are endless.

What you'll be doing..!!
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• Complete the planned work (Method development / Method validation/routine stability sample analysis) in the stipulated time frame given by the sub-department manager.
• Perform all the testing and data recording of API samples, Development Product samples, Validation Samples, Stability samples, Bulk hold samples, RLD samples, PDR samples, etc. according to the draft/approved Method of analysis or current Pharmacopoeia.
• Operate the different instruments like HPLC, GC, Balance, Auto titrator, Karl Fisher Titrator, pH meter, etc. as per approved standard operating procedures.
• Calibrate the Instruments (Daily/as per schedule) like HPLC, GC, Balance, Auto titrator, Karl Fisher Titrator, pH meter, etc. as per approved standard operating procedures.
• Make entries in respective logbooks, when starting the analysis and after the Analysis.
• Use live reference standards, working standards, and Impurity Standards for analysis and maintain their records.
• Verify the shelf life of chemicals and reagents before performing an analysis of the material or product.
• Follow good documentation practices.
• Follow the good Laboratory Practices in the Department.
• Follow the instructions and procedures as mentioned in the approved protocol.
• Keep track of routine requirements. Inform and ensure timely procurements of the same to the respective person or Department.
• Report and investigate any failure / abnormal observation/deviation / Non-Compliance to the sub-department manager and seek solutions.
• Communicate project-related issues to the sub-department manager and follow the action plans.
• Check the trend of results before reporting the results.
• Keep the status of daily work and report to the sub-department manager on a daily basis.
• Prepare standard operating procedures (SOPs) and standard formats for Documentation.
• Verify the instruments after maintenance of the Instruments.
• Check preventive maintenance, Breakdown Maintenance and perform risk assessment. To report preventive maintenance and Breakdown Maintenance to the sub-department manager.
• Represent subject matter expertise in the areas of analysis internally and externally as needed.
• Make Analytical problem-solving efforts to meet urgent business needs.
• Focus on innovation, process improvement, and/or operational excellence.
• Optimally manage projects/programs, and apply established methods, techniques, or approaches.
• Implement new or improved techniques and procedures around specific tasks; write and implement SOP's.
• Maintain knowledge of relevant regulatory requirements related to R&D to ensure compliance in all research, data collection, and reporting activities.
• In addition to having an in-depth knowledge and understanding of cGxP and related regulations and guidance.

What you'll bring..!!
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• Education qualification in M. Pharm./M.Sc. with a minimum of 6-8 years of proven experience in analytical method development.

Equal Employment Opportunity
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Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

EEO is the Law
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EEO is the law - Poster Supplement


Pay Transparency Policy

Recruitment Fraud Notice
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Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Reasonable Accommodations



Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice



Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.


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