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.
Essential Duties and Responsibilities:
This section contains a list of five to eight primary responsibilities of the work. The incumbent will perform other duties as assigned.
To complete the planned work (Method validation/Submission Studies/Regulatory query) in stipulated time frame given by sub-department manager.To 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 draft/approved Method of analysis or current Pharmacopoeia.To operate the different instruments like HPLC, GC, Balance, Auto titrator, Karl Fisher Titrator, pH meter etc. as per approved standard operating procedures.To calibrate the Instruments as and when required (Daily/as per schedule) like HPLC, GC, Balance, Auto titrator, Karl Fisher Titrator, pH meter etc. as per approved standard operating procedures.To use live reference standards, working standards and Impurity Standards for analysis and maintain their records.To verify the shelf life of chemicals and reagents before performing analysis of material or product.To follow good documentation and ALCOA++ practices.To follow the good Laboratory practices in the Department.To follow the instruction and procedure as mentioned in the approved protocol.To keep track of routine requirements. Inform and ensure timely procurements of the same to respective person or Department.To Report and investigate any failure / abnormal observation / deviation / Non-Compliance to sub-department manager and seeking for the solutions.To communicate project related issues to sub-department manager and follow the action plans.To check the trend of results before reporting the results.To keep the status of daily work and report to sub-department manager on daily basis.To prepare standard operating procedures (SOPs) and standard formats for Documentation.To verify the instruments after maintenance of the Instruments.To check preventive maintenance, Breakdown Maintenance and perform risk assessment. To report preventive maintenance and Breakdown Maintenance to sub-department manager.To represent subject matter expertise in the areas of analysis internally and externally as needed.To make Analytical problem-solving efforts to meet urgent business needs.To focus on innovation, process improvement, and/or operational excellence.To execute and manage projects/programs utilize established methods, techniques, or approaches.To Implement new or improved techniques and procedures around specific tasks; write and implement SOP's.To complete the training as per the quality matrix targets.To 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.Equal Employment Opportunity
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.
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
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