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To complete the planned work (Method development / Method validation/routine stability sample
analysis) in the stipulated time frame given by the 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, Zeta sizer, Dissolution test apparatus-IV, etc. as per approved standard operating procedures.
• To 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.
• To make entries in respective logbooks, when starting the analysis and after Analysis.
• 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 an analysis of the material or product.
• To follow good documentation practices.
• To follow the good Laboratory Practices in the Department.
• To follow the instructions and procedure as mentioned in the approved protocol.
• To keep track of routine requirements. Inform and ensure timely procurements of the same to the respective person or Department.
• To Report and investigate any failure / abnormal observation/deviation / Non-Compliance to the subdepartment manager and seek solutions.
• To communicate project-related issues to the 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 the sub-department manager on a 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 and breakdown Maintenance and perform risk assessment. To report

preventive maintenance and Breakdown Maintenance to the 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 utilizing established methods, techniques, or approaches.
• To Implement new or improved techniques and procedures around specific tasks; write and implement SOP\'s.
• 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. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com 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. 124915