Research Assoc I, R&D

5 months ago

Ahmedabad, India Baxter Full time

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.

To complete the planned work (Method development / Method validation/routine stability sample 
analysis) 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 (Daily/as per schedule) like HPLC, GC, Balance, Auto titrator, Karl Fisher 
Titrator, pH meter etc. as per approved standard operating procedures. 
• To make entry in respective logbook, when start the analysis and at completion of 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 analysis of material or product.
• To follow the good documentation practices. 
• To follow the good Laboratory Practices in Department. 
• To follow the instruction and procedure as mentioned in the approved protocol. 
• To keep the 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 subdepartment 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 bases. 
• 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 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.

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