Research Assoc I, R&d

1 week ago


Ahmedabad, Gujarat, 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 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 apparatusIV, 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 projectrelated issues to the subdepartment 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 subdepartment 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 make Analytical problemsolving 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

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