Research Associate at Baxter! MPharma Apply Online
Research Assoc I, R&D – ADL
Req # JR – 142273
Location: Ahmedabad, Gujarat, India
Job Category: Research and Development
Date posted: 08/06/2024
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
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.
At Baxter, we understand 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..!!
- Complete planned work (Method validation/Submission Studies/Regulatory query) in the stipulated time frame given by the sub-department manager.
- Operate different instruments like HPLC, GC, Balance, Auto titrator, Karl Fisher Titrator, pH meter, etc. as per approved standard operating procedures.
- 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.
- 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 and ALCOA++ practices.
- Follow good Laboratory practices in the Department.
- Follow the instructions and procedure 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.
- Maintain regular communication with the sub-department manager regarding daily tasks and progress.
- 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. 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.
- Manage and oversee projects/programs using established methods, techniques, or approaches.
- Implement new or improved techniques and procedures around specific tasks; write and implement SOPs.
- Maintain knowledge of relevant regulatory requirements related to R&D to ensure compliance in all research, data collection, and reporting activities.
What you’ll bring..!!
Education qualification in M. Pharm./M.Sc. with a minimum of 6-8 years of proven experience in analytical method development.
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