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Research Associate Iii

3 months ago

Bengaluru, Karnataka, 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.

Essential Duties and Responsibilities:

  • The Research Associate III is responsible for contributing to all phases of Extractable & Leachable studies carried out IH and at CROs. This would include prepare study design, protocol for sample preparation, analysis and data interpretation.
  • Independently or with support of department manager, author and contribute to the experimental protocols, process and interpret data, author technical reports.
  • Ensure technical output of the team is of the highest quality, scientifically sound and appropriately addresses the business need.
  • Ensure compliance in all research work, data collection and reporting activities.
  • Guide and direct the lab work for junior scientists.
  • Maintain current knowledge of relevant Quality Management System and other regulatory requirements related to research and development (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.
  • Support the build out of the R&D
  • E&L laboratory.
  • Develop and enhance technical capability through training and on job experience.
  • Ensure laboratory is equipped with instrumentation that is qualified to appropriate standards, maintained in a functional state and aligns with the business needs.
  • Key contributor during experimental study designs, execution and review/approval at IH & CROs study.
  • Competent in interpreting complex analytical data and presenting in a form that is suitable for a wideranging audience
  • Create innovative products/processes/methods through novel combinations of expertise within the organization.
  • Coach and mentor junior members working in analytical method development in chromatography, Mass spectrometry, and identification/quantification of impurities.
  • Influence the regional external regulatory environment in the areas of Extractables & Leachables, Elemental Impurities, and Structure Elucidation.
  • Author, review and verify technical reports, protocols and reports, Laboratory process/ SOPs

Reasonable Accommodations

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