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.
As a Research Associate, you will play a significant role in driving innovation and advancing our understanding of healthcare. We are looking for a highly motivated and analytical individual with a passion for healthcare and research. Strong communication and project management skills are critical, as well as the ability to work independently and in teams.

This is where your dedication drives success !

As a Research Associate at Baxter Healthcare, you will plan and supervise the development and optimization of analytical methods for raw materials and finished products, with support from technical subject matter experts (SMEs). You will also define and propose validation/transfer designs, ensure testing follow-up and communication of results, and write comprehensive protocols and reports in English. Additionally, you will own the evaluation, validation, or transfer of analytical methods within Baxter or in partnership with contract research organizations (CROs), both domestically and internationally. You will routinely provide advice and assistance to analytical team members, interpret experimental data, lead investigations and present conclusions to supervisors, project leaders, and management. Finally, you will act as analytical lead for existing products or products under development, by collecting information related to product and product specification, assessing existing method validation versus current regulation requirements, and contributing to innovative ideas for improvement. You will adhere to quality system requirements, including good manufacturing practice (GMP) and good documentation practice (GDP) standards.