Junior Study Director – Extractables & Leachables (E&L)
Req \# 203492 Location Braine\-l'Alleud, Wallonia, Belgium Job Category Research and Development Date posted 06/09/2026
Overview
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This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives.
- Support for Parents
- Continuing Education/ Professional Development
- Employee Heath \& Well\-Being Benefits
- Paid Time Off
- 2 Days a Year to Volunteer
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What makes a successful Research and Development team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.
- Courage
- Action Oriented
- Collaborates
- Cultivates Innovation
- Manages Ambiguity
- Drives Results
At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.
Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.
Here, you will find more than just a job—you will find purpose and pride.
Grow Your Career in a High\-Impact Scientific Environment
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Looking to develop your expertise in Extractables \& Leachables (E\&L) and contribute to the safety of medical devices and pharmaceutical packaging?
Join Baxter and work alongside experienced scientists on cutting\-edge studies in a collaborative and fast\-paced environment.
Your Role
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As a Junior Study Director, you will contribute to the design, coordination, and execution of E\&L studies, ensuring compliance with regulatory standards while developing your scientific and project management skills.
What You Will Do:
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- Support the design and execution of E\&L studies with internal teams and external laboratories
- Contribute to protocol writing, data analysis, and reporting
- Ensure alignment with industry standards (ISO 10993\-18, USP \<1663/1664\>)
- Collaborate with cross\-functional teams (analytical chemistry, toxicology, regulatory, manufacturing)
- Participate in compound identification and data interpretation
- Support scientific investigations and continuous improvement initiatives
- Ensure compliance with quality and regulatory requirements
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- Education \& Experience (including internships):
+ Master’s degree with \~2–3 years of experience, OR
+ PhD in a relevant scientific field
- Background in Chemistry, Analytical Sciences, or related discipline
- Knowledge or exposure to analytical techniques (LC\-MS, GC\-MS, ICP\-MS)
- Interest in regulated environments (medical devices, pharmaceuticals)
- Strong team spirit and good communication skills
- Fluent in English (French is a plus)
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- Work on meaningful projects impacting patient safety
- Develop expertise in a highly specialized field
- Benefit from a collaborative environment with strong learning opportunities
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice
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