Quality Manager, R&D

This is where your work makes a difference.

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. 

Join Baxter and Help Us Save and Sustain Lives

At Baxter, we are united by a mission to improve patient outcomes through innovative healthcare solutions. Our R&D site in Braine-l’Alleud is at the heart of developing therapeutic products and medical devices that make a real difference. We are currently seeking a Quality Manager to lead our Product Quality System team and ensure excellence in compliance, product development, and continuous improvement.

Your Impact:

As Quality Manager, you will:

• Act as Site Quality Head and Quality Management Representative for Baxter R&D Europe.
• Lead the implementation and maintenance of the Quality System, ensuring compliance with global regulations (ISO 13485, ISO 14971, ICH, 21 CFR, MDR, MDSAP).
• Provide quality leadership for new product development and lifecycle management projects.
• Serve as a Subject Matter Expert in Risk Management, Design & Development, and Quality by Design (QbD).
• Oversee laboratory operations, change control, CAPA/NCR processes, and audit readiness.
• Drive continuous improvement through data analysis, internal audits, and cross-functional collaboration.
• Manage and develop a high-performing Quality team, fostering a culture of excellence and innovation.

What You’ll Bring

• A degree in Engineering or Physical Sciences with 8+ years of experience in Quality roles.
• Strong knowledge of pharmaceutical and medical device regulations, including GMP, ISO standards, and FDA/EMEA requirements.
• Experience in project management, risk analysis, and quality systems development.
• Fluent both in English and French.
• Proficiency in tools such as Minitab, TrackWise, TcU, and Microsoft Office.
• Certification in CQE or Six Sigma Green Belt is a plus.

Why Baxter?

At Baxter, we are united by a shared purpose: to save and sustain lives. Joining our R&D team in Braine-l’Alleud means becoming part of a global organization that values innovation, integrity, and collaboration. You’ll work in a dynamic environment where your expertise will directly contribute to the development of life-changing therapies and medical technologies. We foster a culture of continuous learning and improvement, offering opportunities for career growth, recognition, and meaningful impact. At Baxter, your work matters — every day, you’ll help shape the future of healthcare.

Equal Employment Opportunity

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.

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