This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
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. Shape the Safety of Life‑Saving Therapies At Baxter, our mission to save and sustain lives is driven by scientific rigor and regulatory excellence. As an R&D Sterility Assurance Project Lead, you act as a technical focal point, defining and executing robust sterility assurance strategies to ensure product safety, quality, and compliance. You lead sterility assurance activities across complex R&D programs, applying advanced engineering and regulatory principles to solve non‑routine challenges and support multidisciplinary teams that develop, commercialize and support products on the market.
Job Responsibility:
Act as the Sterility Assurance Project Lead / Focal Point for R&D programs
Define and execute sterility assurance strategies, including test method validation plans, rationale statements, and sterilization parameters
Provide interpretation and guidance on GxP and global sterility regulations
Support regulatory submissions related to sterility assurance
Lead sterility assurance activities with a high degree of autonomy across projects of broad scope
Contribute to project planning, budgets, product requirements, and design decisions
Communicate status, risks, and recommendations to cross‑functional teams and leadership
Serve as a technical liaison with manufacturing facilities (domestic and international)
Evaluate and adapt sterilization approaches to optimize quality, safety, and cycle time
Support microbiology test method validations
Assess technical feasibility of complex product and process concepts
Introduce new technologies and methods to improve existing and future products
Support complex investigations, troubleshooting, and CAPAs
Support product development studies across the R&D lifecycle
Provide technical support to R&D, Regulatory Affairs, Manufacturing, and internal Sterility Assurance teams
Mentor junior team members and contribute to Baxter’s leadership in sterility assurance
Requirements:
B.S. in Engineering with 5–8 years of experience, or M.S. with 2–4 years, or Ph.D. with 1–2 years of relevant industry experience
Strong understanding of engineering principles and cross‑disciplinary collaboration