Pluvigner, Brittany, France
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Common questions about this position
This is a full-time position.
This information is not specified in the job description.
The role involves supporting R&D project teams throughout new product development for medical devices, ensuring design control, regulatory compliance, verification and validation, root cause analyses, design reviews, risk management, and CAPA activities.
Baxter colleagues are united by a mission to Save and Sustain Lives, driven by a culture of courage, trust, and collaboration, where individuals are empowered to take ownership and deliver exceptional results.
Strong candidates have expertise in design control, regulatory compliance for medical devices, risk management tools like DFMEA and PFMEA, root cause analysis, design reviews, and experience supporting R&D teams in new product development.
Provides essential medical products and services
Baxter International provides a wide range of medical products and services essential for healthcare. The company operates in several areas, including critical care, hospital care, nutritional care, renal care, and surgical care. Its products are used in various settings, from emergency rooms to home healthcare, helping to meet the needs of patients and healthcare professionals. Baxter develops, manufactures, and distributes medical devices, pharmaceuticals, and biotechnology products, generating revenue through sales to healthcare providers and institutions. A key aspect that sets Baxter apart from competitors is its recent acquisition of Hillrom, which enhances its ability to offer comprehensive healthcare solutions. The company's goal is to improve care outcomes and increase access to healthcare through continuous innovation and a focus on patient needs.