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The Principal Engineer, Software at Baxter is responsible for overseeing end-to-end software project delivery, collaborating with teams globally, managing project risks, and ensuring Agile methodologies are followed. This role includes interacting with various stakeholders, continuous improvement initiatives, and vendor management within the medical device or Healthcare IT sectors.

As a Hospital Delegate for Baxter in the Bordeaux region, you will promote adult parenteral nutrition products to hospital users and home service providers, negotiate tenders, maintain relationships with opinion leaders and major accounts, provide on-site training, analyze sales data, and implement action plans while regularly inputting data into Salesforce CRM.

The Sr. Associate in QA is responsible for overseeing in-process quality assurance activities, including line clearance, sampling, compliance checks, and documentation. They will perform routine checks, handle training records, initiate batch numbers, and support corrective actions, ensuring compliance with manufacturing protocols and data integrity throughout the production process.

The Associate Engineer will oversee the operation, maintenance, and calibration of laboratory and manufacturing equipment, ensuring compliance with industry standards. Responsibilities include SOP preparation, conducting audits, handling shifts independently, and ensuring adherence to safety protocols while managing routine work and vendor personnel.

As a Key Account Manager - Distributors at Baxter, you will manage strategic relationships with key distributors, ensuring satisfaction and collaboration to achieve business goals. Your responsibilities include implementing distribution strategies, analyzing sales data, managing stock, and overseeing tender processes. Building strong relationships in the market and developing competitive pricing strategies are also key components of this role.

Join Baxter as a Process Operator, where you'll ensure compliance with safety and quality standards while operating machinery in a fast-paced GMP environment. Responsibilities include maintaining equipment, identifying quality defects, participating in improvement programs, and collaborating with the team to meet production targets. Ideal candidates are detail-oriented, punctual, and flexible in their roles.

The Analyst, Quality Documentation supports the Quality Management System (QMS) by developing and revising standard procedures, training materials, and facilitating internal assessments. They lead project initiatives, manage documentation processes, provide training on documentation systems, and ensure compliance with regulatory standards while participating in QA/QC projects.