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Do you want to be part of Baxter Healthcare Corporation as a Quality Validations Engineer I? You will help maintain outstanding quality and safety standards in our workflows. You will plan, prepare, coordinate, and lead tasks related to the Validations System, ensuring they align with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDP). Emphasizing regulatory consistency and perfection, you will participate in and encourage ICare's initiatives, promoting solutions that improve product quality, safety, and efficiency. Your keen focus on detail and dedication to regulatory perfection will secure accurate execution and steady process refinement.
Job Responsibility:
Evaluate, build, and improve procedures related to your areas of responsibility
Collaborate with personnel from other areas to develop and complete projects, validations, periodic reviews, continuous improvement initiatives, and analysis of exception documents
Maintain and supervise validation quality indicators
Ensure alignment with the standards of the Safety, Health, and Environmental Protection Program
Provide required support to internal customers to improve the fulfillment of plant goals.
Requirements:
A degree or equivalent experience in Materials Engineering, Production, Industrial, Chemical, Systems, Electrical, Electronic, Electromechanical Engineering, or a related field