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Baxter Healthcare Sr. Manufacturing Engineer in St. Paul, Minnesota

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission. Summary Sr Manufacturing Engineer leads initiatives for daily support to manufacturing teams for tissue products, processes, materials and equipment in order to integrate new products within production goals (i.e., quality, delivery, cost, productivity and safety). Lead engineering improvement projects and participate in R&D activities as assigned. Lead and/or support key development and continuous engineering projects, continues KPI implementation and follow up. Lead conversion loss projects. Design Solid works. Lead investigations into nonconformism and CAPAs. Essential Duties and Responsibilities Provide engineering support to manufacturing lines, including floor support, non-conforming product investigations, change order control requests reviews, and new equipment qualifications. Perform return product investigations for product complaints. Own key deliverables in support of development and continuous/sustaining engineering R&D projects, which may include:first articles, mold tool qualifications, component qualifications, process validations. Work with quality and R&D engineers to prepare manufacturing work instructions, material specifications, and inspection documentation.Set inspection requirements, set inspection methods and inspection sampling plans. Support quality control inspectors with new product inspections and quality issues that arise during inspections. Provide leadership for non conformance investigations and CAPAs and assigned. Support internal audits and supplier audits. Qualifications Self-motivated worker, persistent, curious Strong communication skills Working knowledge and understanding of mechanical drawings Strong problem solving, technical writing, and statistical analysis skills Preferred experience with supporting a manufacturing product line Preferred experience with tissue products Education and/or Experience B.S. degree in Engineering or Science (Biomedical Engineer, Chemical Engineer, Chemistry, Biochemistry, Materials Science, Electromechanic) 3+ years in an engineering role within a Medical Device company. Must have working experience of GMP and ISO 13485 requirements. Physical Demands: Sitting/standing 8 hours per day. Light lifting may be required on occasion. Ability to work using a microscope Ability to be in a clean room environment with varying humidity levels Ability to travel occasionally. #IND-USOPS #LI-TV1 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 here and let us know the nature of your request along with your contact information. 044695 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. EEO is the Law EEO is the law - Poster Supplement Pay Transparency Policy

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