Overview
This is where new knowledge is discovered. Baxter’s Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives.
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Success Profile
What makes a successful Research and Development team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.
- Courage
- Action Oriented
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Principal Engineer, Containers R&D
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.
As a Principal Engineer, you will display engineering principles to resolve difficult problems, from conception to final design with team input. You will plan, schedule, and leads project assignments in the evaluation, selection and adaptation of various engineering techniques, procedures and criteria with minimal guidance within the Medication Delivery business unit.
This position will work on flexible filled container systems, leading design concept selections, as well as verification and validation efforts. You will collaborate within a cross-functional global team environment supporting projects for on-market product. You will collaborate with colleagues from other functional areas including Project Management, Stability, Sterility, Manufacturing, Regulatory, Material Science, Quality, Integrated Supply Chain, Human Factors, and Packaging Engineering.
As a Principal Engineer, you will contribute to the development and sustaining support of container drug products with the following responsibilities:
Execute engineering assignments in primary drug container / delivery system design including developing engineering requirements and conducting design, verification / validation activities and undertaking risk management activities (dFMEA, Use Error Analysis, Risk Assessment & Control table, etc.).
Select sound techniques to solve problems and make design recommendations.
Collaborate with manufacturing facilities to design and execute production of experimental units for testing
Provide technical review for component and material specifications.
Evaluate the impact of supplier change notifications (SNC’s) on NPD and on-market products
Stay abreast of regulatory and compendial requirements for packaging components, systems and testing requirements.
Conduct risk assessments to evaluate components, systems, suppliers, and processes.
Occasional travel to Baxter / Customer sites within the United States and internationally may be required.
Perform root cause investigations related to design issues
Primary responsibilities
Act independently with minimal supervision to conduct smaller approved projects. Expected to make suggestion on improvements based on recent technical knowledge.
Must have experience or advanced training and demonstrate proficiency in Design History File’s and other key areas, such as: quality processes, statistical methods, problem analysis and resolution, materials science, design inputs, design outputs, etc.
Change control owner for engineering design and/or material changes
Must have experience performing complex statistical analysis using Minitab software
Ability to convince management on courses of action with minimal assistance using both written and verbal methods.
Effectively operate in and may facilitate cross-functional teams with guidance.
Must be able to provide solutions that reflect understanding business objectives and cost implications
Qualifications
BS in Engineering (Mechanical, Biomedical/Bioengineering, Chemical) Materials Science or related field with 5+ years of experience.
2+ years of experience working in the pharmaceutical, medical product, or packaging industries.
Your Additional Skills are a plus, but not required!
CAD / CAE experience using CREO / Solidworks.
Experience in molding, extrusion, and/or RF sealing of medical grade plastics.
Fluent in Spanish or Portuguese
- Six Sigma Green Belt Certified
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The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.
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.
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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 link here and let us know the nature of your request along with your contact information.
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