Principal Engineer, R&D
About The Position
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.
Requirements
- B.S. in engineering discipline (preferably Biomedical /Mechanical Engineering) M.S or Ph.D. preferred, with at least 5+ years proven success in product development environment
- Experience in creating/managing design documentation and transfer of products into manufacturing.
- Proficient in 3D CAD Software
- Experience in prototyping, testing, and evaluating mechanical designs
- Skilled at written and verbal presentations within the business/technical community.
- Demonstrated ability to contribute to technical projects through successful outcomes.
- Must be self-motivated, resourceful, flexible. A self-starter is imperative.
- Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.
Nice To Haves
- Preferred experience with TQM, statistical methods, problem analysis and resolution, materials science, and design of experiments.
Responsibilities
- Achieves desired technical outcomes through the direct completion of Design Control, CAPA, CC project deliverables or programs within the boundaries of timing and budget.
- Responsible for technical oversight of a constantly changing portfolio that impact R&D, Operations, Quality Systems (QS), Process, Customer or Supply Chain.
- Lead and collaborate with cross-functional teams to meet schedule & project demands.
- Based on technical expertise, reviews and approves design changes and provides technical product direction for the project team.
- Fosters an environment of rigor, completeness and compliance when participating on CAPA, CC or FCA investigations/assessments.
- Embraces accountability for critical decisions as a technical subject matter expert within a cross-functional team to drive product development deliverables, such as formulation development, process development, or tech transfers.
- Demonstrates understanding of and adherence to FDA, ISO, and IEC design control procedures and standards.
- Creates design concepts and research methodologies that best meet current and future customer & business needs for a product or process domain area.
- Uses critical thinking and teamwork to contribute to the resolution of competing constraints.
- Create and maintain technical documents found in a DHF, such as verification/validation reports, technical drawings, and specifications.
- Develop and execute study plans and reports.
Benefits
- medical and dental coverage that start on day one
- basic life insurance
- accident insurance
- short-term disability insurance
- long-term disability insurance
- business travel accident insurance
- Employee Stock Purchase Plan (ESPP)
- 401(k) Retirement Savings Plan (RSP)
- Flexible Spending Accounts
- educational assistance programs
- paid holidays
- paid time off ranging from 20 to 35 days based on length of service
- family and medical leaves of absence
- paid parental leave
- commuting benefits
- Employee Discount Program
- Employee Assistance Program (EAP)
- childcare benefits
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Principal
