Baxter
Healthcare
PrincipalEngineer
Neural analysis suggests this role is
optimal for Senior candidates.
“Principal Engineer at Baxter. Skills: Automation systems, Control systems, Pharmaceutical manufacturing, GMP compliance. Lead automation initiatives. Lead control system initiatives”
What You'll Achieve.
Enhance manufacturing performance; Enhance manufacturing reliability; Increase operational efficiency; Enhance product quality; Reduce operational costs
Industry & Context.
Root Cause Analysis; Troubleshooting; Problem-solving
5% remote work
What They're Looking For.
Must Have
Bachelor's degree in Engineering, 5 years of related experience, Assess facility and equipment, Develop project execution plan, Plan and manage capital projects $10M, Manage savings $1M, Execute FDA/MoH regulated Change Management, Use Value Stream Mapping, Use Root Cause Analysis, Site SME for automation equipment, Demonstrated familiarity with GMP, Experience operating in regulated environment, Lead multidisciplinary team activities, Develop project approval documentation, Deliver presentations to executive committees, Manage installation of production line serialization systems, Supervise cross-functional team members
Nice to Have
Experience with robotics, Experience with data analytics platforms, Experience with proprietary equipment, Experience with IV bag filling equipment, Experience with pouching equipment, Experience with packing equipment, Experience with Trackwise8 Management, Experience with pharma qualification protocols IQ, Experience with pharma qualification protocols OQ, Experience with pharma qualification protocols PQ, Experience with EUFMD, Experience with DSCSA, Experience with UDI
What You'll Do.
Lead automation initiatives
Lead control system initiatives
Define technical vision
Provide architectural guidance
Evaluate advanced technologies
Recommend advanced technologies
Integrate advanced technologies
Manage project lifecycles
Manage capital requests
Manage design development
Manage validation commissioning
Manage launch of automation systems
Identify technical risks
Assess technical risks
Mitigate technical risks
Manage external vendors
Support negotiation processes
Ensure GMP compliance
Ensure FDA regulation compliance
Ensure 21 CFR Part 11 compliance
Apply quality standards
Supervise engineer work
Supervise technician work
Provide technical guidance
Support troubleshooting
Support problem-solving
Support skills development
How You'll Work.
Team & Collaboration
Multidisciplinary team activities; Cross-functional team members; Operations; Maintenance controls; Validation
Communication Scope
Executive presentations
Process & Methodology
Project lifecycles, Capital requests, Project execution, Implementation plan, Capital expenditure projects, Change Management
Full Job Description
**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. **JOB LOCATION:** Marion, NC **POSITION** : Principal Engineer **POSITION DESCRIPTION:** Baxter Healthcare Corporation is seeking a Principal Engineer with the following duties: * Responsible for leading complex automation and control system initiatives within a highly regulated pharmaceutical manufacturing environment. * Define the technical vision and provide high‑level architectural guidance for automation systems to ensure alignment with business objectives and regulatory requirements. * Evaluate, recommend, and integrate advanced technologies—including robotics, data analytics platforms, and proprietary equipment—to enhance manufacturing performance and reliability. * Manage full project lifecycles, including capital requests, design, development, validation, commissioning, and launch of automation systems in GMP‑regulated environments. * Identify, assess, and mitigate technical and project risks; manage external vendors and support negotiation processes when necessary. * Ensure all automation and control initiatives comply with Good Manufacturing Practices (GMP), FDA regulations, and 21 CFR Part 11 requirements. Learn, understand, and consistently apply rigorous quality standards, Standard Operati
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