Senior Engineer Validation Specialist
Core
Senior Process Engineer leading engineering maintenance, process upgrades, and validation activities in a manufacturing environment to ensure compliance and operational efficiency.
Role type
Senior Process Engineer (Manufacturing)
Builds
Manufacturing processes, equipment upgrades, and validated production systems
Domain
Healthcare manufacturing / Medical devices
Required skills
Project management, technical troubleshooting, design change evaluation, budget control, cGMP compliance, SOP development, audit execution, cross-functional collaboration, shift flexibility, material procurement (via careerplan.io/jobs/JR-211174-senior-engineer-validation-specialist-at-baxter)
Preferred skills
Master's degree or PhD in Engineering/Sciences, leadership/mentoring experience, travel readiness
Technologies
Project management tools, engineering design software, validation protocols
Responsibilities
Coordinate engineering maintenance and process upgrade tasks; direct integration of technical activities; evaluate and approve design changes; control project expenditures; develop and implement systems for cGMP and FDA compliance; audit areas for compliance; support validation processes; maintain manufacturing documentation and reports.
Seniority
Senior, hands-on IC with supervisory responsibilities
