Senior Continuing Cost Engineer

Agiliti is a leading provider of healthcare technology management and service solutions, helping healthcare organizations access, manage, and maintain medical equipment to enhance patient care. We partner across engineering, supply chain, manufacturing, and quality to deliver compliant, innovative, and cost-effective solutions that support clinical environments.

• Drive measurable cost savings on impactful medical device products
• Collaborate cross-functionally with engineering, operations, and supply chain leaders
• High-visibility role influencing product lifecycle and cost strategy
• Opportunity to apply value engineering and design-for-cost principles in a regulated industry
• Competitive compensation and benefits
• Meaningful work that supports better healthcare delivery and patient outcomes

• Lead cost-reduction initiatives across released medical device products (BOM optimization, material substitutions, design simplification, supplier changes)
• Identify cost drivers through BOM analysis, supplier spend, labor studies, and field/service data
• Own engineering changes (ECRs/ECOs) in Solid Works, ensuring compliance with ISO, IEC, FDA, and QMS requirements
• Partner with Supply Chain, Manufacturing, and Quality on alternate sourcing, materials, tooling, and process improvements
• Collaborate with mechanical and electrical engineers to evaluate feasibility and risk of cost-down changes
• Conduct structured trade studies balancing cost, quality, manufacturability, and risk
• Support DFM, DFA, and DFC improvements on legacy and released products
• Apply DFMEA, PFMEA, and RCA to drive sustainable improvements
• Analyze warranty and service data to uncover recurring cost opportunities
• Coordinate validation and phased implementation to minimize production and field disruption
• Track savings, implementation progress, and risks; communicate results to leadership

• Bachelor’s degree in Mechanical Engineering or related engineering discipline; advanced degree preferred
• 8+ years of engineering experience supporting manufactured products; medical device or regulated industry experience strongly preferred
• Demonstrated experience leading cost-reduction, value engineering, or design-to-cost initiatives on released products
• Proficiency with CAD tools (Solid Works preferred), PDM systems, BOM management, and tools such as Jira
• Strong knowledge of manufacturing processes (injection molding, machining, sheet metal, welding, assembly, etc.)
• Experience with supplier-facing engineering changes, alternate sourcing, and material/process substitutions
• Working knowledge of ISO 13485, ISO 14971, IEC standards, and FDA design controls
• Ability to perform technical risk assessments and root cause analysis
• Strong analytical and financial acumen with the ability to quantify savings and trade-offs
• Excellent communication and stakeholder influence skills