Senior Mechanical Engineer

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W2 Regular Full Time Danvers, MA, US

7 days ago Requisition

Samsung HME America (Healthcare and Medical Equipment) is Samsung’s U.S. medical imaging organization, delivering advanced diagnostic solutions across Ultrasound, Digital Radiography, and Computed Tomography. We lead nationwide sales, marketing, service, and distribution of Samsung’s imaging technologies, partnering with healthcare providers to strengthen diagnostic capabilities, streamline clinical workflows, and support better patient care. Samsung HME America also serves as the global manufacturing center for Samsung’s mobile Computed Tomography (mCT) business, leading the development of advanced CT systems used by healthcare providers worldwide.

Backed by Samsung Electronics’ global technology leadership, our teams work closely with clinicians to translate real‑world challenges into innovative imaging solutions. Our culture combines a sense of urgency, customer focus, and clinical collaboration to advance the future of medical imaging.

Responsible for identifying and executing cost‑reduction initiatives for legacy products. This role balances manufacturing efficiency, design optimization, and material substitution without compromising product performance, safety, or quality. Focus on sustaining engineering for machined parts, sheet metal components, and machined castings.

• Cost Optimization:
  Independently identifying cost‑saving opportunities in parts in existing product lines
• Design Modification:
  Redesign mechanical parts and assemblies using Solid Works
• Supplier Engagement:
  Work directly with vendors to evaluate manufacturing capabilities and cost structures and then resolve their bottlenecks and adopt lower‑cost manufacturing methods
• Material Substitution:
  Research and qualify alternative, lower cost materials
• DFMA Application:
  Apply Design for Manufacturing and Assembly principles to simplify production
• Cross‑Functional
  
  Collaboration:
  
  Partner with Procurement, Product Quality, and Manufacturing Engineering teams to implement changes
• Testing & Validation:
  Plan and execute mechanical testing to validate redesigned components and prepare technical reports to document the results
• Engineering Change Orders:
  Author, review, and release ECOs with updated documentation into the PLM system
• Comply with regulatory and quality requirements for medical devices
  • Participate in design reviews and documentation control so as to satisfy QSR/ISO/CMDR and harmonized standards requirements for design history files

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

• BS in Mechanical Engineering strongly preferred
• 10+ years of experience in manufacturing engineering, mechanical design, or value engineering required
• Strong understanding of CNC machining, sheet metal, sand castings, and associated tooling constraints
• 3+ years of experience with Solid Works required; proficient in part modeling, assembly constraints, and detailed drawings
• Experience preparing ECOs in PLM system (i.e. Arena)
• Experience with mechanical FEA and GD&T
• Familiarity with Six Sigma, VAVE methodologies, or Root Cause Analysis are a bonus
• Experience with complex medical devices is preferred

• Must be able to analyze and solve drafting problems
• Must be able to assemble facts from various areas, analyze data, and provide informed recommendations
• Must be able to work with minimal supervision, take charge of projects, and work effectively in a demanding, fast‑paced environment
• High attention to detail
• Understanding of terminology and ability to share and communicate effectively within the group
• Ability to organize and prioritize tasks…