Senior Supplier Development Engineer - Medical Devices

Hamilton-Medical; Reno (NV); On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Medical insurance

401(k) plan

Tuition reimbursement

Job summary

Hamilton Medical, Inc. seeks a Senior Supplier Development Engineer to lead supplier qualification, development, and performance management within a regulated medical device environment in Reno, NV.

You will collaborate with Materials, Quality, and Production teams to meet technical, quality, and regulatory requirements. You will drive CAPA, supplier audits, change management, and risk mitigation, guiding cross‑functional teams toward continuous improvement and supply continuity in support of

Qualifications

• Knowledge of medical device regulatory requirements (FDA QMSR, ISO 13485) and supplier quality systems.
• Ability to read engineering drawings and GD&T and interpret technical documentation.
• Experience with supplier audits, FAI, and change management in a regulated environment.

Responsibilities

• Evaluate, qualify, and requalify suppliers based on technical capability, quality, and regulatory compliance.
• Conduct supplier audits and support onboarding, qualification, and design transfer activities.
• Drive supplier capability improvements through analysis, capability studies, and structured improvement plans.
• Implement supplier quality requirements in collaboration with QA and Engineering.
• Monitor supplier performance and mitigate risks with cross-functional teams.
• Lead investigations of supplier nonconformances and support SCAR activities.

Skills

Supplier development

Quality systems

Auditing

GD&T

Process improvement

Statistical tools

Regulatory compliance

Root cause analysis

Education

Bachelor’s degree in Manufacturing/Mechanical/Biomedical Engineering

Tools

D365

SAP

MS Office

Job description

Hamilton Medical, Inc. seeks a Senior Supplier Development Engineer to lead supplier qualification, development, and performance management within a regulated medical device environment in Reno, NV.

You will collaborate with Materials, Quality, and Production teams to meet technical, quality, and regulatory requirements. You will drive CAPA, supplier audits, change management, and risk mitigation, guiding cross‑functional teams toward continuous improvement and supply continuity in support of