Actalent
US - Colorado - Littleton
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Lead remediation design activities and technical documentation for medical devices to ensure compliance with FDA and ISO standards. Collaborate cross-functionally to execute verification and validation testing and manage product risk assessments.
Requirements: Requires a Bachelor's or Master's degree in Mechanical, Biomedical, or Electrical Engineering with R&D experience in the medical device industry. Must have proven expertise in FDA design controls, risk management tools like FMEA, and proficiency in SolidWorks.
Key Skills: FDA Design Controls, Medical Device Design, Risk Management, FMEA, Verification and Validation, Technical Writing, SolidWorks, Windchill, ISO Standards, IEC Standards, CAPA, Design History Files, Fault-tree Analysis, Product Lifecycle Management, Engineering Studies, Regulatory Compliance
Benefits: Medical, Dental, Vision, Critical Illness, Accident, Hospital, 401(k) Retirement Plan, Life Insurance, Short and long-term disability, Health Spending Account (HSA), Transportation benefits, Employee Assistance Program, Paid Time Off
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