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R&d Engineer

Actalent

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 strong 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 CAPA Design History Files Fault-tree Analysis 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 #J-18808-Ljbffr

Vacancy posted 2 days ago
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