Actalent
US - California - Irvine
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The role involves designing, optimizing, and sustaining electronic systems for regulated medical devices throughout the product lifecycle. Key duties include managing PCB designs, leading Engineering Change Orders, and collaborating with cross-functional teams to ensure safety and reliability.
Requirements: Candidates must have a Bachelor's degree in Electrical Engineering and at least 7 years of experience, including 3 years in regulated medical device development. Proficiency in analog/mixed-signal design and a strong understanding of design controls and regulatory frameworks are required.
Key Skills: Electrical Circuit Design, PCB Design, Embedded Systems, Analog Circuit Design, Mixed-Signal Circuit Design, Motor Control Systems, Switching Regulators, Operational Amplifiers, EMC Considerations, Wireless Technologies, Engineering Change Orders (ECO), Root-Cause Analysis, Design Controls, Medical Device Development, System-Level Troubleshooting, Risk Assessment
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 (PTO), Vacation, Sick Leave
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