A
Electrical Engineer
Accepting applicationsAkkodis · Blue Ash, OH
Contract Mid_senior AnalogDFTMATLABanalog
Posted
1d ago
Category
Verification
Experience
Mid_senior
Country
United States
Job Summary:
We are seeking a Senior Electrical Engineer to lead electrical engineering activities supporting sustaining and legacy medical device products. The role will focus on electrical design, troubleshooting, component obsolescence, supplier changes, verification/validation, root-cause analysis, and regulatory compliance. The engineer will work closely with Quality, Regulatory Affairs, Manufacturing, Test Engineering, and Supply Chain teams.
Pay Range: $48/hr. to $53/hr.; The pay may be negotiable based on experience, education, geographic location, and other factors.
Required Experience:
Bachelor’s or Master’s degree in Electrical Engineering or a related field.
6–8+ years of electrical engineering experience, including at least 3 years in medical devices or another regulated industry.
Strong knowledge of analog and digital circuit design, schematics, PCB layout, and troubleshooting.
Hands-on experience with sensors, drivers, microcontrollers, and communication methodologies including onboard, wired, and wireless.
Experience with medical-device standards such as IEC 60601, ISO 13485, and FDA QSR / 21 CFR Part 820.
Must-Have Technical Skills:
Analog & Digital Circuit Design – design, debugging, and troubleshooting.
Schematic & PCB Design/Layout – experience with tools such as Altium and OrCAD.
DFM/DFA/DFT knowledge.
Component Engineering – component obsolescence, alternate sourcing, and supplier changes.
Medical Device Compliance – IEC 60601, ISO 13485, FDA 21 CFR Part 820.
Electrical Testing and troubleshooting.
Sensors, Drivers, and Microcontrollers.
Embedded Systems – basic understanding of firmware/hardware integration.
MATLAB / LabVIEW experience is desirable.
Key Responsibilities:
Lead electrical engineering activities for sustaining and legacy medical-device products.
Investigate and resolve electrical component obsolescence, supplier changes, and field issues.
Perform root-cause analysis and implement corrective and preventive actions (CAPA).
Support design changes, verification/validation, and technical documentation updates.
Ensure designs and changes comply with FDA, ISO 13485, and IEC 60601 requirements.
Participate in FMEA, risk assessments, design reviews, and change-control processes.
Collaborate with QA, Regulatory Affairs, Manufacturing, Test Engineering, and Supply Chain.
Provide technical support for manufacturing and testing activities.
Maintain technical documentation including schematics, BOMs, test protocols, and reports.
Support sustaining engineering activities and design updates for legacy products.
Ensure compliance with regulatory requirements and internal quality systems.
Failure Analysis / V&V:
Root-cause analysis using FMEA, 5 Whys, Fishbone, etc.
Verification & Validation (V&V) – test planning, execution, and documentation.
Troubleshooting of electrical/electronic product issues.
Corrective and preventive action implementation.
Documentation / PLM
Experience with:
BOMs
ECOs
DHF
PLM systems
Agile
Windchill
Functional / Managerial Skills:
Strong written and verbal English communication.
Ability to manage multiple projects and prioritize activities.
Strong problem-solving and decision-making skills.
Ability to understand and follow complex written procedures.
Effective cross-functional and team collaboration.
Project management, multitasking, prioritization, and milestone tracking.
Lean/Six Sigma knowledge preferred.
If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at Atal.Rai@akkodisgroup.com
Equal Opportunity Employer/Veterans/Disabled
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client.
To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit https://www.akkodis.com/en/privacy-policy.
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
· The California Fair Chance Act
· Los Angeles City Fair Chance Ordinance
· Los Angeles County Fair Chance Ordinance for Employers
· San Francisco Fair Chance Ordinance
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We are seeking a Senior Electrical Engineer to lead electrical engineering activities supporting sustaining and legacy medical device products. The role will focus on electrical design, troubleshooting, component obsolescence, supplier changes, verification/validation, root-cause analysis, and regulatory compliance. The engineer will work closely with Quality, Regulatory Affairs, Manufacturing, Test Engineering, and Supply Chain teams.
Pay Range: $48/hr. to $53/hr.; The pay may be negotiable based on experience, education, geographic location, and other factors.
Required Experience:
Bachelor’s or Master’s degree in Electrical Engineering or a related field.
6–8+ years of electrical engineering experience, including at least 3 years in medical devices or another regulated industry.
Strong knowledge of analog and digital circuit design, schematics, PCB layout, and troubleshooting.
Hands-on experience with sensors, drivers, microcontrollers, and communication methodologies including onboard, wired, and wireless.
Experience with medical-device standards such as IEC 60601, ISO 13485, and FDA QSR / 21 CFR Part 820.
Must-Have Technical Skills:
Analog & Digital Circuit Design – design, debugging, and troubleshooting.
Schematic & PCB Design/Layout – experience with tools such as Altium and OrCAD.
DFM/DFA/DFT knowledge.
Component Engineering – component obsolescence, alternate sourcing, and supplier changes.
Medical Device Compliance – IEC 60601, ISO 13485, FDA 21 CFR Part 820.
Electrical Testing and troubleshooting.
Sensors, Drivers, and Microcontrollers.
Embedded Systems – basic understanding of firmware/hardware integration.
MATLAB / LabVIEW experience is desirable.
Key Responsibilities:
Lead electrical engineering activities for sustaining and legacy medical-device products.
Investigate and resolve electrical component obsolescence, supplier changes, and field issues.
Perform root-cause analysis and implement corrective and preventive actions (CAPA).
Support design changes, verification/validation, and technical documentation updates.
Ensure designs and changes comply with FDA, ISO 13485, and IEC 60601 requirements.
Participate in FMEA, risk assessments, design reviews, and change-control processes.
Collaborate with QA, Regulatory Affairs, Manufacturing, Test Engineering, and Supply Chain.
Provide technical support for manufacturing and testing activities.
Maintain technical documentation including schematics, BOMs, test protocols, and reports.
Support sustaining engineering activities and design updates for legacy products.
Ensure compliance with regulatory requirements and internal quality systems.
Failure Analysis / V&V:
Root-cause analysis using FMEA, 5 Whys, Fishbone, etc.
Verification & Validation (V&V) – test planning, execution, and documentation.
Troubleshooting of electrical/electronic product issues.
Corrective and preventive action implementation.
Documentation / PLM
Experience with:
BOMs
ECOs
DHF
PLM systems
Agile
Windchill
Functional / Managerial Skills:
Strong written and verbal English communication.
Ability to manage multiple projects and prioritize activities.
Strong problem-solving and decision-making skills.
Ability to understand and follow complex written procedures.
Effective cross-functional and team collaboration.
Project management, multitasking, prioritization, and milestone tracking.
Lean/Six Sigma knowledge preferred.
If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at Atal.Rai@akkodisgroup.com
Equal Opportunity Employer/Veterans/Disabled
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client.
To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit https://www.akkodis.com/en/privacy-policy.
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
· The California Fair Chance Act
· Los Angeles City Fair Chance Ordinance
· Los Angeles County Fair Chance Ordinance for Employers
· San Francisco Fair Chance Ordinance
Show more Show less