CyberCoders
Senior Quality Engineer (Electrical Engineer)
CyberCoders, Fort Lauderdale, Florida, us, 33336
Senior Quality Engineer (Electrical Engineer)
4 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Title:
Senior Quality Engineer - Electrical Industry:
Implantable Medical Devices Location:
Co HQ is South East Florida (Hybrid preferred) Intended Compensation Range:
$100-130K base + bonus (for qualified candidates) NOTE:
while hybrid work is preferred, we are open to remote arrangements for qualified candidates Are you an electrical engineer with implantable device quality experience? Join a fast-growing medtech company revolutionizing pain management through wearable neuromodulation. As a Senior or Principal Quality Engineer, you'll lead design control, supplier quality, and manufacturing efforts, driving risk management and compliance with ISO 13485 and FDA 21 CFR Part 820. Help bring a breakthrough device to market. Apply now! Key Responsibilities
Lead implementation and maintenance of the Quality Management System (QMS) Support new product development and design control compliance (DHFs, V&V protocols, risk analysis) Drive manufacturing process validations, test method qualifications, and design changes Manage supplier quality: audits, SCARs, NCMR investigations, and performance monitoring Lead CAPA investigations, root cause analysis, and corrective/preventive actions Support regulatory submissions (FDA 510(k), global) and internal/external audits (FDA, Notified Body) Collaborate cross-functionally with Engineering, Operations, and Software teams Analyze quality data and KPIs to drive continuous improvement initiatives Act as Quality lead for equipment validations, change control, and document reviews Qualifications
BS in Electrical Engineering (hard requirement) 8+ years in medical device quality engineering (implantables) Strong knowledge of ISO 13485, FDA 21 CFR 820, ISO 14971, and design control principles Experience with risk management, FMEAs, and statistical analysis, V&V Skilled in CAPA, Lean/Six Sigma, and supplier quality management $100-130k base depends on experience + bonus Regular Company Functions Vacation/PTO Full Benefits: Medical, Dental, Vision HUGE room for growth (lucrative startup) A team of sharp people on the same mission Must be authorized to work in the US without Sponsorship 401(k)
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4 days ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Title:
Senior Quality Engineer - Electrical Industry:
Implantable Medical Devices Location:
Co HQ is South East Florida (Hybrid preferred) Intended Compensation Range:
$100-130K base + bonus (for qualified candidates) NOTE:
while hybrid work is preferred, we are open to remote arrangements for qualified candidates Are you an electrical engineer with implantable device quality experience? Join a fast-growing medtech company revolutionizing pain management through wearable neuromodulation. As a Senior or Principal Quality Engineer, you'll lead design control, supplier quality, and manufacturing efforts, driving risk management and compliance with ISO 13485 and FDA 21 CFR Part 820. Help bring a breakthrough device to market. Apply now! Key Responsibilities
Lead implementation and maintenance of the Quality Management System (QMS) Support new product development and design control compliance (DHFs, V&V protocols, risk analysis) Drive manufacturing process validations, test method qualifications, and design changes Manage supplier quality: audits, SCARs, NCMR investigations, and performance monitoring Lead CAPA investigations, root cause analysis, and corrective/preventive actions Support regulatory submissions (FDA 510(k), global) and internal/external audits (FDA, Notified Body) Collaborate cross-functionally with Engineering, Operations, and Software teams Analyze quality data and KPIs to drive continuous improvement initiatives Act as Quality lead for equipment validations, change control, and document reviews Qualifications
BS in Electrical Engineering (hard requirement) 8+ years in medical device quality engineering (implantables) Strong knowledge of ISO 13485, FDA 21 CFR 820, ISO 14971, and design control principles Experience with risk management, FMEAs, and statistical analysis, V&V Skilled in CAPA, Lean/Six Sigma, and supplier quality management $100-130k base depends on experience + bonus Regular Company Functions Vacation/PTO Full Benefits: Medical, Dental, Vision HUGE room for growth (lucrative startup) A team of sharp people on the same mission Must be authorized to work in the US without Sponsorship 401(k)
#J-18808-Ljbffr