Product Development and Engineering Manager
Full-timeSeniorProduct Development and Quality EngineeringMedical DevicesUnknownMasters
Market Rate — Compliance Officers
25th
$59K
Median
$76K
75th
$101K
BLS 2024 data (national)
Description
The Product Development and Quality Engineering Manager will lead Agile software development and documentation initiatives with internal and external engineering teams, aligned with IEC 62304 and SaMD requirements. Manage sustaining engineering projects and production planning with contract manufacturers, focusing on product and production improvements, cost reductions, and supply continuity. Maintain integrated schedules, risks, and cross-functional alignment across engineering and production teams. Facilitate sprint planning, technical reviews, and cross-functional coordination to drive on-time execution. Track and report on project status, risks, and key milestones to senior leadership. Collaborate with the Quality & Compliance Manager to maintain and improve the QMS in accordance with FDA 21 CFR Part 820, ISO 13485, and EU MDR. Lead requirements management to ensure all specifications are complete, testable, and aligned across disciplines. Drive risk management activities in accordance with ISO 14971, including updates to risk files and mitigation tracking. Develop and maintain V&V protocols and reports for software updates and product improvements. Own traceability between design inputs, risk controls, and V&V activities. Maintain design documentation such as DHF, DMR, and ECOs. Lead design reviews and support software and hardware root cause investigations. Participate in post-market surveillance activities by investigating and resolving issues.
Requirements
Bachelor’s or Master’s degree in Engineering (Biomedical, Electrical, Mechanical, or related field). 7+ years of experience in medical device development, design engineering, quality engineering, or technical project management. Strong knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and EU MDR. Experience with IEC 62304 and IEC 60601. Proven ability to manage cross-functional projects, ideally in a sustaining context. Hands-on experience with design control, requirements management, risk analysis, and V&V documentation. Familiarity with CAPA processes and leading root cause investigations. Experience working with external design firms and contract manufacturers.
DermaSensor
BIOTECHNOLOGY
Skin Cancer Diagnosis Device
LocationFL - Miami
Open Jobs1
OncologyDermatology
View Company Profile