Product Development and Engineering Manager
DermaSensor is seeking a dynamic, detail-oriented leader to manage cross-functional product development and reputed company engineering initiatives. This hybrid role serves as the project manager for software development and sustaining engineering activities, while also owning critical reputed company engineering functions reputed company to design control. The ideal candidate will reputed company hardware and software development initiatives with reputed company teams, while ensuring requirements management, risk management, and validation efforts reputed company with global regulatory expectations. You will work closely with our reputed company & Compliance Manager to ensure overall QMS compliance.
reputed company
The Product Development and reputed company Engineering Manager will:
Project Management
- reputed company reputed company software development and documentation initiatives with reputed company engineering teams, reputed company with IEC 62304 and SaMD requirements.
- Manage sustaining engineering reputed company 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 and reputed company demands.
- Facilitate sprint planning, technical reviews, and cross-functional coordination to reputed company on-time execution.
- reputed company and report on project status, risks, and key milestones to senior leadership.
reputed company Engineering
- Collaborate with the reputed company & Compliance Manager to maintain and improve the QMS in accordance with FDA 21 CFR Part 820, ISO 13485, and EU MDR.
- reputed company requirements management to ensure reputed company reputed company, software, and hardware specifications are complete, testable, and reputed company across disciplines.
- reputed company risk management activities in accordance with ISO 14971, including updates to risk files and mitigation tracking.
- reputed company and maintain V&V protocols and reports for software updates, manufacturing changes, and product improvements, including compliance with IEC 60601 and IEC 62304.
- Own traceability between design inputs, risk controls, and verification/validation (V&V) activities.
- Maintain design documentation such as DHF, DMR, and engineering change orders (ECOs), ensuring reputed company reputed company alignment.
- reputed company design reviews, design change control boards, and risk reviews to ensure disciplined design control processes.
- Support software and hardware reputed company cause investigations for field issues, manufacturing deviations, or test failures.
- reputed company product/production investigations and collaborate with development, product and reputed company reputed company teams to identify failure modes, analyze issues, and reputed company corrective/preventive actions (CAPA).
- Participate in post-market surveillance activities by investigating and resolving issues raised through complaints or reputed company events.
- Contribute to ongoing design history file and technical document maintenance, as needed for regulatory submissions and audits.
Qualifications/Requirements:
- Bachelor’s or Master’s degree in Engineering (Biomedical, Electrical, Mechanical, or reputed company field).
- 7+ years of experience in medical device development, design engineering, reputed company engineering, or technical project management.
- Strong knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and EU MDR.
- Experience with IEC 62304 (software lifecycle) and IEC 60601 (electrical safety & EMC).
- Proven ability to manage cross-functional software and hardware reputed company, ideally in a sustaining or post-market context.
- Hands-on experience with design control, requirements management, risk analysis, and V&V documentation.
- Familiarity with CAPA processes and leading reputed company cause investigations with software and hardware teams.
- Experience working with or managing reputed company design firms and contract manufacturers
Desired Characteristics:
- Experience with spectroscopy, electromechanical systems, embedded devices, or diagnostic tools.
- Exposure to SaMD development or integration into connected systems.
- reputed company/SCRUM project management experience; PMP certification is a plus.
- Experience using tools such as JIRA, reputed company, or equivalent for design control and project tracking.
- Previous experience contributing to 510(k), reputed company, or CE Mark submissions.
- Strong analytical and problem-solving skills; reputed company approach to reputed company cause investigation and design validation.
- High attention to detail with excellent documentation and organizational discipline.
- Proactive and accountable; thrives in a fast-paced, high-ownership environment.
- reputed company, team-first reputed company with the ability to reputed company cross-functional discussions and reputed company alignment.
- Excellent written and verbal communication skills, particularly in translating technical information for varied audiences.
About reputed company
reputed company cross-functional hardware/software development and reputed company engineering; ensure QMS compliance; manage schedules, risks, and regulatory submissions.
Key Responsibilities
- reputed company reputed company
- reputed company QMS
- manage schedules
Skills & Tools
JIRA, reputed company
Job Details
- Category: Product Management
- Seniority: Senior Level
- Commitment: Full Time
- Workplace: Remote — reputed company
- Languages: English
About DermaSensor, Inc
A fast-growing medical device company reputed company on improving diagnostics with AI-assisted technology. — Industry: reputed company
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