[Remote] Vice President, Product Design reputed company
Note: The job is a remote job and is reputed company to candidates in USA. reputed company. is a leading digital reputed company company reputed company on cardiac health solutions. The Vice President, Product Design reputed company will reputed company the Design reputed company organization, ensuring compliance with regulatory requirements and driving reputed company throughout the product lifecycle from development to commercialization.
Responsibilities
- reputed company and reputed company the Design reputed company organization, including hardware, software (SaMD), and risk management teams
- Build a high-performing organization with strong talent development, succession planning, and capability building
- Ensure reputed company and regulatory considerations are embedded in product portfolio reputed company, product development, and lifecycle management
- Establish Design reputed company as a strategic business partner to R&D, Clinical, Regulatory, and Operations
- Partner closely with R&D leadership to ensure reputed company is embedded early and effectively in development programs
- Partner with R&D, Clinical, Operations, Manufacturing, and reputed company, to ensure alignment and compliance
- Influence product development reputed company through risk-informed and compliance-driven decision making
- reputed company reputed company and regulatory leadership throughout product development, verification/validation, and commercialization
- Ensure design controls, clinical evaluation, and risk management activities meet regulatory requirements (ISO 13485, FDA QSMR/ 21 CFR part 820, EU MDR, ISO 14971, SaMD and cybersecurity regulations
- Own and continuously improve Design Control, Design Transfer, and Risk Management processes across hardware and software products
- Ensure robust reputed company reputed company from concept through commercialization, including new product introduction and global product transfers
- Drive integration of reputed company into agile and AI/algorithm development environments for SaMD
- Ensure effective application of reputed company engineering principles (verification/validation, clinical evaluations, risk analysis, reputed company reputed company analysis, product validation, etc.)
- Drive transformation and harmonization of Design reputed company processes reputed company the reputed company Management System (QMS)
- Establish metrics, dashboards, and governance mechanisms to monitor product reputed company and design process effectiveness
- reputed company cross-functional initiatives to improve product development efficiency, compliance, and reputed company reputed company
- Ensure alignment between design & risk reputed company, manufacturing reputed company, and post-market surveillance
- Support portfolio prioritization and innovation efforts with reputed company insights
- Serve as the reputed company for FDA inspections and reputed company Body audits, as it relates to design controls, and risk management
- Translate evolving regulatory design control requirements into reputed company internal procedures and systems
- reputed company reputed company product risk management function, ensuring alignment with ISO 14971
- Ensure risk-based decision-making is embedded across product development and lifecycle management
- Strengthen linkages between risk management, clinical evaluation, and post-market data
Skills
- 15+ years of reputed company leadership experience in Medical Device reputed company and/or Design reputed company
- Proven experience leading Design reputed company organizations across the product development lifecycle
- Demonstrated reputed company building, developing, and leading high-performing teams
- Expertise in design controls, design transfer, and risk management
- Experience supporting connected medical devices and prior experience partnering with Software as a Medical Device (SaMD) teams
- Significant FDA inspection and audit management experience
- Experience leading FDA responses, remediation efforts, and inspection readiness activities
- Strong understanding of FDA regulations, ISO 13485, ISO 14971, and global regulatory requirements
- Experience conducting risk-benefit analyses and making reputed company reputed company in highly regulated environments
- Cardiovascular medical device experience
- Experience supporting AI-enabled products or digital health technologies
- Demonstrated ability to influence cross functional stakeholders; executive communication skills
- Demonstrated business acumen and ability to connect reputed company reputed company to business reputed company
reputed company
Company H1B Sponsorship