Compliance Engineer ensuring regulatory compliance for health technology at Resmed. Collaborating with product development teams in audits and improving compliance processes.
Responsibilities
Lead critical design control activities including Safety risk analysis
Security risk analysis
Requirements traceability
Design review
SOUP/CSV management
Represent the team in audits, including medical device audits such as MDSAP and EU MDR and security audits such as HITRUST, SOC, and ISO 27001
Perform gap analyses to new and upcoming compliance standards and regulations
Make improvements to Resmed's Quality Management System procedures
Provide input on product regulatory strategy and be involved in communication with regulators and notified bodies
Requirements
2+ years of experience navigating technical products through audits like MDR, SOC2, MDSAP, HDS, or any other regulatory framework.
Proficiency in report writing, analysis, and compliance procedures.
Thorough understanding of regulatory frameworks.
Solid technical knowledge and understanding of product/process design.
An understanding of Software Development Lifecycle
B.S or M.S degree (Nice to Have)
At least 4 years of working in a regulatory environment in the healthcare industry (Nice to Have)
Benefits
A supportive environment that focuses on people development and best practices
Opportunity to design, influence, and be innovative.
Work with global teams and share new ideas.
Be supported both inside and outside of the work environment.
The opportunity to build something meaningful and seeing a direct impact on people's lives
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