Job Information
Philips Senior Risk Management Engineer in Shenzhen, China
In this role, you have the opportunity to:
- Be an integral part of the monitoring solutions development team and have the opportunity to work with the group of world-class R&D team who develop products that help save lives all over the world.
You are responsible for:
Overall accountable of product safety risk management throughout the whole of lifecycle of active medical device, as well, responsible of overall compliance to medical device risk management standards and regulations, typically ISO 14971.
In order to ensure “state-of-the art”, periodically and timely identify and collect standards and regulations of medical device risk management and gather corresponding intelligence, and introduce and decompose into risk management system
In order to ensure SAFETY for a medical device, as product safety risk management owner, organize, plan, lead, coordinate and control the implementations of medical device safety risk management activities:
Identify participants from various functions to form risk management team
Develop risk management plan
Implement risk analysis
Conduct risk evaluation
Evaluate overall residual risks
Coordinate risk management review
Risk management reporting
As one member of cross functional team in design and development projects, participates in design review and provides objective advice on product safety risk, such as:
Intended use and user needs
Product development requirement/specification
Verification and validation
Compliance demonstrations
As product risk expert, provides response and supports to production and post-production risk management activities
As one of stakeholders, provides response and support to medical device registration and certification
As risk management specific SME (Subject Matter Expert), take account in continuous improvements on capability and process of product safety risk management.
You are a part of:
- A professional R&D team with around 100+ team peers in Shenzhen China, a key player in Philips global R&D organization.
To succeed in this role, you should have the following skills and experience:
Bachelor, master or higher degree in engineering, e.g., electronic, industry automation, computer, biomedicine etc.
5+ years’ experience on medical device industry, and at least 3+ years’ experience on product safety risk management/assessment.
Be familiar with medical device risk management standard (e.g., ISO 14971) and/or regulation (e.g., EU-MDR).
Be familiar with FMEA/dFMEA and other assessment tools
Be familiar with development process and design controls of active products, medical device would be better
Be familiar with medical device general safety and performance requirement standards, e.g., IEC 60601-1, , preferred not required
Be familiar with clinical applications, usability, cyber security or software risk, preferred not required.
With competencies of product and design quality and compliance, conflict managements and communication effectiveness
Good English writing and speaking
Strong sense of responsibility, team works, good communication skills, self-learning ability.
Continual improvement focused, self-directed and creative.
About Philips
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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.
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