Not specified; benefits: annual leave 30 days; mob...
3-5 years medical or clinical affairs experience
Bachelor's or master's degree in medical science
Clinical experience in icu, or, or telemetry
This role ensures patient safety and regulatory compliance across the full product lifecycle through proactive risk management and adverse event reporting
Job Summary
This role ensures patient safety and regulatory compliance across the full product lifecycle through proactive risk management and adverse event reporting.
The position requires analyzing safety data from clinical trials and post-market sources to identify emerging risks and support timely regulatory submissions.
Philips offers a comprehensive benefits package including 30 days of annual leave, subsidized mobility options, and extensive professional development opportunities.
Matching Summary
This role ensures patient safety and regulatory compliance across the full product lifecycle through proactive risk management and adverse event reporting.
Salary
Not specified; Benefits: Annual leave 30 days; Mobility: Subsidized Germany ticket and leasing opportunities
Skills & Requirements
Must-have
3-5 years Medical or Clinical Affairs experience
Bachelor's or Master's degree in Medical Science
Clinical experience in ICU, OR, or telemetry
Adverse event reporting and signal detection
Risk-benefit analysis and regulatory compliance
Nice-to-have
Certified Professional in Patient Safety (CPPS)
Willingness to travel internationally 10-25%
Strong stakeholder communication skills
Experience with clinical study reports
Proactive risk mitigation strategies
Key Requirements
Bachelor's or Master's degree in Medical Science
3-5 years experience in Medical Devices industry
Clinical background in adult/pediatric ICU or OR
Knowledge of global medical device safety regulations