Serve as a Subject Matter Expert (SME) and local technical authority for product safety of ultrasound probes following and sharing best practices and supporting global consistency across programs.
Partner with the Safety & Risk Engineer and the local Install Base Engineer to apply ISO 14971 throughout the product lifecycle covering hazard identification risk analysis risk control strategies benefitrisk justification and final safety signoff. Maintain and update product Cause & Mitigation Tables (CMT) to ensure all mitigations remain effective and implemented incorporating postmarket feedback and periodic review inputs in a timely manner.
Lead productsafetyrelated interactions with Notified Bodies (NB) including owning safety document submissions preparing technical safety justifications responding to NB questions or nonconformities and representing product safety as a SME during NB audits and technical file reviews.
Own the definition flowdown and verification of product safety requirements ensuring they are appropriately incorporated during concept development requirements definition architecture decisions NPI design changes and sustaining activities.
Act as the local expert for IEC IEC 606011 IECand related ultrasound safety standards providing authoritative interpretation and ensuring compliance across design and verification activities.
Drive resolution of safetycritical issues including investigation of safety escalations evaluation of field data review of design changes and leadership of cross-functional safety assessments and safetyimpact decisions.
Provide safety engineering leadership for audits inspections design reviews and regulatory submissions ensuring safety documentation is complete accurate and compliant with global regulatory expectations.
Mentor and develop engineers and support personnel building safety engineering capability through training coaching and technical guidance on standards safety analyses and test methodology.
Monitor and interpret evolving global regulations and safety standards assessing their impact on product development and work proactively with the Safety & Risk Engineer to integrate new requirements into organizational processes and designs.
Bachelors degree in engineering physics or related technical discipline and 5 years of medical device development experience;
OR 10 years in medical device engineering/compliance with at least 3 years of hands-on IEC compliance and safety testing experience.
Demonstrated expertise in IEC 60601 series IEC IEC 60529 and other applicable medical electrical equipment standards.
Strong working knowledge of ISO 14971 including experience leading or contributing to formal device risk management activities.
Proven ability to lead crossfunctional teams influence technical decisions and communicate complex safety concepts across diverse technical and cultural environments.
Experience in medical ultrasound diagnostic imaging systems or related highreliability medical devices.
Familiarity with GE HealthCares QMS design control processes and product development workflows.
Demonstrated ability to manage multiple priorities drive complex technical issues to closure and make sound safetycritical decisions under time constraints.
Strong analytical troubleshooting and problemsolving skills with the ability to distill complex information into clear technical documentation.
Excellent written and verbal communication skills including the ability to author safety justifications riskbenefit analyses and regulatory documentation.
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We will not sponsor individuals for employment visas now or in the future for this job opening.GE HealthCare offers a great work environment professional development challenging careers and competitive compensation. GE HealthCare is anEqual Opportunity Employer. Employment decisions are made without regard to race color religion national or ethnic origin sex sexual orientation gender identity or expression age disability protected veteran status or other characteristics protected by law.
GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19 some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.
Relocation Assistance Provided: No
Required Experience:
IC
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