GE HEALTHCARE·1 month ago
1 month ago
Sr. Associate Specialist, Product Surveillance, Clinical WHXR
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What you'll do
- Apply clinical product knowledge and product surveillance expertise to review customer complaints, assess potential risk, and determine whether a complaint represents a potentially hazardous situation.
- Use an understanding of clinical workflows and how products are used in real-world settings to support accurate complaint evaluations and enhance team knowledge.
- Evaluate complaints from patient safety perspective and identify complaints that require further evaluation under 21CFR part 803 (MDR)
- Clearly communicate complex clinical or technical information in a way that is easy for others to understand.
- Build strong working relationships with colleagues across the Complaint Handling Unit and provide guidance and support to new team members.
- Collaborate with cross-functional teams including Medical Safety, Engineering, Regulatory Affairs, and hospitals to gather information and support complaint investigations / determine reportability in alignment with regulatory requirements.
- Work independently on day-to-day responsibilities while following established procedures and knowing when to seek guidance on more complex situations.
- Use clinical expertise, analytical thinking, and sound professional judgment to investigate issues, solve problems, and make well-supported decisions that impact patient safety.
- Draw on resources and subject matter experts across the organization as needed.
- Timely complaint handling, reporting, and training
- Contribute to improving team processes, projects, and standard ways of working within Product Surveillance
What they're looking for
- Bachelor's degree from an accredited university or college (or a high school diploma / GED with at least 8 years of experience in Medical Device Manufacturing Industry or working in a clinical setting)
- Minimum 2 years of experience in a clinical setting interfacing with X-Ray, Bone Mineral Density, or Mammography medical devices.
Nice to have
- Product specific knowledge and/or experience using X-Ray, Mammography, or Bone Mineral Density GEHC manufactured medical devices
- Prior experience working with Microsoft Office products (particularly Excel)
- Demonstrated knowledge of 21CFR Part 820
- Experience working with cross-functional teams and facilitating teams to identify and implement solutions to complex problems, even amongst competing priorities
- Demonstrated experience prioritizing conflicting demands in an extremely fast paced environment
- Excellent interpersonal, organizational, and influencing skills
- Ability to analyze and process data, and draw the appropriate conclusions
- Experience with Lean principles or demonstrated experience implementing process improvements
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Job Description Summary
Gère les activités de traitement des réclamations et prend en charge les zones clés de qualité et de réglementation pour garantir des produits sûrs et efficaces dans la base d'installation de GE HealthCare Healthcare. Responsable de la qualité de son travail. En règle générale, il bénéficie d'une supervision fonctionnelle directe et d'instructions de travail et/ou de vérification système. Le travail est exécuté dans un cadre de fonctions habilitantes bien défini. Il y dispose généralement d'une séquence détaillée des tâches standard à suivre pour obtenir les résultats finaux.Job Description
Roles and Responsibilities
- Apply clinical product knowledge and product surveillance expertise to review customer complaints, assess potential risk, and determine whether a complaint represents a potentially hazardous situation. Use an understanding of clinical workflows and how products are used in real-world settings to support accurate complaint evaluations and enhance team knowledge.
- Evaluate complaints from patient safety perspective and identify complaints that require further evaluation under 21CFR part 803 (MDR)
- Clearly communicate complex clinical or technical information in a way that is easy for others to understand.
- Build strong working relationships with colleagues across the Complaint Handling Unit and provide guidance and support to new team members.
- Collaborate with cross-functional teams including Medical Safety, Engineering, Regulatory Affairs, and hospitals to gather information and support complaint investigations / determine reportability in alignment with regulatory requirements.
- Work independently on day-to-day responsibilities while following established procedures and knowing when to seek guidance on more complex situations.
- Use clinical expertise, analytical thinking, and sound professional judgment to investigate issues, solve problems, and make well-supported decisions that impact patient safety. Draw on resources and subject matter experts across the organization as needed.
- Timely complaint handling, reporting, and training
- Contribute to improving team processes, projects, and standard ways of working within Product Surveillance
Required Qualifications
- Bachelor's degree from an accredited university or college (or a high school diploma / GED with at least 8 years of experience in Medical Device Manufacturing Industry or working in a clinical setting)
- Minimum 2 years of experience in a clinical setting interfacing with X-Ray, Bone Mineral Density, or Mammography medical devices.
Desired Characteristics
- Product specific knowledge and/or experience using X-Ray, Mammography, or Bone Mineral Density GEHC manufactured medical devices
- Prior experience working with Microsoft Office products (particularly Excel)
- Demonstrated knowledge of 21CFR Part 820
- Experience working with cross-functional teams and facilitating teams to identify and implement solutions to complex problems, even amongst competing priorities
- Demonstrated experience prioritizing conflicting demands in an extremely fast paced environment
- Excellent interpersonal, organizational, and influencing skills
- Ability to analyze and process data, and draw the appropriate conclusions
- Experience with Lean principles or demonstrated experience implementing process improvements
GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal 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).
Nonobstant le fait que GE HealthCare ne requiert actuellement pas des salariés américains (USA) qu'ils soient vaccinés contre la COVID-19, certains clients de GE HealthCare appliquent des règles de vaccination qui pourraient toucher certains salariés de GE HealthCare.
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Company
GE HEALTHCARE
Waukesha, United States of America
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