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Responsibilities:
- Evaluate escalation data for potential Field Actions.
- Support business investigation teams with thorough reviews.
- Collect and analyze data related to product corrections.
Qualifications:
- Bachelor’s or master’s degree in engineering or a Scientific/Technical discipline.
- 8+ years in Medical Device, In Vitro Diagnostics, Pharmaceutical, or related Life Science.
- Strong knowledge of FDA, EU MDR, and Health Canada field action regulations.
Agilent Technologies, Inc.
Agilent Technologies, Inc. is a global leader in laboratory and clinical technologies, providing advanced instruments, software, and consumables. With 18,000 employees worldwide, they foster a dynamic and inclusive workplace that values diversity and innovation.