Offres d'emploi : quality engineer
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À propos
Review and assess design transfer documentation for compliance Identify documentation gaps and support remediation activities Collaborate with Engineering, Quality, Manufacturing, and Regulatory teams to ensure documentation accuracy
Required qualifications:
Bachelor's degree in Engineering, Quality, Life Sciences, or a related technical discipline 10-15+ years of experience within the Medical Device industry Strong experience with Design Transfer activities in medical device development Demonstrated experience leading or supporting DHF remediation projects In-depth knowledge of FDA Design Control requirements and ISO 13485 standards
Compétences linguistiques
- English
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