Senior Design Quality Engineer - North Chicago, IL
(e.g., FDA, ISO 13485, MDD/MDR) and industry best practices. Prepare and review documentation for regulatory submissions...
(e.g., FDA, ISO 13485, MDD/MDR) and industry best practices. Prepare and review documentation for regulatory submissions...
(e.g., FDA, ISO 13485, MDD/MDR) and industry best practices. Prepare and review documentation for regulatory submissions...
Compliance: Ensure all design and development activities adhere to applicable regulatory requirements (e.g., FDA, ISO 13485, MDD...
(e.g., FDA, ISO 13485, MDD/MDR) and industry best practices. Prepare and review documentation for regulatory submissions...
(e.g., FDA, ISO 13485, MDD/MDR) and industry best practices. Prepare and review documentation for regulatory submissions...
(e.g., FDA, ISO 13485, MDD/MDR) and industry best practices. Prepare and review documentation for regulatory submissions...
requirements (e.g., FDA, ISO 13485, MDD/MDR) and industry best practices. Prepare and review documentation for regulatory...
compliance with ISO 13485, ISO 14971, FDA 21 CFR Part 820, EU MDD, EU MDR and other relevant regulations and standards. Ensure...
range of mental health conditions across all age groups, including but not limited to Major Depressive Disorder (MDD), Generalized...
; Experience and knowledge of Canadian Medical Device Regulations, MDD, MDSAP and ISO standards preferred; Minimum of three years...