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Actalent is seeking an engineer to lead remediation design activities for medical devices, ensuring compliance with FDA and ISO standards. You will collaborate cross-functionally to execute verification and validation testing and manage product risk assessments.
The role requires a strong background in FDA design controls, risk management (FMEA), and hands-on SolidWorks expertise, with a focus on robust documentation and design history files.
Actalent is seeking an engineer to lead remediation design activities for medical devices, ensuring compliance with FDA and ISO standards. You will collaborate cross-functionally to execute verification and validation testing and manage product risk assessments.
The role requires a strong background in FDA design controls, risk management (FMEA), and hands-on SolidWorks expertise, with a focus on robust documentation and design history files.