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DescripciónDescription
Manufacturing Documentation Support role plays a key part in ensuring that all manufacturing documentation for medical devices is properly created, maintained, and compliant with regulatory standards.
Responsibilities:
Ensure that all documents are up to date, accurate, and in compliance with relevant regulatory standards.
Assist in the creation of documents for product specifications, protocols, and history files.
Support the compliance of manufacturing documentation with regulatory requirements and internal quality standards. |
Requisitos Requirements
Associate's degree or higher in a relevant field (e.g., Manufacturing, Engineering, Sciences, Business Administration, etc.).
2-4 years of experience in a manufacturing or quality assurance role in the medical device industry, with a focus on documentation or regulatory compliance.
Bilingual (English & Spanish, written and spoken)
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