Manufacturing Documentation Support
Jornada completa
QRC Group, LLC
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.
- Coordinate with the Quality Assurance (QA) team to ensure the manufacturing processes and documentation adhere to industry regulations and company policies.
- Assist in internal audits and document reviews to ensure compliance with regulations.
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)
Vacante publicada el Hace un mes
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