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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.
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.
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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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Con Alguna Experiencia
Requires Intermediate Experience
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ClasificadosOnline Warning
Employers DON'T ask for money or deposits for work, if they do is a bussiness, invertion or Fraud.
DON'T send money for work, neither offer personal information, by phone or email. Avoid the Fraud |
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