Manufacturing Documentation Support

• 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.

• 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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