Documentation Specialist

Company Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Job Description

The Documentation Specialist is responsible for maintaining accurate, up-to-date documentation in compliance with regulatory standards and internal quality requirements.

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.
• Assist in internal audits and document reviews to ensure compliance with regulations
• Ensure all documentation aligns with internal quality systems and external regulatory requirements.
• Collaborate with cross-functional teams to manage document control processes and improve documentation workflows.

Qualifications

• Bachelor's degree in a relevant field (e.g., Manufacturing, Engineering, Sciences, Business Administration, etc.).
• 5 years of experience with a focus on documentation or regulatory compliance in the pharmaceutical or medical device industry. 
• Bilingual (English & Spanish, written and spoken)
• Technical Writing 

Additional Information

All your information will be kept confidential according to EEO guidelines.