Quality Systems Documentation Specialist for Validation Area
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.
Average salary estimate
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