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Documentation Specialist at QRC Group, Inc
Vega Baja, Puerto Rico, United States -
Full Time

Start Date

Immediate

Expiry Date

19 Dec, 25

Salary

0.0

Posted On

20 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Documentation, Regulatory Compliance, Technical Writing, Cross-Functional Collaboration, Internal Audits, Quality Systems, Bilingual, Document Control

Industry

Staffing and Recruiting

Description
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.
Responsibilities
The Documentation Specialist is responsible for maintaining accurate, up-to-date documentation in compliance with regulatory standards and internal quality requirements. This includes ensuring all documents are accurate and assisting in the creation of product specifications and protocols.