QC Document Control Specialist (GMP/QA Records)

The Sunrider Corporation; Midlothian (TX); On-site; USD 25,000 - 26,000; Full time

Job summary

The Sunrider Corporation is seeking a QC Document Control Associate in Midlothian, TX. This role maintains document control procedures, updates SOPs and batch records, and supports the QC/QA department to ensure regulatory compliance.

You will manage document distribution, track data like COAs and SDS, and assist in audits and production paperwork with a focus on accuracy, GLP/GMP alignment, and training records.

Qualifications

• High School Diploma or GED and some college (science-based courses preferred). Minimum 3 years of hands-on experience as Quality Assurance documentation in cGMP environment; preferably in a pharmaceutical, nutraceutical or food manufacturing industry.
• Experience with document control, batch record review.
• Fluent in reading, writing and speaking English; knowledge of Spanish a plus; strong technical writing skills.
• Ability to read, analyze, and interpret technical instructions or writings; ability to write reports and procedures.
• Proficient with Microsoft Word, Excel and archiving software; familiarity with Oracle inventory systems.

Responsibilities

• Issue, review, and update company documents (SOPs), manufacturing batch records and regulatory procedures.
• Distribute revised documents to users and departments.
• Maintain records of QC specs, COAs and safety data sheets.
• Update part numbers, shelf life, etc. in Oracle inventory system.
• Assist with artwork approvals and product registration documents.
• Support QA audits and review production paperwork for accuracy and completeness.

Skills

Attention to detail

Quality documentation

Communication

English fluency

Education

High School Diploma or GED

Some college (science-based courses)

Tools

Oracle inventory system

Microsoft Excel

Microsoft Word

Archiving software

Job description

The Sunrider Corporation is seeking a QC Document Control Associate in Midlothian, TX. This role maintains document control procedures, updates SOPs and batch records, and supports the QC/QA department to ensure regulatory compliance.

You will manage document distribution, track data like COAs and SDS, and assist in audits and production paperwork with a focus on accuracy, GLP/GMP alignment, and training records.