QA Compliance & Food Safety Analyst

Digitailor; Midlothian (TX); On-site; USD 55,000 - 85,000; Full time

Job summary

Sunrider seeks a QA/QC professional to conduct internal audits, control documentation, investigate quality issues, deviations, and customer complaints. You will file, update, and create QC, production, and training records, and ensure only current revisions are in use.

You will manage change control on SOPs, batch records, and regulatory procedures; assist with CAPA investigations; coordinate training records; support supplier qualification and calibration programs; and help prepare for FDA,

Qualifications

• B.S. in a scientific field with 2+ years QA/QC experience.
• Experience reviewing batch records, CAPA and customer complaints.
• Food/dietary supplement facility experience preferred.
• High school diploma with extensive relevant experience may be accepted.

Responsibilities

• Administer change control on SOPs and batch records; ensure current revisions.
• Audit production paperwork, batch records and QC inspections for accuracy.
• Prepare and support monthly GMP audits and reports.
• Prepare rework, deviation, OOS and NCMR documentation.
• Assist investigations of product failures and customer complaints.
• Maintain training records; assist supplier qualification reviews.
• Support calibration and preventive maintenance programs.
• Assist with external audits (FDA, NSF, ISO, Kosher, Halal).

Skills

Quality Assurance

Quality Control

Documentation control

CAPA investigation

Regulatory compliance

Education

Bachelor's degree in a scientific discipline

2+ years QA/QC experience

High school diploma with 7+ years experience

Tools

Database software

Spreadsheet software

Word processing software

Job description

Sunrider seeks a QA/QC professional to conduct internal audits, control documentation, investigate quality issues, deviations, and customer complaints. You will file, update, and create QC, production, and training records, and ensure only current revisions are in use.

You will manage change control on SOPs, batch records, and regulatory procedures; assist with CAPA investigations; coordinate training records; support supplier qualification and calibration programs; and help prepare for FDA,