Gummy QA Specialist — Quality & Compliance

College of American Pathologists

La Mirada (CA)

On-site

USD 55,000 - 75,000

Full time

9 days ago

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Job summary

College of American Pathologists is seeking a QA Technician to ensure safety, quality, and regulatory compliance of vitamin and mineral gummy products on the production floor. You will monitor CCPs, review batch records, and address non-conformances through NCRs, deviations, and CAPAs.

In a fast-paced SQF-certified and NSF GMP environment, you will perform in-process testing, assist with audits, and collaborate across production, QA, sanitation, and R&D to uphold cGMP standards and product

Qualifications

  • High school diploma or equivalent; an Associate's or Bachelor's in Food Science, Microbiology, or related field is a plus.
  • 2+ years experience in quality assurance preferred but not required.
  • Experience in food/dietary supplement manufacturing with gummy products preferred.
  • Familiarity with SQF, HACCP, and GMP requirements.
  • Attention to detail and proficiency with quality testing equipment (pH meters, moisture analyzers, refractometers).
  • Ability to perform root cause analysis and implement CAPAs.

Responsibilities

  • Monitor CCPs and in-process testing to ensure product quality and safety.
  • Review Production Batch Records (PBRs) and NCRs, deviations, and CAPAs.
  • Assist with audits and maintain SQF and GMP documentation.
  • Collaborate with production, QA, sanitation, and R&D to uphold cGMP standards.
  • Conduct in-line inspections at key production stages and ensure calibration records are up to date.

Skills

cGMPs & FDA regulations
Detail-oriented
Quality testing equipment

Education

High school diploma
Associate's or Bachelor's in Food Science or Microbiology

Tools

pH meters
Moisture analyzers
Refractometers

Job description

College of American Pathologists is seeking a QA Technician to ensure safety, quality, and regulatory compliance of vitamin and mineral gummy products on the production floor. You will monitor CCPs, review batch records, and address non-conformances through NCRs, deviations, and CAPAs.

In a fast-paced SQF-certified and NSF GMP environment, you will perform in-process testing, assist with audits, and collaborate across production, QA, sanitation, and R&D to uphold cGMP standards and product

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