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Quality Control Analyst

LocationMiami, Florida, United States
TypeOnsite

Title:


Quality Control Analyst

Reports to:


 Quality Control Supervisor

Position Summary


The Quality Control Analyst will be trained in secondary packaging and cosmetic filling operations. This role works cross-functionally with Production to ensure all quality specifications are met. The Analyst demonstrates strong attention to detail, situational awareness, and a commitment to ensuring product quality and compliance with established standards and regulatory requirements.

Key Responsibilities


  • Execute and document applicable in-plant quality processes, programs, and functions within a cosmetic manufacturing environment.
  • Ensure SOPs are followed to meet and exceed quality standards and specifications.
  • Perform in-process product checks, sampling, and verification during filling and secondary packaging to ensure finished goods meet specifications.
  • Log relevant information and maintain QC databases (Excel) for assigned production areas.
  • Prepare deviation and non-conformance reports when products do not meet specifications.
  • Partner with Production to support continuous quality compliance.
  • Complete and sign QC documentation for production areas.
  • Perform daily line cleaning and sanitization verification checks.
  • Collect samples for microbiological and bulk analysis.
  • Review batch records to ensure compliance with GDPs.
  • Conduct bulk testing in the laboratory to confirm specifications are met.
  • Assign appropriate product status labels (Release, Quarantine, Reject) based on test results.
  • Communicate Out-of-Specification (OOS) results and document findings in the bulk lab database.
  • Provide coverage in the Raw Materials lab as needed.
  • Perform tank cleaning & sanitization (C&S) verification using ATP swabs when required.
  • Prepare customer approval documentation and samples when requested.
  • Perform other duties as assigned.

Minimum Job Requirements


Education, Knowledge & Experience


  • Bachelor’s degree required, BS in Chemistry or related field preferred.
  • 2–4 years of related experience; at least 1 year of Quality Control experience in a manufacturing environment preferred.
  • Working knowledge of cGMP, GDP, FDA 21 CFR, and ISO 22716 standards.
  • Proficiency with Microsoft Office (Excel, Word) required.

Skills


  • Strong attention to detail and documentation accuracy.
  • Ability to communicate clearly and professionally in English (Spanish is a plus).
  • Ability to read, analyze, and interpret SOPs, batch records, and technical documentation.
  • Strong interpersonal and teamwork skills.

Physical Requirements


  • Ability to stand, walk, sit, and use hands for handling and inspection tasks.
  • Ability to lift up to 50 pounds.
  • Must be able to work in manufacturing environments, including exposure to humidity, heat/cold, moving machinery, chemicals, and varying environmental conditions.

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