Quality Control Analyst performing quality checks and documentation in cosmetic manufacturing. Collaborating with Production to uphold quality standards and regulatory compliance.
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.
Requirements
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.
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