Quality Control Analyst

Alcora Corporation•Palmetto Bay, FL

About The Position

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.

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.
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.
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.

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.