Quality Assurance Assistant

NAVAJO MANUFACTURING CO INC•Denver, CO

3d•$20 - $22•Onsite

About The Position

We are seeking a detail-oriented and organized Quality Assurance Assistant to support our Quality Assurance (QA) team in maintaining compliance with FDA regulations and internal quality standards. This role is essential to ensuring the safety, quality, and consistency of our consumer packaged goods (CPG) products. The ideal candidate will have a strong understanding of FDA requirements, excellent documentation skills, and the ability to thrive in a fast-paced environment.

Requirements

High school diploma or equivalent required.
Minimum of 1–2 years of experience in a quality assurance role, preferably in the pharmaceutical, medical device, food, and/or cosmetic industry.
Familiarity with FDA regulations and GMP is required.
Strong attention to detail and organizational skills.
Excellent written and verbal communication skills.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Knowledge of quality management systems and documentation practices.
Ability to work effectively in a team-oriented environment.
Problem-solving skills with the ability to manage multiple tasks and priorities.
Ability to stand, sit, or walk for extended periods.
Ability to lift up to 50 pounds occasionally.

Responsibilities

Assist in ensuring all processes, products, and documentation comply with FDA regulations, including GMP.
Maintain and organize quality-related documents, including SOPs, test records, specifications, and audit reports.
Assist in preparing for and supporting FDA inspections, internal audits, and customer audits. Document findings and follow up on corrective actions as needed.
Coordinate with QA team members to conduct routine product inspections and quality checks. Document and report results accurately.
Assist in identifying, documenting, and following up on non-conformances, deviations, or customer complaints. Support root cause analysis and corrective action plans.
Help in training employees on quality processes, GMP, and FDA compliance requirements.
Participate in quality improvement initiatives to enhance product quality and operational efficiency.
Work closely with production and supply chain teams to address quality concerns and implement solutions.