| Job Title | |||||
| Internal Audit Quality Assurance | |||||
| Position Location | |||||
| Miramar | |||||
| Pay/hours for position | |||||
| $20 to $25/HR | |||||
| Requirements of position | |||||
| QualificationsEducationBachelor’s degree in Life Sciences, Chemistry, Biology, Food Science, or a related field required.Experience3–5 years of Quality Assurance experience in a nutraceutical, pharmaceutical, food, or regulated laboratory environment.Hands-on experience conducting internal cGMP audits.Strong working knowledge of FDA dietary supplement regulations.Knowledge & SkillsIn-depth understanding of:FDA cGMPs (21 CFR Part 111 & 117)Internal audit principlesCAPA and root cause analysisLaboratory quality systems and data integrityExcellent documentation, writing, and analytical skills.Strong attention to detail and ability to work independently.Proficiency with QMS software and Microsoft Office.Preferred QualificationsInternal Auditor certification or ASQ Quality Auditor (CQA) preferred.Experience with third-party audits (NSF, USP, ISO).Bilingual (English/Spanish) a plus in South Florida environments.Physical & Work RequirementsAbility to walk production and laboratory areas.Occasional lifting up to 25 lbs.Ability to work in manufacturing and lab environments following PPE and safety requirements. | |||||
| Job SummaryThe Internal Audit – Quality Assurance professional is responsible for planning, conducting, and reporting internal audits to ensure compliance with current Good Manufacturing Practices (cGMP), FDA regulations, and company quality standards within a nutraceutical laboratory and manufacturing environment. This role supports continuous improvement, regulatory readiness, and product quality by identifying compliance gaps and recommending corrective and preventive actions (CAPAs).Key ResponsibilitiesInternal Audits & CompliancePlan, schedule, and conduct internal cGMP audits of laboratory, manufacturing, warehousing, sanitation, documentation, and quality systems.Audit compliance with FDA 21 CFR Part 111 (Dietary Supplements), Part 117 (FSMA), SOPs, and internal quality standards.Evaluate laboratory practices including testing methods, equipment calibration, data integrity, and documentation.Prepare clear, accurate audit reports detailing observations, risks, and recommendations.Track audit findings and verify completion and effectiveness of CAPAs.Quality SystemsSupport and monitor the effectiveness of the Quality Management System (QMS).Review and audit SOPs, batch records, test methods, specifications, and logbooks.Ensure document control, change control, deviation, and CAPA systems are properly implemented.Participate in management review meetings and quality metrics reporting.Regulatory ReadinessSupport FDA, state, and third-party inspections (NSF, USP, SQF, ISO, etc.).Perform mock audits and pre-inspection readiness assessments.Assist in responding to regulatory observations (e.g., FDA 483s, warning letters).Training & Continuous ImprovementProvide cGMP and audit-related training to laboratory and production staff.Identify trends, recurring issues, and opportunities for continuous improvement.Promote a culture of compliance, quality, and data integrity | |||||
Internal Audit Quality Assurance
Contract Type:
Contract to Perm
Location:
Miramar - FL
Industry:
Quality Control
Date Published:
14-Feb-2026
The JobSquad Solutions Team is currently looking for a Internal Audit Quality Assurance to work at a company located in the Miramar, FL area!
The JobSquad Solutions Team is made up of experts around the country. Serving our local workforce communities is our passion.
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