Corporate Policies, Current Good Manufacturing Practice (cGMP), Detail Oriented, Documentation, English Language, FDA Requirements, Maintain Compliance, Manufacturing, Mathematics, Multilingual, Operations Processes, Quality Assurance, Quality Control, Regulatory Compliance, Regulatory Requirements, Safety/Work Safety, Sampling Inspection, Spanish Language, Standard Operating Procedures (SOP), Testing, United States Drug Enforcement Agency (DEA)
Position Summary
We are seeking a detail-oriented QA Inspector to join our team on the night shift. This role is responsible for performing in-process inspections, ensuring compliance with cGMP standards, and maintaining accurate documentation in accordance with internal procedures and regulatory requirements.
Schedule: Monday – Friday | 9:30 PM – 5:15 AM
Pay Rate: $20.37 –$22 per hour
Essential Functions & Responsibilities
- Perform inspection of in-process and finished products, ensuring proper documentation.
- Ensure compliance with cGMP regulations at all times on the production floor.
- Conduct QA tasks including sampling, inspections, and testing to verify compliance with: Internal SOPs, Company policies, Safety initiatives, FDA and DEA regulations
- Inspect and approve rooms, production lines, and equipment prior to use.
- Approve components for in-process operations.
- Monitor manufacturing and packaging areas for compliance with SOPs and regulatory standards.
- Document all work in batch records, logs, and forms accurately and thoroughly.
- Sample in-process materials and finished products; distribute samples as required.
- Review documentation for accuracy and compliance with cGMP and Good Documentation Practices.
- Inform management of deviations, problems, or failures.
- Apply disposition status to components and in-process materials.
- Issue QA Alerts when questionable materials or products are identified.
- Perform other duties as assigned by the supervisor.
Qualifications
- Associate degree or equivalent work experience.
- 1–3 years of experience in Quality Control within a manufacturing environment.
- Bilingual (English/Spanish) required.
- Knowledge of cGMP regulations and FDA guidelines.
- Detail-oriented with strong documentation skills.
- Basic computer and math skills.