Corporate Policies, Current Good Manufacturing Practice (cGMP), Detail Oriented, Documentation, English Language, FDA Requirements, Lift/Move 50 Pounds, Maintain Compliance, Manufacturing, Mathematics, Multilingual, Operations Processes, Pallet Jack, Procedure Development, Quality Assurance, Quality Assurance Methodology, Quality Control, Regulations, Regulatory Compliance, Research & Development (R&D), Safety Compliance, Safety/Work Safety, Sampling Inspection, Spanish Language, Standard Operating Procedures (SOP), Testing, United States Drug Enforcement Agency (DEA), Warehousing
We're currently seeking a bilingual QA Inspector for one of our client in Davie, FL. This is an excellent opportunity for a detail-oriented quality professional with experience in a cGMP manufacturing environment who is looking to join a growing organization committed to quality, safety, and regulatory compliance.
Location:
Davie, FL
Schedule:
Monday–Friday, 5:30 AM – 2:00 PM (1st Shift)
Employment Type:
Full-Time, Temp-to-Hire
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
- Responsible for performing inspections of in-process products and completing the appropriate documentation.
- Ensure cGMP compliance at all times on the production floor.
- Perform Quality Assurance tasks such as sampling, inspections, and testing to ensure manufactured products comply with internal SOPs, safety initiatives, company policies, and FDA and DEA regulations.
- Document all work performed, ensuring accuracy and completeness.
- Inform management of any deviations from established standards or procedures.
- Inspect and approve rooms, production lines, and equipment prior to use by Manufacturing and R&D personnel.
- Approve components for in-process operations.
- Monitor manufacturing and packaging areas for compliance with internal SOPs, cGMP regulations, and FDA/DEA requirements.
- Document all work activities in batch records, forms, and logs to ensure accuracy and compliance.
- Sample in-process materials and finished products. Perform required inspections and testing, then process and distribute samples to the appropriate departments.
- Review records for cGMP compliance, accuracy, completeness, and Good Documentation Practices (GDP).
- Inform management of problems, failures, and deviations from internal and regulatory standards.
- Apply disposition status to components and in-process materials.
- Issue QA Alerts whenever questionable components, in-process materials, or finished products are identified during production or storage.
- Perform other duties as assigned by the immediate supervisor.
QUALIFICATIONS
- Associate degree or equivalent work experience.
- 1–3 years of Quality Assurance or Quality Control experience in a manufacturing environment.
- Previous warehouse experience preferred.
- Experience operating a
manual or electric pallet jack
preferred.
- Bilingual (English/Spanish) required.
- Knowledge of cGMP regulations and FDA guidelines.
- Detail-oriented.
- Basic computer and math skills.
PHYSICAL REQUIREMENTS
Requires standing, walking, bending, lifting, and handling chemicals, as well as using computers and monitoring equipment.
Must be able to lift and carry boxes weighing up to 50 pounds on a regular basis.
Must be able to wear appropriate PPE, including face masks, respirators, safety goggles, and hearing protection.