Job Details

Job Title: Quality Technician – Intermediate Location: Port Allen, LA Pay Range: $22-25/hr on W2 Shift: Two shift options— 1st: 6-4:30pm M-Th with Fri having OT potential (This is the normal shift) 2nd: 2pm-12am M-Th. Fri OT potential (New shift that they are adding. Must be able to train 1st shift, which goes about 6 weeks) Job Summary The Quality Control Inspector is responsible for ensuring that all activities related to the manufacturing, processing, packaging, and holding of active pharmaceutical ingredients (API), drug products, and medical devices are compliant with current Good Manufacturing Practices (cGMPs) and company procedures. This role supports product quality and regulatory compliance across Port Allen, LA and Coppell, TX manufacturing sites. Key Responsibilities If assigned to Incoming Laboratory / In-Process Inspections: Perform area clearances/line clearances and in-process inspections. Inspect and disposition incoming materials. Monitor manufacturing process performance in relation to SPC/SQC and general compliance. Ensure proper control and labeling of components, products, and equipment under evaluation. Verify labels after final printing is completed. Execute activities per production schedule and assist with planning, as needed. Support development, implementation, and maintenance of site quality procedures. Conduct investigations for nonconformances or deviations; assist with CAPA. Perform other assigned tasks to ensure product quality and efficacy. Complete special projects as assigned. If assigned to Analytical Laboratories: Perform chemical analysis on raw materials, in-process materials, finished products, stability, validation, and R&D samples. Collect, handle, and document materials and reagents in accordance with OSHA, EPA, FDA, and cGMP standards. Handle compressed gas cylinders as needed. Conduct calibration and preventive maintenance of analytical instruments. Review work performed by other analysts. Perform routine housekeeping; submit HOLD alerts and work orders as applicable. Carry out special projects to meet departmental and company objectives. Minimum Requirements Education: Associate's Degree in a technical or scientific field (Required) Bachelor's Degree in a science-related field (Preferred) Experience & Certifications: Experience in a regulated work environment (Preferred) ASQ certification (CQE, CQA, etc.) (Preferred) Key Competencies Working knowledge of cGMPs, OSHA, EPA, and FDA regulations Proficiency in Microsoft Word and Excel Strong mathematical and mechanical aptitude Excellent oral and written communication, interpersonal, and organizational skills High attention to detail and team-oriented mindset Ability to collaborate across departments and levels Confidence in enforcing regulations and SOPs Basic knowledge of laboratory analyzers and inspection equipment