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 regulationsProficiency in Microsoft Word and ExcelStrong mathematical and mechanical aptitudeExcellent oral and written communication , interpersonal , and organizational skillsHigh attention to detail and team-oriented mindsetAbility to collaborate across departments and levelsConfidence in enforcing regulations and SOPsBasic knowledge of laboratory analyzers and inspection equipment