Calibration, Continuous Improvement, Detail Oriented, Documentation, FDA (Food and Drug Administration), Hazardous Materials/Substances, High School Diploma, Lift/Move 25 Pounds, Manufacturing, Materials Analysis, Mathematics, Microsoft Office, Product Documentation, Product Testing, Quality Assurance, Quality Control, Quality Metrics, Reporting Skills, SAP, Safety Process, Technical Writing, Testing
This role involves performing and documenting final inspections of production slides, vials, kits, and labels to ensure quality standards are met.
- Conduct incoming material inspections and analyze results against specifications.
- Ensure accurate documentation of released materials and production records.
- Complete QC testing, determine product disposition, and document nonconformities.
- Support lab functions such as preparing standards, reagents, and handling hazardous waste.
- Manage retention samples and device history records.
- Follow safety procedures, including PPE use, and participate in continuous improvement.
Experience: High school diploma with 2+ years QC or manufacturing experience; familiarity with SAP and FDA-regulated environments preferred.
Skills: Proficiency in Microsoft Office, sampling techniques, basic math, technical report writing, attention to detail, decision-making, and knowledge of validation/calibration.
Qualifications: Ability to stand for long periods, lift 25 lbs, perform repetitive tasks, and work flexible hours including overtime.