Quality Control Inspector, Lead
Job in
Santa Clarita, Los Angeles County, California, 91382, USA
Listed on 2025-12-01
Listing for:
huMannity Medtec
Full Time
position Listed on 2025-12-01
Job specializations:
-
Quality Assurance - QA/QC
Quality Control / Manager, Quality Technician/ Inspector -
Manufacturing / Production
Job Description & How to Apply Below
Overview
Job Title:
Quality Control Inspector, Lead. The QC Inspector Lead reports to the Sr. Quality Systems Manager and oversees the QC team. Also, tests and inspects materials and products at various stages of incoming inspection, work in progress, and final inspection. Compiles and evaluates data to determine and maintain quality and reliability of products by performing the following duties.
Base pay range $32.00/hr - $38.00/hr
Essential Duties And Responsibilities- Oversees QC Inspectors, inspections of components and completed assemblies at various phases of production and throughout the manufacturing processes.
- Creates and edits Keyence Programs
- Interprets engineering drawings, schematic diagrams including GD&T.
- Tests and/or inspects dimensions, performance, and mechanical, electrical, or chemical characteristics per written procedures.
- Reviews and approves Inspection Sheets for accuracy against drawings.
- Updates and maintains QC Inspection SOPs and Department Procedures.
- Assists with creation of inspection criteria.
- Distributes the workload within the QC department.
- Documents nonconforming material; clearly and accurately.
- Prepares and maintains Quality records for review of completeness and accuracy to meet both internal and external expectations.
- Able to use general inspection tools such as multi-lens stereo microscope, micrometer, caliper, thread and pin gauges, Smart Scope, profilometer, multisensor measurement systems.
- Associate's degree (A.A.) or equivalent from two-year college or technical school; or a minimum of 5 years of related experience and/or training; or equivalent combination of education and experience in the medical device industry.
- Former Lead or Supervisory Experience
- Strong computer skills and knowledge of Microsoft Word and Excel.
- Familiar with ISO 13485 Standard is a plus.
- Attention to detail, accurate and concise.
- Must have excellent written and oral communication skills, and able to read and write in English.
- IPC 610 Training Preferred
9/80 workweek. 7:00 - 4:30 every other Friday off.
Seniority level- Mid-Senior level
- Full-time
- Quality Assurance
- Medical Equipment Manufacturing
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