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Quality Control Technician

Job in Ivyland, Bucks County, Pennsylvania, USA
Listing for: ClinLab Solutions Group
Full Time position
Listed on 2026-06-18
Job specializations:
  • Quality Assurance - QA/QC
    Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager, Quality Engineering
  • Manufacturing / Production
    QA Specialist / Manager, Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: Ivyland

Summary

The Quality Control Technician is responsible for testing and evaluating finished devices, printed circuit board assemblies, and mechanical/electronic sub-assemblies. This role involves reviewing records, ensuring compliance with documentation standards, and supporting product release processes.

Responsibilities
  • Perform inspections and testing at various production stages, including incoming, in-process, and final product checks.
  • Evaluate printed circuit board assemblies for defects such as solder quality and visual damage.
  • Review and verify production and quality records to ensure compliance with acceptance criteria and documentation standards.
  • Manage batch record systems, including data collection, closure, disposition, and archiving of records.
  • Log batch record data into quality metrics databases and generate reports on yields and defects.
  • Support defect tracking and product acceptance processes, escalating discrepancies as needed.
  • Utilize measurement tools such as multimeters, calipers, and micrometers for quality assessments.
  • Collaborate with team members to maintain compliance with regulatory and quality management requirements.
Qualifications
  • Associate’s degree in a science or technical field, or high school diploma with relevant work experience.
  • Minimum of 2 years of experience in a QA or QC role within medical device manufacturing or a related industry.
  • Experience with manufacturing quality record review is strongly preferred.
  • Direct knowledge of Good Documentation Practices (GDP) and quality management systems.
  • Familiarity with regulatory compliance requirements such as FDA Quality System Regulation and ISO 13485 is preferred.
  • Experience with PCB assembly and/or electronics manufacturing.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Strong organizational skills, attention to detail, and ability to manage multiple priorities independently.
  • Excellent communication and interpersonal skills.
  • Experience using measurement tools including multimeters, calipers, and micrometers.
  • Ability to use standard office equipment (computer, mouse, keyboard, printer, etc.).
  • Advanced fine motor skills and specific vision abilities (close vision, color vision, peripheral vision, depth perception, and focus adjustment).
  • Must be able to lift up to 30 lbs.

Published Category:
Quality & Validation

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