More jobs:
Quality Control Technician
Job in
Ivyland, Bucks County, Pennsylvania, USA
Listed on 2026-06-18
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
Job Description & How to Apply Below
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.
- 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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