Quality Control Inspector — Medical Devices (GMP)

Branch Medical Group

Eagleville (PA)

On-site

USD 55,000 - 75,000

Full time

6 days ago
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Job summary

Branch Medical Group in the United States is seeking a Quality Control Inspector to perform inspections at multiple production stages, ensuring product and raw material quality in alignment with GMP and internal standards.

The role collaborates with QA and engineering to maintain accurate documentation, manage device history records, and support regulatory compliance across US operations. Strong attention to detail and the ability to read complex documents are essential.

Qualifications

  • Three+ years of direct quality inspection experience in a medical device environment.
  • Experience with FDA QSRs and ISO 13485 preferred.
  • Ability to read and interpret documents, plans, sketches, and diagrams.
  • IPC-A-610 certification or knowledge is a plus.

Responsibilities

  • Carries out inspection activities to ensure the quality of products and raw materials used in production.
  • Responsible for the correct handling of fixtures and equipment.
  • Uses quality inspection records following GMP requirements.
  • Maintains and archives documents in an organized state for compliance.
  • Schedules periodic document reviews to ensure compliance with internal and external requirements.
  • Interfaces with cross-functional teams to ensure compliance requirements are followed.
  • Supports release of subassemblies, assemblies, and final products via DHRs and ERP transactions.

Skills

Quality inspection
Documentation control
GMP/QSR knowledge
Microscope inspection
Medical device quality

Education

Technical degree

Tools

QAD system

Job description

Branch Medical Group in the United States is seeking a Quality Control Inspector to perform inspections at multiple production stages, ensuring product and raw material quality in alignment with GMP and internal standards.

The role collaborates with QA and engineering to maintain accurate documentation, manage device history records, and support regulatory compliance across US operations. Strong attention to detail and the ability to read complex documents are essential.

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