Find a jobRecruiters

Manufacturing Quality Technician

Exclusive opportunity

Onsite

Manufacturing Quality Technician

Katalyst CRO

Manufacturing Quality Technician

Skills

Testing & QAInternal AuditProcess ImprovementCompliance

1 month ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

Important information


Contract type:

Freelance / Contract

Location:

New Kensington, PA, USA

Work mode:

Onsite

Published on:

16 September 2026

What they need


Provide quality and manufacturing support for production operations, supplier quality, validation, and process improvement initiatives. This role will assist with manufacturing transfers, quality system compliance, and continuous improvement efforts within a regulated production environment.

Responsibilities

  • Support daily manufacturing quality activities and ensure compliance with established quality standards.
  • Assist with process validation, verification activities, and production readiness initiatives.
  • Perform inspections, maintain quality documentation, and support process monitoring activities.
  • Participate in CAPA, Non-Conformance (Client), deviation investigations, and corrective action tracking.
  • Collaborate with Supplier Quality, Manufacturing Engineering, and Production teams to resolve quality issues and support ongoing manufacturing operations.
  • Collect, analyze, and document quality metrics, validation results, and production data.
  • Assist with internal audits, compliance initiatives, and continuous improvement projects.
  • Support manufacturing process transfers, equipment qualifications, and product transition activities.

Requirements

  • 2+ years of experience in Manufacturing Quality, Quality Assurance, Supplier Quality, Process Quality, or Validation.
  • Hands-on experience with CAPA, NCRs, quality documentation, inspections, and audit support.
  • Familiarity with manufacturing quality systems, process validation, and regulated production environments.
  • Strong documentation, organizational, and problem-solving skills.

Preferred Qualifications

  • Experience in the medical device or other regulated manufacturing industry.
  • Exposure to manufacturing transfers, process validation, supplier quality, or new product introduction (NPI) activities.
  • Experience with respiratory care, ventilator, CPAP, sleep therapy, or similar healthcare products is a plus.

Other offers great for you!

These companies are also looking for great profiles

skiils

Senior Quality Engineer (H/F)

Freelance

Lille, France

Hybrid

Skills

Playwright

5 days ago

Quick apply

skiils

Senior Quality Engineer (H/F)

Permanent contract

Lille, France

Hybrid

Skills

Playwright

5 days ago

Quick apply

B/Acceptance

QA Automatisation Playwright

400-450

Freelance

Paris, France

Hybrid

Skills

Testing & QAPlaywrightSalesforceSalesforce Service CloudSalesforce Sales Cloud

2 hours ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools