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Quality Technician

Job in Zürich, 8058, Zurich, Kanton Zürich, Switzerland
Listing for: HCLTech
Contract position
Listed on 2026-02-18
Job specializations:
  • Manufacturing / Production
    Quality Engineering, QA Specialist / Manager
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Technician/ Inspector, Quality Control / Manager, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below
Location: Zürich

🔬 Quality Technician – Medical Devices (6-month Contract)

We are looking for a Quality Technician to join our Quality Management Team within a medical devices manufacturing environment
.

You will play a key role in ensuring the accuracy, completeness and compliance of manufacturing documentation during ongoing production activities.

Key Responsibilities
  • Review manufacturing and production quality documentation for completeness, accuracy and regulatory conformity
  • Identify non-compliant, incomplete or incorrect documents and communicate findings to relevant production stakeholders
  • Coordinate and track documentation improvement actions related to quality processes
  • Ensure timely implementation of updates and improvements in existing quality documents
  • Collaborate closely with manufacturing and production teams to support accurate and compliant documentation
  • Perform document scanning, archiving and filing in accordance with quality system requirements
  • Participate in continuous improvement initiatives related to quality and documentation processes
Required Skills & Experience
  • 2–3 years of experience in a medical devices manufacturing environment
  • Proven experience in quality documentation review in production (mandatory)
  • Good understanding of GMP / ISO 13485 and regulated manufacturing environments
  • Strong attention to detail and documentation accuracy
  • Ability to communicate effectively with production and quality teams
  • Well-organized, autonomous and process-oriented
Nice to have
  • Experience with electronic document management systems (EDMS)
  • Prior exposure to process improvement or CAPA activities
  • English professional level (German is a plus)
  • Work in a highly regulated and impactful medical devices environment
  • Gain experience within a structured Quality Management System
  • Be part of a collaborative team focused on continuous improvement
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