More jobs:
Quality Technician
Job in
Zürich, 8058, Zurich, Kanton Zürich, Switzerland
Listed on 2026-02-18
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
Job Description & How to Apply Below
🔬 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
- 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
- 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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