CAPA remediation Specialist - Swiss MedTech - 1 yr contract
CAPA remediation Specialist - UDI labeling - Swiss Med Tech - English & German both important - 1 year project
Our client is a large and well respected manufacturer of Class III Medical Device products, globally. As part of their committment to the FDA and UDI based timelines, they are looking to find 2 CAPA remediation specialists for label verification tasks, QC, identifying potential roadblocks to reaching UDI goals, escalating these, and finding solutions.
This is a key role and will require interacting and communicating with other sites and departments including Legal, Trademarks, Packaging, Development, Product Management, Regulatory Affairs, Sterilization & Biological Evaluation, Post Market Surveillance, Custom Product Department, and IT.
German and English are both important.
A start pf July 1 is scheduled - can you make it happen? Apply now
KEY WORDS: Labeling, bar coding, Quality Assurance, QA, CAPA, remediation, QC, visual inspection, Compliance, Medical Devices, Switzerland, USA, ISO 13485, ISO 9001, GMP, ISO 14971, CAPA, Medical Devices Directive, MDD, QMS, Medical Device jobs, nonstop recruitment.
For more information on this vacancy, and other Quality roles in the Swiss medical devices sector, please contact the Senior Consultant Andrew Boroky on 0041 43 50 80 816, and email him your resume in WORD format to firstname.lastname@example.org including Zeugnisse / Employment records and scanned copies of training certifications.
For industry news and new opportunities in QA within the Medical Devices & Diagnostics sectors, please join my Linked group ch.linkedin.com/in/qaswitzerland/en
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