Description
To support a customer project, we are looking for a Quality Engineer (m/f) featuring the below stated skills and experience:Your Tasks:
Our client is looking for Quality generalists, who will need to work on the remediation of the quality system, not only as consultants, but hands-on.
Support/training of the project members onsite
CAPA Management
Qualifikation:
Relevant working experience in Quality Management /Regulatory Affairs
Experience in the implementation of international regulatory processes, quality management, in compliance with DIN EN ISO 13485 and CFR 820.
Need to have knowledge within Medical Devices or equivalent area (Pharma, Lifescience,..)
Production-knowledge is important as well.
CAPA is a must have experience
Very good English and German-knowledge (spoken and written) is a must.
Please send your CV in English and give us a rating of the below listed skills.
Qualification Rating 1 to 5 Years:
21 CFR Part 820
CAPA
ISO 13485
experience with medical devices
Location: Lake of Constance
Project time scale: 4 months
Details about this project can be provided. Please don't hesitate to contact us.
If you are interested in this employment opportunity, please send your profile and information about your availability and hourly rate to
NEWS under www.twitter.com/SoftpaceGmbH
Softpace GmbH