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Product Quality Engineer Serie- GxP/Quality Control/German

Posted on Oct 30, 2019 by ITech Consult

Luzern, Switzerland
Engineering
Immediate Start
Annual Salary
Contract/Project

Product Quality Engineer Serie- GxP/Quality Control/German

Project/Role:
For our client, a renowned pharmaceutical company in Switzerland, we are looking for a Product Quality Engineer.

Main Tasks:
-Preparing, updating, reviewing and Training of specification documents, instructions and reports as well as technical Review of Validation and qualification documents
-Processing and technical review of Deviations as well as technical release of the assigned products.
-Ensuring and checking the product quality during the system development and the subsequent system production
-Support the staff with the Compliance with GPS regulations regulated activities in accordance with the SOP
-Support of quality management and ensure that regulated activities efficient, effective and in accordance be executed
-Support with troubleshooting at the assigned analysis system in the case of Complex deviation messages
-Securing and verification of the Product quality during the system development and the subsequent system production
-Identification and presentation of Improvement measures and implementation in consultation with the product team
-Coordination of the tasks in the equipment management process and Support for the responsible bodies
-Interface between R&D, assembly, System check and QA in case of deviations to find constructive solutions and to develop a achieve smooth release
-Development and maintenance of Quality standards and metrics for key activities
-Mainly responsible for the Variance management one or more products
-Responsible for the evaluation and Analysis of quality data (eg Right First Time, deviation messages) as well as the Management of corresponding meetings in the product team

Skills/Requirements:
-At least 3 years' experience in Quality control
-Experience in the regulated GxP environment ideally medical technology (ISO 13485, GMP, FDA 21 CFR 820) in the range of Deviation management
-You have a pronounced Quality awareness and a structured, scientific approach is for you of course

Nice to Have:
-In-depth IT knowledge (MS Office, MiniTab)
-SAP knowledge
-Understanding of complex hardware and software Architectures
-You appreciate independent and responsible work in a company that is versatile product and project environment

Education:
-University of Applied Sciences degree in a natural science subject or other related area or Training as a laboratory technician with at least 3 years of professional experience in the diagnostic or Molecular Biology Laboratory

Languages:
-German- Fluent speaker/comparable Level
-English- Fluent.

Reference No.: 918705C
Role: Product Quality Engineer Serie- GxP/Quality Control/German
Industry: Pharma
Location: Lucerne und Region
Workload: 100%
Start: ASAP
Duration: 30.11.2020++

Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. If the position is not a perfect match and you wish to receive other opportunities directly, you can send us your CV anyway via this advert.

About us:
ITech Consult is a certified ISO 9001:2008 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.

Reference: 785573304

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