Overview
I am looking for a manufacturing engineer for my client based in the canton of Fribourg, specialized in in vitro diagnostic products. The contract is for a duration of 9 months.
Responsibilities
* Qualification / Validation: lead on qualification / validation strategy and development
* Execution of qualification / validation
* Work with external companies to drive specific qualification / validation projects
* Project Management: manage development and continuous improvement projects related to the function
* Develop a Lean Six Sigma approach to its activities
* Document Management: keeps the documentation of the related activities up to date
* Support Calibration coordination tasks and projects
Qualifications
* Bachelor\'s degree in engineering or equivalent.
* 3 - 5+ years of experience in validation / qualification in a GMP environment (medical diagnostic / food industry / pharmaceutical).
* Good project management skills. Resilient, pragmatic and analytical thinking.
* Expertise in GMP requirements.
#J-18808-Ljbffr