Senior Validation Engineer

SENIOR VALIDATION ENGINEER

On behalf of our client, a leading global company within medical, we are looking for a SENIOR VALIDATION ENGINEER. For this contract position based in Solothurn in Switzerland our client is looking for an English and German speaking candidate who can start as soon as possible. Are you looking for an exciting new opportunity with a market leading global company then please have a look at the details:

Your main responsibilities will be:

- Compile a traceable process validation documentation for medical devices in respect of cleanliness and biocompatibility
- Support the manufacturing sites in implementing the biocompatibility and cleanliness process
- Prepare the complete and traceable electronic documentation of the cleanliness validation and Biological Safety Evaluation (part of the Device Master Record (DMR)
- Review and incorporation of manufacturing process validation and test data into documentation management systems
- Interface between different functions (manufacturing, process validation, material testing, risk management)

The skills and experience needed for this position are:

- Experiences of Good Manufacturing Practice (GMP)
- Background in process and cleanliness validation
- Proficient with MS Office Tools (Word, Excel) as well as SAP
- Fluent in German and English
- Place of work at different manufacturing sites in Switzerland, travel to Southern Germany and Austria necessary

Apply today to secure your chances in this interesting opportunity for a Swiss fast growing Global Company.

Please don't hesitate to send your CV in English to Ms. Andra Weiland or if you should have any questions, please don't hesitate to call her.

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