Beschreibung
We are looking for an experienced Validation Engineer to join a market leading Medical Device company in Baden-Württemberg on a 6 month contract with a good chance of extension.As a Validation Engineer you will:
- Create, execute, and report validation activities, i.e. DR, IQ, OQ and PQ qualifications
- Develop and execute Clean in Place (CIP) & Sterilisation in Place (SIP) Validations
- Ensure validating test equipment is current standard and calibrated to date
- Provide validation support to process development projects
- Update and create relevant validation SOP's & QOP's
The successful Validation Engineer is likely to have experience in the following areas:
- Technical / Scientific / Engineering Degree or equivalent
- Clean in Place (CIP) Validation Strategy and Protocol Execution experience
- Sterilisation In Place (SIP) Validation Strategy and Protocol Execution experience
- Extensive experience of protocol & Report writing (DR, IQ, OQ, PQ)
- Competent computer skills including: MS Office, CAD, MS Project
- Minimum 5 years industry experience in the Medical Devices Industry
Please do not hesitate to contact me should you fulfill all requirements and be interested.
Ivan Seleme
i.seleme[at]realstaffing.com
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