DSP Validation Engineer (Netherlands) (Contract until March 2019)

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I am working via an EPCM Client on a Biotech facility in Holland who have a need for a CQV Engineer, on a contract basis at least until the end of March 2019.The role is a senior Validation Specialist DSP with pharma experience.Do you have in-depth knowledge of process validation and experience with projects in a pharmaceutical environment?Available in the short term for a challenging project?Your tasks:                           Responsible for process validations on Down Stream Processing                           Transform process validations into workable protocols.                           Have documents drawn up that are critical for process progress                           Collaborate with and manage the Quality department so that the right data is available at the right timeRequired background for a Senior Validation DSP Engineer:                           Experienced as Validation Specialist in the field of process validation pharmacy                           Experienced within a pharmaceutical production environment, preferably with biological, bacterial, viral or biochemical products                           Strong substantive knowledge of column chromatography and UF concentration                           As a person you have an independent and structured attitude, you work solution-oriented and you are strong in communication.  If these roles are of interest, my client is getting feedback within 1-2 days so there is a quick turnaround for the EPCM and Client here. They want somebody on board quite quickly so will be reviewing CVs as they receive them.Therefore do not hesitate in applying if you are interested as no doubt compeititon will be rife.