CQV Engineer - Düsseldorf

We are recruiting on behalf of our client, an Engineering Consultancy specialized in C&Q projects in the (bio)phamaceutical industry CQV Engineers. This is a temporary position for 12+ months. Requirements: – Strong experience with SAT/Commissioning, IQ and OQ, Design Review (DR) process – GMP Risk Assessment (FMEA) experience – Identify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities required – Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirements – Technical problem solving skills – Mechanical Completion procedure and Construction scope of work (Walkdown, system acceptance, punch list and follow up) – Schedule preparation and progress review – Management and coordination of Contractors and Vendors – Final Handover reports to the Client users Preferred Requirements: - Degree or equivalent in an engineering related discipline – 5+ years experience in the pharma and/or biotech industry – Fluent in English, any other language an advantage – Strong leadership and team player ability, liaising directly with client and other project key functions