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Our client is a global vaccine research, development and production company, that employs over 11,200 people worldwide, of which 7,500 in its three Belgian sites: Rixensart, Wavre and Gembloux. Notre client est une entreprise qui recherche, développe et produit des vaccins. Elle emploie environ 11200 personnes dans le monde et près de 7500 personnes sur ses 3 sites belges: Rixensart, Wavre et Gembloux.
Nous sommes activement à la recherche d'un process engineer pour une mission ( freelance - consulting - CDI) chez l'un de nos clients pharmaceutique. Si vous interessé par de nouveaux challenge, n'hésitez surtout pas à me contacter : firstname.lastname@example.org
• Individually or as part of a project team, you will be responsible for solution design & qualification to be implemented in primary & secondary process. • You will be responsible for the execution, coordination and follow-up of solution designs and technical matters related to Single Use Systems to ensure production, transformation, commissioning and qualification of the solution meets agreed cost, timing, technology and quality standards in line with the Engineering standards. • Key activities include: o Define functional, technical and quality requirements. o Ensure preparation and update of the project qualification and coordinate qualification activities of the systems. o Ensure coordination of a multifunction team to enable the creation of single use articles following the internal procedures. o Ensure correct systems implementation through training, SOP writing and assistance to the production team. Environment See request for offer
Engineer with experience post-graduation in cGMP environment and key activities described above
Demonstrates deep knowledge in design and implementation of engineering projects. Good project management skills: organisation, cost, time, schedule, contracting, procurement, qualification, validation, technologies Practical experience in project supervision and people management Good communication skills Perform his/her work in a cGMP consistent manner.