Qualification and Validation Specialist (French)
You will be working in a dynamic environment, where you have to multitask with lots of projects, so you have to know how to work under pressure. It is a fast growing company, with it's own manufacturing capability. It is an enriching environment where you can develop yourself and learn a lot to further your career. The company designs and manufactures a lot of different products.
The role entails the design of the aseptic process simulation and to supervise the annual program "Media Fills". And you also have to ensure that all activities are performed according to schedule and that it is all properly documented. You also need to know how to write validation protocols and reports and investigate deviations and execute CAPA's. And to participate in customer and authority audits, so it is a role with a lot of responsibility and with a lot of variation, where can also be involved in other validation activities.
You need a Master degree in Pharmacy/Biology/Bio-Engineering or something similar and also Experience in the pharmaceutical industry (sterile manufacturing and GMP's). Since the company language is French you need to be Fluent in French and English. You are expected to fill the role without a problem, so you need to be experienced in the role. And also have excellent communication skills and since there are a lot of projects you need to have project management and leadership skills.
For more information please contact me on +31 207 09 1070 and send an updated CV to B.Bihari@nonstop-recruitment.com.