You will have to help our customer from pharmaceutical industry on equipment qualification projects.
Your responsibilities will be:
-Ensure the qualifications related to your project(s) and write or supervise the writing of qualification documents : protocols, reports, testing sheets ;
-Implement the various tests in the field : FAT/SAT/IQ/OQ/PQ, and analyse the results ;
-Coordinate the various stakeholders and qualification operations according to the schedule progress and ensure the implementation as well as the follow-up of the actions plan in case of non-conformities and deviations
With an engineer background, ideally specialized in chemical engineering or process engineering, you have a first experience in this field.
You have a real knowledge of applicable standards and rules in the pharmaceutical and biotechnologies industry (GMP, BPF…).
Your interpersonal skills enable you to work in team with all of your interlocutors while being autonomous in your activity.
Your rigour, your ability to analyse and summarize and your initiative are essential assets for your success in this function.
If you are interested, please send your application to: firstname.lastname@example.org under the following reference: