QC Validation Supervisor Akkodis is an organization with more than 1,000 engineering, scientific and digital experts in Belgium. Our mission is clear: create a smarter future together! We are a one stop shop for engineering, IT, Life Science, and new technologies. Our combined passion for talent and technology allows us to look at the world differently. With our 360 offer we support companies in all sectors in implementing Smart Industry solutions, from the up and reskilling of entire teams to the delivery of complete projects.Our added value? We make incredible happen! What do you do all day? As QC Validation Supervisor, you actively participate to the validation process of analytical methods, used in the QC department of a global biopharmaceutical company. You participate to the implementation of validation design, coordination of laboratory tests, data analysis and redaction of related documents linked to the validation of the analytical methods, subjected to cGMP standards. This function means that you will regularly interact several stakeholders of the validation project, like laboratory technicians, tests supervisors, validation manager, QA specialist, products coordinators, and others. It''s a hybrid job that will allow you to combine work at home and on customer site. You will also be required to go to the laboratory when necessary (without performing any manipulation). This job lets you to start project management approach, while keeping a job with scientific thinking. Your responsibilities: As QC Validation Supervisor, you are in charge to: o Participate to the reflection of the validation design and the treatment of experimental data in collaboration with different stakeholders. o Coordinate laboratory tests which can take place in various QC laboratories. o Write validation documents (validation protocols/reports, qualification protocols/reports, rational documents, comparability documents, revalidation assessment reports, etc.). o Participate to the investigation phases in case of acceptance criteria unmet. o Depending on your expertise, you may be required to participate to troubleshooting activity and decision making with other customer experts. o Provide support to the management of quality elements (CAPA, eCC, Deviation, etc.), without being task owner. o Participate to the administrative tasks of the team (complete follow up files, continuous improvement, etc.). o Guarantee the application and maintenance of adequate cGMP rules in his work area. Your profile: o You are graduated as a bachelors or masters degree in pharmaceutical, bioengineering or chemistry, with a good expertise in chemistry, biochemistry, virology, cell biology, immunology, physicochemistry, or other related science. o You have a good knowledge in validation of analytical methods. o Thorough knowledge of cGMP expectations. o You have advanced written and verbal communication skills. You are French fluent, and you have good knowledges in English (mainly writ