Codev Technician

Location: Louvain-la-Neuve

As a Co-Development Technician (technician CODEV) you are responsible for the support of multiple clinical projects. Our department manufactures clinical/development batches in Puurs and your responsibility is to make sure that those batches and critical samples are supplied in time to the clinical studies, pack and label sites and testing labs all across the world. You work closely with Project Engineers, who are responsible for each project.
In order to make an application, simply read through the following job description and make sure to attach relevant documents.
A codev technician can provide support with:
- Technical/administrative support in manufacturing clinical supply
- Follow up of production activities (formulation, filling, inspection), executed by operators from production
- Write supporting documents for production activities (request for lab analysis,…)
- Responsible for sampling during production and sample handling afterwards
- Write request documents for shipment activities (Checklists, NSSG forms,…)
- Responsible for timely shipping and storage conditions of samples and clinical batches to R&D and clinical studies
- Working in computer applications (SAP, IPL, …)
- Communicate efficiently with different stakeholders (Customs, Receiving Site, CoDev Project Engineers, Import/Export departments, Couriers…)
- Correct labeling and packaging of samples to different receiving sites xlxgzvr
- Responsible for the correct pick up of samples by the courier
Desired experience
- Bachelor's degree in a scientific field
- Couple of years’ experience in a GMP industry (e.g. lab / production / hospital environment)
- Experience in pharmaceutical industry
- Experience in GMP documentation
- Experience and skilled with MS Office systems (Word, excel)
- Hands-on
- Positive mindset, real team player