July 25th 2022
Quality Assistance is a leading European Contract Research Organisation providing the pharmaceutical industry with all the analytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products. We assist our clients from candidate selection, through non-clinical and clinical studies, to marketing authorisation, using our state-of-the-art, product-dedicated expertise in analytical sciences.
You will report to the Technical Leader
You will be part of a team of 5/6 people.
You will work on the bench and you will perform daily laboratory activities related to the application of analytical methods in the context of GLP/GcLP bioanalysis studies, and also stability studies and Quality control (GMP).
After a training period and depending on your level of expertise, you could also be requested to work on projects related to development and validation of analytical methods based on a protocol and under the supervision of the Technical Leader.
You could also be accountable for protocols and analysis reports writing.
You have a scientific background (Bachelor or Master)
Required:
- UPLC (Waters Alliance, BioAlliance)
- UPLC - Acquity, H-Class, I-Class
- UPLC - MS/MS (Waters Xevo TQ)
Pluses:
Send your application (reference JOB296) now to Isabelle Lebrun, Talent Acquisition Manager, to recrutement@quality-assistance.be or consult the Careers page on our website http://www.quality-assistance.com/careers/jobs.
Address: Technoparc de Thudinie 2, 6536 Donstiennes, Belgium