We are currently actively looking for a Laboratory Associate.
You will be part of a team involved in projects outsourced by our clients.
Those projects are related to the development, validation and/or application of analytical methods based on a protocol for the characterisation and quality control of biomolecules.
You will be part of a team of 5/6 people and report to the Technical Leader Chromatography.
You will work on the bench and you will perform daily laboratory activities related to the application of analytical methods and/or stability studies analyses.
Depending on your level of expertise, you could also be requested to work on projects related to validation of analytical methods.
You have a scientific background.
You have hands-on technical expertise (application of analytical methods) in either:
HPLC / (U)HPLC
Capillary Electrophoresis (cIEF, cGE)
You are fluent in French.
First experience in a regulated environment is a plus.
Knowledge of Empower is an asset.
Why join Quality Assistance?
We are a true career partner.
We accelerate people’s access to new medicines.
We offer an inspiring work-life balance in a human scale environmeant.
We care about mutual respect, assistance and communication.
We listen to your needs and your suggestions.
We offer a market-competitive remuneration package including numerous fringe benefits.
Visit https://www.quality-assistance.com/quality-assistance/life-quality-assistance to learn more.
About Quality Assistance
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.
For each client project, we design customised solutions, define analytical protocols, develop and validate specific new analytical methods and perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing, in order to evaluate the Quality, Safety and Efficacy of the given drugs.
The company holds a unique position on the market with all its laboratories on one site, 210 highly qualified professionals and over 35 years’ expertise at the forefront of analytical sciences.
The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant.
Visit https://www.quality-assistance.com/quality-assistance/leading-analytical-cro to learn more.