We are currently actively looking for a Laboratory Analyst – LC-MS / HPLC
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 bioanalysis of small molecules, as well as quality control of small molecules and biomolecules.
You will report to the Technical Leader.
You will be part of a team of 5/6 people.
In this role you will be accountable for :
Working on the bench
Performing 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's or Master's degree)
First experience in a similar laboratory role
Good theoretical knowledge and hands-on technical expertise of :
HPLC (Waters Alliance, BioAlliance)
UPLC – Acquity, H-Class, I-Class
UPLC-MS/MS (Waters Xevo TQ)
Fluent in French
English level (A2-B1)
Knowledge of Empower and MassLynx
First experience in a GLP and/or GcLP environment
Knowledge of ICP-MS
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, 220 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.