To face our constant growth, we are currently actively looking for a Laboratory Analyst LC/MS.

You will work on innovative (bio)pharmaceutical products under development (preclinical and clinical phases). 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 (bio)molecules.

Your mission

You will report to the Technical Leader LC/MS.

You will be part of a team of 5/6 people.

In this role, when starting at Quality Assistance you will be accountable for:

  • Applying methods for non-clinical and clinical studies

  • Performing daily laboratory activities such as

    • Performing analyses

    • Processing data

    • Writing reports and associated supporting documents

    • Presenting/discussing results

Your profile

Bachelor’s degree or Master’s degree.


  • First experience in a similar role

  • Good knowledge of HPLC, (U)HPLC

  • Very good command of French (spoken and written)

  • Working experience in a regulated environment


  • Good knowledge of LC/MS

  • First experience in development, validation of analytical methods is an asset

  • Knowledge of GMP, GLP, and GcLP

  • Good command of English (spoken and written)

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.

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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.

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