We are currently actively looking for a R&D Scientist – Molecular Biology.

You will work on innovative biopharmaceutical products under development (preclinical and clinical phases).

You will work in a team involved in Quality Assistance's in-house analytical development projects. 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 (bio)molecules.

Your mission

Working in a team involved in Quality Assistance's in-house analytical development projects, you will:

  • take up the technical, scientific and regulatory challenges of method development and participate in writing reports on experiments

  • be involved in the communication of scientific results via webinars and conferences

You may also participate in projects outsourced by our clients.

Your profile

You have a good theoretical and practical knowledge of Next Generation Sequencing (NGS).

In addition, you have relevant experience in methods development and validation with one of the following techniques:

  • Flow cytometry (FACS)

  • qPCR

You are fluent in French.

You have a good English level allowing you to:

  • Follow trainings

  • Read and write reports and/or mails

You are a team player.

You have strong organisational skills with ability to manage projects through wise planning, time optimisation, detail orientation and prioritisation.


  • Practical experience in Cell-based assays, immunoassays and Elispot

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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