To face our constant growth, we are currently actively looking for an Immunoassays Scientist - Bioanalysis GLP.

You will work on innovative biopharmaceutical 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 bioanalytical methods for the study of large molecules in biological matrices by ligand-binding assays in the frame of preclinical and clinical pharmacokinetic and immunogenicity studies.

Your mission

In this role, after a training period you will be accountable for:

  • Performing laboratory activities related to method development, validation and transfer depending on the client project:

    • Performing analyses

    • Processing data

    • Writing reports and associated supporting documents

    • Presenting/discussing results

  • Taking part in the writing/preparation of protocols

  • Supporting audits and investigations

  • Validation of raw data

  • Bringing scientific expertise and develop team spirit and collaboration in the method development and the setting-up of new analytical platforms

Your profile

Master's / Engineer's degree with a specialisation in Biology or Biochemistry.


  • Relevant experience working with ELISA on bioanalytical methods

  • Practical experience working in a GLP or GLP like environment

  • A previous practical experience in development and/or validation and/or method transfer of Ligand Binding Assays

  • Very good communication skills both in French and English (writing scientific documents, reports, protocols and mails, phone conferences, contacts with clients)

  • Good team player

  • Very good organisation skills and ability to manage priorities


  • Good knowledge of the Pharmaceutical sector in a GLP / GCLP environment

  • Good theoretical knowledge and practical experience of MSD, Luminex and/or Cell-based assays

  • Knowledge of biological medicinal products (mAbs, ADCs, proteins, recombinant peptides) and associated regulations (EMA and FDA).

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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