We assist our clients through non-clinical and clinical studies to marketing authorisation, using our state-of-the-art, product-dedicated expertise in analytical sciences. For each customer and each 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.

To face our constant growth, we are currently actively looking for a SPACIALIST - Bioassay.

You will be requested to work on projects related to the characterisation and quality control of Biomolecules.

Your mission

You will report to a Technical leader and you will be part of a team of 5/6 people composed of Laboratory technicians, Analysts, Scientists.

According to the client’s projects and your level of expertise, you may be required to ensure different tasks such as: 

  • Performing daily laboratory activities related to method application, development, validation and transfer

    • Performing analyses

    • Processing data

    • Writing reports and associated supporting documents

    • Presenting/discussing results

    • Validating raw data

    • Validating experimental results and ensuring protocols are respected

  • Applying methods for QC and stability studies

  • Communicating with clients

  • Training team members and others on technical skills if needed

Your profile

Bachelor's / Master's degree or PhD in Sciences


  • Good knowledge and relevant working experience in cell lines amplification

  • Good knowledge of Cell-based assays and relevant working experience with one of the following tests

    • Cytotoxicity testing (Antibody-Dependent Cell-mediated Cytotoxicity (ADCC), and Complement Dependent Cytotoxicity (CDC), …)

    • Reporter gene assays

    • Cell death,

    • Proliferation

  • Working experience in development, validation and/or application of analytical methods

  • Working experience in a regulated environment ideally in the pharmaceutical industry within a GMP environment

  • Good level of French and English (writing scientific documents, reports, protocols and mails)


  • Good knowledge of 

    • SPR (Biacore)

    • ELISA

    • qPCR

What we offer

  • A sector compliant remuneration package including numerous fringe benefits (luncheon vouchers, hospitalisation and ambulatory insurance, pension plan, etc.)

  • In addition to the fringe benefits received by all the personnel, you will also be provided with a company car.