Immunoassays Scientist Bioanalysis GLP (M/F)

August 14th 2020

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 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. The company holds a unique position on the market with all its laboratories on one site, 190 highly qualified professionals and over 35 years’ expertise at the forefront of analytical sciences

Mission Description

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
  1. Perform analyses
  2. Process data
  3. Write reports and associated supporting documents
  4. Present/discuss results
  • Taking part in the writing/preparation of protocols
  • Support audits and investigations
  • Validation of raw data
  • Bring scientific expertise and develop team spirit and collaboration in the method development and the setting-up of new analytical platforms.


Candidate profile

Master / Engineer, specialisation 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 organization 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).


  • 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 environment.
  • We care about mutual respect, assistance and communication.
  • We listen to your needs and your suggestions.
  • We offer a market-competitive salary and package including numerous fringe benefits. About Quality Assistance

Contact Details

Send your application now (JOB221) to Mrs Isabelle Lebrun, Talent Acquisition Manager, to or consult the Careers page on our website
Address: Technoparc de Thudinie 2, 6536 Donstiennes, Belgium