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Scope

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 (non-clinical 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

ELISA

Your profile

Scientific background with a specialisation in Biology or Biochemistry.

Required

  • 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

Plus

  • 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).

ELISA

Why join Quality Assistance?

Do you want to thrive in a professional setting that still maintains a human touch? Are you looking for a working environment based on mutual respect, communication and support, where it is good to live and work?

Apply now to join our analytical CRO! We are pursuing a common goal: to accelerate access to new medicines.

You will benefit from a competitive compensation package in line with the industry, including many fringe benefits (meal vouchers, hospitalisation and outpatient care insurance, group insurance, bonuses, a company car and petrol card).

As soon as you start your job, you will follow a comprehensive training programme adapted to your profile and role.

Did you know that in 2022 we welcomed, and trained 35 new colleagues? We also promoted 21 team members (vertical mobility). 12 positions were filled by internal candidates.

We offer multiple opportunities so that you can integrate yourself into your new work environment and get to know your new colleagues (after-works, sports and recreational activities, team building, department dinners, end-of-year parties, BBQs, events for families, etc.). We pamper our team members and take care of them: free sports lessons, free fruit and sugar-free drinks, daily delivery of lunches and bread, free car wash, ironing service via service vouchers, books and board games available, and much more….

You will join a company that listens to your needs and your suggestions!

 

10 reasons to join

About Quality Assistance

Quality Assistance is a leading European Contract Research Organisation (CRO) 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.

From candidate selection, through non-clinical and clinical studies, to marketing authorisation, Quality Assistance provides customised solutions for its clients: 

  • We define analytical protocols;

  • We develop and validate specific new analytical methods;

  • We perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing.

These tests are performed in order to evaluate the Quality, Safety and Efficacy of the given drugs.

With 40 years’ expertise at the forefront of analytical sciences, Quality Assistance holds a unique place on the market thanks to:

  • All of its laboratories located on one site (Donstiennes, Belgium);

  • 240 highly qualified professionals;

  • A wide range of analytical methods and state-of-the-art equipment.

The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant.

Visit https://www.quality-assistance.com/quality-assistance/leading-analytical-cro to learn more.

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Bernard Adant

Isabelle Lebrun

Celia Cosseddu

Rachel Vanhoutte

Talent Management

+32 71 890 156

recrutement@quality-assistance.be