Scope

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 client 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.

Your mission

You will report to the Analytical Team Manager.

You will be part of a team of 25 people.

In this role, you will support Project Leaders into their daily management activities with the following tasks:

  • Writing the technical agreement

  • Being involved in the planning of the work

  • Supervising the allocation of the samples and standard references

  • Monitoring the execution of all project-related activities

  • Ensuring protocols and contracts are respected

  • Managing communication internally and with clients

  • Being involved in addressing technical issues

  • Checking the final reports: trends analysis, conclusions, conformity of QA documents, respect of the technical agreement, …

  • Maintaining records and files

  • Meeting customers during visits and audits

Project leader

Your profile

University degree with a scientific orientation.

Required

  • Strong communication skills in French and English to interact internally with colleagues and externally with clients.

  • Strong organisational skills with ability to manage projects through wise planning, time optimisation, detail orientation and prioritisation.

  • Knowledge of GMP.

  • Resilience under pressure.

  • Team Player.

Pluses

  • Knowledge of compendial testing (Ph. Eur. and USP) and some practical experience in the characterisation, stability testing and/or quality control of pharmaceutical products.

  • Knowledge of following products : Proteins, Antibodies, ADCs.

  • Good understanding of Drug Development Process.

Project leader

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, and for certain positions, 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 2021 we welcomed, and trained 45 new colleagues? We also promoted 23 team members (vertical mobility). 13 positions were filled by internal candidates. We provided 1,275 general and technical training sessions as well as 696 practical training courses.

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);

  • 230 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.

ApplyFor this job
In compliance with the European Union’s General Data Protection Regulation (GDPR), Quality Assistance processes personal data lawfully, fairly and in a transparent manner, and only in the context of Quality Assistance services and activities. We do not transfer personal data to, or share personal data with, third parties, except in compliance with legal obligations or with your prior authorisation. You can ask for your data to be rectified or deleted, or you can withdraw your consent to receive information from us at any time, by sending an e-mail to contact.compliance[at]quality-assistance.be

More info about Terms of Use and Privacy Policy
Type of jobs