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 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.

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 manage projects and assist the Analytical Team Manager in his daily management activities.

You will ensure the following tasks:

  • Writing technical agreements

  • 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, etc.

  • Maintaining records and files

  • Meeting customers during visits and audits

Your profile

Scientific background (PhD or Master's degree / Engineer)

Required

  • Strong communication skills in French and English interacting internally with peers and externally with clients

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

  • Relevant working experience in the pharmaceutical industry more specifically in a GMP environment

  • Very good knowledge in antibody testing and characterisation

  • Relevant experience in a project management role

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.

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. 

Visit https://www.quality-assistance.com/quality-assistance/life-quality-assistance to learn more.

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.

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

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