PROJECT MANAGER

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 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 thetechnical agreement

• Being involved in the planningof the work

• Supervisingthe allocation of the samples and standard references

• Monitoringthe execution of all project-related activities

• Ensuring protocols and contracts are respected

• Managing communicationinternally 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

Your profile

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

Required

• Strong communication skills in Frenchand Englishinteracting internally with peers and externally with client

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

• Relevant work experience in the pharmaceutical industry more specifically in a GMPenvironment

• 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.

• Very good knowledge in antibody testing and characterisation.

Why join Quality Assistance?

We are a true career partner.

• We acceleratepeople’s access to new medicines.

• We offer an inspiring work-life balancein a human scale environmeant.

• We careabout mutual respect, assistance and communication.

• We listento your needs and your suggestions.

• We offera market-competitive remuneration package including numerous fringe benefits.

Visithttps://www.quality-assistance.com/quality-assistance/life-quality-assistanceto 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 EMAand FDAregulations for the development and marketing ofinnovative human medicinal products.

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 isGMP, GLP and GCLP/GCP compliant.

Visithttps://www.quality-assistance.com/quality-assistance/leading-analytical-croto learn more.