Analytical Project Leader

Location: Belgium

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Brussels Hoofdstedelijk Gewest Belgium.

The Company

Le laboratoire est spécialisé dans le développement, la validation et le transfert de méthodes analytiques pour tous les produits entrant sur le site.
Le laboratoire est également spécialisé dans la génération des données requises pour les dossiers d'enregistrement de nos nouveaux produits (détermination du profil de dégradation, détermination de la stabilité du produit dans des conditions normales / sous contraintes, etc.).

Role Description

To strengthen our Process Development & Scale-up department, we are currently offering two permanent positions of Analytical Project Leaders. The successful candidates will report directly to the Deputy Head of Process Development & Scale-up.

Responsibilities

The analytical project leader

• Leads analytical activities (within Corden Pharma Brussels or in collaboration with other Corden sites) for the development and qualification of analytical methods for specific projects.
• In collaboration with lab assistants, generates experimental data in the frame of analytical method development, pre-qualification and qualification of analytical methods (mainly HPLC/UPLC), analytical method transfer to other Corden sites and/or QC department, trouble-shooting for running productions, analyses of non GMP products
• Manages stability studies of non GMP products (protocol, study, report)
• Integrates cGMP requirements in analytical development lab and analytical activities
• Provides adequate technical reporting
• Provides technical input for the preparation of regulatory documents
• Provides technical input for new project evaluations
• Prepares power point presentations summarizing analytical outcome for specific projects
• Participates as analytical expert to regular teleconferences and meetings with customers, internal team meetings or meeting with other Corden sites
• Reports to the Deputy Head of Process Development & Scale-up

Requirements

• Master degree in analytical sciences. PhD is a plus.
• Several years of experience in analytical development in chemical or pharmaceutical industry is a plus
• Experience with HPLC/UPLC
• Knowledge or experience in peptide chemistry appreciated
• Ability to work in team
• Autonomous and proactive
• Good communication skills
• Hands-on and result-oriented
• Languages:
o A satisfying English level is mandatory (written and spoken) to be able to interact with customers and other Corden Pharma sites, and for technical documents drafting
o French (or willing to learn French), as this is the official language of the site

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Ewout de Jong.