Functie

• As a project manager you are the single point of contact for our pharma/biotech customers.
• You advise the customer in the analytical part of their drug development. You translate their needs into laboratory assignments and make estimates of the workload.
• You actively maintain knowledge of current regulatory requirements and serve as a subject matter expert (SME) in regulatory or customer’s audits.
• You manage phase appropriate and GMP/ICH compliant analytical method development, validation and release/stability testing (writing, set-up, review, data management).
• You actively work together with your fellow project managers, scientists and group leads to kick-off, execute and finalize the projects in accordance with customer expectations.
• You are responsible for the interpretation of the results and reporting to the clients.
• You closely follow working methods and procedures and you are able to proactively detect issues and propose optimizations.
• You will be leading or participating in improvement projects as part of our continuous improvement company culture.
• Finally, you keep your scientific knowledge up-to-date through literature and attendance at scientific seminars.

Jouw profiel

• You have a scientific education (e.g. bio-engineer, analytical chemist, biotechnology, pharmaceutical sciences, …) or equivalent by experience. Practical lab experience in an analytical environment is an advantage.
• You have at least 5 years of experience in a laboratory environment within the pharmaceutical industry and you understand the analytical needs in the different phases of drug development.
• You have in-depth experience in techniques and instruments used in the analysis of synthetic or biological drugs, like chromatography (LC-UV/ELSD/CAD/MS and GC-FID). Experience with other methodologies as Dissolution, KF, ELISA, … are a plus.
• Experienced in or good knowledge of a GxP regulated environment is a big advantage.
• You are highly motivated to work in an environment with a lot of variety and learning opportunities. Flexibility and agility are in your DNA.
• You can plan, organize and coordinate well, taking into account the timing and budget.
• Your colleagues and clients know you as a good communicator.
• Finally, you are fluent in English and you have a working knowledge of Dutch.

• Rapporten, publicaties en scripties opstellen
• Onderzoeksgegevens en –resultaten bestuderen en analyseren
• Wetenschappelijk onderzoek en ontwikkelingen voorstellen en verklaren
• Methodes voor onderzoek en voor de gegevensverzameling en –analyse bepalen en ontwikkelen
• Wetenschappelijke, technologische, technische, reglementaire, … informatie opvolgen en actualiseren
• Het verloop en de vooruitgang van wetenschappelijke experimenten en observaties leiden en controleren
• Onderzoekers, instituten, ondernemingen adviseren en wetenschappelijke steun bieden

Aanbod

• You will be part of the anacura group, a warm and family owned, long term focused and ambitious laboratory organization.
• You will join a science-driven, dynamic team and have a position with autonomy and responsibility with opportunities to take initiatives to support further growth.
• You will be offered a competitive salary with fringe benefits, a green work environment and the possibility to join our bike lease program, flexible working hours, a healthy lunch, and a pleasant fun club.
• You are stimulated in your personal growth; we build on your talents in accordance with our ambitions.

Solliciteren

Jill Colaers
09 257 15 07
jobs@anacura.com