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.