QC Project Coordinator - Elisa methods

Akkodis is an organization with more than 1,000 engineering, scientific and digital experts in Belgium. Our mission is clear: create a smarter future together! We are a one-stop-shop for engineering, IT, Life Science, and new technologies. Our combined passion for talent and technology allows us to look at the world differently.

With our 360° offer we support companies in all sectors in implementing Smart Industry solutions, from the up and reskilling of entire teams to the delivery of complete projects. Our added value? We make incredible happen!

Your responsibilities:

As a QC Project Coordinator, your main responsibilities will be:

• Drive transversal scientific projects and will interact with different internal and/or external stakeholders.
• Evaluate and analyze project and business issues.
• Centralize information on one or more projects to provide visibility on its progress (implementation Dashboard, Timeline, etc.).
• Put in place risk management strategies to proactively prevent the risk inherent in the execution of the project.
• Create and maintain comprehensible and consistent project documentation.
• Maintain continuous scientific awareness to ensure the project relevance and competitiveness.
• Demonstrate problem solving capabilities to resolve situation promptly and efficiently to ensure on time delivery and to maintain high level of customer satisfaction.
• Depending on your expertise, you may be required to participate in decision-making with other customer experts.
• Guarantee the application and maintenance of adequate cGMP rules in his work area.

Your profile:

• You are graduated as a bachelor’s or master’s degree in pharmaceutical, bioengineering or chemistry, with a good expertise in biochemistry, virology, cell biology, immunology, analytical chemistry, or other related science.
• You have a strong expertise enzyme-linked immunosorbent assay (ELISA).
• You are familiar with QC environment of a pharmaceutical company and cGMP environment.
• You have experience in project management.
• You are fluent in French and English.
• You have good organizational skills and can plan and prioritize your activities.
• You enjoy meeting and speaking with people, presenting your results, and advising costumers.
• You are proactive, solution-oriented, open-minded, and flexible.
• Which can be seen as a plus:
  Knowledges pharmaceutical guidelines (ICH, USP, EP, etc.).
  Knowledge in the use of SAP, Veeva, LIMS software.
  Knowledge in the field of analytical methods or equipment validation.
  Good basis in Microsoft® Office software used.

What’s the offer you can’t refuse?

As an AKKODIS Team member, you will be:

• Onboarded in your position via a buddy process and supported in your career by your Business Manager.
• Actor of your training plan and your personal and professional development.
• Benefit from a full time permanent AKKODIS contract with competitive salary package including several extra-legal benefits.
• In a nice work environment & atmosphere within an international group.
• Invited to attractive events calendar including afterwork, life sciences meeting, and other professional gatherings.

Do you have any questions? You can contact me at marie.defruit@akkodis.com