QC Project Manager

Job content

QC Project Manager

First, did you know that AKKA Belgium is going to be AKKODIS soon? Because of the merger with MODIS.

AKKODIS is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation.

As part of the development of the activities at one of our clients, we are looking for a QC Project Manager.

What are your responsibilities?

• Drive one or more transversal projects (in the field of analytical methods) and will interact with different stakeholders
• Monitor the implementation of new requirements, in the analytical domain, within the client’s site
• Centralize information on one or more projects in order to provide visibility on its progress (implementation dashboard, timeline, status by PMUs, resource needs, etc.)
• Evaluate and analyze project and business issues
• 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 management documentation
• Demonstrate problem solving capabilities to resolve situation promptly and efficiently to ensure on time deliveries 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
• Participate to transversal interactions with other teams in QC Department and different other stakeholders
• Participate to the administrative tasks of the team (continuous improvement, complete the follow-up files, etc.)
• Guarantee the application and maintenance of adequate cGMP rules in his work area.

What skills do you bring to the table?

• You are graduated as a bachelor’s and/or master’s degree in scientific field (chemistry, biochemistry, bioengineer or pharmaceutical) and you have a working experience in project management
• You are familiar with industrial/pharmaceutical manufacturing and cGMP environment
• You have the laboratory experience, in analytical method validation and/or method transfer
• You have good analytical and coordination skills
• You are fluent in French and English (mainly writing and reading)
• You enjoy meeting and speaking with people, presenting your results, and advising customers
• You are proactive, solution-oriented, open-minded, organized and flexible
• You master the Microsoft Office software
• Which can be a plus:
• Knowledge in project management tools
• A working experience in the field of sterility
• Knowledge and use of Eudralex

What’s the offer you can’t refuse?

As an AKKODIS Team Member, you will be:

• In charge of diverse transversal analytical validation projects in a cGMP environment
• Part of a dynamic and collaborative team of validation supervisors under the direction of a Service Manager
• Onboarded in your position via a buddy process
• Supported in your career by your Business Manager
• Actor of your training plan and your personal and professional development
• Benefiting from a permanent contract
• Benefiting from a competitive salary package including several extra-legal benefits

Do you any questions? You can contact me at marie.defruit@akka.eu