QC Project Manager

Vacancy details

General information

Reference

2023-26818  

Publication date

08/03/2023

Position description

Category

OPERATIONS - PROJECT MANAGEMENT

Job title

QC Project Manager

Contract

Permanent contract

Job description

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.

So, what do you do all day?

As QC Project Manager, you will be able to perform project management, while keeping a job with scientific thinking. Plans, directs, and coordinates project activities to ensure that the defined objectives are meet within the timeline, the quality and the budget.

It’s a hybrid job that will allow you to combine work at home and on customer site. You will participate to regular teleconferences and meetings with customer and internal team as appropriate.

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

Business Industry

Life sciences

Profile

What skills do you bring to the table?

·       You are graduated as a bachelor’s and/or master’s degree in Chemistry, Biochemistry, Bioengineer or Pharmaceutical

·       You have a working experience in project management

·       You have also good knowledge in validation of analytical methods and cGMP environment

·       You are fluent in French, and you have a good knowledge of English (mainly, written and reading)

·       You enjoy meeting and speaking with people, presenting your results, and advising costumers

·       You are proactive, solution-oriented, open-Minded, and flexible

·       You master the Microsoft® Office software

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@akkodis.com

Position location

Job location

Europe, Belgium, Wallonia, Walloon Brabant

Location

Avenue Jules Bordet 168 1140 Bruxelles

Telework

1-2 days per week

Candidate criteria

Minimum level of education required

6. Master Degree

Diploma specialisation

  • Biotechnology
  • Chemistry / Biochemistry / Petrochemistry
  • Pharmaceutics

Level of experience

3 to 5 years