About us:
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!


What do you do all day?
As a Business Analyst, within the 'Lab Data Operations' department, you are in charge of analyzing the risks of data traceability of the testing methods used in the QC department of a global biopharmaceutical company. You work under the supervision of a Project Manager, and you are in daily contact with many players in the QC environment. It's a hybrid position that allows you to combine work at home and on customer site.


You are also an integral part of an Akkodis platform, within our customer teams, which means you'll have daily follow-up and support from people who know your work environment. In addition, you will also be encouraged to propose initiatives to diversify the activities of this platform and improve its functioning. Just as, depending on your availability and level of expertise, you could provide support to other Akkodis platforms.



Your responsibilities:
As Business analyst, you are in charge to:
Understand how data are captured and generated from analytical methods by analyzing the QC department's internal procedures and conducting laboratory observations with operational teams.
Create DPM (Data Process Mapping) of analytical methods to visually represent the data flow.
Identify and list in a DVA (Data Vulnerability Assessment) the GMP/GDP data (raw data and metadata) involved in the method's process.
Assess data vulnerability (based on criticality, technical/procedural controls in place, etc.).
Assess risks to determine the controls to implement (if any are lacking).
Maintain accurate and up-to-date documentation related to the project.
Participate to the administrative tasks of the team (complete follow-up files, continuous improvement, etc.) and weekly follow-up meetings.

Your profile:

You have minimum 2 years of work experience. 
You have scientific background with knowledge in laboratory analysis technics, like biochemistry, physicochemistry, microbiology and/or cell biology.
You have excellent analytical and synthesis skills to interpret complex data and propose appropriate solutions.
You are familiar with the QC environment of pharmaceutical companies.
You have knowledge of cGMP expectations and, especially, in data integrity.
You have experience or affinity with data management.
You are proficiency in French and English, both written and spoken.
You know how to handle pressure situations, and you could respond resiliently to an emergency event.
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