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Qc data process mapping consultant

Akkodis
Publiée le 29 avril
Description de l'offre

QC Data Process Mapping ConsultantAkkodis is an organization with more than 1,000 engineering, scientific and digital experts in Belgium. 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. As a QC Data Process Mapping Consultant, 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. 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. As QC Data Process Mapping Consultant, 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.).Participate to the administrative tasks of the team (complete follow-up files, continuous improvement, etc.) 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 have strong interpersonal skills, excellent communication abilities, team spirit, and the ability to work in a dynamic, multidisciplinary environment.You are familiar with the use of laboratory softwares and/or equipments.You master the Microsoft Office software, and you have already used Microsoft Visio.You already have experience using SAP and/or Documentum/Veeva.

As an AKKODIS Team member, you will be:

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.

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