Join a forward-thinking and innovative environment focused on enhancing manufacturing processes through digital transformation. We are looking for a dedicated professional to make an impact in the manufacturing sector by supporting essential MES (Manufacturing Execution System) projects.
The ideal candidate for this role is a knowledgeable
TechnoFunctional Consultant
with a passion for streamlining operations and improving efficiency in bio-manufacturing processes. If you are driven by precision and possess a keen understanding of both technical and functional aspects in a regulated environment, this position could be the right fit for you.
* You collect and write User Requirements (URS) for MES on specific process steps.
* You understand and translate complex biomanufacturing processes into functional requirements.
* You test electronic batch records directly within the MES environment.
* You perform Performance Qualification (PQ) of MES solutions.
* You interact with IT and validation teams throughout the MES lifecycle.
* You collaborate with other MES team members during the ramp-up phase.
* You manage assigned packages autonomously over time.
What are we looking for?
* You have experience in regulated / GxP environments.
* You possess knowledge of the validation lifecycle (URS, PQ, basic IQ/OQ understanding).
* You have experience with MES systems.
* You exhibit strong communication and stakeholder management skills.
* You are able to work independently after onboarding.
* You are proficient in
English
and have at least an understanding level of
French
.
* You are willing to work mostly onsite.
* You have experience in biomanufacturing or pharmaceutical production (nice to have).
* You possess knowledge of OSIsoft PI (nice to have, not mandatory).
* You have a Technofunctional / Business Analyst profile.
* You have experience working closely with production teams (nice to have).