• Defining the production constraints for RPS consumables
• Identify and support teams and customer in the regulatory applicable rules

• Defining and maintaining the “rules of the game” for the consumables production for the RPS chemistry modules with main focus on ISO 9001/14001 by setting up processes and related procedures. Active followup, training and support during implementation.
• Ensure consistency, awareness, maintenance and validation of the associated QMS
• Support Bid Teams with refined project specific regulatory constraints
• Develop the associated services
• Define and issue business performance reporting, create and define dedicated KPIs, advise and implement corrective actions to improve or secure services

• QA and RA experience (3 years minimum)
• Excellent analysis capabilities
• Hands-on solutions finding skills
• Networking skills
• QA/RA experience in medical context is a plus
• English : Fluent
• Portuguese is an plus

• Very autonomous & proactive
• An excellent communicator at all organization levels
• A good team-player
• Eager to learn continuously about Products, Market & Organization changes
• Well-organized and to the point
• Based or will be based in Belgium