Consultant MedTech (m/w/d)

StingOrg’s mission is to create organizations that improve themselves. Our goal is to transform organizations, so they not only excel in quality and efficiency but also nurture responsible, empowered individuals.

We are implementation-oriented consultants specialized in managing Quality implementation and improvement projects. We operate mainly in Life Sciences, Automotive and Industrial engineering sectors.

We’re looking for a Consultant MedTech to strengthen our StingOrg BV team in Belgium.

• You will report to the Consulting Manager and additionally, when engaged in a project, to the respective customers.
• Consulting/Project Management
• Provide expert advice and implement it at the customer location
• Project Scoping, Planning & Execution Management
• Project Team Leadership & Coordination
• Risk & Issue Management
• Stakeholder Communication & Reporting
• Quality & Performance Monitoring
• Note: Operational involvement in the customer processes is not excluded
• As examples, customer-related projects could include:
• Advising on Company strategies e.g. Quality, Regulatory, Data Governance, etc.
• Optimizing Production and Supply Chain processes
• Developing or refining technical documentation to meet Industry Sector requirements, and end-to-end business process mapping
• Establishing or improving Quality Management Systems, conducting internal audits and addressing found CAPAs and gaps
• Manage implementation of business-critical software tools
• Development of customer teams and individuals in Quality and/or Project Management methods
• Business Development
• Actively promote the StingOrg services to your network
• Identify new sales leads and partnership opportunities
• Participate in or attend industry events
• Identify project opportunities during active projects at customers
• As examples, other StingOrg internal tasks may include:
• Establish or improve internal processes
• Deliver training sessions in light of team knowledge-sharing
• Support marketing activities
• Organise small-scale events

• Master’s degree in engineering or sciences, ideally with a focus on Life Sciences or Medical Technology
• At least 10 years of working experience in a regulated environment (MedTech, BioTech, or Pharma)
• Strong practical knowledge of international regulations and standards: MDR, IVDR, ISO 13485, ISO 14971, FDA Q(M)SR
• Practical knowledge of ISO 27001 is a plus
• Experience in Project Management (e.g. PMP, AgilePM), Quality Management, and Risk Management
• Skilled in planning and motivating others
• Assertive, analytical, and hands-on approach to problem-solving
• Willingness to travel internationally
• Fluent in English and Dutch (written and spoken); French or German is a plus
• You are located in Belgium