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.Your ResponsibilitiesConsulting/Project ManagementProvide expert advice and implement it at the customer locationProject Scoping, Planning & Execution ManagementProject Team Leadership & CoordinationRisk & Issue ManagementStakeholder Communication & ReportingQuality & Performance MonitoringNote: Operational involvement in the customer processes is not excludedAs examples, customer-related projects could include:Advising on Company strategies e.g. Quality, Regulatory, Data Governance, etc.Optimizing Production and Supply Chain processesDeveloping or refining technical documentation to meet Industry Sector requirements, and end-to-end business process mappingEstablishing or improving Quality Management Systems, conducting internal audits and addressing found CAPAs and gapsManage implementation of business-critical software toolsDevelopment of customer teams and individuals in Quality and/or Project Management methodsBusiness DevelopmentActively promote the StingOrg services to your networkIdentify new sales leads and partnership opportunitiesParticipate in or attend industry eventsIdentify project opportunities during active projects at customersAs examples, other StingOrg internal tasks may include:Establish or improve internal processesDeliver training sessions in light of team knowledge-sharingSupport marketing activitiesOrganise small-scale eventsThe profile we are looking for:Master's degree in engineering or sciences, ideally with a focus on Life Sciences or Medical TechnologyAt 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)SRPractical knowledge of ISO 27001 is a plusExperience in Project Management (e.g. PMP, AgilePM), Quality Management, and Risk ManagementSkilled in planning and motivating othersAssertive, analytical, and hands-on approach to problem-solvingWillingness to travel internationallyFluent in English and Dutch (written and spoken); French or German is a plusYou are located in BelgiumWhat we offer you:Competitive salary with performance-based bonusesComprehensive benefits package, including a company car, meal vouchers, Eco cheques, Hospital insurance32 holidays per year (40h/week contract in PC200)A flexible hybrid work environment (subject to customer requirements)Tailored program for professional developmentOpportunities for continuous learning and knowledge-sharing with global colleaguesA dynamic, open-minded, and team-oriented cultureChallenging projects in an international environmentThe opportunity to further shape your role according to your preferences, in line with the company's business strategyThe opportunity to be at the forefront of a growing unique service companyDoes this sound like you? Or perhaps not 100% like you, but you tick several boxes and are eager to learn?Your mindset, attitude and personality match is more important to us than the knowledge match.Interested?Let's talk