Senior Director of EMEIA - Quality Varian

Senior Director of EMEIA - Quality Varian page is loaded Senior Director of EMEIA - Quality Varianremote type: Office Basedlocations: CEY BO: KEMtime type: Full timeposted on: Posted Todayjob requisition id: R-25449Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Then come and join our global team as Senior Director of EMEIA-Quality Varian (f/m/d) to ensure the highest quality in Finland, Germany, Hungary, and India - with a focus on R&D in the global VARIAN radiotherapy portfolio. location: UK (Crawley) or Germany (Kemnath) Your tasks and responsibilities: As Head of Quality, EMEIA, you will provide strategic leadership to multiple global quality teams, developing a high-performing organization, fostering a culture of accountability, continuous improvement, and effective cross-functional collaboration. You are responsible for developing the quality management strategy for the EMEIA region in alignment with global quality management systems, quality, and corporate goals. You will work with various business areas/line teams to achieve these You handle communication with authorities and are responsible for processes to meet internal and external regulations You are responsible for budget planning for global quality programs and coordinate the budget plan with the organizational unit You analyze and develop local quality data to identify problems or deviationsTo find out more about the specific business, have a look at Your qualifications and experience: You have a degree in engineering, life sciences, regulatory affairs, or a comparable field You have many years of relevant professional experience in quality management in a highly regulated environment, ideally in medical technology, imaging, diagnostics, or similar You also have extensive professional and disciplinary leadership experience in large, geographically distributed teams in a matrix organization, ideally with a focus on quality, R&D, regulatory affairs, and post-market You have solid experience working with authorities and solving complex regulatory issues Ideally, you are familiar with agile, lean, and digital transformation processes in a regulatory environment In-depth knowledge of EU MDR/IVDR, ISO 13485, MDSAP, and relevant national regulations, as well as experience with integrated quality/regulatory management systems and digital tools, complete your profile Your attributes and skills: You have fluent English skills (and German if you are Kemnath based) as well as excellent communication, problem-solving, and negotiation skills in both languages You are implementation-oriented and ensure the sustainable anchoring of innovative solutions and processes - you are passionate about continuously developing existing processes using digital and AI tools You stand out with decisiveness, transparency, and leadership strength in uncertain or changing regulatory environments Personally, you pursue the overarching goal of creating a world without fear of cancer every day. Therefore, you strive for continuous improvement, quality is close to your heart, and you are happy to implement our high standards together with the team Your profile is rounded off by a strong motivation for continuous process improvement and openness to changeAs an equal opportunity employer, we welcome applications from individuals with disabilities.We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities. Who we are : We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways. How we work : When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.To find out more about Healthineers' specific businesses, please visit our company page .As an equal opportunity employer, we welcome applications from individuals with disabilities. Data Privacy : We care about your and take compliance with GDPR as well as other data protection legislation seriously. For this reason, we ask you not to send us your CV or resume by email. 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Siemens Healthineers is not responsible for any fees related to unsolicited resumes. As an equal opportunity employer, we welcome applications from individuals with disabilities.