Then come and join our global team as Senior Manager (m/f/d) for Technical and International Standards Management in the central Quality Department, supporting our Business Areas, Business Lines, Business Horizontals, and Technology Units as well as the country organizations in the development, analysis, and application-oriented interpretation of international and national standards, as well as relevant laws and guidelines regarding in-vivo medical devices and in-vitro diagnostic products.

Choose the best place for your work – Within the scope of this position, it is possible, in consultation with your manager, to work mobile (within Germany) up to an average volume of 60% of the respective working hours.

Even more flexibility? Mobile working from abroad is possible for up to 30 days a year under certain conditions and in selected countries.

Your tasks and responsibilities:

• You act as the central point of contact and oversee the management of technical regulations and standards of organizational units and countries to ensure compliance with legal requirements and support business growth.
• You independently develop our standardization strategy for global market access and advise your counterparts in the business units as well as in the countries.
• You take responsibility for advising on standardization mechanisms and support the organizational units in implementing normative and legal requirements.
• You ensure legal clarity for market access by monitoring and evaluating relevant standards and regulations, particularly in Europe, and by providing comments on drafts.
• You proactively participate in committees of standards organizations (SDOs), preferably at a strategic level, to ensure a practical standardization landscape.
• You represent us in industry associations to ensure effective and sustainable exchange with stakeholders and decision-makers.
• You are responsible for optimizing and maintaining the company-wide process for managing standards and technical regulations in a digitally evolving environment.
• You drive our internal reporting, organize workshops and training sessions for colleagues, and create globally valid company policies relevant to compliance with legal requirements.

To find out more about the specific business, have a look at https://www.siemens-healthineers.com/de/products-services

Your qualifications and experience:

• You have a university degree in natural sciences or in the field of engineering.
• You have extensive professional experience with technical standards in the areas of Regulatory Affairs, Quality Management, R&D, or conformity assessments, ideally for medical or in-vitro diagnostic electrical devices and systems as well as related safety standards such as the IEC 60601-1 or IEC 61010-1 series.
• You impress with in-depth knowledge and a strategic perspective on standardization and are active and well-connected in national and international committees as well as working groups of industry associations.
• Ideally, you have already contributed to the development of standards and gained experience in leading working groups in an international environment.
• Do you already have extensive, long-standing professional experience and additional qualifications in this field but no university degree? Then we would also be happy to receive your application.

Your attributes and skills:

• You are a natural networker, complemented by strong communication skills in German and English.
• You can analyze complex topics and set clear goals and priorities.
• Your working style is results-oriented and assertive, and you know how to use your experience to lead working groups with diverse cultures and personalities in the role as chair.
• Your personal strengths include a high degree of initiative, flexibility, and service orientation.
• You are open to digitalization in an environment characterized by increasing regulatory and normative complexity.
• International business travel (approx. 25%) is a welcome change for you.
• We learn passionately – a high level of motivation for continuous process improvement and your openness to change are a matter of course for you.

Depending on the experience and qualifications background of the applicant, task enrichment into the area above the general pay scale is possible.