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Website: zeiss.com
Zeiss is a German manufacturer of optical systems and optoelectronics, founded in Jena, Germany, in 1846 by optician Carl Zeiss. Together with Ernst Abbe and Otto Schott he laid the foundation for today's multinational company. The current company emerged from a reunification of Carl Zeiss companies in East and West Germany with a consolidation phase in the 1990s. Zeiss is active in four business segments with approximately equal revenue in almost 50 countries, has 30 production sites and around 25 development sites worldwide.
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Join ZEISS as a Senior Advisor, Regulatory and Clinical Affairs in a full-time position in the United States. This role offers the opportunity to shape regulatory strategy and advance clinical innovation at one of the world's most respected science and technology organizations. About the Role As Senior Advisor, Regulatory and Clinical Affairs at ZEISS, you will serve as a strategic leader responsible for navigating complex regulatory landscapes and driving clinical affairs initiatives forward. You'll partner across cross-functional teams to ensure compliance, develop regulatory strategies, and support clinical programs that transform healthcare and scientific advancement in a dynamic, innovation-focused environment. What You'll Do Develop and execute regulatory strategies aligned with organizational goals and evolving regulatory requirements Lead clinical affairs initiatives, from program development through implementation and stakeholder engagement Prepare regulatory submissions, manage documentation, and oversee compliance activities Collaborate with research, quality, medical, and commercial teams to drive regulatory excellence Maintain deep expertise in relevant regulations and industry standards, advising leadership on compliance and strategic opportunities Support planning for new products, technologies, and market entry strategies What We're Looking For Extensive experience in regulatory affairs or clinical affairs within life sciences, medical devices, healthcare, or related industries Demonstrated expertise in regulatory submission processes, compliance frameworks, and agency interactions Strategic mindset with ability to influence and align cross-functional teams Strong written and verbal communication skills Comprehensive understanding of regulatory agencies and evolving healthcare regulations Proven success managing complex regulatory and clinical projects About ZEISS For nearly 180 years, ZEISS has pioneered optical systems, optics, and optoelectronics on a global scale. We drive innovation at the intersection of science and technology, delivering solutions that advance human progress and create lasting impact on global challenges. Excellence, innovation, and sustainability define our commitment to the future. How to Apply To apply for this Senior Advisor, Regulatory and Clinical Affairs opportunity with ZEISS, submit your application through this listing along with your resume and any supporting materials that highlight your regulatory and clinical expertise.
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