Your Talent, our Vision – together we see beyond. Your start at ZEISS Vision Care. As a leading manufacturer of ophthalmic lenses, we help people around the world achieve a clearer vision – sustainable and with focus on the future.
Our products are as diverse as the career paths we offer, from tailored lenses to award-winning measurement systems. Become part of our team and shape a future in which clear vision and professional success go hand in hand.

Your Role

• Track and analyze regulatory changes, guidelines, and policy trends in key EMEA markets (e.g., EU, MOEL, SEE, META) to stay informed and proactive
• Identify and assess new and evolving requirements for the Vision Care Portfolio, supporting the development of innovative solutions and competitive advantages
• Maintain a regulatory intelligence database and provide timely updates to internal teams to ensure alignment with current regulations
• Develop EMEA regulatory framework strategies for Vision to ensure compliance with regulatory requirements for Quality Management Systems (QMS) and products
• Represent the company in EMEA industry associations and regulatory forums, building relationships with key regulators and policymakers
• Prepare position papers and execute advocacy strategies to influence regulatory policies in alignment with business objectives, while identifying regulatory opportunities and risks
• Conduct training for internal teams to anticipate regulatory requirements, develop clear summaries of complex regulatory issues, and create trend reports for upcoming challenges

Your Profile

• Bachelor’s degree in Life Sciences, Pharmacy, Regulatory Affairs or related fields; advanced degree (MSc, MBA) or RAC (Devices) certification preferred
• Profound experience in Regulatory Affairs within the Life Sciences or Medical industry, with a strong understanding regulatory requirements (e.g., FDA, MDR, ISO 13485, MDSAP) as well as EMEA regulatory frameworks and strategies (e.g. EU MDR)
• Proven knowledge in managing multiple parallel projects across geographies and functional areas including the interaction with authorities and external stakeholders with strong communication, negotiation, and collaboration skills
• Proficiency to leverage digital tools and platforms to enhance regulatory processes and communication
• Ability to think strategically with analytical skills and strong problem-solving capabilities to navigate complex regulatory challenges in a multicultural environment
• Proficiency in German and English; additional languages are an advantage

Your ZEISS Recruiting Team:
Hannah Beutle

• Track and analyze regulatory changes, guidelines, and policy trends in key EMEA markets (e.g., EU, MOEL, SEE, META) to stay informed and proactive
• Identify and assess new and evolving requirements for the Vision Care Portfolio, supporting the development of innovative solutions and competitive advantages
• Maintain a regulatory intelligence database and provide timely updates to internal teams to ensure alignment with current regulations
• Develop EMEA regulatory framework strategies for Vision to ensure compliance with regulatory requirements for Quality Management Systems (QMS) and products
• Represent the company in EMEA industry associations and regulatory forums, building relationships with key regulators and policymakers
• Prepare position papers and execute advocacy strategies to influence regulatory policies in alignment with business objectives, while identifying regulatory opportunities and risks
• Conduct training for internal teams to anticipate regulatory requirements, develop clear summaries of complex regulatory issues, and create trend reports for upcoming challenge