Regulatory Affairs Manager 80-100%

About the job

Curaden AG, based in Kriens near Lucerne, is more than just a company – we embody a vision, a system, and a philosophy that sets global standards. Under our brand CURAPROX, we are revolutionizing dental care and striving for nothing less than a healthier and happier society. Our promise "Better health for you" drives us to develop innovative and pioneering dental products that inspire in over 90 countries on six continents.

For more than seven decades, we have also stood by dental professionals in practices and laboratories. We offer tailored solutions and all necessary products for an exceptionally patient-oriented practice management. Our goal? A true win-win-win situation between patients, dentists, and Curaden – thus laying the foundation for lifelong healthy teeth.

We are aware that achieving our goals requires employees who are ready to exceed the ordinary and think unconventionally!

To further advance our mission and make the world a better place, we are looking for creative personalities and courageous innovators like you. Let’s explore new paths together and shape the future of oral health!

To strengthen our team in Kriens, we are immediately or by arrangement looking for a

Regulatory Affairs Manager 80-100%

Your tasks

• You lead international projects for the registration and approval of cosmetic products and consumer goods
• You ensure that all required documents are complete and organize certifications by external bodies if necessary
• You create and update regulatory and technical documents, e.g., product data sheets, safety data sheets, self-declarations, or FSC
• You manage relevant documents in IQSoft and SAP
• You review packaging layouts and other labeling elements for regulatory compliance, e.g., INCI declarations
• You are the contact person for regulatory questions from partners and distributors
• You handle error reports in IQSoft as well as CAPA and act as the link between internal departments, suppliers, and external partners
• You contribute to maintaining and further developing the quality management system
• You perform general administrative tasks within the Regulatory Affairs and R&D area
• You actively participate in the further development of the department

Your profile

• You have training in medical technology, quality management, regulatory affairs, or a comparable field
• Ideally, you already have professional experience in the registration of cosmetics; experience with medical devices is an additional advantage
• You want to make a difference, are reliable, communicative, and have a high sense of responsibility and quality awareness
• You have good German and English skills; additional knowledge of Spanish and/or Italian is an advantage
• You have an organized and structured way of working, think outside the box, and have an eye for detail

Curaden convinces through

• challenging, versatile, and exciting tasks
• a rapidly growing corporate group
• a family-like working atmosphere and a dynamic work environment
• various training and development opportunities
• trust in employees with the opportunity to contribute themselves
• attractive employee conditions and offers

We look forward to getting to know you!

CURADEN AG | Human Resources | Amlehnstrasse 22 | 6010 Kriens | Phone: +41 41 319 45 59