At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.

Regulatory Affairs Officer (m/f/d) 

The Consumer Health division of Bayer S.p.A. is looking for a passionate and curious Regulatory Affairs Officer to join the Italian team.

He/she/they will be responsible for managing regulatory activities for our local Consumer Health portfolio including drugs, food supplements, medical devices and cosmetics.

This is a unique opportunity to build regulatory expertise across different product categories and collaborate with highly engaged cross‑functional teams.

MAIN TASKS AND RESPONSIBILITIES:

• Develop, manage and maintain regulatory activities for the assigned Consumer Health portfolio including lifecycle management, license and registration maintenance, submissions, product information updates and promotional compliance
• Prepare, submit and coordinate country‑specific regulatory documentation and approval processes with internal stakeholders and external authorities
• Support and maintain RA IT and lifecycle systems (e.g., DORIS, Synaps, eDAM), ensuring accurate labeling data and statutory text management
• Review and approve promotional materials to ensure full compliance with regulatory requirements and applicable codes of practice
• Monitor, interpret and communicate regulatory intelligence, evaluating impacts for both local and global stakeholders
• Collaborate with cross‑functional teams in Italy and at enterprise level to align national and European regulatory processes and to ensure compliance during products’ lifecycle management
• Contribute independently to operational decision‑making while learning from senior regulatory experts
• Develop and implement local best practices to streamline and enhance regulatory operations
• Broaden regulatory expertise across medicinal products, medical devices, cosmetics and food supplements through hands‑on portfolio engagement

WHO YOU ARE:

• Master’s degree in Life Sciences or a related scientific discipline
• At least 2 years of experience in Regulatory Affairs in Consumer Health/OTC. Experience with food supplements will be a plus.
• Ability to work cross‑functionally and across countries; naturally collaborative and curious
• Strong organizational skills, high attention to detail, and excellent communication abilities
• Creative problem‑solver, able to balance technical rigor with practical business needs
• Exposure to cross‑functional projects (e.g., Marketing, QA, Legal, Supply Chain) and interactions with EU regulatory environments
• Tech‑savvy, with confidence using regulatory databases and digital collaboration tools
• Excellent knowledge of Office, Excel and PowerPoint
• Residence or domicile in Lombardy
• Fluent knowledge of English and Italian mother tongue

Location: Milan

Type of Contract: Permanent