Regulatory Affairs Specialist

We are growing and looking for a Regulatory Affairs Specialist to join the Regusole team.

About Regusole:

Regusole is a growing Regulatory Affairs service provider helping pharmaceutical companies navigate complex regulatory requirements. From early strategic planning and regulatory submissions to post-approval and lifecycle management, we support our clients throughout the product journey. Our work is built around regulatory excellence, practical solutions and close collaboration with clients across Europe and CIS countries.

Your responsibilities will include:

• Managing regulatory submissions, variations and renewals.

• Preparing and reviewing regulatory documentation.

• Reviewing Product Information, labelling and artwork.

• Communicating with Health Authorities and local partners.

• Monitoring regulatory intelligence and country-specific requirements.

• Supporting other day-to-day regulatory activities throughout the product lifecycle.

For this position, you will need:

• A degree in Pharmacy, Life Sciences or a related field.

• At least 2–3 years of hands-on Regulatory Affairs experience in the pharmaceutical industry.

• The ability to work independently and take responsibility for your projects.

• A curious and solution-oriented mindset.

• The ability to identify practical solutions, not only regulatory challenges.

We offer:

• A salary of EUR 2,800–3,900 gross per month, depending on experience and competencies.

• A fully remote working model - open to candidates based in Europe.

• A full-time position.

• The possibility of freelance collaboration.

• The opportunity to work directly on diverse pharmaceutical regulatory projects.

Please send your CV to info@regusole.com

We look forward to hearing from regulatory professionals who would like to grow together with Regusole.