Junior Regulatory Affair Officer

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Location: Zagreb, Croatia

Would you like to start or further develop your career in Regulatory Affairs and help ensure that medicines reach patients in line with the highest regulatory and quality standards? We are looking for a motivated and detail-oriented Junior Regulatory Affairs Officer to join our team in Croatia.

In this role, you will support local regulatory activities throughout the product lifecycle, working closely with experienced colleagues and local and global cross-functional teams. You will contribute to timely submissions, accurate product information, and compliance with Croatian, European, and company requirements.

Key responsibilities

• Support the preparation, submission, and follow-up of regulatory documentation for new registrations, variations, renewals, and product maintenance activities.
• Maintain regulatory databases, submission records, approvals, and correspondence in accordance with local procedures and company standards.
• Assist with local labelling, packaging materials, product information, and implementation of approved changes.
• Track regulatory changes, gather regulatory intelligence and translate it into practical guidance for colleagues
• Support communication with competent authorities and respond to requests in cooperation with senior colleagues.
• collaborate with cross-functional teams, and contribute to pharmacovigilance activities and quality/recall actions
• Contribute to inspections, audits, SOP updates, training, and continuous improvement of regulatory processes

What we are looking for

• University degree in pharmacy
• Initial experience or a strong interest in Regulatory Affairs within the pharmaceutical industry.
• Basic understanding of Croatian and European pharmaceutical regulations is an advantage.
• Strong attention to detail, organisational skills, and the ability to manage documentation accurately.
• Clear written and verbal communication skills.
• Good command of English and confidence using standard digital tools.
• A collaborative, responsible, and proactive approach, with a willingness to learn and develop.

Why join us?

This is an opportunity to build your Regulatory Affairs expertise in a supportive and collaborative environment. You will gain exposure to varied regulatory activities, learn from experienced colleagues, and contribute to work that supports compliant operations and timely access to medicines for patients.

Interested?

If you are motivated to grow your career in Regulatory Affairs and contribute through accurate, high-quality work, we would be pleased to hear from you. Apply via LinkedIn and join us in helping make a meaningful difference for patients.

Whatever your area of expertise, your work within the Servier Group helps advance therapeutic progress for the benefit of patients. You will be part of teams recognised for their scientific excellence and reach your full potential in a professional environment that encourages you to develop yourself. Tailor-made onboarding journeys, mobility opportunities, quality trainings, responsible management, team spirit... All this and more in a workplace focused on your well-being.

At Servier, we are committed to therapeutic progress to serve patient needs. We put the diversity of our employees as a source of richness for the fulfillment of this vocation.