On-site position based in Zaragoza, Spain. Plan, coordinate and manage product registration processes across international markets.

Prepare and manage technical dossiers and regulatory documentation required to obtain product registrations and authorisations.

Coordinate regulatory procedures with international distributors, external consultants and competent regulatory authorities.

Assess country-specific regulatory requirements and ensure compliance with applicable legislation.

Manage and monitor existing registrations, including renewals, variations and ongoing regulatory maintenance.

Work closely with R&D;, Quality, Production and Commercial departments to ensure the accuracy and compliance of technical documentation.

Set priorities, monitor deadlines and registration timelines, track regulatory changes and optimise internal regulatory processes.

Candidate Profile:

University degree in Veterinary Medicine, Pharmacy, Chemistry, Biology, Biotechnology or a related discipline.

Previous experience in Regulatory Affairs, preferably involving international product registrations within the livestock, veterinary, biocides or animal nutrition sectors.

Sound knowledge of product registration procedures, technical dossier preparation and regulatory documentation management.

High level of English , both written and spoken, essential for international communication.

Strong organisational and planning skills, with the ability to manage multiple projects across different markets simultaneously.

Ability to work independently, results-oriented mindset, attention to detail and excellent communication skills.

The following will be considered an advantage:

Experience in the registration of biocides, disinfectants, animal feed additives and animal health-related products.

Knowledge of regulatory requirements in Latin America, Asia, Africa and the Middle East.

Experience working directly with international distributors and regulatory authorities.

Knowledge of additional languages, particularly French.

What We Offer:

Working arrangement: On-site.

Working hours: Monday to Thursday, 8:00 am–5:00 pm, and Friday, 8:00 am–3:00 pm.

Summer working hours (July and August): 8:00 am–3:00 pm.

A stable, collaborative and professional working environment with genuine opportunities for career development.

Direct involvement in international projects and SomVital's expansion into new markets.

A position offering autonomy, responsibility and the opportunity to make a meaningful contribution to the company's growth.

📌 International Regulatory Affairs Manager (Zaragoza)
🏢 SomVital
📍 Zaragoza