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.

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📌 International regulatory affairs manager (Aragón)
🏢 SomVital
📍 Aragón