On-site position based in Zaragoza, Spain.

Recuerde revisar su CV antes de enviar la solicitud. Además, asegúrese de leer todos los requisitos relacionados con este puesto.

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- 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:

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- 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:

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- 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:

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- 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. xghoner

- 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