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. #J-18808-Ljbffr

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