International Regulatory Affairs Manager
- Zaragoza (Spain)
- Regulatory Affairs
- On-site
Key responsibilities
- Plan, coordinate and manage product registration processes in international markets.
- Prepare and manage the technical dossiers and regulatory documentation required to obtain product registrations and marketing authorisations.
- Coordinate regulatory procedures with international distributors, external consultants and competent authorities.
- Analyse the specific regulatory requirements of each country and ensure compliance with applicable legislation.
- Manage and monitor existing registrations, including renewals, variations and regulatory maintenance.
- Work closely with the R&D&I, Quality, Production and Sales departments to ensure the accuracy and regulatory compliance of technical documentation.
- Set priorities, manage registration deadlines and schedules, monitor regulatory changes and optimise internal regulatory processes.
Candidate profile
- University degree in Veterinary Medicine, Pharmacy, Chemistry, Biology, Biotechnology or a related field.
- Previous experience in Regulatory Affairs, preferably in the international registration of products in the livestock, veterinary, biocides or animal nutrition sectors.
- Solid knowledge of product registration procedures, technical dossier preparation and regulatory documentation management.
- High level of spoken and written English, essential for communication in international environments.
- Strong organisational and planning skills, with the ability to manage multiple projects in different markets simultaneously.
- Autonomy, results orientation, attention to detail and excellent communication skills.
Highly valued
- Experience in registering biocides, disinfectants, feed additives and animal health products.
- Knowledge of the regulatory requirements of markets in Latin America, Asia, Africa and the Middle East.
- Experience dealing directly with international distributors and regulatory authorities.
- Knowledge of other languages, especially French.
What we offer
- Working arrangement: on-site.
- Working hours: Monday to Thursday, 8:00 am to 5:00 pm, and Friday, 8:00 am to 3:00 pm.
- Summer hours (July and August): 8:00 am to 3:00 pm.
- A stable, collaborative and professional working environment, with real opportunities for professional development and growth.
- Direct involvement in international projects and in SomVital’s expansion into new markets.
- A role with autonomy, responsibility and the opportunity to make a significant contribution to the company’s growth.
Apply now and become part of SomVital.
#ABetterTomorrow