International Regulatory Affairs Manager
Hace 1 día
Zaragoza, Aragon, España
SOMVITAL
Jornada completa
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Before you read on: If you are interested in this opportunity, please send your CV to talento@somvital.com, stating “International Regulatory Affairs Manager” in the email subject line. This is an on-site position based in Zaragoza, Spain.
🎯Key Responsabilities
• 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. Apply now and become part of SomVital. #ABetterTomorrow
• 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. Apply now and become part of SomVital. #ABetterTomorrow