Regulatory Affairs and Pharmacovigilance Officer at Vetoquinol

Niel, Antwerp, Belgium -

Full Time

Start Date

Immediate

Expiry Date

25 May, 26

Salary

0.0

Posted On

24 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Affairs, Pharmacovigilance, Compliance, Animal Health, Regulatory Reporting, Lifecycle Management, Deontology, Transparency, Quality Assurance, Audits, Training, Stakeholder Management, Dutch, French, English, Continuous Improvement

Industry

Pharmaceutical Manufacturing

Description

Company Description Belgium – Netherlands – Scandinavia Are you a science-driven professional with strong regulatory expertise and a passion for compliance and animal health? Then you may be the Regulatory Affairs & Pharmacovigilance Officer we are looking for ! Who we are We are Vetoquinol BeNeSca (Belgium, Netherlands & Scandinavia), a top‑10 global player in the animal health industry, with the heart and warmth of a family-owned company. Our mission is to improve the lives of pets, their owners and the veterinary teams who care for them. We innovate, we collaborate, and we deliver meaningful value. And you can play a key role in this mission. Job Description In this key position, you ensure the safety, compliance and integrity of Vetoquinol’s products across BeNeSca. You act as the Regional Responsible Person for Pharmacovigilance and play an essential role in Regulatory Affairs, Deontology & Transparency, and Quality Assurance support. Pharmacovigilance (PV) Act as the Local/Regional Responsible Person for Pharmacovigilance (LRRP). Manage and continuously improve the pharmacovigilance system in line with EU and national regulations. Collect, assess, and report adverse events within regulatory timelines, manage PV deviations and if necessary implement corrective and preventive actions. Prepare for and participate in authority inspections and internal PV audits. Deliver PV training to internal teams and third parties. Ensure PV agreements or clauses are in place with all relevant stakeholders. Regulatory Affairs : Regulatory Compliance & Lifecycle Management Ensure compliance with national regulatory requirements. Manage the lifecycle of authorised veterinary medicinal products. Prepare, review and update product information, labelling and regulatory documents. Support new marketing authorisation applications and review promotional materials for regulatory compliance. Translate regulatory documents and package leaflets where required. Deontology & Transparency Provide advice and approvals on gifts, sponsorships and benefits for veterinary healthcare professionals. Oversee accuracy of published product information on platforms such as pharma.be, FIDIN, Vetindex, company website. Prepare and submit annual transparency declarations. Quality Assurance (Back-up Responsible Person) In absence of the acting Responsible Person you will take on some of their responsibilities, such as: supporting recalls, handling customer complaints, CAPA management and documentation. Qualifications You thrive in a scientific, regulatory and quality‑driven environment and enjoy working with multiple stakeholders. You bring: A Master’s degree in veterinary science, pharmacy or biology. Fluency in Dutch, French and English. Strong communication skills and customer‑focused mindset. High technical and professional knowledge standards. Ability to work independently, adapt quickly and deliver high‑quality results. A continuous improvement mindset and strong service orientation. Additional Information Why you will love working with us At Vetoquinol, you will find: A supportive and collaborative international environment. Opportunities to develop advanced expertise in pharmacovigilance, regulatory affairs, deontology and quality assurance. A global business with a warm, people-first culture A meaningful role contributing to veterinary product safety and compliance. Competitive salary and strong benefits Hybrid working and a pet-friendly office (yes, pets are welcome in our office in Niel 🐾) Apply now by reaching out to our HR Manager Sandra Cannaerts via [email protected] or +32 496 59 30 31.

Responsibilities

This role ensures the safety, compliance, and integrity of Vetoquinol’s products across BeNeSca, acting as the Regional Responsible Person for Pharmacovigilance and supporting Regulatory Affairs, Deontology & Transparency, and Quality Assurance functions. Key duties include managing the PV system, handling adverse event reporting, managing product lifecycles, ensuring regulatory compliance, and advising on transparency matters.