Regulatory & PV Manager — Veterinary Medicines (Poland)

Phibro Animal Health Europe; Województwo mazowieckie; On-site; PLN 211,000 - 296,000; Full time

Job summary

A global animal health company is seeking a Regulatory Affairs Manager in Poland, responsible for managing regulatory activities, ensuring compliance, and acting as Pharmacovigilance Local Representative. Applicants should have a DVM or pharmacist qualification, at least 3 years’ experience in the pharmaceutical field, and be fluent in English. This full-time role offers a diverse work environment and the opportunity to contribute to animal health solutions.

Benefits

Competitive benefits package

Qualifications

• At least 3 years’ experience in a multinational pharmaceutical company or similar position.
• Computer literate, including Teams.
• Experience working in culturally diverse teams.

Responsibilities

• Manage local and EU regulatory activities and liaise with authorities/distributors.
• Prepare VNRA/VRA/MAA submissions and track progress with Global Vaccines RA.
• Ensure GDP compliance and oversee Quality System.

Skills

Fluent in written and spoken English

Planning skills and detail orientation

Strong accountability and results oriented

Business acumen and project management skills

Experience working in culturally diverse teams

Education

DVM or pharmacist

Postgraduate regulatory affairs course (e.g. TOPRA)

Tools

MS Office

Job description

A global animal health company is seeking a Regulatory Affairs Manager in Poland, responsible for managing regulatory activities, ensuring compliance, and acting as Pharmacovigilance Local Representative. Applicants should have a DVM or pharmacist qualification, at least 3 years’ experience in the pharmaceutical field, and be fluent in English. This full-time role offers a diverse work environment and the opportunity to contribute to animal health solutions.