We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.
PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and becoming one of the global leaders in its fields. We cover all therapy areas including medical devices.
We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.
Come and join us in this exciting journey to make a positive impact in patient’s lives.
The EU QPPV is responsible for:
Why PrimeVigilance?
We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.
To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.
We offer:
Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!
We look forward to welcoming your application.
Gerencia registros, renovações e pós-registros de medicamentos em mercados internacionais, coordenando dossiês e estratégias de submissão, avaliando mudanças regulatórias e apoiando inspeções, lançamentos e projetos de internacionalização.
Leads transit safety and security project tasks for U.S. clients, applying FTA processes and APTA standards to develop safety plans, assess hazards, guide teams, and deliver reviews and training.
Own the end-to-end food safety and quality program for shelf-stable seafood, including HACCP and regulatory compliance, supplier oversight, lot-release decisions, recall readiness, audits, and scalable quality systems.
Independently manages complex industry-sponsored research agreements from drafting and negotiation through execution, balancing legal, financial, and regulatory needs while protecting institutional interests and supporting research.
Execute and operate compliance programs across SOC 2, ISO certifications, and FedRAMP, owning audit delivery, control monitoring, vendor risk, customer security assurance, and compliance automation.
