European Union Pharmacovigilance Expert
Há 6 dias
Pharmacovigilance Lead Role
Tn Portugal invites applications for a highly skilled Deputy European Union Qualified Person for Pharmacovigilance (m/f/d) to join our Lisbon-based team. As a key member of our Global Patient Safety organization, you will play a critical role in ensuring the safe use of our medicines across Europe and contributing to the advancement of pharmacovigilance expertise within our company. This is a fantastic opportunity to make a meaningful impact on patient safety and shape the future of our organization.
Key Accountabilities:
- Develop and implement comprehensive pharmacovigilance strategies aligned with EU regulatory requirements and company goals.
- Lead cross-functional teams to review and approve EU regulatory submissions, PASS protocols, and actions related to emerging safety concerns.
- Maintain collaborative relationships with regulatory agencies, industry partners, and internal teams to advance shared interests and objectives.
- Drive the development of pharmacovigilance policies, procedures, and guidelines to ensure compliance with EU regulations.
- Stay up-to-date with evolving EU regulatory requirements and apply knowledge to inform business decisions and optimize patient safety outcomes.
Personal Qualities:
We seek a motivated and results-driven individual with a strong track record in pharmacovigilance and excellent leadership skills. The ideal candidate will possess a deep understanding of EU regulatory frameworks, exceptional problem-solving abilities, and the capacity to foster a culture of collaboration and innovation within our organization. If you are a seasoned professional looking for a new challenge, we welcome your application to join our team at Tn Portugal.
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