Pharmacovigilance role available to lead GxP audits and quality tasks globally
About the Job
We are looking for a Pharmacovigilance specialist to perform remote and onsite audits of affiliates, external collaborators, service providers, and distributors. This is an exciting opportunity to join our team and work on quality management systems and tools.
Responsibilities
1. Plan, conduct, and report GVP audits
2. Audit CAPA follow-up
3. Risk management and tools
4. Document Management
5. Conduct stakeholder meetings
Requirements
* Bachelor's/Master's degree in Health Science with 5+ years of experience in pharmacovigilance regulated areas
* Strong quality mindset with commitment to maintaining high standards in all quality-related processes
* Excellent cross-cultural communication skills in Danish and English
What We Offer
We offer a dynamic working environment that fosters personal and professional growth. As a global pharmaceutical company, we value professionalism, integrity, and collaboration. You will be part of a committed and enthusiastic team who values skill and knowledge creation.
This is a full-time position with opportunities for flexible working arrangements. We encourage you to apply by attaching your CV and a short letter of motivation.