Qualified Person Responsible for Pharmacovigilance (QPPV) in the EU and UK (homebased)

Ergomed · Zagreb, Croatia

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Role summary

Ergomed seeks a Qualified Person Responsible for Pharmacovigilance to establish and maintain adverse reaction reporting systems, ensure regulatory compliance, and oversee medicinal product safety profiles across the EU and UK from a home-based position.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on SmartRecruiters, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-03). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Life-science education background; medicine or pharmacy degree preferred
Solid knowledge of pharmacovigilance system operations and regulatory functions
Strong knowledge of global regulations and post-marketing pharmaceutical compliance
Proven leadership and project management experience
Extensive pharmacovigilance experience with prior QPPV role
Fluent oral and written English communication skills

What you'll be doing

Establish and maintain systems to collect and collate adverse reaction reports from company personnel and medical representatives
Respond fully and promptly to competent authority requests for product benefit-risk evaluation information
Provide regulatory authorities with relevant safety information and post-authorisation study data
Maintain continuous availability to regulatory agencies and ensure adequate backup procedures
Oversee safety aspects of medicinal products and monitor emerging safety concerns

Privacy & handoff

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What RoleLantern checked

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RoleLantern checked active

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Date posted2 days ago

Last source check1 day ago

Salary listedNeeds clarity

Location clearClear

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