Experteer Overview
In this role, you will support pharmacovigilance quality across the company, driving audits and ensuring regulatory readiness. You work with cross-functional teams to uphold GxP standards and align on compliance in PV activities. You shape audit outcomes, contribute to inspections, and help develop training materials to raise quality awareness. This position offers global exposure and the chance to impact patient safety through rigorous QA practices. Join a mission-driven, collaborative environment focused on safety and continuous improvement.
Retribuzione / Benefits
* Lead planning, execution and reporting of Pharmacovigilance routine audits
* Support non-routine pharmacovigilance audits of activities, data, facilities and processes in GxP areas
* Participate in projects or teams as assigned by supervisor
* Support regulatory inspections in various roles
* Assist in preparing training material if requested
* Provide consultation to business partners on routine tasks with occasional supervision
* Collaborate with partners to address compliance inquiries and ensure a unified departmental position
Responsabilità
* Bachelor's or equivalent degree; focused in natural/biological sciences
* Strong verbal and written communication skills; presentation abilities
* Strong xrdztoy teamwork and analytical skills; ability to work in a collaborative team
* Fluency in English
* Travel 10%-30% domestically and internationally
* Preferred: 2+ years in a GVP-regulated environment with PV experience
Requisiti fondamentali
* annual bonus with target
* vacation days
* parental leave
* bereavement leave
* well-being reimbursement
* insurance plans
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