Experteer Overview

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In this global Pharmacovigilance QA leadership role, you will shape quality and compliance across Pharmacovigilance and Device Vigilance to support patient safety at Novartis. You will influence strategic quality decisions, drive continuous improvement, and ensure inspection readiness in a complex, multinational setting. You will partner with cross-functional stakeholders to mitigate compliance risks and oversee quality activities during transactions and system integrations.

This opportunity offers high visibility, impactful problem solving, and a chance to advance global health by strengthening safety systems.

Compensaciones / Incentivos

- Lead quality oversight of global Pharmacovigilance and Device Vigilance activities to ensure regulatory compliance
- Drive quality improvement initiatives that strengthen compliance, efficiency, and operational excellence
- Identify compliance risks and provide mitigation recommendations to Patient Safety stakeholders
- Support due diligence activities for product acquisitions and business development opportunities
- Lead quality activities supporting mergers, acquisitions, divestments, and system integrations




- Support maintenance of the Pharmacovigilance System Master File and related quality systems
- Guide complex investigations, corrective actions, and preventive action plans to resolution
- Support health authority inspections, inspection readiness activities, and remediation efforts
- Provide quality governance and oversight for global pharmacovigilance operational vendors
- Deputize for the Team Head, providing leadership support and ensuring continuity of critical quality activities

Responsabilidades

- Degree in Life Sciences or a related scientific discipline
- Excellent written and verbal communication skills in English
- Fluency in at least one additional language
- Significant experience in pharmacovigilance quality, pharmacovigilance xugodme operations, or pharmaceutical compliance
- Strong knowledge of global pharmacovigilance regulations, guidelines, and quality requirements
- Proven ability to manage complex compliance issues and drive effective resolutions
- Demonstrated leadership skills with success in cross-functional and global environments
- Quality-focused mindset with strong problem-solving, decision-making, and prioritization capabilities

Requisitos principales

- flexible and hybrid working options
- minimum 14 weeks paid parental leave
- insurance plans
- retirement plans
- wellbeing resources
- bonus and long-term equity awards

📌 Associate Director, Pharmacovigilance QA (Barcelona)
🏢 Novartis
📍 Barcelona