This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Senior Manager QPPV Office based remotely in India.

We are seeking an experienced pharmacovigilance professional to support the oversight and coordination of Qualified Person Responsible for Pharmacovigilance (QPPV) office activities. In this role, you will help ensure the timely preparation of authority-relevant documentation and maintain effective processes for Pharmacovigilance Agreements (PVAs). You will contribute to the development of standardised templates, project-specific documents, and robust operational procedures that support regulatory compliance and quality. Working at the intersection of drug safety, regulatory affairs, and process governance, you will collaborate with relevant stakeholders to maintain consistency and efficiency across global pharmacovigilance activities. This opportunity is suited to a detail-oriented professional with solid coordination skills, sound regulatory knowledge, and a commitment to patient safety.



Your work will help strengthen pharmacovigilance oversight and support the safe use of medicines across international markets.

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Accountabilities

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Oversee and coordinate the timely preparation of documentation relevant to health authorities and pharmacovigilance requirements.

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Act as the process owner for Pharmacovigilance Agreement (PVA) management, supporting consistent and effective agreement-related processes.

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Coordinate global pharmacovigilance activities related to PVA management, ensuring appropriate oversight and alignment with applicable requirements.

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Conceptualise, develop, and maintain standardised templates, project-specific documentation, and operational processes.

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Support the continuous improvement and consistency of QPPV office procedures and documentation practices.

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Collaborate with cross-functional stakeholders to facilitate the preparation, review, coordination,

📌 Senior Manager QPPV Office (India)
🏢 Jobgether
📍 India