Pharmacovigilance Quality & Compliance Manager
Sanofi
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This role on the market
15 open pharmacovigilance roles across 8 companies are on ApplySarthi right now, most of them in Hyderabad (2).
- Patient Safety and Pharmacovigilance SpecialistJobgether
- Associate Director DDIT Development in Patience Safety and Pharmacovigilance Business AnalyticsNovartis
- Gestionnaire principal(e), Pharmacovigilance et sécurité des médicaments/ Senior Manager, Pharmacovigilance & Drug SafetyMckesson
- Pharmacovigilance InternRoche
- Sr Assoc Pharmacovigilance OperationsAmgen · hyderabad
What pharmacovigilance roles keep asking for: Excel (27%), Stakeholder management (13%) — counted across their open postings here.
Sanofi has 1,469 open roles listed here.
- Master Data Managerhyderabad
- Order to Serve (O2S) Protege (Mandarin Speaker)
- Project manager - Project Management Serviceshyderabad
- Chemical technician II
- Maintenance Planner
Counted across 14 company job boards, updated as roles open and close.
Preparing for this interview
Interviews for pharmacovigilance roles keep coming back to Excel, Stakeholder management. Practise those questions before you sit with Sanofi.
Questions you are likely to be asked
- Why do you want to join Sanofi?
- Where do you want to be in three years?
- What is a weakness you are working on, and how?
- Tell me about yourself, and why this role is the right next step.
- Tell me about a problem you solved at work that you are proud of.
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Practise the Pharmacovigilance Quality & Compliance Manager at Sanofi interview free →Job title: Pharmacovigilance Quality & Compliance Manager Location: Tokyo ---------------- Job role Fulfill responsibility that processes to comply with local PV regulations and the global procedures are implemented, documented and followed locally (QD management, self-inspection, etc.) Fulfill responsibility on creation and revision of SDEA, PV contract for safety information exchange and/or GVP and non-GVP agreement. Serves as a consultant/advisor GPV contracts serving Japan PV business. Fulfil responsibility on storage including document transfer at a transfer of approval. Window person of document management in Japan PV. Take control Audit and Inspection and its preparation. Coordination of GVP inspection and GxP Audit. Hard knowledge and experience about Audit/Inspection. Fulfill responsibility to lead Quality in J-PSPV by conducting “self-inspection”, “Change Management, and “Deviation Management /CAPA implementation” . Understand the Global Quality process and implement it to Japan considering local regulation. Within Japan organization, to be a window person of training about general topic and local regulation for safety mutters. Keep communication to global training leader and implement to Japan. Leader of Japan GVP training program. Personal requirements Ability to create and implement appropriate safety processes from quality and compliance standpoint. High level of coordination, communication and negotiation skills. Solid knowledge of audit/inspection, experience with Japan GVP. Commitment and ethical standard to fulfill responsibility in keeping SaKK in compliance with both global and local PV regulatory obligations Pursue progress , discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !
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Listed on workday · posted 2026-10-26. ApplySarthi collects openings and links to application pages; the role is advertised by Sanofi, not by us.