Manager, QPPV Office at Sandoz in India

Manager, QPPV Office Location: Telangana (Sandoz) Job Description Summary Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape! To support the EU-QPPV and Head QPPV Office with activities required to ensure compliance with Guidelines on Good Pharmacovigilance Practices (GVP) and other applicable worldwide PV regulations and to fulfil role requirements as indicated below. Job Description Your Key Responsibilities: Your responsibilities include, but not limited to: Drive PV performance oversight including creation and monitoring metrics, KPI, KQIs for PS and key vendors. Support the development, management and implementation of deviations and associated CAPAs across the Patient Safety organization Support inspection and audit operations, including CAPA development, tracking and management Support the development, implementation and dissemination of PS procedures Support QPPV in meeting legislative requirements as per relevant legislation Writing meeting minutes when required and preparing presentations for allocated areas of work Support other QPPV office Managers when required Any other activities to support the QPPV office as assigned What you’ll bring to the role: Essential Requirements: > five years of pharmacovigilance experience desired (not mandatory), including clinical safety, and closely related areas of development Sound knowledge of global safety and pharmacovigilance regulations worldwide Proven ability to work and handle multiple tasks independently and effectively Ability to lead and deliver cross divisional initiatives Excellent negotiation, conflict resolution, decision making, problem solving, communication (written and verbal) and presentation skills Results driven, self-starter with proactive working style, committed and accountable, transparent working style also under pressure Excellent planning, organizational and computer skills Skills: Clinical safety Employee Training. Pharmacovigilance regulations Project Management. Global safety Safety Science. Why Sandoz? Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more! With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably. Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported! Join us! Skills Desired Databases, Employee Training, Pharmacovigilance, Reporting, Safety Science, Waterfall Project Management