BeOne Medicines
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
💊 Pharmaceuticals
Biotechnology • Healthcare • Pharmaceuticals
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge Management
🕒 June 2
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BeOne Medicines
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
💊 Pharmaceuticals
Biotechnology • Healthcare • Pharmaceuticals
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting the development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
📋 Description
• Managing assigned escalated GxP and Quality incidents in an end-to-end process on global level • Initiating GxP/Quality incident prevention measures • Maintaining (incl continuous improvement) of defined incident management related processes within regulated environments on global level • Leading and overseeing that quality incidents are managed effectively • Ensuring compliance with regulatory requirements (e.g., ICH Q9) • Building and growing the knowledge management processes and tools to enable rapid access to data and knowledge over the entire product lifecycle
🎯 Requirements
• Bachelor’s degree and 8+ years of experience in quality sciences, quality systems, or related fields within a regulated industry (e.g., pharmaceuticals, biotechnology, medical devices) • Master’s degree and 10+ years direct experience preferred • 6 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint) • Experience with regulatory interactions including notification and communication with health authorities on global level for sensitive compliance topics
🏖️ Benefits
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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