
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.
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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.
• Provide coordination and operational support to Process Leads and senior GCPM leadership • Support document review and approval workflows • Coordinate document control activities, including QA alignment, DCC activities, and approval tracking • Gather, prepare, tabulate, and organize inputs for Process Lead review and decision-making • Develop, document, and maintain project plans, including status reviews and follow-up • Maintain stakeholder lists, meeting planning materials, and project charter drafts • Support organizational change management activities and prepare draft communications • Compile data from Veeva Vault or equivalent systems for status reporting and process reviews • Prepare and maintain QE CAPA tables and tracking materials • Prepare and analyze GCPM intake-form data for management review, process improvement, and innovation evaluation
• Bachelor’s degree required • 2+ years of experience in pharmaceutical and/or biotechnology sector preferred • Efficient in Microsoft suite (Excel, Outlook, Word, PowerPoint, Project) • Fluent English (oral and written) • Knowledge of ICH-GCP • Excellent interpersonal and problem-solving skills • Excellent organizational skills and a predisposition to quality management and process improvement • Effective oral and written communication skills
• Annual bonus plan eligibility for non-commercial roles • Incentive compensation plan eligibility for commercial roles • Discretionary equity awards • Voluntary participation in the Employee Stock Purchase Plan • Medical insurance • Dental insurance • Vision insurance • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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