
10,000+ employees
Founded 2010
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 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.
🔥 5 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

10,000+ employees
Founded 2010
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 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.
• Developing, implementing, and advising on global regulatory strategies for development programs • Manage regulatory aspects of compounds through all phases of development • Provide leadership and strategic regulatory oversight for designated projects • Develop the global strategy for interaction with Health Authorities • Interface with business partners regarding development, regulatory, and registration strategies • Recruit, develop, manage and mentor regulatory professionals
• BA/BS Degree with 14 plus years of experience in the biotechnical or pharmaceutical industry • A minimum of 10 years’ experience in a Regulatory capacity • Broad background in a Regulatory capacity • MA/MS/MBA with 10 plus years of overall and Regulatory experience preferred • Experience working as a lead in Regulatory Affairs across two or more major geographic areas • Prior experience with both small molecules and biologics preferred • Thorough understanding of drug development process and the pharmaceutical industry • Excellent interpersonal, oral and written communication skills • Ability to analyze and convey complex issues effectively
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
Apply Now🔥 41 minutes ago
Internal Audit Manager overseeing enterprise SOX compliance and governance framework for AI technology company. Collaborating cross-functionally and ensuring sound financial controls throughout the organization.
🇺🇸 United States – Remote
💵 $135k - $250k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🚔 Compliance
🦅 H1B Visa Sponsor
🔥 52 minutes ago
Manager, United States Regulatory Lead focusing on regulatory strategy in General Medicine for Amgen. Delivering U.S. regulatory executions to enable clinical trials and maintaining compliance.
🇺🇸 United States – Remote
💵 $112.7k - $152.5k / year
💰 $28.5G Post-IPO Debt on 2022-12
⏰ Full Time
🟡 Mid-level
🟠 Senior
🚔 Compliance
🦅 H1B Visa Sponsor
🔥 53 minutes ago
1 - 10
Environmental Compliance Practitioner providing expertise in environmental permitting and compliance auditing for Geosyntec's diverse client base. Joining a dynamic team with a focus on environmental solutions.
🔥 5 hours ago
Enhanced Compliance Consultant offering consulting services on compliance matters for financial services. Collaborating with advisory firms to manage regulatory obligations and mitigate risks.
🔥 6 hours ago
Supporting Mitsubishi Motors' regulatory compliance for vehicle safety. Managing coordination and communication with various stakeholders in the automotive safety domain.