
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
đź’Š 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.
đź•’ February 24
🇺🇸 United States – Remote
đź’µ $204.5k - $274.5k / year
⏰ Full Time
đźź Senior
đźš” Compliance
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10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
đź’Š 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.
• Lead and develop the U.S. Biologics Regulatory CMC team • Provide strategic and operational leadership for global biologics Regulatory CMC strategies • Partner closely with global cross-functional stakeholders on CMC regulatory strategies • Establish and continuously improve Regulatory CMC standard operating procedures (SOPs) • Ensure appropriate Regulatory CMC assessment throughout the product lifecycle • Review and approve Regulatory CMC documentation within the RIM system • Represent the company in external forums and regulatory or scientific conferences
• BA/BS Degree in scientific disciplines, MS/PhD preferred • 12+ years of relevant pharmaceutical or biopharmaceutical experience • At least 10 years of direct Regulatory CMC experience • Demonstrated track record of leading Health Authority interactions • Proven experience leading and developing teams of 10+ or more professionals • Advanced scientific training with hands-on expertise in at least one core pharmaceutical or biologics discipline • In-depth knowledge of ICH guidelines and global Regulatory CMC requirements • Extensive experience authoring, reviewing, and managing complex technical documentation
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
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