
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.
đ February 24
đşđ¸ United States â Remote
đľ $204.5k - $274.5k / year
â° Full Time
đ Senior
đ Compliance
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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.
⢠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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