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Global CMC Regulatory Affairs Program Lead

Gilead Sciences, San Francisco, California, United States, 94199

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A global biopharmaceutical company is seeking a CMC Regulatory Affairs Project Manager in San Francisco, California. The role involves coordinating regulatory activities for global programs, managing project timelines, and ensuring compliance with submission standards. A Bachelor’s degree and 4–6 years of experience in regulatory affairs or project management is required. Strong problem-solving and communication skills, along with experience with project management tools, are essential. This position offers a competitive salary between $157,590.00 - $203,940.00, plus bonuses and benefits. #J-18808-Ljbffr