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We are seeking an experienced and strategic Director of Regulatory Operations to lead and oversee global regulatory submission processes, electronic publishing, and regulatory systems management, with a particular focus on Veeva Regulatory Information Management (RIM) systems. This leadership role will drive regulatory submission excellence, process optimization, and system innovation, ensuring the timely execution of regulatory filings across multiple health authorities, including FDA, EMA, Health Canada, MHRA, and other global agencies. The ideal candidate will be a subject matter expert in Veeva RIM, with a strong background in electronic Common Technical Document (eCTD) submissions, global regulatory compliance, and document management best practices. This position is based in our South San Francisco headquarter offices and required to be onsite four days per week per our company policy.