Regulatory Submissions Specialist at AbCellera

AbCellera is hiring a Regulatory Submissions Specialist to lead the electronic publishing and validation of clinical development submissions across regional regulatory authorities. The role involves compiling, formatting, quality-checking, version-controlling, and optimizing submissions for authorities including the United States, Canada, Australia, and the European Union. Candidates need at least five years of regulatory operations experience, a bachelor’s degree or equivalent experience, eCTD publishing expertise, and extensive Veeva RIM experience. The position offers a CAD 93,000–116,000 annual base salary plus equity, bonus, RRSP contribution, lifestyle allowance, vacation, professional development, and health benefits.