AbCellera is seeking a meticulous Regulatory Submissions Specialist to lead electronic publishing of clinical development submissions. You will format, compile, and ensure compliance across global health authorities, coordinating with internal stakeholders to meet tight timelines.
You’ll apply 5+ years in regulatory operations, a Bachelor’s degree, and strong experience with eCTD, Veeva RIM, submission gateways, and regulatory processes to ensure high-quality submissions and seamless lifecycle
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Global Regulatory Submissions Lead — eCTD & Publishing in Vancouver employer: AbCellera
AbCellera is an exceptional employer that fosters a collaborative and innovative work culture in the vibrant city of Vancouver. With a strong focus on employee growth, we offer numerous opportunities for professional development and advancement within the rapidly evolving field of biologics. Our commitment to meaningful work and cutting-edge projects ensures that you will be part of a team that is making a significant impact in the biopharmaceutical industry.
