Regeneron
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Recently posted jobs
Biotech • Pharmaceutical
Lead and manage global aggregate safety reporting (PSURs/PBRER, PAER, DSURs, local periodic reports, SUSARs). Oversee planning, production, vendor oversight, regulatory submissions, SOPs, KPIs, and cross-functional collaboration to ensure timely, compliant, high-quality aggregate safety deliverables and drive process improvements and automation.
Biotech • Pharmaceutical
Manage a finance operations accounting team, improve and automate accounting processes, develop process models, track performance metrics, deliver reports/dashboards, and partner with offshore teams to meet close deliverables.
Biotech • Pharmaceutical
The Associate Director will lead international product launches, managing timelines, resources, and stakeholder coordination across teams, while ensuring project delivery aligns with company goals.
Biotech • Pharmaceutical
Lead global pharmacovigilance operations and governance, define global-to-local scope for regional PV hubs, ensure compliance and quality, drive strategic risk insights, embed patient-centered safety, scale teams, and influence cross-functional leaders to align regional and global priorities.
Biotech • Pharmaceutical
The Senior Manager Regulatory Intelligence monitors and interprets global regulatory changes, focusing on EU regulations and pharmacovigilance, while collaborating with cross-functional teams.
Biotech • Pharmaceutical
Manage day-to-day payroll operations across multiple European and Asian countries; review payroll inputs/outputs; oversee reconciliations; lead cross-functional payroll meetings; drive process improvements and SOP updates; support new country payroll implementations; resolve queries and escalations; prioritize to meet payroll deadlines.
Biotech • Pharmaceutical
The Director of Government Affairs Europe will lead public policy activities, manage stakeholder relationships, and align advocacy efforts with Regeneron's business objectives across European healthcare systems.
Biotech • Pharmaceutical
Lead and execute risk-based GCP audit strategy across therapeutic areas and studies, manage audit programs and outcomes, represent QA on cross-functional initiatives, deliver reports and metrics, and collaborate with global stakeholders to ensure regulatory compliance and inspection readiness.
