STEMCELL Technologies
Jobs at STEMCELL Technologies
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Biotech
Coordinates recruitment workflows, including onsite interview scheduling, candidate and requisition documentation, communication among hiring stakeholders, and Workday-based recruiting dashboards and reports. Supports the talent team with administrative tasks while maintaining accuracy, organization, deadlines, and a professional candidate experience.
Biotech
Designs, develops, operates, and continuously improves scalable AWS cloud applications, tools, services, and infrastructure. Owns service lifecycles, production troubleshooting, reliability improvements, incident response, and escalated issue resolution. Partners with technology and project teams as a systems subject matter expert while promoting effective operating practices and new technologies. Requires expertise in AWS, cloud infrastructure, automation, infrastructure as code, networking, monitoring, and hybrid connectivity.
Biotech
Leads STEMCELL’s diversity, equity, inclusion, and corporate social responsibility programs. Responsibilities include managing Employee Resource Groups, coordinating global CSR events and sponsorships, overseeing budgets and logistics, driving employee volunteerism and community outreach, developing organization-wide communications, partnering with leadership on DEI policies, and tracking program performance metrics.
Biotech
Partner with HR and business teams to design, evaluate, and administer global compensation programs and job architecture. Maintain the enterprise job-leveling framework, oversee job evaluation and documentation, ensure market competitiveness, and provide compensation guidance and education. Analyze confidential compensation data, advise on organizational design challenges, maintain program governance, and monitor market trends and best practices.
Biotech
Implement, configure, test, and enhance Workday HR system functionality. Lead cross-functional requirements, design, deployment, upgrades, integrations, security, reporting, process redesign, vendor selection, and RFP activities. Manage downstream system impacts, maintain documentation and data quality, identify continuous improvement opportunities, and train stakeholders and end users on new functionality.
Biotech
Lead upstream biologics process development from experimental design through scale-up and technology transfer. Serve as a subject matter expert for cGMP protein manufacturing, analyze experimental data, develop SOPs, investigate non-conformances, support CAPAs, and collaborate with R&D, Quality, Regulatory, and CDMO partners to establish robust, efficient manufacturing workflows.
Biotech
Reviews, drafts, negotiates, and manages contracts while monitoring contractual obligations, identifying commercial risks, supporting renewals and amendments, and coordinating with legal, procurement, finance, suppliers, customers, and business stakeholders across jurisdictions.
Biotech
Design, build, and maintain FP&A planning, forecasting, and reporting solutions using SAP Analytics Cloud and related BI tools. Partner with Finance to translate requirements into scalable SAC models, dashboards, and automation; ensure data integrity, governance, and user adoption through documentation and training; troubleshoot and drive continuous improvements across the FP&A systems ecosystem.
Biotech
Lead SEO, GEO, and PPC strategy and execution to increase brand discoverability across search and generative AI platforms. Manage paid advertising budgets, optimize high-traffic global websites, enable analytics and reporting (Google Ads, Analytics, Search Console, seoClarity), and provide data-driven recommendations to drive measurable inbound marketing outcomes.
Biotech
Lead downstream process development and technology transfer for cGMP protein/antibody production. Create development plans, guide transfers to manufacturing or CDMOs, collaborate with R&D, QC, QA and Regulatory, author process and manufacturing documentation, and support manufacturing campaigns and CAPA/NCR investigations.
Biotech
Lead upstream process development and technology transfer for cGMP protein production. Create development plans, guide transfers to manufacturing/CDMOs, author regulatory and batch documentation, support manufacturing campaigns, and collaborate with R&D, QC, QA, and Regulatory on critical quality attributes and process parameters.
Biotech
Responsible for preparing complex reconciliations, journal entries, and audit-ready schedules across balance sheet, P&L, and cash. Develops management and compliance reports, analyzes financial trends to support forecasting and risk identification, manages period-end close, ensures compliance with accounting standards and tax/regulatory requirements, and leads process improvements.
