Jobs at STEMCELL Technologies

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.

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.

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.

Designs, tests, troubleshoots, and improves analogue and digital electronics for cell-sorting scientific instruments. Responsibilities include sustaining engineering, root-cause investigations, component obsolescence management, PCB design, FPGA and embedded-system support, prototype development, design verification, manufacturing transfer, and compliance with safety, EMC, and regulatory standards. The role collaborates across engineering, manufacturing, quality, service, software, and supply chain teams.

Supports mechanical design, CAD development, prototyping, testing, production troubleshooting, root-cause investigations, technical documentation, and continuous improvement for cell-sorting instruments. Collaborates with R&D, Manufacturing, and Quality teams on product development and compliance activities. Uses SolidWorks to create components and drawings, builds test rigs, analyzes results, and contributes to next-generation instrumentation under senior-engineer mentorship.

Serves as the first point of contact for visitors, managing calls, emails, visitor logs, access badges, parking passes, office supplies, mail, deliveries, and courier packages. Supports Facilities operations by tracking service requests and work orders in JIRA. Provides new-hire assistance by preparing badges and nameplates and maintaining seating charts. The role requires strong organization, customer service, problem-solving, computer, and time-management skills in an onsite, collaborative environment.

Serve as the first point of contact for visitors by managing reception, calls, emails, visitor logs, access badges, parking passes, office supplies, mail, deliveries, and courier packages. Support facilities operations by tracking service requests and work orders in JIRA. Assist with new-hire preparation, including badges, nameplates, and seating charts, while providing organized, responsive customer service.

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.

Lead design control and risk-management activities for instrumentation and single-use consumables used in GMP cell and gene therapy manufacturing and research applications. Review technical and validation documentation, support vendor qualification and design transfer, develop inspection plans, perform incoming and final inspections, and maintain quality metrics. Manage QMS activities including nonconformance investigations, CAPAs, change controls, document management, audits, and factory inspections while ensuring compliance with applicable medical-device, quality, and regulatory standards.

Perform and troubleshoot laboratory experiments to support development and validation of pluripotent stem cell products. Document and analyze data, present findings, contribute to technical documentation and literature reviews, and help maintain R&D lab operations, including equipment, inventory, and training. Weekend availability required.

Manage and grow assigned territory by developing business plans, prospecting new customers, maintaining relationships, providing technical support, preparing quotations, documenting interactions in CRM, and representing STEMCELL at conferences to achieve revenue targets.

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.

Manage and grow key accounts independently by developing long-term revenue strategies, gathering customer intelligence, coordinating internal teams (Sales, R&D, PMs, Scientific Marketing), and serving as an expert liaison to drive product development, licensing opportunities, and effective inventory management.

Lead sustaining engineering and DFM for cell-sorting instruments, managing design changes, supplier technical partnerships, root-cause investigations, and design verification. Collaborate with optics and electronics teams to ensure mechanical designs meet tolerance, stiffness, and thermal stability requirements; design and test precision mechanical, opto-mechanical, and electro-mechanical assemblies using SolidWorks.

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.

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.

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.