Jobs at Aspect Biosystems

Supports procurement, logistics, and supply chain operations across company locations. Responsibilities include purchase order creation, requisition processing, vendor and ERP data management, shipment scheduling and tracking, customs documentation, inventory transactions, invoice matching, recordkeeping, and cross-functional operational support. The role also provides reception and delivery support at the Vancouver office.

Support and strengthen GMP quality assurance programs for bioprinted cell therapies. Responsibilities include QMS implementation, document control, training, change management, vendor qualification, investigations, CAPA, batch record review, raw material approval, equipment qualification, risk assessments, and collaboration with R&D, CMC, and QC teams.

Supports manufacturing and process development of bioprinted tissue therapeutics for GMP and research goals. Responsibilities include preparing materials, optimizing and scaling processes, maintaining bioprinting equipment, executing qualification studies, analyzing process data, collaborating with R&D, CMC, quality, and regulatory teams, and creating controlled documentation such as SOPs and batch production records.

Lead development and characterization of aseptic cell therapy manufacturing workflows, including fluidic systems, bioreactor scaling, automated cell processing, risk assessments, mathematical modeling, and DOE. Support technology transfer, process qualification, validation, clinical manufacturing, troubleshooting, deviations, regulatory filings, and patentable process improvements. Mentor colleagues and promote rigorous, data-driven technical decision-making.

Supports development and characterization of aseptic biomanufacturing workflows for bioprinted tissue therapeutics. Responsibilities include fluidic and bioreactor system development, automated cell processing, risk assessments, DOE and process modeling, technology transfer, qualification, troubleshooting, deviation investigations, validation support, and regulatory documentation. The role collaborates across process development, bioengineering, engineering, and manufacturing teams to improve cell therapy yield, purity, robustness, and scalability.

Lead and scale the QA organization and GxP compliance for bioprinted tissue therapeutics. Establish a phase-appropriate GMP QMS, oversee Document Control, CAPA, deviations, inspection readiness, regulatory interactions (FDA/EMA/Health Canada), QA oversight of GMP cell manufacturing, support QC and data integrity, and author/review quality sections for regulatory submissions.

Manage and scale corporate IT infrastructure for a clinical-stage biotech, securing Google Workspace, networks, endpoints and IDS, governing IT assets and vendors, driving safe AI use, enforcing cybersecurity posture, and providing technical support and documentation to enable secure, high-performing tools and processes.

Manage and improve a centralized project management system for technical operations in biotech. Support planning, tracking, reporting, risk identification/mitigation, cross-functional coordination, meeting facilitation, and development of decision-support materials and dashboards to drive progress toward clinical development milestones.

Design and run in vitro and ex vivo vascularization studies for bioprinted tissues, optimize vascular and immune-related assays (flow cytometry, imaging, immunostaining, multiplex cytokine analysis), analyze datasets with computational teams, integrate vascularization insights into product design, maintain ELNs/SOPs, and support regulatory and IP deliverables.

Develop, optimize, and qualify bioanalytical methods (ddPCR, qPCR, flow cytometry, ELISA, cell-based assays) to characterize bioprinted tissue therapeutics. Execute and troubleshoot assays, perform routine testing, author SOPs/protocols/reports, ensure GxP compliance, maintain instruments, and work cross-functionally to support product characterization and clinical readiness.