Jobs at Aspect Biosystems

Develops, optimizes, qualifies, and validates analytical methods for bioprinted tissue therapeutics. Performs cell-based assays, flow cytometry, ELISA, routine testing, stability studies, data analysis, and technical documentation under GxP requirements. Troubleshoots analytical methods, maintains instruments, supports quality systems, and collaborates with process development, quality control, research, development, and manufacturing teams.

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.

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.

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.