Teams at Natera

Supports quality operations under supervision by collecting metrics, administering CAPAs, deviations, SCARs, complaints, and NCRs, reviewing documents, tracking qualification and training records, coordinating eQMS access, and assisting with audit preparation and logistics. The role provides exposure to FDA, ISO 13485, CLIA, and CAP requirements in a regulated biotech and diagnostics environment.

Deploys, optimizes, troubleshoots, repairs, and supports laboratory automation systems, including liquid handlers, workcells, and analytical instruments. Leads medium-complexity engineering and continuous-improvement projects, supports verification and performance qualification, drafts SOPs, and provides production floor support. Collaborates with Production, R&D, Quality, Service Engineering, and vendors while maintaining documentation, change control, safety, and regulatory compliance.

Plans demand, production capacity, raw materials, work orders, and inventory for manufactured and purchased parts. Coordinates with production, purchasing, quality, R&D, laboratory, and product development teams to achieve milestones, maintain accurate ERP and planning master data, support new product introductions, and optimize supply strategies. Analyzes supply and demand trends, reduces excess and obsolete inventory, manages work-in-process, and replans schedules to meet manufacturing and marketing requirements.