Jobs at Resilience (resilience.com).

Administers the site learning management system, maintaining training documents, role assignments, course content, compliance records, and data integrity. Supports audits, regulatory inquiries, SOP assessment submissions, instructional design, training materials, learning events, reporting, and KPI tracking. Collaborates with leaders, quality teams, process owners, and SOP authors to ensure accurate training requirements and effective learning processes. Provides LMS support, guidance, and continuous improvement across the learning community.

Drives new business growth for Resilience’s biologics and drug product CDMO offerings across the West Coast. Responsibilities include prospecting, pipeline development, consultative selling, proposal creation, pricing, contract negotiation, closing, client relationship management, market intelligence, Salesforce reporting, and collaboration with commercial and operational teams. The role requires technical knowledge of biologics and drug product development and manufacturing, including sterile fill/finish, plus up to 50% regional and national travel.

Leads capital and manufacturing projects from initiation through closeout across biomanufacturing sites. Manages scope, schedules, budgets, risks, stakeholders, suppliers, contractors, commissioning, qualification, technology transfer, GMP compliance, and operational handover. Oversees equipment and packaging line installations, utility upgrades, automation integration, construction activities, quality change controls, documentation, and continuous improvement. Provides PMO governance, project reporting, coaching, and cross-functional leadership.

The Senior Analyst, QC Microbiology performs microbiological testing and ensures GMP compliance, authors SOPs, and leads investigations in QC processes.

Performs and coordinates environmental monitoring in classified and non-classified areas up to Grade A at a sterile pharmaceutical manufacturing site. Reviews QC data and documentation for trends and cGMP compliance, schedules sampling workflows, leads investigations and process improvements, and coordinates QC and Operations activities. Trains EM technicians, provides technical guidance, troubleshoots methods, and supports laboratory and manufacturing processes with limited supervision.

Supports supply chain and program management activities, including SAP implementation, procurement, vendor onboarding, inventory management, logistics documentation, data validation, system testing, user acceptance testing, process improvement, and reporting. The intern will help maintain master data, prepare procurement materials, monitor inventory levels, and coordinate cross-functional initiatives during an approximately eight-month placement.

Lead and execute validation activities for automated equipment and GxP computer systems (PLC/SCADA/DCS), authoring IQ/OQ/PQ, ensuring 21 CFR Part 11 and data integrity compliance. Serve as technical advisor, coach junior staff, manage validation lifecycle, resolve complex issues, support audits, and maintain validated state through change control and requalification in a cGMP biomanufacturing environment.

Owns and improves assigned biomanufacturing equipment processes, including process capability, validation, troubleshooting, change control, risk management, and technical documentation. Partners with Manufacturing, Quality, Maintenance, suppliers, and project teams to resolve issues, improve yield and efficiency, manage equipment lifecycle, support regulatory inspections, and deliver projects. Develops training for Operations, Engineering, and Maintenance personnel. The role requires work in a GMP or regulated manufacturing environment and occasional travel.

Lead technical execution of technology transfer and process validation to manufacturing, deliver and maintain capable processes, drive continuous improvement (yield, OEE, reliability), author validation and GMP documentation, support troubleshooting, change control, risk management, supplier collaboration, and act as technical owner for regulatory inspections.

The Automation Engineer II role involves optimizing, validating, and maintaining automation systems in a biomanufacturing setting while collaborating across departments and ensuring compliance.

Lead and manage the site Investigation Team to conduct timely, compliant root cause analyses for deviations and complaints. Set investigation standards, coach staff, author reports, maintain procedures and metrics, align cross-functional partners, drive CAPAs, and promote continuous improvement and regulatory compliance.

Serve as the sole FP&A business partner for the RBI site, owning site P&L, budgeting, forecasting, capital tracking, COGS and batch costing analysis, reporting, ERP migration support, FP&A systems/super-user duties, and financial business partnering to drive accountability and decision-making across manufacturing and site leadership.