Jobs at Resilience (resilience.com).

Manage lifecycle, reliability, and maintenance of PET/Facility assets at a GMP biomanufacturing site. Lead technical troubleshooting, validation, documentation, compliance (EHS/GMP), supplier relations, CAPA/root cause analyses, and engineering support for operations. Supervise and develop engineering/technical staff and support inspection operations.

Lead site-level delivery and support of SAP/ERP and other business applications (R&D, manufacturing, lab, quality). Manage incidents via ServiceNow, drive continuous improvement, support ERP deployments and post-go-live, ensure compliance and security, facilitate audits, and collaborate with global application teams and site stakeholders to prioritize enhancements and training.

The MRO Project Coordinator oversees project activities related to maintenance and spare parts, ensuring timely delivery, documentation compliance, and support for maintenance readiness. The role involves collaboration with engineers, managing inventory, and facilitating audits while adhering to internal quality and safety standards.

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.

Lead technology transfers from feasibility through PPQ and commercial introduction, drive continuous improvement and risk management, author and approve validation and controlled documents, mentor junior engineers, manage technical projects and supplier relationships, and support regulatory inspections in a GMP biomanufacturing environment.

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.

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

The Quality Control Systems Engineer oversees LabVantage LIMS, leading enhancements and validations, ensuring compliance and effective system operations in a regulated environment.

Support QC Microbiology by performing and documenting microbiological testing of raw materials, in-process and finished products, stability, utilities, and environmental samples. Author and review cGMP documentation, participate in investigations and CAPAs, troubleshoot, monitor equipment, coordinate cross-functional and qualification activities, and use CMMS for logistics.

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.

Lead reliability activities for packaging and inspection assets in a cGMP biomanufacturing site: develop reliability strategies, optimize PMs, perform RCAs, manage spare parts and BOMs in SAP/CMMS, support capital projects, ensure GMP compliance, train and mentor staff, and drive continuous improvement and shutdown coordination.

The Supply Chain Analyst I supports supply chain master data activities, assists in documentation and processes, and collaborates with various teams to ensure data accuracy and compliance.