Jobs at Resilience (resilience.com).

Lead full-cycle recruiting for a biotech manufacturing company: design search strategies, partner with hiring teams, source and close candidates across levels, improve processes using metrics, and ensure an equitable candidate experience. Act as trusted advisor to senior leaders and cross-functional stakeholders.

Supervise QC Microbiology team to ensure timely, compliant execution of microbiological testing (endotoxin, bioburden, sterility, microbial ID) and environmental monitoring. Oversee equipment qualification, documentation, deviations/CAPAs, SOPs, training, and support regulatory inspections while managing staffing, resources, and GMP compliance.

Perform GMP microbiology testing (LAL/endotoxin, bioburden, sterility, microbial ID), environmental monitoring, data analysis, and equipment maintenance. Lead investigations, author SOPs and reports, drive change control and CAPAs, and mentor junior analysts. Support validation media fill training and maintain required certifications and gown qualifications. Work in classified and non-classified cleanroom environments following aseptic technique and cGMP.

Lead night-shift environmental monitoring and aseptic control activities for a biomanufacturing site. Manage and train a team of leads and technicians, ensure cGMP and regulatory compliance, review production and lab documentation, drive investigations, trending, EMPQ updates, process improvements, and ensure employee safety and training across 24/7 operations.

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.

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 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.

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.

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.

The Reliability Engineer III is responsible for developing reliability strategies, optimizing maintenance plans, performing RCA, and collaborating across departments to ensure effective asset management in a biomanufacturing environment.