Search the 8 jobs at Resilience (resilience.com).

The Automation Engineer III will lead engineering activities in manufacturing operations, ensuring effective use and maintenance of automation systems. Responsibilities include collaboration with teams, process improvement initiatives, technical troubleshooting, document authoring, and support for regulatory inspections.

The MSAT Process Engineer IV is the technical expert responsible for executing and improving product and process technology transfers at the manufacturing site. Key duties include overseeing visual inspection processes and leading continuous improvement efforts. The role involves collaboration with various departments to ensure successful implementation and validation of processes in compliance with corporate standards.

The Senior Associate in Upstream MSAT will act as a technical expert in upstream process manufacturing for biopharmaceuticals, focusing on process design, GMP documentation, and equipment qualification. Responsibilities include leading manufacturing projects, troubleshooting processes, and supporting continuous improvement initiatives while ensuring compliance with industry standards.

The Associate II, Quality Assurance position involves supporting QA activities for process execution, including batch release, documentation, equipment validation, and supplier management. The role requires collaboration with quality professionals, compliance with regulatory standards, and participation in continuous improvement processes. Training is provided to develop skills in all responsibilities of the role.

The PI Historian Analyst will support and enhance data historian systems in a biomanufacturing environment, collaborating with manufacturing teams to improve data integrity and visualization. Responsibilities include architectural design, troubleshooting, training, documentation, and ensuring compliance with regulatory standards.

The Senior Analyst II, Quality Control (Potency) ensures compliance in testing lentiviral vector and CAR-T products, designs method qualifications and validations, investigates anomalies, and mentors junior staff. This role collaborates with various teams to meet organizational testing needs while adhering to cGMP standards.

The Automation Engineer II leads and advises on automation projects at the West Chester Site, collaborating with cross-functional teams. Responsibilities include designing, optimizing, and validating equipment, providing technical guidance, troubleshooting issues, ensuring compliance, and supporting manufacturing operations.

The Manager, Quality Control Analytical oversees the QC Analytical laboratory, ensures compliance and timely execution of testing, manages a team of QC Analysts, and collaborates with other teams to address quality control issues. Responsibilities include approving deviations and driving continuous improvement initiatives.