The Senior Specialist in Supply Chain and Procurement is responsible for tactical procurement and materials planning, managing supplier relationships, ensuring timely delivery of materials, analyzing supply patterns, and overseeing the procurement team's activities while supporting continuous improvement initiatives.

The Specialist Network Engineer is responsible for the design and implementation of network infrastructure, including firewalls, routers, and switches. This role involves network planning, optimization, and troubleshooting, as well as working with managed service providers and ensuring network security and performance.

The Senior Director for Sales and Business Development oversees the West Coast region, managing a team to drive revenue growth through strategic customer relationships and lead generation in the biomanufacturing industry. This role involves sales strategy development, contract negotiations, market intelligence, and collaboration with various internal teams to ensure business success.

The Senior Specialist, Technical Quality, ensures operational excellence and compliance in biomanufacturing by providing quality oversight during investigations, validations, and technology transfers. This role involves leading cross-departmental initiatives, approval of quality documents, participating in audits, and driving continuous improvements in manufacturing processes.

The Director of Downstream Process Development will lead the Downstream Process Development function for Biologics, Vaccines, and Gene Therapy at Resilience. Key responsibilities include overseeing technical development, process transfer, manufacturing and ensuring successful regulatory submissions, while mentoring staff and driving a scientific culture.

The Senior Associate in Upstream MSAT at Resilience is responsible for supporting upstream process manufacturing, technology transfer, and continuous improvement in biomanufacturing. This includes designing processes, creating GMP documentation, and training staff while acting as a subject matter expert in upstream processes for therapeutic proteins.

The Director of Sales & Business Development will drive profitable revenue for the Commercial Services Organization by building a sales strategy for assigned territories, developing new business opportunities and managing customer relationships within the pharma and biotech sectors.

The Senior Director will oversee sales and business development in the East Coast, focusing on biologics, gene therapy, and cell therapy. Responsibilities include managing a team, driving revenue growth, maintaining customer relationships, and leading market strategy efforts while attending trade shows and industry events.

The Director of Sales and Business Development is accountable for driving profitable revenue across various technology platforms. This role involves building customer relationships, generating new business, leading sales strategies, and collaborating with internal teams to ensure business needs are met while maintaining accurate data and reports.

The Scientist I, QC Microbiology leads lab investigations, verifies QC data, develops and validates new methods, and serves as a technical leader for microbiological testing and processes within a sterile manufacturing environment.

The Automation Engineer II leads projects to enhance automation systems across departments in a biomanufacturing site. Key responsibilities include designing and optimizing equipment, troubleshooting automation systems, reviewing specifications, providing training, and ensuring compliance with regulatory standards. Collaboration with cross-functional teams is essential to support manufacturing operations in a regulated environment.

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.

As a PI Historian Analyst, you will design and maintain historian systems, support manufacturing data capture and visualization, and lead cross-department collaborations for process improvements. The role involves technical troubleshooting, training, documentation, and compliance adherence in a GMP environment.

The Senior Analyst II, Quality Control (Potency) will perform testing and validations for lentiviral vector and CAR-T products, collaborate with teams to ensure compliance with testing procedures, investigate anomalies, and mentor junior analysts. Works under cGMP conditions to maintain quality control standards and documentation.

The Manager, Quality Control Analytical oversees the QC Analytical laboratory, coordinating laboratory activities, managing a team of QC Analysts, ensuring compliance with quality standards, and leading investigations on QC issues. They will collaborate with various departments to meet testing schedules and drive operational excellence within the organization.

The Process Engineer IV will lead the Process Execution Team by driving standardization, continuous improvement, and performance enhancements in biomanufacturing processes. Responsibilities include developing standards, coaching team members, problem-solving, and ensuring compliance with regulatory standards, while spending significant time in hands-on operational roles.