The Scientist II will lead upstream cell culture process development for biopharmaceutical production, involving bioreactor operations and technical support to teams.

The Process Engineer III leads technical improvement initiatives, manages projects, ensures compliance, and oversees process validations in a biomanufacturing setting.

The Scientist II will develop, validate, and optimize bioanalytical methods for protein therapeutics, ensuring compliance with quality standards while conducting thorough documentation and analysis of results.

The Automation Engineer IV is responsible for leading automation initiatives, optimizing equipment, overseeing compliance in a cGMP environment, and providing technical support across systems. The position involves managing specifications, training personnel, troubleshooting signal issues, and ensuring productivity improvements while participating in audits and acting as the interim manager when needed.

The Senior Specialist II in QA Systems & Training will manage daily operations of the LMS, ensure training compliance, support training material development, and assist during regulatory inspections and audits. This role involves leading training programs and metrics reporting for performance assessment.

This Administrative Assistant role focuses on providing various administrative and project support tasks for the Process Execution Team. Responsibilities include scheduling meetings, managing travel arrangements, processing purchase orders, maintaining supplier relationships, and assisting with data management and reporting.

The Process Engineer IV serves as the aseptic filling Subject Matter Expert, focusing on standardization, continuous improvement, and performance enhancements within the Process Execution Team. Responsibilities include developing standards, leveraging performance data, ensuring regulatory compliance, and coaching operators, with more than 50% of the time spent on the floor for hands-on support and training.

The Senior Specialist, Technical Quality is responsible for ensuring operational excellence and compliance in manufacturing processes. This role includes providing quality oversight for investigations, validation, and technology transfer, leading cross-functional collaboration, and driving continuous improvement initiatives to enhance product quality and operational efficiency.

The Process Engineer will develop specifications for systems in biopharmaceutical manufacturing. Responsibilities include designing cleanrooms, overseeing compliance with FDA regulations, executing Factory Acceptance Testing, and supporting production optimization. Additionally, the engineer will coordinate projects with clients and assist in manufacturing troubleshooting and improvements.

The Director of Downstream Process Development will lead the downstream process development function for Biologics, Vaccines, and Gene Therapy at Resilience. Responsibilities include overseeing technical development, process transfer, manufacturing, and regulatory submissions, as well as mentoring and driving a team of downstream process scientists.

The Director of Sales and Business Development leads the Commercial Services Organization for specific territories, driving profitable revenue through relationship cultivation and new business generation within the biomanufacturing sector. The role requires knowledge in Biologics, Vaccines, and Gene Therapy, as well as involvement in sales strategy, lead generation, and closure of deals to foster sustainable client relationships.

The Specialist Network Engineer will focus on designing, deploying, and managing core route/switch and data center networks using Cisco equipment. Responsibilities include network planning, installation, maintenance, and troubleshooting to ensure optimal performance of Resilience's network infrastructure.

The Senior Analyst II, Quality Control will provide technical expertise and ensure compliance with testing for lentiviral vector and CAR-T products. Responsibilities include method development, testing execution, and investigation of any out-of-specification results while collaborating with other teams and mentoring junior analysts.

The Automation Engineer III at Resilience will manage automation projects, improve manufacturing processes, and provide technical support for equipment. This role requires collaboration with various teams to enhance equipment operations, train personnel, and maintain compliance with regulatory standards.

The Aveva PI Engineer III will design, architect, troubleshoot, and enhance the data historian systems, support manufacturing, train users, and improve processes at the site. Responsibilities also include reviewing documentation, ensuring compliance, and leading cross-functional investigations to enhance data integrity and productivity.

The Director, Sales and Business Development is responsible for driving profitable revenue through relationship building and lead generation within the assigned territory, particularly in the biotech and pharmaceutical industries. This includes managing customer relationships, attending industry events, and collaborating with commercial development and marketing to optimize growth strategies.

The Senior Associate in Upstream MSAT is a technical expert responsible for managing upstream process manufacturing for biopharmaceuticals. Key duties include designing and implementing manufacturing processes, creating GMP documents, overseeing technical operations, and providing training to staff. The role also involves continuous process improvement and compliance with quality standards.

The End User Support Analyst provides technical support to end-users, manages digital asset systems, assists with onboarding and offboarding, and supports conference room technology. Responsibilities include troubleshooting device issues, managing digital operations, and contributing to continuous improvement initiatives.

The Analyst II in QC Microbiology is responsible for testing pharmaceutical products, writing and reviewing SOPs, conducting troubleshooting, and participating in quality investigations. The role involves data trend analysis, compliance monitoring, and equipment oversight while adhering to cGMP standards. This position requires an understanding of production operations and problem-solving skills.

The Specialist I, Technical Services is responsible for supporting technology transfer activities, assisting in engineering and GMP runs, and optimizing processes. tasks include drafting protocols, preparing technology transfer plans, participating in risk assessments, supporting training compliance, and ensuring adherence to safety standards.