Seeking a VP of Operations to oversee the launch and operations of a cGMP cell therapy manufacturing facility. Responsibilities include leading a team, ensuring compliant operations, collaborating with key stakeholders, and driving continuous improvements and efficiencies.

The Systems Engineer will develop and manage verification plans for a QC testing platform, collaborating with teams to enhance automated solutions and troubleshoot issues. Responsibilities include monitoring system performance, authoring technical documentation, and implementing improvements in laboratory automation systems.

The Supervising Scientist will lead process characterization studies to validate cell therapy manufacturing. Responsibilities include developing experimental designs, analyzing datasets, collaborating with cross-functional teams, authoring technical documentation, and mentoring junior staff in a fast-paced environment.

The Scientist will lead process characterization studies, develop statistically sound experimental designs, analyze complex datasets, and collaborate with cross-functional teams to optimize cell therapy manufacturing processes, ensuring high-quality outputs. They will also provide mentorship to junior members and serve as a subject matter expert in cell and gene therapy processes.

The Senior Applications Scientist will support process development in cell therapy, interacting with various teams to optimize manufacturing processes. They will design experiments, provide technical training, and communicate results effectively to different audiences. Hands-on expertise in cell therapy manufacturing is essential, alongside strong collaboration skills.

The Executive Assistant will maintain executives’ calendars, coordinate meetings and travel, manage expenses, and organize company records. This role requires strong organizational skills, attention to detail, and the ability to handle confidential information while supporting various tasks in a fast-paced environment.

The Consumable Qualification Engineer leads the testing and validation of consumables for regulatory compliance. Responsibilities include designing and executing biocompatibility tests, managing external labs, collaborating with multiple departments, analyzing results, and preparing technical reports. The role demands a strong understanding of regulatory standards and effective communication skills.

The CMC Program Manager will manage project timelines and activities for Cell Therapy Manufacturing, acting as a bridge between cross-functional teams. Responsibilities include strategy generation, budget management, regulatory preparation, vendor management, and process improvement, with an emphasis on communication and relationship building.

The Senior Controls Engineer will design, implement, and verify control systems for an advanced cell therapy manufacturing platform. Responsibilities include leading development of integration systems, collaborating with cross-functional teams, and developing PLC control software and test software. The position demands innovation and a proactive approach within a fast-paced environment.

The LIMS Developer will design, develop, and implement LIMS solutions for cell therapy manufacturing and QC testing, manage user requirements, create documentation, and coordinate on data management tools. They will collaborate with cross-functional teams to develop digital architecture and work with LIMS providers for feature implementation.

The Logistics Specialist oversees shipping and receiving, manages logistics operations, ensures compliance with trade regulations, and improves inventory accuracy. Responsibilities include developing best practices, analyzing shipping costs, and maintaining supplies for cell therapy manufacturing. This hands-on role requires effective communication and proactive problem-solving in a fast-paced environment.

The Automation Scientist will develop and optimize lab automation systems for high-throughput cell therapy manufacturing QC testing, collaborating with teams to establish automated methods, troubleshoot issues, and ensure quality control. They will manage assay development and validation while addressing workflow bottlenecks efficiently.

The Senior Quality Control Analyst is responsible for performing routine and non-routine analytical testing, peer reviewing results, investigating discrepancies, maintaining compliance with cGMP guidelines, and supporting method validation and quality systems. This role involves hands-on work with cell therapy products and various analytical assays, ensuring laboratory standards and training associates.

The Automation Engineer will support the deployment and optimization of automated QC testing workflows, including the validation of liquid handling methods and system performance monitoring. Responsibilities include collaborating with teams, conducting system troubleshooting, and developing documentation and training materials.

The Senior Quality Control Analyst, Microbiology will oversee routine and non-routine quality control testing, ensuring compliance with cGMP guidelines. Key responsibilities include conducting environmental and microbiological testing, reviewing test results, maintaining training records, and participating in audits and validations.

The Senior Manager of Finance Operations will lead the company’s Operating Plan process, partner with executives for financial planning, and analyze key metrics for profitability and cash flow. The role involves strategic decision-making and financial modeling to improve operational performance and support expansion initiatives.

The Senior Manager of Financial Planning and Analysis will lead the company's financial planning processes, develop and monitor key financial models, and provide strategic financial analysis to guide executive decision-making. Responsibilities also include improving profitability through comprehensive analysis, engaging in discussions around resource allocation, and collaborating with various teams to achieve financial targets.