Search the 28 jobs at Cellares

The Human Resources Manager will establish and implement HR best practices, maintain daily functions of the HR department, assist employees with benefits and payroll inquiries, draft company policies, ensure compliance with employment laws, and manage employee relations.

The Senior Systems Integration Engineer will lead integration testing, troubleshooting, and improve advanced cell therapy systems. Responsibilities include executing complex experiments, generating technical documentation, and collaborating with cross-functional teams to enhance performance and efficiency of technology platforms.

The Senior Applications Scientist will work on cell therapy manufacturing processes, design experiments, provide technical support, and collaborate across departments. They will also analyze data, train junior members, and author technical documents.

The R&D Engineer will contribute to the development of a cell therapy manufacturing platform, focusing on the design, prototyping, and verification of plastic injection molded components. Responsibilities include component selection, design tasks, quality assurance, and collaborating with interdisciplinary teams. The role requires hands-on experience and strong analytical skills to handle complex biomedical device designs.

The Consumable Quality Engineer will lead the testing and validation of consumables, ensuring compliance with ISO 10993 and USP Class VI standards. Responsibilities include developing qualification plans, executing a range of tests, coordinating with external labs, analyzing test results, and collaborating across departments.

The Associate Scientist will support cell therapy manufacturing by designing and executing experiments aimed at process development and improvement. Responsibilities include maintaining cell lines, generating process documentation, addressing project challenges, and performing laboratory activities. The role requires strong technical writing skills and knowledge of cell therapy methods.

Seeking a Senior Analytical Transfer Specialist to lead analytical method transfers, evaluation, and support for cell therapy QC operations. Responsibilities include authoring procedures, contributing to regulatory submissions, and providing technical leadership. Requires a Bachelor's degree and 4+ years of experience in biologics/gene therapy with knowledge of QC principles and relevant analytical methods.

The Automation Engineer will support the deployment and optimization of automated QC testing workflows, validate methods for sample preparation and analysis, monitor system performance, conduct validation testing, and develop troubleshooting methodologies. They will work collaboratively with cross-functional teams and contribute to system documentation and training.

The Senior Manager of Operational Technology will oversee technical operations and infrastructure in an industrial and cell therapy lab, ensuring 24x7 operational support. Responsibilities include managing OT systems, developing implementation plans, ensuring compliance with security best practices, troubleshooting production issues, and delivering training for OT staff, while interacting with senior leadership and business functions to align priorities.

Seeking a VP, CMC Process Sciences to oversee establishment and execution of CMC development plans for cell and gene therapy products. Responsible for providing CMC leadership, collaborating with stakeholders, and driving effective communication and coordination across functional groups.

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.

Seeking a Senior Process Engineer to contribute to the development of an advanced cell therapy manufacturing platform. Responsibilities include technology transfer, process development, compliance, scalability, and driving process automation solutions. Must have 5+ years of experience in biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy.

Seeking an experienced Senior Data Engineer to lead the design, development, and management of scalable data pipelines and architecture for a cell therapy manufacturing platform. Responsibilities include data pipeline implementation, collaboration with cross-functional teams, data preprocessing for machine learning models, and documentation of processes. Requirements include a Bachelor's or Master's degree in Computer Science, 6+ years of data engineering experience, proficiency in Azure services, programming skills in Python or C#, and experience in data visualization tools and data governance.

The CMC Program Manager at Cellares is responsible for managing project timelines and coordinating activities related to cell therapy manufacturing, acting as a liaison between multiple cross-functional teams. Responsibilities include budget management, risk mitigation, regulatory filings support, and ensuring customer satisfaction through effective communication and problem-solving.

The Manager of Analytical Operations will oversee a team of scientists and analysts, manage assay execution and data analysis, ensure compliance with regulatory standards, and troubleshoot operational issues. Responsibilities include method transfer, team management, and aiding in regulatory submissions.

The Director of Product Management will oversee the entire product lifecycle, from ideation to launch, collaborate with the R&D team, analyze market trends, and ensure alignment with company strategy. The role requires both high-level strategy and hands-on execution in a dynamic environment.

The Senior Process Engineer will lead technology transfer activities for cGMP manufacturing, focusing on process automation, compliance, and scalability. Responsibilities include developing project plans, supporting late-stage process development, defining user requirements for equipment, conducting root cause analyses, and collaborating with stakeholders. This role requires expertise in technology transfer and manufacturing science.

The Senior Client Systems Engineer will design, upgrade, and maintain client systems while implementing new systems and providing training to team members. Responsibilities include resolving end user help requests, managing IT systems like Intune and Zoom, and providing support for desktop and mobile devices. They will also manage company assets and collaborate with the network team.

Seeking a Senior Manager, Logistics to manage clinical and commercial vein-to-vein logistics activities for autologous and allogeneic client programs. Responsible for on-time shipment management, vendor performance monitoring, and budget tracking. Key role in coordinating logistics across manufacturing sites and stakeholders to deliver client products. Must ensure compliance with cGMP requirements and regulatory agencies. Multidisciplinary role interfacing with various departments.

Seeking a Senior Controls Engineer to lead the design, implementation, and testing of control systems for a cell therapy manufacturing platform. Responsibilities include developing PLC control software, collaborating with cross-functional teams, and validating automation systems. Requires 5+ years of industry experience and expertise in control systems development.