Search the 14 jobs at Cellares

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 Senior Data Engineer will architect, design, and implement scalable data pipelines and infrastructure while collaborating with teams to support data analytics and AI solutions for cell therapy manufacturing. Responsibilities include managing data ingestion, transformation, and storage systems, ensuring data quality and performance, and documenting processes.

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 Staff Process Engineer will support the development and scalability of advanced cell therapy manufacturing at Cellares, focusing on technology transfer and process automation. Responsibilities include overseeing GMP documentation, training staff, conducting investigations, and ensuring compliance in operational practices. The role involves high-level interaction with stakeholders to drive operational excellence in a fast-paced environment.

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 Staff Technical Product Manager will develop requirements for advanced cell therapy manufacturing by understanding user needs and workflows, collaborating with technical teams, and synthesizing a product roadmap that aligns with business goals. This role involves acting as a customer advocate, managing product development phases, and ensuring high-quality standards are met while staying current with industry trends.

The Manager of Quality Control oversees GMP manufacturing processes, ensures compliance with GxP standards, manages analytical testing and method validation, and leads a quality control team. Responsibilities also include training staff, collaborating on specifications, and representing Quality Control in cross-functional meetings.

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, 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 Systems Engineer will develop and manage system verification and validation plans for lab automation, troubleshoot issues, enhance automated solutions, and collaborate with cross-functional teams on continuous improvement projects. Responsibilities include monitoring system performance, analyzing workflows, and documenting technical processes.

The Scientist in Analytical Development will develop and optimize assays for cell therapy products, execute analytical procedures for drug characterization and stability testing, guide fellow team members, and contribute to cell therapy manufacturing improvements.