Search the 31 jobs at Cellares

Seeking a LIMS Developer to design, develop, and implement LIMS solutions for high-throughput cell therapy manufacturing. Responsibilities include software requirements capture, custom script development, creating technical documentation, and collaborating on digital architecture. Company Cellares is an IDMO focused on accelerating access to cell therapies through integrated technologies and automation.

Seeking an experienced DevOps Engineer to contribute to the development of a cell therapy manufacturing platform. Responsibilities include continuous integration, release management, automation, and pipeline management. Requires a Bachelor's degree in computer science or engineering and 5-7 years of experience.

Senior Quality Control Analyst responsible for routine and non-routine QC testing according to SOPs. Conduct analytical testing, peer review, investigate deviations, compile data, support method validation, and maintain QC procedures. Requirements include Bachelor's degree in science, 5+ years of cGMP/cGxP experience, method development/validation, and knowledge of pharmaceutical cGMP. Strong communication, organizational, and interpersonal skills.

Seeking a collaborative Director of Quality Assurance for Cell & Gene Therapy operations in South San Francisco. Lead cGMP compliance activities, manage quality aspects of customer projects, oversee quality management system, and develop SOPs. Requires 10+ years of experience in pharmaceutical or biopharmaceutical industries with leadership experience and knowledge of cGMP regulations.

Seeking an innovative and highly motivated Associate Scientist in Analytical Development to contribute to the development of a cell therapy manufacturing platform. Responsibilities include analytical method development, testing, and automation, as well as collaboration across departments. The company, Cellares, is focused on accelerating access to life-saving cell therapies through integrated technologies.

The Staff Technical Product Manager will lead the development of an advanced cell therapy manufacturing platform by understanding user needs, defining product vision, and working closely with cross-functional teams. This role requires expertise in product management in biotechnology/medical device industries with a focus on automation, instrumentation, and cell therapies.

The Manager of Quality Control will be responsible for managing the quality control lab and ensuring compliance with GxP and safety standards. They will oversee routine and non-routine analysis, review and approve documentation, manage stability programs, and serve as a subject matter expert between Quality Control and other departments. The position requires a bachelor's degree in a science discipline with at least 7 years of experience in a cGMP or cGxP environment, including 2 years in a managerial role.

Lead process development efforts and implement new cell therapy processes to drive continuous improvement of the Cellares platform. Provide technical training and guidance to team members and perform routine laboratory activities.

Manage payroll operations and maintain accurate books and records. Lead payroll functions and transactions, reconcile payroll and bank transactions, analyze payroll accuracy, manage payroll accounting matters, collaborate with HR, Legal, Accounting, and Finance, and update payroll changes in ADP.

This position is responsible for supporting the activities involved in analytical process transfers, compliance, and scalability for Cellares’ Quality Control (QC) operations.

The Scientist in Process Development will design and execute experiments to improve the cell therapy manufacturing platform. They will collaborate with various teams, author technical documents, analyze results, and support troubleshooting. The ideal candidate has a degree in bioengineering, chemical engineering, biology, or related field and experience in the cell and gene therapy field. Strong communication, technical skills, and a self-motivated mindset are required.

Seeking a detail-oriented Senior Scientist with extensive experience in flow cytometry-based assays for cell therapy products. Responsible for method development, assay transfer, data analysis, and troubleshooting. Collaborate with cross-functional teams and serve as a subject matter expert on multicolor flow cytometry.

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.

Seeking a Senior Controls Simulation Engineer to lead the development of virtual commissioning tools and simulation strategies for advanced cell therapy manufacturing platforms. Responsibilities include designing virtual commissioning tools, integrating PLCs and robots, developing simulation capabilities, and collaborating across teams. Requires 5+ years of experience in developing systems with industrial robotics and motion control systems.

Seeking a highly motivated Logistics Specialist to oversee shipping and receiving processes in a fast-paced, mission-driven environment. Responsible for managing logistics and distribution of supplies, improving operational efficiency, and ensuring compliance with trade regulations. Requires on-site full-time work and experience in customs trade, cGMP warehouse, and life sciences field.

Seeking an Automation Scientist to contribute to the development, implementation, and optimization of lab automation systems for high-throughput cell therapy manufacturing QC testing. Responsibilities include designing automated QC methods, troubleshooting technical issues, and coordinating assay method validation. Requires a Master's or Ph.D. in related fields, experience with assay method development, analytical instruments, LIMS, and GMP compliance. Must have strong technical writing skills and be self-motivated.

The VP of Legal & General Counsel will oversee the legal department, manage complex commercial transactions, provide legal advice to the company's senior management and board of directors, and ensure compliance with legal regulations.

Seeking a detail-oriented Scientist for Analytical Development role in South San Francisco. Responsibilities include method development, assay execution, training associates, data analysis, laboratory maintenance, and inventory management. Must have extensive experience in immune cell phenotyping and cell-based assays, as well as a BS, MS, or PhD in a related field. Company is focused on accelerating access to cell therapies through innovative manufacturing technologies.

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.

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.