The Senior Quality Control Analyst will conduct tests, analyze results, manage laboratory compliance, and oversee equipment maintenance. Responsibilities also include authoring procedures, documentation according to cGMP guidelines, and training junior analysts, all while ensuring product quality and safety standards are met.

As a Senior Operation Quality Assurance Specialist, you will conduct internal audits, review batch records, and ensure compliance with regulatory standards for cell and gene therapy products. You will oversee quality checks, collaborate with teams to resolve quality issues, and mentor junior staff while maintaining procedures and supporting regulatory inspections.

The Director of Process Development will lead a team to develop TCR-T programs for solid tumor treatment, manage process optimization for commercial manufacturing, and drive innovation in manufacturing processes. They will provide leadership for CMC activities, oversee GMP implementations, and ensure alignment with regulatory standards.

The Senior Microbiologist oversees the microbiology laboratory, performing assays and qualifications for environmental monitoring and product testing. Responsibilities include authoring protocols, managing test releases, and performing microbial identifications. They will also maintain equipment and conduct various qualification studies, ensuring compliance with regulations and standards.

The MSAT Associate II is responsible for facilitating and optimizing technology transfers between Process Development and GMP Manufacturing. This role involves performing specialized cell manipulations, conducting analytical tests, maintaining laboratory supplies, and managing project-specific inventories, all while adhering to cGMP regulations.

The Senior Director of Quality Control provides strategic leadership for the quality control department, ensuring compliance with industry standards, managing laboratory functions, developing processes for product quality, and leading continuous improvement initiatives across various teams.

The Senior Accountant is responsible for processing accounts payables, cash posting, account reconciliation, and ensuring compliance with GAAP. This role includes preparation of financial statements and managing vendor inquiries. Candidates are expected to maintain internal controls aligned with Sarbanes-Oxley Act requirements and assist with month-end and year-end closing.

The Environmental Monitoring Supervisor oversees Quality Control and Microbiology personnel, managing daily environmental monitoring activities in aseptic production areas. Responsibilities include training staff, managing schedules, performing environmental monitoring, authoring quality documents, and ensuring effective communication within the team.

The Research Associate will support clinical trials by performing product characterization assays. Responsibilities include executing flow cytometry assays, conducting aseptic cell culture, maintaining documentation, assisting with data analysis, and equipment calibration. Candidates should have basic lab skills and attention to detail.

The Quality and Documentation Specialist I is responsible for ensuring the accuracy and compliance of documentation in a clinical laboratory. Key tasks include reviewing lab process documentation, quality control, overseeing patient records, and preparing for audits. The role also involves maintaining instruments, implementing change control processes, and conducting training sessions.

The Research Associate I will support clinical trials by performing product characterization assays, executing flow cytometry assays, conducting aseptic cell culture, and assisting with data analysis and documentation updates. Maintaining laboratory equipment and ensuring compliance with SOPs are also responsibilities of the role.

The VP of CMC Commercial Strategy oversees the development of commercial capabilities for Immatics' cell therapy portfolio. This role involves designing the CMC commercial organization, ensuring supply chain readiness, managing procurement, and collaborating cross-functionally for successful commercial launches. The VP will also lead the onboarding of clinical sites, optimization of patient journeys, and manage external vendor relations.

The Operational Quality Systems Specialist I supports the quality systems team by managing training and document control. Responsibilities include ensuring compliance with policies, leading quality system projects, monitoring quality management systems, and performing quality metrics analysis. The role requires independent work and strong communication skills to collaborate with cross-functional teams and improve quality processes.

Responsible for environmental monitoring services in aseptic production areas, conducting microbiological testing, validating equipment, and supporting safety testing for drug product release within a GMP compliant lab environment.

The Quality Control Analyst I executes various analytical methods for product release within the Quality Control laboratory, including assays for cell product identity and safety. Responsibilities include data extraction, reporting results, maintaining compliance with regulations, and assisting with quality documentation processes.