cGMP Flow Cytometry Specialized Laboratory Technician

Responsibilities

• Performs moderate to complex laboratory procedures focused on the development and execution of multiparametric flow cytometry assays to support testing and characterization of cell and gene therapy products.
• Sample preparation, antibody staining, instrument setup, and daily quality control.
• Data acquisition and basic data analysis.
• Maintains and calibrates laboratory equipment and ensures strict adherence to SOPs, documentation practices, and quality control requirements.

Requirements

• Assists in the design, optimization, and execution of multiparametric flow cytometry assays for immune phenotyping, cell characterization, and quality control testing.
• Performs laboratory procedures associated with flow cytometry workflows and related cell culture activities, including cell handling and culture, panel setup, antibody titration, staining optimization, and data review.
• Performs sample handling activities including collection, processing, storage, and tracking of specimens for flow cytometry analysis.
• Maintains accurate records and ensures proper handling, labeling, and tracking of samples.
• Supports troubleshooting and ensures consistent instrument performance.
• Trains investigators and students in specialized laboratory techniques.
• Provides technical consulting in area of expertise.
• Assists in protocol or policy development.
• Performs other highly specialized laboratory tests as appropriate.
• Complies with any quality control policies and procedures and maintains required documentation.
• Maintains a safe environment in accordance with standards, policies and safety regulations.
• Ensures compliance with infection control policies.
• Handles and disposes of hazardous and non-hazardous materials in accordance with safety protocols.
• Creates and maintains databases and/or spreadsheets to manage and process information or data.
• May supervise unit employees and/or student workers as assigned.
• Sets appropriate goals and deadlines.
• Ensures timely completion of unit's work.
• Schedules, assigns, and prioritizes workloads on a daily basis.
• Assigns and oversees progress of special projects for staff and student workers.
• Assists in budget preparation by gathering historical data in a limited area, such as materials and supplies or salaries.
• Tracks and monitors assigned budget expenditures and reports on variances.
• Organizes and maintains supplies.
• Maintains inventory levels, prepares purchase orders as needed.
• Provides advice on equipment upgrades and acquisitions.
• Keeps informed of developments in field.
• Reads journals and other relevant publications, attends professional association meetings and seminars as appropriate.
• Performs other related duties as assigned or requested.

Qualifications

• Minimum Education: Bachelor's degree in Biological Science or Biotechnology.
• Minimum Experience: 2 years in cell therapy development.
• Preferred Education: Master's degree.
• Preferred Experience: 3 years in cell therapy development.

Skills

• Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality control testing.
• Strong attention to detail and ability to follow standard operating procedures (SOPs) and quality assurance principles meticulously.
• Excellent communication and teamwork skills to collaborate effectively with cross-functional teams.
• Ability to troubleshoot and resolve technical issues in a timely manner.
• Knowledge of regulatory requirements and guidelines (e.g., FDA, EMA) related to cGMP.

Pay

The hourly rate range for this position is $34.32 - $36.05/hr.