Cell Processing Specialist

The Cell Therapy Processing Specialist I will receive on-the-job training to perform a variety of tasks to provide the highest quality products for patients undergoing stem cell transplant and other cellular therapies. Regular work schedule is 1pm-9:30pm.

PRIMARY DUTIES AND RESPONSIBILITIES

Process minimally manipulated clinical human therapeutic cellular products by various methods using manual and/or automated aseptic technique in a regulated clean room environment according to standard operating procedures and applicable regulations. Achieve and maintain competency in routine procedures including cryopreservation/thawing, centrifugation/washing, handling of genetically modified cells, labeling, and transportation. Review and evaluate test results for acceptability including automated and manual cell counts, viability results, flow cytometry histograms, and sterility testing results. Identify and escalate problems related to product processing and quality data of products. Appropriately communicate outcomes. Perform quality check and cleaning of equipment and instrumentation. Identify the need for repair or referral as required. Respond to REES alarm system alerts and document corrective action. Participate in validation of new instruments. QA/Regulatory Duties and Responsibilities Work within cGMP and cGTP guidelines and adhere to all regulatory standards within the Cell Manipulation Core Facility.

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED

Ability to learn to perform routine cell processing for all allogeneic and autologous products. Ability to apply critical decision-making skills, good judgment and attention to detail. Communicate effectively and professionally with other health care providers involved in the patient’s care. Ability to continually upgrade job skills. Ability to work effectively, independently and as a member of a team. Good interpersonal and communication skills. Capable of working in a fast-paced and rapidly changing environment. Capable of producing accurate results within strict time constraints. Ability to adapt to changing technology.Ability to perform complex mathematical calculations using scientific notation. Knowledge of lab safety and infection control; clinical/research GCP knowledge. Familiarity with operation and performance of basic lab equipment, i.e., centrifuge, microscopes, program freezers, etc.

SUPERVISORY RESPONSIBILITIES

None.

PATIENT CONTACT

None.

MINIMUM JOB QUALIFICATIONS

Minimum Education: BS/BA in a Biological Science, Medical Technology or related field preferred. Associate Degree in related science with MLT and clinical lab experience may substitute for bachelor’s degree. Minimum Experience: Clinical lab experience preferred. One year in a clinical laboratory setting required with Associate Degree. License/Certification/Registration: Medical Lab Technician (MLT) certification required with Associate Degree. EEO Statement Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law. Pay Transparency Statement The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications. For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA). $68,200.00 - $76,500.00 #J-18808-Ljbffr Dana-Farber Cancer Institute