Cell Processing Specialist
Company: Dana-Farber Cancer Institute
Location: Boston
Posted on: November 6, 2024
Job Description:
The Connell and O'Reilly Families Cell Manipulation Core
Facility (CMCF) assists DF/HCC members in developing new cell-based
therapies for patients with cancer who are enrolled in novel
therapeutic clinical research protocols. It also supports clinical
research studies designed to evaluate the safety and efficacy of
these novel treatments. Please visit .The Cell Therapy Processing
Specialist II performs a variety of tasks to provide the highest
quality products for patients receiving more than minimally
manipulated cellular therapy products on clinical trials. These
trials include Gene Therapy, Cancer Vaccines, Immuno-effector Cells
including CAR-T cells, Induced Progenitor Cells (iPS), Mesenchymal
Stromal Cells, Adoptive Immunotherapy and other innovative
therapies. The Cell Therapy Processing Specialist II is competent
in all routine processing procedures with the ability to
troubleshoot and participate in complex processing. May serve as
Project Lead on Cell Therapy Trial without complex processing.Work
Location:100% on-site at our Boston Campus in the Longwood Medical
area.Scheduling Requirements:Full Time, 40 hours per weekWeekend,
evening, and on-call coverage will be required on a rotating
basis.Located in Boston and the surrounding communities,
Dana-Farber Cancer Institute is a leader in life-changing
breakthroughs in cancer research and patient care. We are united in
our mission of conquering cancer, HIV/AIDS, and related diseases.
We strive to create an inclusive, diverse, and equitable
environment where we provide compassionate and comprehensive care
to patients of all backgrounds, and design programs to promote
public health particularly among high-risk and underserved
populations. We conduct groundbreaking research that advances
treatment, we educate tomorrow's physician/researchers, and we work
with amazing partners, including other Harvard Medical
School-affiliated hospitals.Cell Processing
- Process more than 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 and complex
processing procedures, including:
- cell culture, including aseptic technique,
- cryopreservation/thawing,
- cell selection (Miltenyi CliniMACS),
- centrifugation and washing,
- manufacture gene manipulated products using semi-automated
platform,
- labeling and transportation.
- Review and evaluate test results for acceptability including
automated and manual cell counts, viability results, flow cytometry
histograms, sterility testing results.
- Accurately enter and maintain records of procedures and enter
data, both manually and on electronic data capture systems.
- Identify, evaluate, and troubleshoot or correct problems
related to product preparation, including issues with
instrumentation, reagents, and documentation. Appropriately
communicate outcomes, including escalating problems to supervisors
and managers.
- Perform environmental monitoring of work area and
laboratory.
- Assist in validation studies, including implementation, of new
procedures and working with vendors/trial sponsors.
- Serve as project lead for at least one cell therapy trial, not
requiring complex processing.
- Write and review Standard Operating Procedures.
- Upgrade job skills to stay relevant and to progress in the
field.Equipment
- Perform preventive and corrective maintenance of equipment and
instrumentation. Identify the need for repair or service, as
required.
- Respond to REES alarm system alerts and document corrective
actions appropriately.
- Participate in validation of new instruments, including
collaborating with development of SOPs and other
documentation.QA/Regulatory Duties and Responsibilities
- Work within the cGMP and cGTP guidelines and adhere to all
regulatory standards within the Cell Manipulation Core
Facility.
- Recognize and report deviations from standard operating
procedures.
- Initiate and document corrective actions when
required.Training
- Participate in training of new Specialists and assist
management to assess competency.Minimum Education:BS/BA in a
Biological Science, Medical Technology or related field
required.Minimum Experience:
- 2 years experience in a clinical laboratory setting or 1 year
in a Cellular therapy or cGMP environment.
- Demonstrated Cell Processing Specialist I competency.KNOWLEDGE,
SKILLS, AND ABILITIES REQUIRED:
- Capable of working in a fast-paced and rapidly changing
environment and technology.
- Ability to communicate and interact effectively with team
members and stakeholders.
- Capable of producing accurate results within strict time
constraints.
- Ability to apply critical thinking skills and possess good
judgment, problem-solving skills, and attention to detail.
- Good analytical reasoning and ability to perform complex
mathematical calculations using notation.
- Well versed in clinical Good Clinical Practice/research GMP,
GTP, Good Laboratory Practice.
- Well versed in lab safety and infection control.
- Knowledge of operation & performance of basic lab equipment,
e.g., centrifuge, microscopes, program freezers, etc., and the
ability to troubleshoot problems.
- Ability to achieve level of subject matter expert when training
on new processes.
- Demonstrate organizational skills and leadership qualities to
serve as project lead for at least one Cell Therapy Trial.
- Able to identify process improvements and make recommendations
to management.
- Actively pursues and participates in continuing education of a
minimum of 5 hours of professional development annually.
- Ability to compile and/or present data for presentations to
staff, project collaborators, or Trial Sponsors.At Dana-Farber
Cancer Institute, we work every day to create an innovative,
caring, and inclusive environment where every patient, family, and
staff member feels they belong. As relentless as we are in our
mission to reduce the burden of cancer for all, we are equally
committed to diversifying our faculty and staff. Cancer knows no
boundaries and when it comes to hiring the most dedicated and
diverse professionals, neither do we. If working in this kind of
organization inspires you, we encourage you to apply.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.EEOC Poster
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Keywords: Dana-Farber Cancer Institute, Revere , Cell Processing Specialist, Other , Boston, Massachusetts
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