Job Description
The Mammalian Cell Processing Specialist is responsible for executing detailed and precise cell processing tasks in a flexible and sometimes unpredictable work schedule. This role requires specialized training in GMP grade conditions, as well as proficiency in both manual and automated processing. The candidate must possess knowledge of cell culture and flow cytometry and adhere to GMP/GDP documentation guidelines.
ResponsibilitiesAdhere to GMP guidelines in cleanroom (ISO7) environment.Perform flow cytometry to assess cell viability and count.Perform isolation of HSCs, NK, and T-cells.Conduct calculations during processing to assess product yields.Utilize aseptic techniques while performing cell processing procedures.Investigate and resolve problems with procedures or processes.Execute validation processes on new instruments and equipment.Perform sterility and environmental monitoring testing with QC specialist.Collaborate closely with QC specialist and QA department.Ensure documentation is accurate, complete, comprehensive, and maintained.Collect and label required laboratory samples and maintain accurate and complete result reports, processing worksheets, and cryopreservation records.Perform quality control and preventative maintenance on instruments and equipment and maintain complete and accurate records.Practice proper safety techniques and report any unsafe conditions.Perform other duties and procedures as assigned.Essential SkillsCell cultureCell therapyFlow cytometryMammalian Cell CultureELISAResearch & DevelopmentAssayCleanroom operationsCell IsolationCell BiologyHEK, CHO, MSCAdditional Skills & QualificationsExperience in cGMP requirements highly preferred.Experience in flow cytometry assays and interpretations preferred (Cytoflex).Knowledge of sterile techniques required.Knowledge of the use of liquid nitrogen for cryogenic environments.Experience with microbiological testing preferred.Experience with CliniMACS Prodigy preferred.Work Environment
The work environment is an ISO 7 cleanroom, requiring adherence to GMP guidelines. It is a family-oriented, growing team setting, offering opportunities to collaborate closely with QC specialists and the QA department.
Pay and Benefits
The pay range for this position is $25.00 - $28.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Boca Raton,FL.
Application Deadline
This position is anticipated to close on Aug 20, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.