Cell Therapy Specialist

Date Posted: 05/01/2026Hiring Organization: Rose InternationalPosition Number: 500664Industry: Biotech/HealthcareJob Title: Cell Therapy SpecialistJob Location: Frederick, MD, USA, 21704Work Model: OnsiteShift: Role is full time 4/10 role but the roles and shifts can change with the needs of the dept. Shift times will be directed by the manager or dept leadsEmployment Type: TemporaryFT/PT: Full-TimeEstimated Duration (In months): 7Min Hourly Rate($): 20.00Max Hourly Rate($): 34.00Must Have Skills/Attributes: Cell Culture, GMPExperience Desired: cGMP experience (2+ yrs); Cell culture or Cell line experience (2+ yrs)Required Minimum Education: High School Diploma or equivalent**C2C is not available**Job DescriptionImportant Shift Information: For the first 6-8 weeks of the assignment, work hours are Mon-Fri (0730-1600) to complete New Hire Orientation and Manufacturing On-boarding Technical Training After the training is completed, you'll be deployed onto a specific shift as needed by the department leadershipRequired Education Bachelor's Degree in Science FieldOR Associate's Degree with 1+ years of cGMP experienceOR High School Degree/equivalent and 2+ years of cGMP experienceThe Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance.Responsibilities Successfully troubleshoots processing and equipment issues while communicating said issues to management Completes required training assignments to maintain necessary technical skills and knowledge and to ensure compliance with cGMP requirements Authors and/or revises SOPs that are technically sound, provides clear instructions to align with cGMP requirements and supports efficient operations Routinely monitors, cleans, prepares and operates sophisticated automated cell processing, cell expansion and filling equipment in Grade B/C clean roomsall required PPE and gowning for classified GMP manufacturing areas is provided by the company Finds opportunities for improvement in manufacturing efficiencies and compliance while assisting with investigations/deviations and change controlsAre you passionate about making an impact on people’s lives? Would you be excited to work for a company leading the way in developing and producing unique, innovative immunotherapies? Do you have a background in cGMP manufacturing? If the answer is yes, we’d like to consider you!**Only those lawfully authorized to work in the designated country associated with the position will be considered.****Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**BenefitsFor information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website. California Pay EquityFor information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here. Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances. If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department. Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).