job summary: The Senior Manufacturing Technician, Cell Therapy position is responsible for the hands-on manufacturing of clinical cell therapy product according to current Good Manufacturing Practices (cGMPs) and procedures. The position will work directly with a team of manufacturing technicians, specialists and scientists in Cell Therapy Manufacturing and Process Development. location: Arcadia, California job type: Temporary salary: $34 - 38 per hour work hours: 9 to 5 education: Bachelors responsibilities: Participates in the hands-on manufacture of cell therapy products, using state-of-the-art cell manufacturing technologies (i.e., CliniMACS Prodigy, Xuri Bioreactor, M1 Fill and Finish System, etc.), media preparation, cell culture maintenance, sampling and cell counting (i.e., NC200 and CellDrop).Follows and executes batch records and standard operation procedures.Performs aseptic and closed manipulations within Biosafety Cabinet and Grade B, C and D Cleanrooms.Performs manufacturing process steps in accordance with cGMP, procedures and relevant regulations.Performs delegated work assignments in a timely and complete manner.Supports Process Development and Manufacturing Sciences, as needed.Authors and maintains controlled documents including but not limited to SOPs, forms and batch records.Assists with deviation investigations and implementing CAPAs.Assists with qualification and validation activities including equipment qualification, gown qualification, aseptic process validation and process qualification/validation.Maintains manufacturing facility in a 5S and inspection-ready state.Cross trains in other areas including Vector Manufacturing, Manufacturing Sciences, Process Development, QC and QA to perform additional job functions, as necessary.Trains and leads other Technician I on all processes and equipment functionality.Responsible for assisting with startup activities in area of responsibility.Assists in commissioning & qualification of production equipment.Assists in the review & creation of operation documents by providing input to technical composition of documents.Operates on the manufacturing floor in accordance with cGMP's and standard operating procedures.Prepares equipment for manufacturing operations and monitors equipment to ensure process specifications are met.Uses and maintains bench top equipment in accordance with relevant procedures.Effectively demonstrates understanding of cGMPs & applies to specific responsibilities.Follows accurate oral & written procedures when operating production equipment & performing processing steps.Maintains orderliness of process area.Practices safe work habits and adheres to Resilience's safety procedures and guidelines.Assists in training of new and junior staff.Utilizes manufacturing knowledge to improve process operations and affect positive change.Escalates issues related to product and safety to senior staff. qualifications: Associates/Bachelor's (science preferred) degree with 4+ years in cGMP manufacturing environment or Bachelor's degree and 3+ years experience. skills: Biology, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.