Cell Therapy Specialist Position Available In Suffolk, Massachusetts

Job Description:

By clicking the “Apply” button, I understand that my employmentapplication process with Takeda will commence and that theinformation I provide in my application will be processed in linewith Takeda’s Privacy Notice and Terms of Use . I further attestthat all information I submit in my employment application is trueto the best of my knowledge. Job Description Pursuant to Section 20C.F.R. 656.10, you are hereby notified that an application forAlien Employment Certification will be filed by Takeda DevelopmentCenter Americas, Inc.

for the following job opportunity:

JOBLOCATION

Cambridge, MA

POSITION

: Cell Therapy Specialist

POSITIONDESCRIPTION

Takeda Development Center Americas, Inc. is seeking aCell Therapy Specialist with the following duties: Execute unitoperations for manufacturing of patient therapies according tostandard operating procedures and cGMP, regulatory and safetyrequirements which includes basic cell culture as well asspecialized techniques for cell selection, activation,transduction, and purification; perform operations in a cleanroomenvironment, using proper controls to assure aseptic processingincludes gowning, cleaning, and isolation procedure; performsupporting operations as needed including preparation ofconsumables, media blending, cleaning, and environmentalmonitoring; complete manufacturing tasks following standardoperating procedures and batch document instructions, completingforms, reports, logs and records of equipment, and batches asrequired; ensure all training assignments are complete and up todate, to maintain necessary technical skills and knowledge; ensureprocessing equipment and required materials are available,maintained, and qualified as required for the differentmanufacturing activities; support investigations in manufacturingand technical deviations; participate in problem identification,problem solving, and change initiatives in cooperation with otherteams and function.; up to 20% remote work allowed.

REQUIREMENTS

Bachelor’s degree in Biology, Engineering, Biomedical Engineering,or related field plus 1 year of related experience.

Priorexperience must include:

Develop GMP compliant documents such asbatch records and procedures for use in a manufacturing setting;Process and culture mammalian cells in a lab environment; Preparematerials for and perform analytical methods in support of clinicalmanufacturing; Execute GMP activities in support of clinicalmanufacturing; Media preparation/reagent prep (media/interleukins).Full time. $80,000 to $130,000 per year. Competitive compensationand benefits.

Qualified applicants can apply athttps:

//jobs.takeda.com . Please reference job

R0151592 . EOE

Anyindividual may provide documentary evidence bearing on thisapplication, with information on available workers and informationon wages and working conditions, to the Certifying Officer, U.S.Department of Labor, Employment and Training Administration, Officeof Foreign Labor Certification, 200 Constitution Avenue, NW, RoomN-5311, Washington, DC 20210. Locations Boston, MA Worker TypeEmployee Worker Sub-Type Regular Time Type Full time