Cell Therapy Specialist

Takeda Pharmaceuticals; Boston (MA); Hybrid; USD 80,000 - 130,000; Full time

Job summary

An established industry player is seeking a dedicated Cell Therapy Specialist to join their innovative team. This role involves executing critical manufacturing operations for patient therapies, ensuring compliance with stringent GMP standards. With a focus on cell culture and analytical methods, you'll play a vital role in supporting clinical manufacturing efforts. The position offers a dynamic work environment with up to 20% remote work flexibility, making it an exciting opportunity for professionals passionate about advancing therapeutic solutions. Join a forward-thinking company that values your expertise and commitment to excellence.

Qualifications

• 1+ years of experience in a manufacturing setting with GMP compliance.
• Experience with mammalian cell culture and analytical methods.

Responsibilities

• Execute manufacturing operations for patient therapies per SOPs.
• Perform cleanroom operations and maintain aseptic processing.

Skills

Cell Culture

GMP Compliance

Analytical Methods

Problem Solving

Education

Bachelor's Degree in Biology

Bachelor's Degree in Engineering

Bachelor's Degree in Biomedical Engineering

Tools

Laboratory Equipment

Media Preparation Tools

Job description

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sPrivacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:

JOB LOCATION: Cambridge, MA

POSITION: Cell Therapy Specialist

POSITION DESCRIPTION: Takeda Development Center Americas, Inc. is seeking a Cell Therapy Specialist with the following duties: Execute unit operations for manufacturing of patient therapies according to standard operating procedures and cGMP, regulatory and safety requirements which includes basic cell culture as well as specialized techniques for cell selection, activation, transduction, and purification; perform operations in a cleanroom environment, using proper controls to assure aseptic processing includes gowning, cleaning, and isolation procedure; perform supporting operations as needed including preparation of consumables, media blending, cleaning, and environmental monitoring; complete manufacturing tasks following standard operating procedures and batch document instructions, completing forms, reports, logs and records of equipment, and batches as required; ensure all training assignments are complete and up to date, to maintain necessary technical skills and knowledge; ensure processing equipment and required materials are available, maintained, and qualified as required for the different manufacturing activities; support investigations in manufacturing and technical deviations; participate in problem identification, problem solving, and change initiatives in cooperation with other teams 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. Prior experience must include: Develop GMP compliant documents such as batch records and procedures for use in a manufacturing setting; Process and culture mammalian cells in a lab environment; Prepare materials for and perform analytical methods in support of clinical manufacturing; Execute GMP activities in support of clinical manufacturing; Media preparation/reagent prep (media/interleukins).

Full time. $80,000 to $130,000 per year. Competitive compensation and benefits.

Qualified applicants can apply at https://jobs.takeda.com. Please reference job # R0151592. EOE

Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.

Locations

Boston, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time