Cell Therapy Specialist
Company | Takeda |
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Location | Cambridge, MA, USA |
Salary | $80000 – $130000 |
Type | Full-Time |
Degrees | Bachelor’s |
Experience Level | Entry Level/New Grad, Junior |
Requirements
- Bachelor’s degree in Biology, Engineering, Biomedical Engineering, or related field plus 1 year of related experience
- 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)
Responsibilities
- Execute unit operations for manufacturing of patient therapies according to standard operating procedures and cGMP, regulatory and safety requirements
- Perform operations in a cleanroom environment, using proper controls to assure aseptic processing
- 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.
Preferred Qualifications
-
No preferred qualifications provided.