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Job Description

About the Role:

As a Manufacturing Technician II, you will implement all processes in production while strictly following cGMP, environmental health and safety guidelines and any applicable related regulations. You will have technical and administrative competence to organize and lead production activities. You will participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include assisting with the movement of Flexbumin between the different stages of inspection to packaging within the value stream. In this role, you may act as line lead, and will ensure the line operates smoothly and keeps up with daily goals. In addition, you will document your process activities on routers or in the electronic batch management system (EBM). You will report to the Supervisor, Manufacturing. The role supports Takeda's mission by ensuring efficient and high-quality production processes.

How you will Contribute:

• Maintain a safe and quality working environment
• Participate in Continuous Improvement Teams.
• Support manufacturing operations.
• Lead Manufacturing Technicians I in daily tasks.
• Operate general production equipment (such as Downstream Automated Packaging {DAP} lines, forklifts, and hoists).
• Move pallets to different rooms within the value stream.
• Communicate and work with other departments.
• Receive and distribute supplies into the production area.
• Follow cGMP, environmental health and safety guidelines, and any other regulations.
• Complete relevant paperwork and electronic system prompts/tasks, following GDP/GMP guidelines.
• Perform daily cleaning of the production area to maintain in GMP fashion.
• Train our employees/contractors on procedures.
• Communicate issues related to safety, quality, compliance and equipment to the manufacturing lead operator and supervisor.
• May perform other duties as assigned to enable team success and contribute toward professional development.

What you bring to Takeda:

• High school diploma or GED 2+ years of experience or AA or higher and 1+ years of related work experience.
• Good interpersonal skills and ability to work effectively and efficiently in a team environment.
• Can speak, read, write, and follow detailed written and oral instructions in English.
• Understanding of cGMP regulations in a pharmaceutical manufacturing environment.
• Ability to remain professional at all times.
• Meet the deadlines of individual production tasks during shift.
• Follow the company's safety and quality guidelines.

Important Considerations

At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product. In this role, you may:

• Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.
• Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.
• Work in a cold, wet environment.
• Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.
• Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and b