What are the responsibilities and job description for the Technical Production Assistant position at Takeda Pharmaceutical?
As a Manufacturing Technician II at Takeda Pharmaceutical, you will play a critical role in ensuring the smooth operation of our production facilities.
About the Position:
The ideal candidate will have a strong background in manufacturing and experience working in a fast-paced production environment. They will be responsible for implementing all production processes, including those related to cGMP guidelines and regulations.
Responsibilities will include assisting with the movement of Flexbumin between stages of inspection and packaging within the value stream. The individual may act as line lead and ensure the smooth operation of the line, meeting daily goals. They will also be responsible for documenting process activities on routers or in the electronic batch management system (EBM).
Key Responsibilities:
- Implement all production processes while adhering to cGMP guidelines and regulations
- Assist with the movement of Flexbumin between stages of inspection and packaging within the value stream
- Act as line lead and ensure the smooth operation of the line, meeting daily goals
- Document process activities on routers or in the electronic batch management system (EBM)
- 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 cross-functionally 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 following GDP/GMP guidelines
- Perform daily cleaning of the production area to maintain in GMP fashion
- Review and revise pertinent documentation as appropriate
- Train new and existing employees/contractors on procedures
- Communicate issues related to safety, quality, compensation and benefits, and equipment to the manufacturing lead operator and supervisor
Requirements:
- Good interpersonal skills and ability to work effectively and efficiently in a team environment
- Must be able to speak, read, write, and follow detailed written and oral instructions in English
- Knowledge of cGMP manufacturing
- A self-starter with a positive attitude and good time management skills
- Ability to remain professional at all times
- Meet the deadlines of individual production tasks during shift
- Follow the company's safety and quality guidelines
