What are the responsibilities and job description for the Cell Therapy Process Manager position at AmplifyBio?
About the Role
The Process Engineer will be responsible for managing the transfer of CGT manufacturing processes from our clients into the AmplifyBio GMP facility. They will provide leadership and training of the manufacturing staff on cell and gene manufacturing processes and equipment. Additionally, they will support the manufacturing staff during technical transfer, start up, and in routine processing.
This position requires close collaboration with other operational groups to ensure that all GMP requirements are met for the implementation of processes into the AmplifyBio facility. The successful candidate will also work closely with Supply Chain, Quality Control, Validation, Engineering, and Quality Assurance functions internally to ensure the facility meets all appropriate standards and cell therapy manufacturing processes are performed per client and GMP requirements.
Key Responsibilities:
- Manage the transfer of CGT manufacturing processes from clients into the AmplifyBio GMP facility
- Provide leadership and training of the manufacturing staff on cell and gene manufacturing processes and equipment
- Support the manufacturing staff during technical transfer, start up, and in routine processing
- Work closely with internal functional departments and external clientele to ensure deliverables are met
The Process Engineer will be responsible for managing the transfer of CGT manufacturing processes from our clients into the AmplifyBio GMP facility. They will provide leadership and training of the manufacturing staff on cell and gene manufacturing processes and equipment. Additionally, they will support the manufacturing staff during technical transfer, start up, and in routine processing.
This position requires close collaboration with other operational groups to ensure that all GMP requirements are met for the implementation of processes into the AmplifyBio facility. The successful candidate will also work closely with Supply Chain, Quality Control, Validation, Engineering, and Quality Assurance functions internally to ensure the facility meets all appropriate standards and cell therapy manufacturing processes are performed per client and GMP requirements.
Key Responsibilities:
- Manage the transfer of CGT manufacturing processes from clients into the AmplifyBio GMP facility
- Provide leadership and training of the manufacturing staff on cell and gene manufacturing processes and equipment
- Support the manufacturing staff during technical transfer, start up, and in routine processing
- Work closely with internal functional departments and external clientele to ensure deliverables are met
