Specialist – CAR-T Production Planning and Scheduling
| Company | Bristol Myers Squibb |
|---|---|
| Location | Summit, NJ, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Mid Level |
Requirements
- Bachelor’s degree required. An equivalent combination of education, experience and training may be considered.
- 2 to 3+ years of relevant work experience required, preferably in a regulated pharmaceutical manufacturing environment in Cell Therapy, Cryopreservation, or Manufacturing Operations.
- 1+ years of experience supporting ERP systems (preferably Oracle EBS and SAP).
- Understanding of cell culture, cryopreservation, purification, and aseptic processing or lab techniques.
- Knowledge of cGMP/Pharmaceutical regulations.
- Understanding of ERP systems and analytics/reporting tools.
- Experience in MS Office applications.
- Proficient written and verbal communication skills.
- Proficient presentation development and delivery skills.
- Technical writing capability.
Responsibilities
- Create and maintain detailed site plans for operations including apheresis receipt, material kitting, media process intermediates, manufacturing, and drug product shipments.
- Point of contact for the Manufacturing Operations team to provide support, facilitating operational continuity and addressing issues as they arise.
- Monitor and report KPI’s.
- Work with the Systems and Technology, Manufacturing Sciences and Technology team on system implementations and continuous improvement projects.
- Collaborate with IT Business Partners in support of modeling and scheduling simulation implementations.
- Support the S&OP process by providing site level manufacturing capacities and operational capabilities.
- Maintain and update site procedures for CAR-T material management functions.
Preferred Qualifications
- Experience in a regulated pharmaceutical manufacturing environment in Cell Therapy, Cryopreservation, or Manufacturing Operations is preferred.