Senior Production Scheduling Specialist

il y a 2 semaines

Gent, Belgique Legend Biotech EU Temps plein

**Company Information**

Legend Biotech entered into a global collaboration agreement with Janssen Biotech, Inc. to develop, manufacture and commercialize ciltacabtagene autoleucel (cilta-cel). Through our strategic partnership, we look to advance the promise of an immunotherapy in the treatment of multiple myeloma.

**Role Overview**

The Senior Production Scheduling Specialist will be part of the Manufacturing Technical Operations team responsible for detailed scheduling within the end-to-end Supply Chain for the production of a personalized cell therapy and supporting both clinical and commercial requirements in the cGMP environment in accordance with company policies and procedures.

The position requires strong analytical and advanced system and tool based skills with the ability to quickly analyze data, schedules resources and partner with Vein-to-Vein (V2V), Manufacturing Operations, Planning and Procurement to understand production slots availability to meet patients demand while providing an optimal service level and performance.

**Major Responsibilities**
- Based on the master production schedule, develop a coordinated floor schedule, including daily work schedules, across multiple areas.
- Perform and communicate activities such as material consumption and process orders release status, to enable on-time production plan execution and scheduling attainment
- Develop, interconnect, maintain, and actively manage functional stakeholder relationships to enable assembly and execution of an optimized/aligned plan
- Lead and/or participate in regular plant planning meetings to successfully execute against the MPS (Master Production Schedule) and LRP (Long Range Planning)
- Collaborate with other planners and schedulers within the team that support areas or functions and those plans into a master plant production schedule
- Monitor progress-to-plan by proactively identifying threats/challenges that jeopardize the production plan and work to pull functional stakeholders together in order to prioritize and develop contingency/mitigation strategies to ensure manufacturing operations and scheduling continuity
- Partner, support and communicate frequently with V2V, Manufacturing Operations, Planning & Procurement counterparts to ensure daily and longer-term production plans are successfully achieved
- Support in developing strategic planning methodologies and tools to integrate all operating and support area activities that is scalable, sustainable and handles high throughput and demand
- Actively participate and contribute to future capacity and scheduling analysis that maintains certain flexibility and optimized resource capacity and utilization
- Prepare, lead and participate in routine planning and communications, meetings, reports, presentations, graphs and metrics
- Serve as S4 HANA key user for D2D manufacturing planning & scheduling activities
- Support the BPO in implementing and testing the system releases, as well as enabling the best business practice adoption and process improvement end-to-end

**Qualification**

**Education**:
Bachelor's degree in Supply Chain Management, Business/Engineering, or related field or equivalent work experience required

**Experience**:

- A minimum of 5 years working within supply chain/operations in a similar planning/scheduling function.
- Operations experience within a cGMP environment in the biotech/biopharma industry preferred.
- SAP - Advanced Supply Chain Planning and D2D best business practices knowledge is highly preferable

**Capabilities, Knowledge, and skills**:

- An ability to build strong partnerships and effectively integrate with external collaborators to drive projects/programs forward in a matrixed environment.
- Ability to work independently and successfully, prioritize and manage multiple tasks simultaneously, integrate cross-functional issues and balance competing priorities effectively.
- Clear and succinct verbal and written communication skills with an attention to detail and the ability to follow procedures.
- Knowledge of supply chain principles (materials management, production planning & scheduling etc.), pharmaceutical operations, and industry practices.
- Knowledge of cGMP regulations and FDA guidance related to manufacturing of cell based products.
- Ability to support as required by the manufacturing and support area processes
- Ability to promote a mindset of continuous improvement, problem solving, and prevention
- Technologically savvy with the ability to quickly adopt new systems and processes. Proficient in Excel (Pivot Tables and Advanced Analytics), Word, Visio, and exposure to ERP and other financial accounting systems.
- Transparent, Passionate, Fearless and Accountable

**Language(s)**:
English/Dutch

LI-AG1

Legend Biotech maintains a drug-free workplace.

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