We are currently seeking a Production Scheduler to join the Clinical Supplies Service Team at this exciting time of continued and sustained growth. The position deals primarily with the master schedule to ensure alignment with requirements between systems, schedules and the CSS site plans as well as manages our Planners/Buyers.

Reporting to the Global Supply Chain Lead, this role as the Supply Chain Production Scheduler will require you to manage the master schedule and materials requirements for standard packaging.

The role will see you create and manage the network planning process and drive resolutions for any immediate, medium or long term risks to supply during the relevant production readiness, scheduling review and S&OP forums when required.

The role will require you to be responsible for assisting the resolution of demand, supply and capacity issues among the sites supply chain ensuring the OTS and OTD dates reflect reality in the short term. Ensuring the production plan is in line with latest demand picture at all times. It is likely you will run ‘what-if’ scenarios to identify risks to the plan and/or identify opportunities to improve efficiencies in line with global inventory objectives and analyze spikes and valleys in demand to understand the key drivers and impact on capacity.

This role will require you to facilitate discussions during the relevant sites supply chain readiness or S&OP meetings, to mitigate risk of supply interruption while achieving the business goals set for inventory management and service levels to customers.

You will also support the JDE and Orchestrate system upgrades, conversions and implementations as necessary.

As the Master Scheduler your role is responsible for managing the Supply Chain Master Schedule for CSS Business in China which will require you to be involved in projects and decisions that impact immediate business performance along with future strategy and performance.

To be successful in this role you must have a thorough understanding of contract services preferably within a GMP environment.

Ideally you will also have validation and a working knowledge of MRP, Finite Planning techniques or systems.

Successful candidates will have a minimum:

• 3 years’ experience in a pharmaceutical manufacturing environment
  

• 5 Plus year’s previous Scheduling/Planning experience required

• Proven track record in motivating and managing direct reports

• APICS Certification a plus

上班地址：外高桥保税区