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Detailed Scheduler (long term temporary)

Req #: 16002132
Location: BOUDRY, NE CH
Job Category: Manufacturing/Technical Operations
Work Location: Boudry, Switzerland Route de Perreux 1 Boudry 2017
Organization: Celgene International SaRL
Schedule: Full-time
Shift: Day Job
Employee Status: Regular
Job Type: Experienced
Job Level: Individual Contributor
Travel: No

Description

In this position the Detailed scheduler will manage within a short-mid term scope the logistical activity for the manufacturing site in Boudry (semi-finish and finish products).

This mission will be lead in close collaboration with the Manufacturing Detailed Scheduler and the internal stakeholders. The Manufacturing Detailed Scheduler acts as the back-up of the Manufacturing Scheduler.

 

DUTIES AND RESPONSIBILITIES

  • Define and guarantee the execution of the short and mid-term plans in a timely and smooth manner.
  • Track the Semi-Finish (SF) and Finish Goods (FG) batches from creation to release (material reservation incl) in Oracle

  • Lead the scheduling meetings related to his/her scope of activities

  • Check the reservation consistency for Bulk reservation

  • Coordinate of routine and non-routine operations: with the different stakeholders (QA, QC, Validation, Production, Warehouse, Supply Chain…

  • Coordinate stability schedule in close collaboration with Quality Control Department

  • Coordinate Make To Order repacking activity

  • Follow-up and define solutions for issues or deviations related to his/her scope of activities

  • Accountable for his/her own KPI for SF and FG

  • Participate to improvement initiatives

*LI-NS1



Qualifications

SKILLS/KNOWLEDGE REQUIRED

  • + 3 years experience in the field of production or supply chain planning
  • Experience in an industrial international environment
  • Capability to work in a changing environment and beyond pre-defined processes and to actively contribute in defining new structures
  • Pro-active personality with an eye for anticipation and continuous improvement
  • Conscientious, reliable in action follow-up
  • Good negotiation, priority management communication (works in transparency), problem solving and decision-making skills
  • Team-player
  • Excellent IT proficiency: MS Office, Excel, ERP, Oracle experience is an asset
  • Knowledge of the pharmaceutical environment and GMP-experience are an asset
  • Fluency both in French and English 
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