Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.
In this position the Manufacturing scheduler will manage within a short-mid term scope the logistics activities for the manufacturing site in Couvet (bulk, semi-finish goods, finish goods). This position will be in based in Couvet and ensures the operational readiness and starts for his/her scope of activities. The first months will be based in Boudry and perform the activities described for the Boudry manufacturing site.
This mission will be lead in close collaboration with key users working in Manufacturing Operations Services and other internal stakeholders (Quality Control, Quality Assurance, GSCP, PLM, Production, Validation).
The Manufacturing Scheduler acts as the back-up of his/her scheduler peer.
Duties and Responsibilities
All tasks assigned to the Manufacturing scheduler are done according to GMP’s and GDP’s.
Define and guarantee the execution of the short and mid-term plans in a timely and smooth manner
Participate to monthly supply plan activities
Check the reservation consistency for production orders managed by his/her peer
Coordinate the out-sourcing activities
Coordinate stability schedule in close collaboration with QC Department
Coordinate the phase out and phase in of the recipes in close collaboration with MEDM Team
Coordinate the make to order (MTO) repacking
Be accountable for the CCR Tasks execution in the frame of change management
Follow-up and define solutions for issues or deviations related to his/her scope of activities
Be accountable for OTIF/KPI for his/her scope of activities
Participate to improvement initiatives and projects
Be accountable to execute his/her activities as per GMP regulations and ensure timeliness for EQRMS record execution.
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Celgene is a global biopharmaceutical company committed to improving the lives of patients worldwide. At Celgene, we seek to deliver truly innovative and life-changing treatments for our patients.