Work Location: Couvet, Switzerland Route des Nasieux 18 Couvet 2108
Organization: Celgene International SaRL II
Shift: Day Job
Employee Status: Regular
Job Type: Experienced
Job Level: Individual Contributor
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 in the area of cancer and other severe, immune and inflammatory conditions.
We look for a Technician Coordinator GMP documentation based in Couvet (NE) to support the Manufacturing organization in the setup of our new plant.
Contract duration: 6 months (temp. mission)
Support the manufacturing teams with quality documentation management.
Support the QC, Production, Packaging and Validation teams with the management of GMP documents such as: Validation Protocols, Methods, Work Practices, SOPs, etc.
Tasks include the inventory, update, page setting, approval follow up and archiving of these documents,
Take care of the document flows in the eSystem (Celdox),
Administrative support to these teams: material ordering, coordination with 3rd parties, coordination with other departments (QA, Warehousing, Logistics, Finance, etc).
Skills & background
Fluent in French and in English (written and oral),
Technician diploma (or equivalent), CFC in business or other relevant education
Proficient in word processing programs,
Experience in GMP documentation in the pharma industry (or related): good documentation practices, document lifecycle management, electronic documentation management system,
Detail oriented and thorough,
Excellent organizational skills,
Team player, autonomous and at ease in a moving environment with multiple internal customers.