Technical Coordinator GMP (temp assignment 6 months)
Req #: 16002185
Location:
COUVET,
NE
CH
Job Category: Manufacturing/Technical Operations
Work Location: Couvet, Switzerland Route des Nasieux 18 Couvet 2108
Organization: Celgene International SaRL II
Schedule: Full-time
Shift: Day Job
Employee Status: Regular
Job Type: Experienced
Job Level: Individual Contributor
Travel: No
Description
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)
Job summary
Support the manufacturing teams with quality documentation management.
Responsibilities
- 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).
*LI-EX
*LI-MONEU
Qualifications
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.
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