Do you want to work for a renowned healthcare company ? Do you have labelling experience in such an environment ?
Our client is looking for the next Supply Chain Specialist for a temporary position of 12 months (with possibility of extension) in the Luzern region.
Creation and approval of label text translations with the aid of systems ( Clinical Label Proof Generator and the electronic document database ).
Creation and approval of the translations and corresponding documents with regards to the study-specific, company-internal and country-specific regulatory requirements.
Creation and monitoring of the project schedule and coordination of projects from the label translation to the delivery of the labels to the packaging department.
Ensures through effective project management that the communication to the relevant locations is guaranteed at all times and the project requirements can be met.
Consultation of the responsible project manager with regards to the determination of the label text in compliance with international regulatory requirements and internal company standards.
Provides input and partners with other work centers to develop the packaging / labeling strategy for the individual clinical products in regards of label text.
Participates regularly in internal and global coordination meetings
Ensures a regular and pro-active collaboration with our booklet vendor.
Maintenance of the label generation documentation according to GMP Standards.
Review of label generation documents according to study specific and regulatory requirements.
Works out proposals for continuous optimization of processes & procedures (SOPs) concerning clinical supply planning and packaging operations.
Investigations of internal and external product complaints regarding labels as well as implementation of corresponding risk assessments and the resulting corrective measures CAPA.
The individual must possess excellent communication skills
Excellent organizational skills, time management skills
Able to work independently
Eye for detail
Able to work in the GMP environment
Do you see yourself in those lines ? Then do not wait a second and apply quickly!