Document Quality Specialist - Switzerland, United Kingdom - CK GROUP
Description
CK QLS are recruiting for a Document Quality Specialist for a renowned Pharmaceutical company based in Basel, Switzerland, on a 1 year contract basis.
In this Document Quality Specialist position, you'll have to perform assessment, quality control and publishing of NIBR scientific documents to ensure consistency with source data and to achieve the technical quality to comply with internal and external guidelinesand requirements.
Other Document Quality specialist's responsibilities:
- Collaborate with external service providers as related to areas of responsibility.
- Collaborate to support timely compilation of highquality submissions for Global Health Authorities.
Qualifications:
- Undergraduate degree preferably in a scientific discipline or equivalent work experience
- Languages: English fluent (oral and written)
- Previous experience with electronic document management systems, document review and with compliance practices (GxP and SOP)
- Knowledge of clinical and nonclinical information
Apply:
Please could you send any correspondence in English. Please quote job reference 55098 in all correspondence.
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