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Job Description
Job Description
Gives support for the preparation of all regulatory and GMP(Good Manufacturing Practise)files,
Responsible for translation and filing of the related parts of the regulatory and GMP submission dossiers,
Gives support to RA specialist and RA manager on her/his daily regulatory tasks with regard to filing, archiving, tracking, documenting, etc.
Gives support to the daily business activities of the units.
Requirements
4th/5th years students or graduates from Pharmacy Faculties,
Able to work during summer, for full time
Good command of written and spoken English is preferred,
Good command of MS Office applications.
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
Job Posting End Date:09/03/2024
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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