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| תיאור: |
For Teva Pharmaceutical Industries which is based in Netanya,scientific document specialist is required Job description:
Document quality control specialist for our Nonclinical development department. The person will Produce high quality nonclincal QC audit of raw data and regulatory deliverables, to ensure the integrity of this information as well as to ensure compliance to submission standards. The nonclinical QC audit must meet nonclinical QA requirements and should be performed using nonclinincal QA and regulatory guidelines.
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| דרישות: |
At least B.Sc.in life sciences/Pharmaceutics or related field
Experience/Understanding of nonclinical toxicology/pharmacology and drug metabolism in pharmaceutical field - Am advantage
Strong organizational skills, ability to work on diverse project load, excellent communication skills.
Exceptional written and oral communication skills, along with a solid command of the English Language including style, spelling/grammar, punctuation.
Commitment to accuracy (according to QA feedbacks), and work under tight deadlines in a fast paced environment. Adapt to and embrace change in a rapidly changing environment. Establish work priorities and manage multiple projects.
Full time position at our Netanya R&D Site
Applications should be submitted through our website (Position no.7507):
https://jobs.teva.co.il/pos7507?referrerId 427
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| היקף המשרה: |
מלאה |
עיר/ישוב: |
נתניה |
תפקיד: |
איש צוות |
שנות ניסיון: |
שנה |
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