Regulation available positions

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חיפוש משרות חופשי  

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היקף משרה

   
   
   
   
   

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סוג משרה

     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     
     

לוח משרות דרושים, נמצאו 1 משרות עבודה Regulation available positions

Positions address both male and female
תיאור תפקיד:
• The main objective for this role is to assist with the management of
the Quality System, audit requests, production records &
certification.
• Prepare quality records and SOP’s for internal production purposes
as per GMP requirements
• Assist with generation of R&D/QC & QA reports and data review.
• Performing GMP audits in Production.
• Participation (as GMP supervisor) during production activities.
• Aseptic Rooms Environment Data review and room release for production
• Preparation of clinical trial materials shipments and sample shipments for different purposes (contract laboratories etc.)
• Connection with laboratories/companies abroad
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דרישות:
• BSC / MS.c in Life science Biology/Biotechnology
• A minimum of 2 years experience in a pharmaceutical /
biotechnology company within a GMP environment
• Experience with writing SOP’s
• Proficient in Microsoft Office suite
• Pedantic
• Good organizational skills
• written communications skills are essential
• English - high level
• High responsibility skills
• Reporting to the Head of QA

היקף משרה: Full-time
קוד משרה: JB-07870
קרא עוד

תן למשרות שלנו לחפש אותך - חינם!