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Title   Company Name     Location   Date  
RA Project Manager 

  omrix    Tel Aviv Area, Nes-Ziona   8/8/2013 
Category: Biotechnology, Pharmacy/Pharmacology, Regulatory Affairs  
Education:   Position type: Full Time Employee  Experience: 2 years 
Area(s) of expertise desired: Biology, GMP, Regulatory Affairs  
Omrix, a J&J Bio-Pharmaceutical company, is seeking RA Project Manager for itsí Nes-Ziona or Jerusalem Site. The position includes Providing Regulatory Affairs support, Generating and managing submission documents for new products or changes to existing files;
Assessing company activities, including new efforts and modifications for existing products, for regulatory impact and creating and executing regulatory strategies for implementation; Tracking requirements of regulatory agencies and implementing file updates accordingly.
Degree in biology, chemistry, or another related field.
At least 2 years of Similar industry experience (QA / Medical Device) -
Experience in biologics Regulatory Affairs an advantage.
Familiarity with regulatory requirements
Working experience with regulatory authorities
Excellent communication, interpersonal and organization skills.
Computer skills: Microsoft Office applications.
Language: mother-tongue level English required

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