XPost: mtl.jobs, ont.jobs, tor.jobs   
   From: careers@jedgarcareers.com   
      
   We are currently searching for a Regulatory Affairs Associate in Montreal.   
      
   The incumbent will be in charge of preparation, review, submission and   
   life cycle management of products locally and internationally.  Ensuring   
   Regulatory submissions are accurate, scientifically sound and in   
   compliance with foreign and local government guidelines.  We’re looking   
   for someone who has maintained up-to-date knowledge and expertise on   
   regulations and guidelines for assigned markets ensuring regulatory   
   compliance for marketed products.   
      
   You must be able to coordinate with functional teams like R+D, Global   
   Op’s, QA/QC, Legal, Biopharmaceutics and Project Management in the   
   preparation/compilation of regulatory documents and execution of   
   additional tests as required.  You must have experience fulfilling   
   additional information requests from assigned Ministries of Health and   
   coordinate internal efforts to ensure that a proper and complete answer   
   is given in a timely fashion.   
      
   Requirements Include:  Bachelors or Masters Degree in Chemistry,   
   Biochemistry, Pharmacology or other relevant disciplines, The RAC   
   -Regulatory Affairs Certificate, 2-4 years of Pharmaceutical industry   
   experience, good understanding of drug development process, knowledge   
   and understanding of ICH guidelines with the ability to interpret and   
   apply them, electronic CTD submission experience, Strong communication   
   skills in French and English – other languages are an asset, good   
   computer skills with Word, Excel, Outlook and Access.   
      
   Salary is to $55K, location is Montreal.   
      
   Call Jason for all the details at 416 225-2628 and check us out at:   
   http://www.jedgarcareers.com   
      
   careers@jedgarcareers.com   
      
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