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Reference # : 17-00714 Title : Scientist
Location : PR
Position Type : Full Time/Contract
Experience Level : 5 Years Start Date / End Date : 07/24/2017 / 04/30/2019  
Description
Working knowledge of appropriate global medical device regulations, requirements, and standards, such as 21 CFR Parts 803, 806, and 820, ISO13485, ISO14971, European Medical Device Directive (93/42/EEC), Canadian Medical Devices Regulation (SOR/98-282), Japanese MHLW Ordinance 169, and ISO 9001.•Ability to analyze large data populations using MS Excel or Minitab, Trackwise, Maximo, EDMQ, and presenting information in a clear, structured manner
Bachelor's degree in Life Sciences or Engineering and 5 years of Parenteral/Biopharma Formulation and Filling experience OR Master's Degree in Life Sciences or Engineering and 3 years of Parenteral/Biopharma Formulation and Filling experience