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      Medical science jobs in Munster 1 -5 of 5 (0.001s)

      Regulatory affairs specialist ii

      CorkBoston Scientific Corporation

      ...and associated ancillary products (medical devices and components) for the administration of drug product.Key Responsibilities:* Review and assess design and CMC changes, and prepare suitable submissions to ensure compliance to pharmaceutical regulatory requirements.* Support and provide regulatory input for pharmaceutical [...]

      Category Office & Administration

      7 days ago in Experteer

      Quality engineer - p2 (defined term)

      ClonmelBoston Scientific Corporation

      ...background.* Experience in the medical device industry.* Working knowledge and understanding of FDA, ISO13485, and the medical device industry quality requirements associated with manufacturing and supplier controls.* Experience in problem solving and process improvement methodologies.* Process Validation, Risk [...]

      Category Engineering & Architecture

      7 days ago in Experteer

      R&d engineer ii

      CorkBoston Scientific Corporation

      ...a relevant discipline including Biomedical, Mechanical, Polymers & Materials, Chemical Engineering.* 5+ years industry experience within a regulated industry environment and with a track record of accomplishments.* R&D/technical experience in the pharmaceutical or medical device industry essential.* Experience [...]

      Category Engineering & Architecture

      7 days ago in Experteer

      Regulatory affairs specialist, p2

      ClonmelBoston Scientific Corporation

      ...(level 8) in life sciences, engineering or related field* Basic knowledge of FDA and international regulations* Ability to communicate complex ideas clearly and simply both orally and in writing* Understanding of medical device regulations, FDA and international regulations.* Team player with excellent [...]

      Category Fashion & Arts

      7 days ago in Experteer

      Associate quality manager - m2

      CorkBoston Scientific Corporation

      ...to cGMP’s of all medical device regulatory agencies (e.g. FDA and TUV). Provide functional expertise to other support functions on quality related issues (e.g. regulatory requirements, statistical techniques, sampling principles). Identification and implementation of appropriate statistical techniques to monitor process [...]

      Category Manufacturing & Production

      29 days ago in Experteer
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