Document Control Specialist, San Diego, Medical Device, $20-$25

This is not an entry-level position, but is best suited for those newly working in medical device industry. The ideal candidate should have basic understanding and comprehension of ISO 13485 and requirements of existing regulations, however they are not yet expected to provide guidance related to compliance other than ensuring consistent adherence to approved processes. A sharp eye for detail, exceptional organizational skills, strong editing and proofreading skills, the ability to learn and superb time-management skills to prioritize multiple deadlines are all necessary to succeed in this role. This is a full time position in a fast-paced expanding organization. Requirements: * Is familiar with a regulated environment and supporting a compliant quality management system * Familiar with ISO 13485 * Understands that regulation is law and varies from country to country * Excellent written and oral English, as well as strong interpersonal skills * Excellent organizational skills with attention to detail and follow-up * Ability and willingness to learn new things * Ability to understand technical topics and discussions and be able to summarize in a logical manner * Dependability and punctuality * Strong analytical skills/problem solving abilities * Proficiency in Microsoft Office Suite * Ability to interact professionally with external resources * Self-Starter with ability to multi-task This is a great opportunity with a fast paced up and coming medical device company. This position needs to be filled ASAP. So please apply immediately to be considered.

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com