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Location:Audubon, PA Job Code:RAPMKB0515 Description The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products.6/26/2016 Audubon, PA Save This Job
Up To Lead Regulatory Affairs Specialist Scientific Protein Laboratories LLC (SPL) is a biopharmaceutical world leader in the development and cGMP compliant manufacturing of pancreatic enzymes and heparin. We have an immediate opening in Waunakee, WI (Madison Area) for an6/2/2016 Waunakee, WI Save This Job
Location:Audubon, PA Job Code:IRPMLB0216 Description The International Regulatory Affairs Specialist writes, submits and gains approval of product registrations and other submissions to international Regulatory agencies. This position entails development of submissions in6/26/2016 Audubon, PA Save This Job
POSITION SUMMARY: The position is responsible for diverse regulatory functions, including but not exclusive to the development of Medical Device submissions and the implementation of Regulatory Compliance. ESSENTIAL DUTIES AND RESPONSIBILITIES: ? Prepare submissions for US and6/7/2016 Sylmar, CA Save This Job
Regulatory Specialist (United States; Russia; Egypt; Turkey; UAE; Israel; Saudi Arabia) Responsibilities Ensure compliance with regulatory agency regulations and interpretations Prepare responses to regulatory agencies? questions and other correspondence Organize and maintains6/19/2016 Westborough, MA Save This Job
ALAMEDA, CAREGULATORY AFFAIRSFULL-TIME APPLY FOR THIS JOB As a member of our Regulatory Affairs team, you will play a key role in expediting the availability of our lifesaving products worldwide by ensuring that they meet all requirements set forth by regulatory bodies in the6/30/2016 Alameda, CA Save This Job
Department: Manufacturing Operations Reports to: Director of Operations and Project Management Scope of Supervision: No Direct Reports EDUCATION, BUSINESS EXPERIENCE, AND PHYSICAL REQUIREMENTS ? Basic computer skills necessary ? Experience in Medical Device assembly and working6/29/2016 Minneapolis, MN Save This Job
Menlo Park, CA, US Worker Category :Full Time Job ClassProfessional Earlens is looking for a regulatory professional who has experience with FDA and worldwide submissions to support a new technology hearing device. The title shall commensurate with candidate?s4/28/2016 Menlo Park, CA Save This Job