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Experience with PMA and/or 510K submissions a plus. At Tempo Therapeutics, we are pioneering a new era in tissue engineering and regenerative medicine with our cutting edge Microporous-Annealed-Particle (MAP) technology platform.
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Requirements: Positive mental attitude (PMA) Enjoy working with a team Enjoy working in a fast-paced environment Drive and determination Desire for personal and professional growthCompany IntroductionThe Arby's brand purpose is Inspiring Smiles Through Delightful Experiences.
$15.5 - $16 an hourFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experience developing firmware for use in regulated medical devices (i.e. 510(k), PMA) is. Biolinq is a venture-backed clinical stage medical device company developing a wearable biosensor platform that measures biomarkers important to the management of many clinical conditions including diabetes.
$110,000 - $130,000 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Experience in Portable Maintenance Aid (PMA) activities such as aircraft forms documentation and supply chain management activities. Possess effective communication skills for coordinating with Contractor Field Team (CFT) Leads, Aircraft Managers/Supervisors, Field Service Reps, System Engineers, Maintenance Logistics Support Managers, Customer (DCMA/GCQA), COR/QAE and maintainers regarding quality issues, Instrumentation System Integration, Deficiency Analysis/Reporting, customer complaints, and other issues related to higher quality as they occur.
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Experience with breakthrough, RMAT, and orphan designation submissions; experience with companion diagnostic submissions (IDE/PMA) a plus. An exciting and innovative clinical-stage biopharmaceutical company dedicated to the development of first-in-class cellular immunotherapies for patients with cancer and autoimmune disease is looking for an Executive Director in Regulatory Affairs to oversee and direct the strategic planning and execution of clinical regulatory activities essential for initiating and conducting clinical trials and securing marketing authorization.
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Minimum of 15+ years of regulatory experience in the diagnostics industry, with a focus on in vitro diagnostics or single site PMA or 510(k) Strong understanding of European regulations, including the European Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR.
$260,000 - $357,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We pride ourselves on approaching all situations with a Positive Mental Attitude (PMA) and encouraging collaboration. With operations in 54 countries, Chubb provides commercial and personal property and casualty insurance, personal accident and supplemental health insurance, reinsurance, and life insurance to a diverse group of clients.
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Positive Mental Attitude (PMA) Cross-Training / Graphic Design and/or Production Specialist. Positive Mental Attitude (PMA) This position involves a hybrid in-store/outside sales as many of our projects require visiting the customer at their facility.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Assist in regulatory submissions (510(k), PMA, and CE) We have a great opportunity for a Regulatory Affairs Specialist to join our team! The Regulatory Affairs Specialist will assist in regulatory submissions, interpret regulations, and provide regulatory guidance.
ExpandApply NowActive JobUpdated 10 days ago
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