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PMA USA, a subsidiary of CNO Financial, has a strong commitment to diversity and inclusion. PMA USA (Performance Matters Associates, INC.) , is a national company that provides insurance benefits solutions and markets voluntary insurance products.
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Positive mental attitude (PMA) Positive mental attitude (PMA) Cleaning the dining room and all areas behind the counter. We at Arby's are committed to delivering a “Cut-Above” restaurant experience to our customers and a stimulating career environment for our employees.
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Experience with high-risk class IVD products (e.g. U.S. BLA/PMA, EU Class D and C, etc. As a Regulatory Affairs Specialist, you will support Bio-Rad's commitment to quality and compliance by coordinating the Domestic and International Registration Requests as a Regulatory Specialist.
$140,100 - $192,600 a yearFull-timeExpandUpdated 2 months ago - UpvoteDownvoteShare Job
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Experience working with Class III medical devices (PMA, IDE, EU MDR) Must demonstrate a history of successful Class III device submissions such as IDEs, PMAs, PMA supplements, 30-day notices, and Annual Reports in the US.
$120,691 - $150,864 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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New Agent Bonus: Earn $400 a week during your first 6 weeks (up to $2,400), in addition to your sales commissions. Our 4 day work week allows you to spend more time with your family. Sales lead management tool that makes it easy to identify existing clients and qualified prospects.
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Major contributions to or the leadership of projects from development through the 510k and PMA approval process. Review and approve quality records (deviations, CAPA/EVs, change controls) The Quality Assurance Manager will also provide Quality oversight of quality records such as Deviations, CAPAs, Change controls and review/approval of physical test methods documents.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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PM280 (Tomahawk Weapons System) is searching for a Production Program Analyst with an active Secret clearance to support the Missile Systems IPT from the PM280 detachments in Tucson, AZ.
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Knowledge of PMA/TSO/STC/OEM qualification and certification. Reporting to the Certification Manager, the Certification Engineer will be responsible for the research, planning, and execution of the regulatory certification process for interior components of airplanes.
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Interact and negotiate with regulatory agencies / Notified Bodies to support product life cycle management, including FDA for Class II and III Pre-Submission Meetings and PMA submissions, Health Canada for Class III/IV submissions, and EU MDR Class I – IV submissions and change notifications.
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Knowledge of FDA regulations, including 21 CFR, 510(k), and PMA requirements. Responsibilities Assist in the preparation, submission, and maintenance of regulatory filings and registrations, including 510(k) and PMA submissions.
$60,000 - $80,000 a yearFull-timeExpandUpdated 26 days ago - UpvoteDownvoteShare Job
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Proficiency in interpretation and application of US regulatory requirements for IVD/Medical Devices/Biologics including submissions experience for PMA and/or BLA products. BIO RAD LABORATORIES - 390 Regulatory Affairs Specialist IV Seattle , Washington Apply Now As a Regulatory Affairs Specialist IV you will support Bio-Rad's commitment to quality and compliance by coordinating the Domestic and International Registration Requests.
$107,200 - $147,400 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Familiarity with wireless charging standards such as Qi (WPC) or PMA. Your dedication to cross-disciplinary collaboration will help develop groundbreaking technologies, such as iOS, macOS, watchOS, and tvOS. By crafting these distinct, holistic user experiences, you’ll continue to uphold and advance the excellence people expect from Apple devices.
$150 - $200ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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As a key member of the Performance Measurement & Analysis (PMA) product area, the Investment Performance Analyst will play a crucial role in driving the technical implementation of performance capabilities, shaping the future of our product roadmap, and maximizing the value of our platform across the enterprise.
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Prepare Pre-Sub, IDE/IDE Supplement, PMA/PMA Supplement, 510(k) submissions, and technical documents to support CE mark/MDR submissions. The Principal Regulatory Affairs Specialist will be vital in launching new products and sustaining the current product portfolio.
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PM290 Senior Logistics Manager
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