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This role must have prior background developing global device and workplace strategies, implementing and supporting Microsoft 365, Intune/SCCM/JAMF, and has a deep passion for modernizing the workforce.
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Medical Device - Wound Care Sales - Biologics. Medical Device Sales selling Biologics, Regenerative Medicine or Wound Care. My medical device client is an innovative company that develops and manufactures regenerative therapies for wound and tissue repair.
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Side-by-side selling to find personalized solutions beyond the bare-bones device and service plan that keep our customers connected to the people and lifestyle they love, including anything from unique accessories cutting-edge IoT devices.
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We specialize in electrical discharge machining (EDM) and precision manufacturing of all mechanical components for the aerospace and medical device industries as well as tooling for the plastics industry and stamping industry.
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Under the Court Executive 2B (Operations Division Manager) and/or other high level manager/supervisor, the successful candidate must be able to interpret in the three modes of interpretation (sight, consecutive and simultaneous) in court proceedings, quasi-judicial hearings, complimentary dispute resolution events and other court related events in person or via a telecommunication device.
$59,141.55 - $111,206.94 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Obtains field uniformity images and spatial resolution checks of gamma camera for non-uniformity and degradation of resolution and assures integrity of photographic recording device. Diagnostic Radiography License or NJ Registered Radiological Technologist License or NJ State Radiography License.
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Intune policies for application deployment, device compliance, and security configurations. Create and manage Intune policies for application deployment, device compliance, and security configurations.
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0 - 2 years of chemical processing experience or batch mixing in the Medical Device or Pharmaceutical manufacturing industry. Responsible for accurately maintaining legible and accurate records, required logs, books, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and Health and Safety requirements.
Up to $22 an hourExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Collaborate with primary container development, device development, marketing, supply chain, procurement, logistics, internal and external manufacturing sites, to successfully develop, tech transfer and launch packaged products for US and export markets that are in compliance with Design Controls, and relevant elements of the Quality System Regulations.
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Lead technical workstreams for lifecycle management of commercial device and combination products, including but not limited to: change controls, technical investigations, technology transfer, supplier management, risk analysis, component and process improvements.
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2+ years of sales experience, having strong experience in B2B or capital equipment sales, medical device preferred. 2+ years of sales experience, having strong experience in B2B or capital equipment sales, medical device preferred.
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TMC is part of Tokyo-based Terumo Corporation; one of the world’s leading medical device manufacturers with $5+ billion in sales, 20,000+ employees worldwide and operations in more than 160 nations.
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Coordinating Technology Team – data cabling, port assignments, patching, VLAN configuration, firewall configuration, device white-listing, CommsSheet maintenance, etc. Coax (SDI, CATV, etc.) Coordinating Technology Team – data cabling, port assignments, patching, VLAN configuration, firewall configuration, device white-listing, CommsSheet maintenance, etc.
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3,000 sign and stay bonusAbout us:At STERIS Applied Sterilization Technologies (AST), We are One Team with One Goal. Through a network of nearly 60 facilities globally, STERIS AST has been committed to patient safety by providing contract sterilization services to the medical device, pharmaceutical, consumer, and industrial communities for over 50 years.
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A minimum of 4 – 15 years of experience in a QA role or regulatory role, (with plant QA experience preferred) in either Food and Dietary Supplements Production, Pharmaceutical, Medical Device, OTC Drug, and/or Cosmetics.
ExpandApply NowActive JobUpdated 9 days ago
device job Company: Genesis Research in Edison, NJ
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