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Reviews and analyzes purchase requisitions. Oversees purchasing activities with manufacturing, planning and engineering departments to acquire inventory in a cost effective and timely manner. Reviews purchase requisitions, purchase change orders and requests for supplier quotes. Responsible for procurement business system data input and integrity. Performs cost analysis a
Posted 20 days ago
The Contract Administrator will be responsible for all aspects of domestic and international assigned regional healthcare account contracts within the Contracts group. The position will support domestic and international assigned regional field sales and partner closely with internal departments, both domestically and internationally, to support the sales teams by providi
Posted 20 days ago
The Helpdesk Support Specialist will be responsible for providing Level 1 technical support for users via phone, email, and web for 'GlobusOne', an inhouse developed ERP System. The individual is responsible for Level 1 problem analysis, documentation, resolution and escalation. Shift Hours 12 00 pm 8 00pm Essential Functions Provides support in person and over phone/vide
Posted 20 days ago
At Globus, we move with a sense of urgency to deliver innovations that improve the quality of life of patients, inspired by the surgeons and healthcare providers who treat them. Our world class engineering works to transform clinical insights into tangible musculoskeletal solutions. We are constantly in pursuit of better patient care, and we understand that speed is criti
Posted 21 days ago
Globus Medical, Inc. (NYSE GMED), is an innovative and fast growing medical device company. We are seeking a bright, motivated individual to join our Finance team! The ideal candidate is a self starter, detail orientated, and able to work in a fast paced environment with the ability to multi task. Strong communication skills, dependability, flexibility and a willingness t
Posted 21 days ago
The Regulatory Affairs Specialist drafts, submits and gains 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. This position entails development of FDA submissions, requires working knowledge of products under review and of relevant regulations and guidance documents. This i
Posted 24 days ago
Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitor
Posted 24 days ago
The Production Planner will be responsible for developing and managing the manufacturing schedule across multiple product lines, ensuring supply to the market and minimizing backorders. The individual will work to optimize operations to maximize efficiency and performance within the department. Hours 7 00 am 4 00pm or 8 00 am to 5 00 pm Essential Functions Develops a prod
Posted 24 days ago
The Compliance Manager works with the Director of Compliance and Chief Compliance Officer to support our Global business on compliance matters relating to adherence to relevant policies, codes, laws, and regulations impacting business operations. The Compliance Manager will assist with various aspects of our compliance program, including compliance training, auditing and
Posted 25 days ago
The Senior Analyst will assist in the analysis, planning and execution of M&A, Corporate Development & Investor Relations initiatives. This is a great opportunity to flex your analytical horsepower and transaction experience to help execute a growing medical device company's strategic plan. As a key member of our dynamic and active Corporate Development team, you will lea
Posted 25 days ago
The EDM Wire Operator wires and operates assigned machines to produce parts, all of which must meet the dimensional specifications of the mechanical engineered drawing. This effort includes, but is not limited to, conducting basic machine changeovers, accurately completing quality control documentation and inspection sheet. Assists operators in the diagnosis of part dimen
Posted 25 days ago
The Associate Model Maker is responsible for prototype fabrication to support product development. This includes bringing a product from idea/concept through design, prototyping, development, testing, design verification and validation, manufacturing, and product introduction. The Model Maker will also be responsible for maintenance of the machines including calibration,
Posted 25 days ago
The Laser Marking Operator is responsible for the setting up and operating the CNC laser equipment to produce finished goods within the Implants/Trauma department. This effort includes, but is not limited to, reading drawings and work instructions. This individual works with the entire department to ensure all finished materials are laser marked correctly and up to compan
Posted 26 days ago
The Lead Regulatory Affairs Specialist leads the preparation of document packages for regulatory submissions for new and sustaining enhanced technologies, software enabling and robotics systems within the Surgical Intelligence (SI) portfolio, to ensure compliance with local and regional registration requirements. The Lead Specialist will be responsible for coordinating pr
Posted 26 days ago
Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitor
Posted 26 days ago
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