- Compass Group, North America (New York, NY)
- …Facilities Management, and Ambulatory EVS. Learn more at www.Crothall.com. Job Summary The Medical Device Integration and Cybersecurity specialist will be ... Utilizing Crothall's cybersecurity framework, technologies and policies and procedures, the Medical Device Integration and Cybersecurity Specialist will… more
- ICU Medical (Albany, NY)
- *Position Summary*// The Device Sales Specialist is responsible for building and maintaining relationships with key decision makers that lead to future business ... increases profitability and expands existing accounts by selling ICU Medical products and extending relationships into new areas with...requires travel 50% of the time * * **Title:** * Device Sales Specialist - New York City… more
- BioFire Diagnostics, LLC. (Morrisville, NC)
- …OR + High School Diploma/GED with 3 years of experience in customer service, medical device , or troubleshooting related military also accepted + Customer service ... and troubleshooting experience preferred. + Clinical laboratory experience and/or medical device industry experience preferred. + Networking or LIS/LIMS… more
- Amazon (Bellevue, WA)
- …TV and Echo Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to ... project teams About the team The Quality & Lean, Medical Devices Operational Compliance Center (MD-OCC), consists...verbal, presentation, and organizational skills. - . Experience with medical device software requirements. - . Ability… more
- ICU Medical (Lake Forest, IL)
- …. Working experience in material compliance and associated regulations, in medical device industry. For eg REACH, RoHS, California Prop 65, Conflict ... Specialist II, Quality Systems will support functional activities associated with material compliance for medical devices managed under ICU Medical … more
- Abbott (Plymouth, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...currently has an on-site opportunity for a **Senior Quality Compliance Specialist ** . This new team member… more
- Integra LifeSciences (Boston, MA)
- …enhance the skills and competencies of employees in a medical device -regulated environment. The Senior Training Specialist will assess training needs, ... and set new standards of care. The Senior Quality Compliance Specialist -Training will create and conduct...or a related field with 5+ years' experience in QA/ Compliance within the medical device … more
- Integra LifeSciences (Boston, MA)
- …and years' experience in QA/ Compliance within the Life Sciences Industry, preferably Medical Device Industry. + Working knowledge of medical device ... and set new standards of care. The Senior Quality Compliance Specialist - Technical Writer will work...Acrobat, EndNote, Reference Manager). Experience with MS-Project preferred. + Medical device experience is preferred (510(k), PMA,… more
- Integra LifeSciences (Boston, MA)
- …in Engineering, Life Science, or a related field with 5+ years' experience in QA/ Compliance within the medical device or similar industry or equivalent ... patient outcomes and set new standards of care. The Senior Quality Compliance Specialist has responsibility for supporting overall site Quality Management… more
- Veterans Affairs, Veterans Health Administration (Grand Junction, CO)
- …Ensures compliance of networked attached clinical systems to all Medical Device Protection Program (MDPP) requirements. Designs, implements and manages ... sub-netting, HL7, DICOM, Access Control List (ACL) and network security across the medical device network. Coordinates and works effectively with other facility… more
- Globus Medical, Inc. (Audubon, PA)
- …to perform these_ essential _functions._ **Qualifications** **:** + Bachelor's Degree + Medical Device experience is a MUST + Experience performing file ... At Globus Medical , we move with a sense of urgency...within the Quality Assurance department to provide review of device /product records to ensure compliance to applicable… more
- Terumo Medical Corporation (Elkton, MD)
- …Complaints Engineering and Compliance functions. + Assists with generation of Medical Device Reports (MDRs) and Vigilance Reports as required. + Assists ... Complaints Specialist I (Temporary) Date: Nov 13, 2024 Req...of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in… more
- Veterans Affairs, Veterans Health Administration (Anchorage, AK)
- …Ensures compliance of networked attached clinical systems to all Medical Device Protection Program (MDPP) requirements. Designs, implements and manages ... Manages complete systems of central computerized networks, databases, analytic servers and medical device networks. Implements and plans for new or emerging… more
- Medtronic (Santa Rosa, CA)
- …degree required. + Minimum of 2 years of experience in regulatory affairs in the medical device industry. + Or advanced degree with a minimum of 0 years ... III and/or class IIb products. Additionally, the Regulatory Affairs Specialist is responsible for assessment of device ...of experience in regulatory affairs in the medical device industry. **Nice to Have (Preferred… more
- Veterans Affairs, Veterans Health Administration (White River Junction, VT)
- …Ensures compliance of networked attached clinical systems to all Medical Device Protection Program (MDPP) requirements. Performs other related duties ... to: Manages complete systems of central computerized networks, databases, analytic servers and medical device networks. Implements and plans for new or emerging… more
- Abbott (Plymouth, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...lives. We are currently hiring an **International Regulatory Affairs Specialist I** to work on-site at our **Plymouth, MN**… more
- Terumo Medical Corporation (Somerset, NJ)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... SAP Extended Warehouse Mgmt Specialist Date: Nov 14, 2024 Req ID: 3766...Removal Strategies, Post Processing Framework, Replenishment, Physical Inventory. + Medical Device /Serialized product experience is required +… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... experience providing training program administration support or training facilitation to a medical device (or other regulated industry) organization. + Program… more
- ICU Medical (Atlanta, GA)
- …weekends/nights, when necessary *Knowledge, Skills & Qualifications* . PriorRespiratory and/or medical device sales experience is a requirement. . Strategic ... Specialist is responsible for building and maintaining ICU Medical 's Respiratory Care business in a given territory. The...with a proven track record of success. Preferably in medical device sales with relationships in key… more
- West Pharmaceutical Services (Exton, PA)
- …support submissions including Premarket Notifications, Technical Documentations under EU MDR ( Medical Device Regulation), and Master Files (DMF/MAF) associated ... Sr. Specialist , Regulatory Project Management (Evergreen Posting) Requisition ID:...skills, as well as demonstrated understanding of pharmaceutical and/or medical device operations (eg, manufacturing, process development,… more