- BD (Becton, Dickinson and Company) (Louisville, CO)
- …assistant personnel **QUALIFICATIONS:** + Must have knowledge of the US and European medical device regulations + Must have excellent written and verbal ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...approval of product labeling and marketing claims for regulatory compliance + Update STED technical files for CE marking… more
- Integra LifeSciences (Plainsboro, NJ)
- …4+ years of experience in a laboratory or manufacturing engineering in a medical device or pharmaceutical environment. + Creative thinking and proactive ... chance to do important work that creates change and shapes the future of healthcare . Thinking differently is what we do best. To us, change equals opportunity. Every… more
- ICON Clinical Research (Raleigh, NC)
- …of outsourced development and commercialisation services to the pharmaceutical, biotechnology, and medical device industries, is seeking a Senior Director, Group ... Blue Bell / Dublin ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to...key advisor on ICON's global accounting and reporting, ensuring compliance with US GAAP and IFRS standards, and providing… more
- Diversified (Washington, DC)
- …traditional SDI (3G/12G) workflows. This role ensures 24/7 reliability and compliance for live production, playout, and multi-platform distribution. The position ... SMPTE ST 2110 systems, including AES67 audio and NMOS IS-04/IS-05 device registration/control. + Configure and troubleshoot multicast routing (IGMP/PIM), VLAN… more
- Merck (West Point, PA)
- …distribution/ transportation technologies for pharmaceutical products including parenteral and/or medical device and combination products. + Demonstrated ... applicable. We offer a comprehensive package of benefits. Available benefits include medical , dental, vision healthcare and other insurance benefits (for… more
- Edwards Lifesciences (Salt Lake City, UT)
- …or related field, with experience in Quality Engineering, Quality Management, or Regulatory Compliance within the medical device industry; prior work in ... optimizing quality engineering practices while ensuring a culture of quality and compliance with global regulatory requirements. **How You'll Make an Impact:** +… more
- WellSpan Health (Chambersburg, PA)
- …current emotional/physiological status regarding the testing procedure, pertinent medical history/social history) and to determine final testing ... therapy. Is supportive and reassuring. Reinforces to the patient the importance of compliance with a treatment plan when established by the physician. 15. Prepares… more
- Philips (San Diego, CA)
- …You have a minimum of 8+ years' experience in FDA regulated, IEC 62304 medical device software environments (SiMD/SaMD), with a focus on Software Design ... software projects (SaMD) as well as software-related aspects of complex medical systems (SiMD). Manages the development, oversight and execution of comprehensive… more
- Edwards Lifesciences (Irvine, CA)
- …of ~15%. **What else we look for (preferred):** * APICS CPIM Certification * Medical device industry experience will be a plus. Equivalent experience in highly ... and discovering lasting solutions for unmet patient needs. Our Principal Compliance Specialist, Product Stewardship position is a unique career opportunity that… more
- Edwards Lifesciences (Naperville, IL)
- …cath lab/OR environment and procedural best practices + Expert understanding of medical device asset creation, regulation requirements for claims and training ... and management of operations for the department, purchase order compliance and processing, and 3rd party vendor compliance...is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all… more