- Cytiva (Miami, FL)
- … engineering or project engineering role, preferably in healthcare manufacturing or medical device production.2+ years experience with regulatory standards and ... into clear, concise language for a non-technical audience.Working in Pharmaceuticals or Medical Device industryExperience with Veeva & Magic systemsCytiva, a… more
- Raytheon (Andover, MA)
- …Summary:An exciting opportunity has opened for a Lead Semiconductor Reliability Engineer to join our Advanced Microelectronic Solutions Department (AMSD) at Raytheon ... to the success on this role. As a lead engineer , you need to communicate efficiently and effectively and...go above and beyondRelentlessly interact with a team of process engineers, technology owners, and project leadsProduce key reliability… more
- Beckman Coulter Life Sciences (Indianapolis, IN)
- …experience in product development, manufacturing and / or quality systems (ISO 9001), medical device (ISO 13485), pharmaceutical, related life sciences or other ... Danaher Business System which makes everything possible.The Staff Quality Assurance Engineer or Scientist is responsible for facilitating application of quality… more
- Raytheon (Mckinney, TX)
- …assembly environment.Experience in design analysis and providing feedback on other engineer 's designsExperience with Windchill and the Common PDM system, ASME BTH-1 ... (Below-the-Hook Lifting Device Design)Active and transferable DoD Security ClearanceWhat We OfferOur...Department of Defense, handles and adjudicates the security clearance process . More information about Security Clearances can be found… more
- Cytiva (Miami, FL)
- …walks.It would be a plus if you also possess previous experience in: Medical Device , eg ISO 13485PharmaceuticalChemicalAutomotive, eg IATF 16949Speaking fluent ... the Danaher Business System which makes everything possible.The Senior Supplier Quality Engineer for Cytiva is responsible to manage supplier defects, be compliant… more
- Beckman Coulter Diagnostics (Miami, FL)
- …a plus if you also possess previous experience in: Experience in IVD Medical device or Pharmaceutical ManufacturingASQ CertificationThe salary range for this ... that address the world's biggest health challenges. The Senior QA Validation Engineer for Beckman Coulter Diagnostics is responsible for assisting in the sustainment… more
- Cytiva (Miami, FL)
- …of experience in Quality or Regulatory in a regulated industry (ISO 9001, medical device , or pharmaceutical preferred).Experience with root cause analysis, CAPA ... the Danaher Business System which makes everything possible.The Quality Assurance Engineer (Design & Manufacturing) is responsible for providing quality leadership… more
- Cytiva (Miami, FL)
- …walks.It would be a plus if you also possess previous experience in: Medical Device , eg ISO 13485PharmaceuticalChemicalAutomotive, eg IATF 16949#LI-OnsiteJoin our ... the Danaher Business System which makes everything possible.The Senior Supplier Quality Engineer (m/f/d) for Cytiva is responsible to manage supplier defects, be… more
- Pentax Medical (Montvale, NJ)
- …Position Opening: Senior Quality Engineer Why JOIN Us? We are an established medical device leader that is preparing for high growth. This means that PENTAX ... Time Off and Holiday policy. Want More INFO? The Medical Device , Senior Quality Engineer ...quality improvement, remediation initiatives, and facilitate the change management process within the PENTAX Medical facility. This… more
- Merck (Rahway, NJ)
- **Job Description** As a Senior Engineer in Device Design and Process Development group, you will be part of our R&D team that designs and develops ... Director responsible for this area, you will partake in device assembly and process development using semi-automated...13485, ISO 14971 etc.) and industry standards related to medical device manufacturing is a plus. +… more
- Amgen (Cambridge, MA)
- …team. Join us and transform the lives of patients while transforming your career. Engineer I - Medical Device Design Control Documentation Specialist **What ... Quality Management - ISO 13485; Risk Management - ISO 14971; EU Medical Device requirements - Council Directive 93/42/EECStrong background in documenting… more
- Lilly (Indianapolis, IN)
- …DOE's, GR&R's or process capability studies. + Previous drug delivery, medical device or pharmaceutical industry experience. + Experience working with ... for new equipment throughout phases of asset delivery. Support the global device network to develop process technology capabilities and synergistically leverage… more
- Integra LifeSciences (Plainsboro, NJ)
- …pathways to advance patient outcomes and set new standards of care. The **Sr.** **Quality Engineer - Medical Device / Pharma** will provide Plant Quality ... corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device … more
- Takeda Pharmaceuticals (Lexington, MA)
- …support lifecycle management of commercial combination product. The Staff Device Engineer has extensive experience in medical devices for drug delivery ... of my knowledge. **Job Description** **Primary** **Role:** The Staff Device Engineer will lead technical efforts for...including combination products, solid understanding of polymeric medical device manufacturing processes via molding and… more
- System One (West Valley City, UT)
- Job Title: Medical Device Quality Assurance Engineer Location: West Valley City, UT Hours/Schedule: Mon- Fri 8am 5pm Type: Contract Responsibilities Will ... issues and communicate effectively to all levels within the organization; a medical device industry professional who is passionate about providing superior… more
- Micron Technology, Inc. (Boise, ID)
- …inspiring the world to learn, communicate and advance faster than ever. Welcome! As a Device Engineer working in the R&D DRAM Device and Cell Technology ... guide process development. + Develop understanding of process and device requirements for current and...prepare for the future. We offer a choice of medical , dental and vision plans in all locations enabling… more
- LCI-Lawinger Consulting (Minneapolis, MN)
- …risks in the development process . Preferred Qualifications: + Experience with medical device combination products or active implantable devices. + Six Sigma ... Job Title: Senior / Principal Design Assurance Engineer Location: Minneapolis, MN Job Type: Direct Hire...in ensuring the safety, effectiveness, and regulatory compliance of medical device products. Key Responsibilities: + Lead… more
- Bausch Health (Bothell, WA)
- …creates it-where your skills and values drive our collective progress and impact. As a Medical Device I-Product Engineer at Solta Medical , the successful ... range of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. Our 7,000 employees share… more
- Global Foundries (Malta, NY)
- …markets. For more information, visit www.gf.com . Summary of Role: As a silicon photonics device engineer , you will be working on the development of CMOS and Si ... theoretical studies by multi-physics modeling of device performance, designing the device , and working closely with process / integration engineering team on… more
- Skyworks (Irvine, CA)
- Senior Principal Engineer SAW Device Development Apply now " Date:Apr 30, 2025 Location: Irvine, CA, US Company: Skyworks If you are looking for a challenging ... communicates. Requisition ID: 74982 Description Skyworks Solutions seeks a Senior Principle Engineer of Surface Acoustic Wave (SAW) device development who will… more
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