- ManpowerGroup (San Antonio, TX)
- …to collaborate with a wide range of disciplines. **Job Title:** Medical Device Product Design Verification and Stability Engineer **Location:** San ... Our client in the medical device industry is seeking a Product Design Verification and Stability Engineer to join their team. As a Product DVnS Engineer… more
- Amazon (San Francisco, CA)
- …infrastructure with a focus on supporting device and architecture theory and device design . You will work closely with other Software Development Engineers, ... source control management, build processes, testing, and operations. - Experience developing design verification and electronic design automation tools -… more
- Pentax Medical (Montvale, NJ)
- …PENTAX Medical provides endoscopic imaging devices and solutions to the global medical community. The Medical Device Quality Engineer is an integral ... Quality System and production of Quality Products. Position Opening: Medical Device Quality Engineer Why JOIN Us?...and manage the Material Review Board process + Support design verification and validation test plans, protocols,… more
- Merck (West Point, PA)
- …development activities including engineering design , engineering analysis and testing, medical device design controls, risk management, test ... leading cross-disciplinary project teams. + Has broad knowledge of medical device development, design controls...risk management, alongside deep knowledge in device design , requirement management, design verification ,… more
- ManpowerGroup (San Antonio, TX)
- …testing protocols and verification documentation as part of a product design change. + Create specifications for device components, assemblies, packaging, ... Our client in the medical device industry is seeking a...**Duration:** 12 month contract? **What's the Job?** + Lead design efforts under the guidance of Senior Engineers on… more
- AbbVie (Pleasanton, CA)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Medical Device Quality Intern Overview Envision spending your summer ... of the most dynamic organizations in the pharmaceutical / medical device industry. This is a reality...deliverables required within the product development process. + Support Design Verification and Validation activities, including review… more
- US Tech Solutions (San Bruno, CA)
- …with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design /Process Verification , ... **Responsibilities:** + Managing cross-functional or cross-team projects to bring regulated medical device products to market. + Ensuring product specifications… more
- AbbVie (North Chicago, IL)
- …of principles and practice of Design Controls (CFR 820.30 / ISO 13485), Medical Device Software Lifecycle (ISO 62304), and Risk Management (ISO 14971) + ... Planning for Design outputs and ownership of Design Output Reviews + Design Verification...of experience (MS preferred) + Experience must include significant device development, with medical device ,… more
- Merck (Columbus, OH)
- …or a related field within the pharmaceutical, biotechnology, or medical device industries. + Demonstrated expertise in the design /development (QA oversight), ... associated with combination products. This role ensures the highest standards of device quality throughout the product lifecycle, from design and development… more
- Merck (Rahway, NJ)
- …partners. **Preferred Experience and Skills:** + Experience with medical device development with understanding of Design Controls (21 CFR 820.30) ... A minimum of a Ph.D. plus 4 years of device design and engineering evaluation experience. +...system for medical use. + Familiarity with Design Verification (DV) strategies and mechanical tests… more
- Micron Technology, Inc. (Boise, ID)
- …preferred_ + _5 plus years industry experience in the field of CMOS device design , simulation, characterization_ + _Experience in developing advanced logic ... cost effectiveness + You define, execute, and analyze silicon experiments for future device generations + Interface with Design Engineers to define transistor… more
- Takeda Pharmaceuticals (Boston, MA)
- …+ Monitors regulatory landscape in US to maintain contemporary knowledge of global medical device and combination product regulations, standards, and guidance + ... reviews design control documentation, including technology transfer protocols, design verification and validation protocols and reports, technical reports,… more
- Motion Recruitment Partners (Lake Forest, CA)
- …Forest, CA **Hybrid** Contract $55/hr - $70/hr Our client is one of the largest medical device companies within the US that focuses on building devices and ... Relibality Device Engineer - Medical , Labview, PCBA,...Collaborates with NPI teams in identifying and executing key pre- verification characterization testing and other activities necessary for continuous… more
- Belcan (Thousand Oaks, CA)
- …System Regulation - 21CFR820 * Risk Management - ISO 14971 * EU Medical Device requirements - Council Directive 93/42/EEC Preferred Qualifications: * Bachelor"s ... risk assessments including hazard and probability analysis * Background in medical device development, commercialization and knowledge of manufacturing processes… more
- Merck (West Point, PA)
- …stage through launch and supply, including mechanical systems design and manufacture, medical device design controls and device risk management, ... 15-20 personnel overseeing technical support and product stewardship for our company's medical device and combination products (approximately 15 in total). This… more
- Merck (Rahway, NJ)
- …stage through launch and supply, including mechanical systems design and manufacture, medical device design controls and device risk management, ... preferred. + Minimum of 15+ years of experience in medical device or combination product engineering, with...human factors evaluations, and design verification /validation. + Significant experience in analytical method development and… more
- AbbVie (Pleasanton, CA)
- …in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... Engineer will work collaboratively with a team to design and develop medical products from initial...(DFMA) and document the DFMA benefits of the chosen design . + Plan, perform, and document verification … more
- AbbVie (Irvine, CA)
- …in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... Engineer will work collaboratively with a team to design and develop medical products from initial...(DFMA) and document the DFMA benefits of the chosen design . + Plan, perform, and document verification … more
- Lilly (Concord, NC)
- …+ Deliver equipment, lines, and supporting systems through user requirements, design , build, verification , qualification, validation, and subsequent operation. + ... wage for this position is $151,500 - $222,200 **Position Description:** The Device Assembly and Packaging (DAP) Operations Sr Director is responsible to provide… more
- Inovio Pharmaceuticals (San Diego, CA)
- …from HPV-related diseases, cancer, and infectious diseases. INOVIO's technology optimizes the design and delivery of innovative DNA medicines that teach the body to ... This individual will need a thorough understanding of the design control process and product life cycle. Design...and activities. The individual shall have lead development of medical devices of similar complexity and scope. A complete… more