- Bausch + Lomb (Kirkwood, MO)
- …Design for Six Sigma [DFSS]. - Medical Device Audits - Design Controls & Risk Management. - Quality Function Deployment [QFD]. - Analytical Hierarchy ... demonstrated technical leadership of cross-functional teams. + Broad understanding of medical device design and development processes, workflows, and tools… more
- Actalent (Foster City, CA)
- Design Control Quality Engineer with Medical Device or Combo Device Experience Description * Act as a quality engineer for medical device ... such as FMEA. Skills Risk management, quality management system, iso 13485, medical device , design control Disqualifiers: - no medical device … more
- ManpowerGroup (San Antonio, TX)
- 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 II, ... collaborate with a wide range of disciplines. **Job Title:** Medical Device Product Design Verification...to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup… 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, ... problems and propose workable solutions. Translate user stories into software design documents demonstrating sensible trade-offs between complexity and delivery. *… more
- Amazon (Seattle, WA)
- …the life As a Senior Design Technologist working on the next generations of device user experiences, no two days are the same. You might start by reviewing a ... Description As part of Amazon's Devices and Services Design Group (DDG), the Futures Design ...to hear from you. Key job responsibilities - Build high- quality , functional prototypes that convey, prove, and advance the… more
- Sanofi Group (Cambridge, MA)
- …or related engineering degree) + 6+ years' experience in medical device product development focused on quality engineering related activities. + 2 ... **Job Title:** Digital Device Quality Expert - SaMD **Location:**...Risk Management and Supplier Control support of Software as Medical Device (SaMD) by leading all cGMP… more
- Eurofins (Boston, MA)
- …Build and lead a team of skilled consultants with expertise in medical device testing, regulatory affairs, and quality management. + Foster a culture of ... vision and team to support our clients in the medical device industry across their product innovation,... industry across their product innovation, regulatory compliance, and quality assurance processes. This role will focus on establishing… more
- US Tech Solutions (San Bruno, CA)
- …and align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design /Process ... to release, manage project schedules, mitigate risks, handle the Design History File, and align with stakeholders. + Collaborate... Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management… more
- Integra LifeSciences (Boston, MA)
- … Engineering/ Quality Compliance/ Quality Assurance experience in the Medical Device or similar FDA regulated industry. Integra LifeSciences is an equal ... documentation). + Knowledge of statistical sampling and analysis. + Working knowledge of medical device regulations (including FDA QSRs, ISO13485). + Ability to… more
- Motion Recruitment Partners (Lake Forest, CA)
- Human Factors Engineer - Medical Device , IEC-60601, HFC Lake Forest, CA **Hybrid** Contract $65/hr - $80/hr Our client is a worldwide medical device ... teams. + Maintain awareness of the state-of-the-art methods as applied to life-sciences / medical device industry. + The contracted service is expected to plan… more
- Sutter Health (West Sacramento, CA)
- …in Northern California within the Sutter Health footprint. Responsible for Cyber Security, Medical Device Vulnerability, Medical Device Integration, and ... comprehensive action plans to address gaps and enable successful execution of medical device integration and technology advancement including testing, release… more
- Mallinckrodt Pharmaceuticals (Madison, WI)
- … Device Engineering to join our senior leadership team at our Madison, WI medical device manufacturing site. This key role is central to driving engineering ... and efficiency. You will play a crucial part in shaping the future of medical device engineering, ensuring regulatory compliance, and fostering a culture of… more
- United Therapeutics (Eden Prairie, MN)
- … Device Development is responsible for leading research and development of medical device products and components used in combination products by applying ... matter expertise. This role involves identifying and solving problems, leading product design and development projects, and supporting the R&D team in developing… more
- Lilly (Indianapolis, IN)
- …11, Parts 210/211, Part 820 QSR, ISO 13485, ISO 14971, Canadian MDR, EU Medical device Directive, JPAL) + Regulatory inspection experience + Knowledge of the ... is $118,500 - $173,800 **Position Brand Description:** The IDM (Indianapolis Device Manufacturing) Quality Assurance Associate Director is primarily responsible… more
- Sanofi Group (Bridgewater, NJ)
- …be responsible to lead the design , development, and implementation of connected medical device technologies and ensuring they meet the specific needs of the ... representatives from the core device platforms and device manufacturing sites, Digital, Global Quality , GRA...work experience in the area of connected & digital medical device technologies or equivalent. + Working… more
- Amazon (Sunnyvale, CA)
- … quality of new products and SW releases. Key job responsibilities * Design and execute comprehensive quality strategies that align with the organization's ... device makers. Basic Qualifications - 6+ years of quality assurance engineering experience - 4+ years of delivering...compensation package, in addition to a full range of medical , financial, and/or other benefits. For more information, please… more
- Amneal Pharmaceuticals (Piscataway, NJ)
- Description: The Medical Device Engineering Manager is responsible for owning the day-to-day Program Management activities of Drug Delivery Device projects. ... Complete the risk management activities to meet project timescales, device performance and quality requirements + Ensure...outputs are thoroughly documented, providing a robust and detailed design history file + Prepare Device related… more
- Amgen (Thousand Oaks, CA)
- …experience with 5+ years of experience in operations/manufacturing environment + Medical device industry experience and regulated work environment experience ... Quality System Regulation - 21CFR820, Risk Management - ISO 14971, EU Medical Device requirements - Council Directive 93/42/EEC + Strong understanding and… more
- Takeda Pharmaceuticals (Boston, MA)
- …fSCIG/cSCIG device launch KPIs and monitoring. + Translate customer feedback into device design and using launch strategies developed for the global ... / external partners, this position will help drive efficiency, quality , and overall success when bringing medical ...+ Background in commercial strategy and leadership within the medical device industry or related field. +… more
- Battelle Memorial Institute (Columbus, OH)
- …under a registered QS and under FDA Design Controls. + Experience in medical device design and testing for regulatory/ compliance (ie IEC 60601) ... welcome all qualified individuals to apply. **Job Summary** The Medical Device Solution team is seeking a...requirements + Background in product development process, operating under Quality System and Design Controls + US… more