- GRAIL (Durham, NC)
- …requires regular on-site presence (5 days a week) **Responsibilities:** + Support medical device Quality Engineering operations through expert ... area. + Minimum of 5 years of experience working within a medical device , pharmaceutical, or biotech quality management system. + Experience working… more
- Micron Technology, Inc. (Boise, ID)
- …to learn, communicate and advance faster than ever. As a Process Integration and Device engineer at Micron Technology, Inc., you will have opportunities to work ... DRAM in the manufacturing Fab, ramp up production yield and deliver high quality DRAM products to customers. You will be offered hands-on experience in semiconductor… more
- Battelle Memorial Institute (Columbus, OH)
- …Creo along with PDM or Windchill vaults **Preferred Qualifications** + Medical device or consumer product design engineer experience + Hands on general lab ... apply. **Job Summary** We are currently seeking a **Mechanical Engineer II** . This position is located in **Columbus,...core team member in the design and development of medical and commercial products and systems. This role contributes… more
- SanDisk (Milpitas, CA)
- …portfolio of products that are recognized globally for innovation, performance and quality . Sandisk has two facilities recognized by the World Economic Forum as ... process, design, reliability, and system groups to ensure timely product device support, memory qualification, and ramp of volume production **Qualifications**… more
- SanDisk (Milpitas, CA)
- …portfolio of products that are recognized globally for innovation, performance and quality . Sandisk has two facilities recognized by the World Economic Forum as ... members from process, design, reliability, and system groups to ensure timely product device support, memory qualification, and ramp of volume production + In this… more
- Terumo Medical Corporation (Elkton, MD)
- NPD Quality Engineer II Date: Dec 8, 2025...+ Demonstrated working knowledge of key medical device related standards including 21 CFR 820 ( Quality ... Design Assurance/ Quality Engineering **Job Summary** The Design Quality Engineer (DQE) II will plan, coordinate,...scientific environment + Minimum of 2 years of experience in a regulated industry ( medical device industry… more
- Caris Life Sciences (Irving, TX)
- …will be quality the subject matter expert for software development of medical device and computerized systems. **Job Responsibilities** + Authors (as needed) ... your impact begins.** **Position Summary** The Staff Software Design Quality Assurance Engineer is a leader that...is a plus. + Working knowledge or familiarity with medical device software (IEC 62304) is a… more
- Teleflex (Olive Branch, MS)
- … certification. - 3+ years of Quality Assurance experience required within medical device / FDA regulated industry preferred. - Bachelor's degree in ... Quality Engineer II, Distribution **Date:** Nov...- Bilingual (Spanish), preferred. - Relevant Experience working within Medical Device , Pharmaceutical, or other FDA-regulated Industry… more
- Teleflex (Chelmsford, MA)
- …investigation teams. Understands the fundamentals of root cause investigation, risk management, and medical device Quality Management Systems per 21 CFR 820, ... Quality Engineer 2, Product Quality... Quality Engineer 2, Product Quality Assurance **Date:**...Engineering (or related technical field) - 2-5 years related ( medical device preferred) experience - Experience with… more
- Caris Life Sciences (Phoenix, AZ)
- …than yourself, Caris is where your impact begins.** **Position Summary** The Process Quality Engineer ensures on-going product quality through continuous ... and continual quality improvement initiatives. The Process Quality Engineer is primarily responsible for the...of 2 years of experience working within FDA regulated ( Medical Device , Pharmaceutical) highly preferred and/or regulated… more
- Integra LifeSciences (Mansfield, MA)
- …industry with knowledge of Risk Management (ISO 14971 2019), MDD ( Medical Device Directive), IEC 62366, ISO 13485 ( Quality Management Systems), FDA QSR and ... standards of care. This **Staff Design & Reliability Assurance Quality Engineer ** is a key functional role...DFSS techniques * 8 years of experience in a Quality Assurance role for medical device… more
- Olympus Corporation of the Americas (Westborough, MA)
- …matter expertise, technical guidance, and leadership for the application of health and medical device SW regulatory standards to the Olympus SDLC, including IEC ... **Job Description** This role provides professional expertise for Software quality and best practices in SW design, development, release,...+ Minimum of 6 years of experience in a medical device setting. + Experience in the… more
- Terumo Medical Corporation (Elkton, MD)
- …Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high- quality medical devices used in a broad range of applications ... of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in...robust manufacturing processes into the Value Streams The Senior Engineer 1 ensures technical quality , contributes to… more
- Caris Life Sciences (Phoenix, AZ)
- …than yourself, Caris is where your impact begins.** **Position Summary** The Supplier Quality Engineer is primarily responsible for ensuring the needs of ... groups help drive corrective action when necessary. The Supplier Quality Engineer acts as a liaison between...of 3 years of experience working within FDA regulated ( Medical Device ) or regulated industries (Automotive, Aerospace)… more
- Integra LifeSciences (Mansfield, MA)
- …(Mechanical Engineering preferred) with minimum of 3 years' experience in the medical device or pharmaceutical industry; strong analytical skills, exceptional ... regulations and standards. + Previous experience in high volume manufacturing environment.( Medical Device preferred) + Demonstrated project management and… more
- Cordis (Miami Lakes, FL)
- …development, quality engineering, or related roles, preferably in medical device or regulated manufacturing environments. **Preferred Qualifications** - ... people who keep saving lives. **Responsibilities** **Summary** As a Supplier Development Engineer at Cordis, you will be the influential coach, analytical thinker,… more
- Terumo Neuro (Aliso Viejo, CA)
- …to five (5) years of quality assurance/compliance related experience in the medical device industry. 3. Must be able to handle multiple projects ... **13069BR** **Title:** Sr. Quality Systems Engineer **Job Description:** This is a hands-on position in which the Senior Quality Systems Engineer is an… more
- Terumo Medical Corporation (Elkton, MD)
- …ability to create a development strategy and technical approach for a large medical device project and coordinate with applicable cross-functional leaders to ... Medical Devices in accordance with global regulatory and quality standards and requirements. o Demonstrated understanding of the...the design and development of a new or novel medical device on a bench top or… more
- Micron Technology, Inc. (Manassas, VA)
- …world to learn, communicate and advance faster than ever. As a Front-End Central Quality Assurance (FECTQA) Engineer , you will play a critical role in supporting ... fabrication facility. You will collaborate extensively with process and product engineering, quality teams, and global partners to ensure the highest standards of … more
- Micron Technology, Inc. (Boise, ID)
- …world to learn, communicate and advance faster than ever. As an Intern DRAM RMA Quality Engineer at Micron Technology Inc., you will assist in testing, debugging ... products as they transition from new product qualification to mass production. Quality Engineers are crucial partner between our Customers, Quality Engineering,… more
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