Register
Recruit Create CV

Senior Device Engineer Jobs

Qa Engineer - Med Device
By Hays At Acton, MA, United States
• Perform quality duties as assigned by Quality Manager III.
• 0-3 years of Medical Device experience
• Knowledge and working application of reading and understanding blueprints and technical drawings.
• Ability to multi-task and methodically manage projects.
QA Engineer - Med Device – Contract – Acton, MA - $39.00-$49.00/hr.
• Complaint Investigations (Time Spent: 45%):
Device Test Engineer Jobs
By TechFetch.com - On Demand Tech Workforce hiring platform At Richardson, TX, United States

"ALL our jobs are US based and candidates must be in the US with valid US Work Authorization. Please apply on our website directly." Job Title: Device Test EngineerLocation: Atlanta, GA (Onsite) Job ...

Device Engineer Ii Jobs
By Pfizer At , Parsippany
Proactive, has experience with high performance teams, strong interpersonal and project management skills
Knowledge and experience with Drug Product processing and equipment
Perform other tasks necessary to support site compliance to Center and regulatory requirements.
Working knowledge of Food and Drug Administration Regulations, and Good Manufacturing Practices
Strong written and verbal communication skills
Demonstrated experience in a relevant manufacturing environment
Senior Security Engineer Ii, Trusted Device Access
By Cruise At , Remote $168,000 - $247,000 a year
Experience in Authentication, Authorization, Federation, and Identity Management.
Experience with other parts of security such as data loss prevention, email security, access control management, logging, and PKI
Building automation to make security more accessible for end users while leveraging open source technologies and configuration management tooling
Infectious enthusiasm for configuration management and automation
Pre-tax Commuter Benefit Plan for non-remote employees
Creating delightful user experiences and interactions with well-integrated security tooling
Microled Device Engineer, Augmented Reality
By Google At , Fremont, Ca
Master's degree in Applied Physics, Materials Science, Optoelectronics, a related field, or equivalent practical experience.
3 years of experience working in a semiconductor fabrication technical environment.
3 years of experience in advanced device architecture.
5 years of direct experience working in a semiconductor fabrication technical environment.
Experience with research and development experiments and advanced data analysis.
PhD or equivalent in Applied Physics, Materials Science, Optoelectronics, or a related discipline.
Optoelectronic Device Test Engineer, Augmented Reality
By Google At Fremont, CA, United States
Bachelor's degree in Electrical Engineering, Computer Engineering, Physics, a related field, or equivalent practical experience.
5 years of experience in optoelectronic device (LED, VCSELs, Lasers, detectors) or module test development.
10 years of experience in optoelectronics device test development in a R&D or manufacturing environment.
Experience with microLED device test, device calibration, and low noise electrical measurements for industrial or consumer products.
Experience driving technical analysis of device test hardware and software issues.
Develop and improve various micro-LED device test capabilities as needed to support the innovative LED technology.
Device Test Engineer/Qa Engineer
By MINDBRIDGE SOLUTIONS INC At Dallas, TX, United States
Required Skills / Preferred hands on experience:
Device Test Engineer / QA Engineer
Dallas, TX (Day 1 onsite)
. If you are interested please share your resume to my mail [email protected]
Job Title: Device Test Engineer / QA Engineer
Location: Dallas, TX (Day 1 onsite)
Device Software Engineer Jobs
By BioSpace At Pleasanton, CA, United States
BS in Software Engineering, Electronics Engineering, Computer Science or related discipline or equivalent combination of education and experience.
We offer comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
Contribute to requirements definition at the functional level.
Experience in medical devices or similarly controlled software environment preferred.
Experience in developing event driven, multi-threaded Windows-based applications using .NET Framework and C# preferred.
Knowledge of software life cycle processes used in regulated development environments. Agile process is preferred.
Manual Device Test Engineer
By Accenture At , Atlanta, Ga
Information on benefits is here.
Minimum 2 years of Manual Device Testing, ADB, Java
High School Diploma or GED
Minimum 2 years of Unix Shell scripting
California – $26.44 - $36.44
Colorado – $26.44 - $36.44
Device Engineer Iii (Contractor)
By Genentech At , San Francisco, Ca $68.19 - $90.39 an hour
Excellent communication skills are required. Experience in working with external partners is also highly desirable.
Plan and execute test-method validation projects, including developing, performing, and documenting test-method validation activities in accordance with cGMP requirements.
At least 8 years of experience in the industry and/or academia (including advanced studies) after receiving their Bachelors degree.
Develop and commercialize devices including interfaces with the primary container.
Provide guidance and input regarding product development using structured product development process.
Regularly interface with staff and leaders in Contract Manufacturing,
Senior Engineer - R&D - Medical Device, Microfluidics
By Novo Nordisk At , Fremont, Ca $98,820 - $172,000 a year
Preparation and management of Design History Files or equivalent
Lead the definition and development of user needs, business needs, use cases and requirements.
Solid experience in product development, especially under Design Controls and for Design Verification & Validation
Experience working with Design Controls systems compliant with ISO 13485, MDR, 21 CFR 820 and other relevant regulations
Experience with combination product medical product development.
Experience managing collaborations, contracts and partnerships with external industry groups. Demonstrated success managing academic and clinical partners.
Device Engineer Ii Jobs
By Teva Pharmaceuticals At , West Chester, 19380, Pa
Present information and data to technical and management teams
Develop and execute feasibility testing in support of product development.
Ensure that every product is robust in design; perform engineering analysis and routinely provide evidence of robustness, reliability and efficacy.
Create technical drawings, reports, data and other documents.
Understanding of solid mechanics and fluid dynamics principles.
Perform risk analysis, FMEA etc.
Senior Sales Representative, Surgical Device
By Teleflex At , Manhattan, Ny $150,000 a year
Specialized Skills / Other Requirements
Participate in a specific amount of surgical procedures as assigned by the regional sales manager on a weekly basis.
Communicate customer requirements and request support from other departments as necessary to assist in achieving established objectives.
Cooperate with finance to assure the collection of accounts receivable due in obtaining of appropriate documents to minimize risk.
Assist in establishing sales objectives for territory in cooperation with Regional Sales Manager.
Attain quota through aligning with corporate objectives and required sales processes.
Principal Ms&T Device/Packaging Engineer
By Teva Pharmaceuticals At , Salt Lake City, 84116, Ut
Masters degree with 7+ years’ relevant experience OR PhD degree with 3+ years relevant experience
Experience with development of drug-device combination (DDC) products and primary packaging
Experience of using CAD and Simulation software
Working experience of managing multiple projects of varying complexity simultaneously.
Liaise with our internal and external manufacturing partners to assess early technology device Design for Manufacturability and Assembly (DFMA).
Identify opportunities and propose potential mitigations during participation in design reviews at critical stages of device and product development.
Optical Device Design Engineer
By M/A Com Technolgy Solutions At , Ithaca, Ny $83,790 a year
Excellent familiarity with CW and high-speed measurements, reliability testing, and qualification standards and strong characterization skills.
Work with process development and product engineering teams to define fabrication process, mask layout, process flow and test requirements.
Minimum 5 years of experience in the optoelectronics/photonic field with a proven track record in laser development/manufacture.
Self-motivated, with strong analytical and problem-solving skills.
Design, simulation, testing and analysis of directly modulated and CW semiconductor laser products.
PhD or MS in Engineering, Physics, or equivalent discipline
Senior Director Global Medical Device
By NSF International At , $150,000 - $330,000 a year
15 years in industry experience Medical Device (from a regulator ex. FDA
Consulting experience ie. FDA, MHRA, EMA
Strong medical device and IVD compliance experience
Experience developing and implementing strategy
Demonstrated experience in managing P&L including allocating resources and managing expenses to achieve or exceed revenue and profit targets
Demonstrated experience leading and developing other leaders
Sr Device Engineer Ii
By Gilead Sciences At , Foster City, 94404, Ca $149,600 - $193,600 a year
Experience with project management methods and tools
Completion of post-market risk management activities
Development of design control and risk management deliverables per 21 CFR 820, ISO 13485, and ISO 14971
Experience/knowledge with drug delivery systems and standards (ISO 11608, ISO 11040, etc.) is desired
Mentor engineers and other functional area team members in technical, regulatory, and compliance best practices and requirements.
Remain current, apply understanding, and mentor others in relevant FDA, ISO, and Quality System Requirements.
Senior Quality Engineer - Medical Device
By Intuitive Surgical At , Sunnyvale, Ca $111,700 - $189,000 a year
Quality Advocacy and Project Management.
Escalates to direct management all quality issues that could impact patient safety or surgical efficacy.
Ensures successful, on-time completion of department projects, communicates constraints to direct management when successful project completion is at risk.
Experience in writing and reviewing Qualification and validation reports
Drive and project manage quality initiatives in one or more of these focus areas:
Minimum 8+ years of working experience in Quality Engineering, or in manufacturing environment