- Inovio Pharmaceuticals (San Diego, CA)
- …tools. For more information, visit www.inovio.com . Job summary The temporary Mechanical Engineer will be responsible for developing, transferring and supporting ... programs in the development of INOVIO's electroporation devices. Development of electro- mechanical mechanisms will support the needs of clinical trials and research.… more
- Motion Recruitment Partners (Lake Forest, CA)
- Relibality Device Engineer - Medical , Labview, PCBA, HALT, Python, C, Analysis Lake Forest, CA **Hybrid** Contract $55/hr - $70/hr Our client is one of the ... locations around the world and are looking for a Medical Reliability device engineer to...manufacturing environment. **(Nice to Have)** + Proven knowledge in mechanical , electrical, or optical design principles. **Education** + BSc.… more
- MicroVention, Inc. (Aliso Viejo, CA)
- …R&D **Job Description:** Support development of products and/or product engineering for medical device with work including writing or verifying specifications; ... documentation. 4. Working knowledge of standard machine shop equipment, processes, and medical device manufacturing equipment. 5. Knowledge of medical … more
- MicroVention, Inc. (Aliso Viejo, CA)
- …requirements (eg, ISO 62304). 7. Strong design experience in designing and developing electro- mechanical medical device and associated test requirements (eg, ... **12084BR** **Title:** Staff Engineer , R&D **Job Description:** Support the design and...Minimum six (6) years of relevant work experience in medical device industry. 3. Strong written and… more
- MicroVention, Inc. (Aliso Viejo, CA)
- …Regulatory Affairs + Quality + Supply Chain Job duties: Support development of medical device products with work including writing or verifying specifications, ... **12538BR** **Title:** Engineer I, Engineer Development Program **Job...machine shop equipment and processes, and working knowledge of medical device manufacturing equipment and processes. 5.… more
- Inovio Pharmaceuticals (San Diego, CA)
- …visit www.inovio.com . Job summary The Temporary Senior Embedded Software Engineer develops and enhances Electroporation Device firmware and associate ... level testing, and compliance. + Design and develop board bring up code, device driver code, boot loaders, firmware update software, software for interfacing with… more
- Edwards Lifesciences (Irvine, CA)
- …. + Strong knowledge of **regulatory requirements** and q **uality standards** in the medical device industry (eg, FDA, ISO 13485, ISO 60601). + Excellent ... are seeking a highly skilled and experienced **Senior Systems Engineer ** to join our dynamic team. The ideal candidate...+ Previous experience with UI/UX software development in the medical device industry. Aligning our overall business… more
- MicroVention, Inc. (Aliso Viejo, CA)
- …of ten (10) years of relevant manufacturing process development experience in the medical device industry. 3. Strong written and verbal communication skills. 4. ... **12591BR** **Title:** Principal Engineer , NPI & Transfers **Job Description:** Responsible for...years of relevant manufacturing process development experience in the medical device industry. 3. Ability to design,… more
- MicroVention, Inc. (Aliso Viejo, CA)
- …of six (6) years of relevant manufacturing process development experience in the medical device industry. 3. Strong written and verbal communication skills. 4. ... **12590BR** **Title:** Staff Engineer , NPI & Transfers **Job Description:** Responsible for...years of relevant manufacturing process development experience in the medical device industry. 3. Proven ability to… more
- Medtronic (Carlsbad, CA)
- …Math * 5+ years industry experience Quality Assurance, R&D, or Regulatory Affairs in Medical Device or Pharmaceutical Industries. * Experience with Medical ... across the Ventilation Service Solutions portfolio. As a Senior Design Quality Engineer , you will apply Design Controls and Risk Management principles to ensure… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …ISO 13485. IEC 60601 and IEC 62304 experience a plus. + Experience in medical device and/or regulated industry (required). + Experience with remediation efforts ... **Job Description Summary** The Staff Engineer - Risk Management is responsible for implementing...8+ years in a regulated industry, particularly within the medical device , bio-pharmaceutical, or biotechnology sectors, with… more
- Actalent (Carlsbad, CA)
- …Management System, FDA 21 CFR Part 820 Quality System Requirements (QSR), and medical device industry requirements. Assist in the implementation of the quality ... Job Title: Quality Engineer Job Description Support and develop forms for...Management System, FDA 21 CFR Part 820 QSR, and medical device industry requirements. + Assist in… more
- Actalent (San Diego, CA)
- …hardware design, risk management, statistical analysis, data interpretation, CGM technology, medical device development, ISO 13485 Additional Skills & ... statistical analysis and data interpretation 2. Experience with CGM technology or other medical device development 3. Familiarity with ISO 13485 and other… more
- General Atomics (San Diego, CA)
- …currently have several exciting opportunities for a mid-level Instrumentation and Control (I&C) engineer as part of the Engineering and Projects team in the Energy ... 30-170 GHz with RF power in magnitudes of mW or MW depending on the device . The position requires a multi-faceted individual who is competent in both the software… more
- Actalent (Carlsbad, CA)
- …Ability to effectively present data to a team. + Assay automation and microfluidic medical device development. + Knowledge of complex life science systems and ... Title: Biomedical EngineerJob Description We are seeking a highly skilled Biomedical Engineer to improve the performance, diagnose failure modes, and verify the… more
- Abbott (San Diego, CA)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... quality, compliance, and adequate documentation is applied to every medical instrument which undergoes the refurbishment/repair process. **Responsibilities** +… more