- Abbott (Milpitas, CA)
- …and implement process improvements. Collaborating with cross-functional teams, they ensure high- quality software delivery and contribute to the full development life ... technical leadership and mentoring for embedded software projects. + Ensure high- quality software delivery within schedule constraints. + Own technical aspects of… more
- Terumo Neuro (Aliso Viejo, CA)
- …(PMP) certification is highly desirable. 3. Strong knowledge of medical device development processes, regulatory requirements, and quality management systems. ... and monitoring of projects, ensuring adherence to timelines, budget, and quality standards. + Manage project risks, issues, and dependencies, implementing proactive… more
- J&J Family of Companies (Santa Clara, CA)
- …portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary ... + Partner with the Adv. R&D and PDP teams to translate finished device requirements to the balloon component level + Survey emerging technologies in the… more
- Medtronic (Northridge, CA)
- …ensuring compliance with ISO 10993 standards and global medical device regulations. This role involves conducting comprehensive biocompatibility assessments, ... and decision-making skills. The role requires the ability to produce high- quality technical documentation and effectively communicate findings. This position also… more
- Teledyne (Camarillo, CA)
- …include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, ... team to solve material growth and processing issues, and to improve device designs, processing methods, and production capabilities. + Assurance of all production… more
- Actalent (Irvine, CA)
- …(FDA, MoH, TUV, etc.). + Thorough knowledge of US and International Medical Device Regulations. + Strong knowledge of Quality Concepts like CAPA, Audits, ... Title: Document Control Specialist Job Description Join our team as a Quality Control Specialist, responsible for ensuring compliance with internal and external… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …commitment to collaborative problem solving, sophisticated design, and the creation of quality products are essential. Your team's primary focus is building core ... deliver software architecture, diagrams, design documents + Ensure the performance, quality , and responsiveness of applications + Unit-test code for robustness,… more
- Abbott (Santa Clara, CA)
- …Responsible for Biocompatibility support to the research & development of new medical device products as well as the maintenance of business activities by ensuring ... the existing and emerging regulatory requirements, particularly the EU Medical Device Regulations (EU MDR) and ISO 10993 series. **Principal Responsibilities** +… more
- Power Device Corp (Poway, CA)
- Software Engineer Sr- Space Department:Space Engineering Location:Poway , CA Power Device Corporation (PDC) is recognized as a world leader in the design and ... for the Aerospace, Defense, and Space industries. Our dedication to supplying quality products, on-time delivery, and superior support, has contributed to the… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …to ensure regulatory compliance, expedition of product clearances and maintain the highest quality standards. Candidates will be expected to work on-site 4 days per ... based multifunction SaMD products to determine compliance with FDA's guidance on device versus non- device functionality. + Prepare, submit, and manage regulatory… more