- Abbott (San Diego, CA)
- …debuggers, unit test frameworks) + Knowledge of design controls and regulations for medical device development is a plus + Understanding of quality software ... visual modeling, multi-threading, formal development methodologies, and source code management + Medical device product development knowledge is a plus + Ability… more
- Hologic (San Diego, CA)
- …environment, ideally in the IVD space. + Working knowledge of Quality Management System for Medical Device Manufacturing FDA 21 CFR 820, ISO 13485 as well as CE ... team member on New Product Development projects to ensure compliance with design controls, as well as identify and...mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management… more
- Kelly Services (South San Francisco, CA)
- …advance your career, join us as we pioneer progress in the biotechnology and medical device industries. **Workplace:** Hybrid, onsite in South San Francisco, CA ... efforts in developing and implementing Quality programs and policies to ensure regulatory compliance . + Collaborate on crafting Standard Operating Procedures for… more
- Silicon Valley Power (Santa Clara, CA)
- …term strategic and operational plans, monitor related legislation, regulations, reporting and compliance and serve as the liaison to various stakeholder groups. The ... understanding of wholesale power market operations, renewable energy, and regulatory frameworks. + _Strong Analytical Skills:_ Proficiency in financial modeling,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …analytics vendors, as well as internal departments such as Marketing, Analytics, Training, Compliance , Medical , Regulatory , and Legal + Liaise with ... care reimbursement practices, Co-pay financial support, and its related compliance and regulatory requirements. It will be...with 10+ years of related experience in the pharmaceutical, medical device , or biotech industry. + Prior… more
- J&J Family of Companies (Irvine, CA)
- …14155, MDR, MEDDEV, ). + Clinical/ medical background is a plus. + Medical device experience is highly preferred. + Good understanding of clinical research ... clinical research; + Cooperation with the necessary stakeholders (clinical study team, medical , clinical sites, regulatory , data management) on safety activities… more
- Philips (San Diego, CA)
- …solutions through product development, integration and V&V, ensuring compliance with medical device standards and global regulatory requirements. + You ... and thorough manner. + You have experience working in the regulated medical device environment: demonstrating practical knowledge and experience with global… more
- Medtronic (Orange, CA)
- …+ **SR4:** 10 years B2B or Healthcare Sales with 5 years experience selling Medical device or medical capital equipment **NICE TO HAVE- DESIRED/PREFERRED ... to company policies and procedures + Adheres to financial, regulatory , quality compliance standards and requirements. **Influence...+ Thorough working knowledge of medical terminology, medical procedures and the medical device… more
- California Energy Commission (Sacramento, CA)
- …Energy Commission seeks an Attorney I in the Chief Counsel's Office - Advocacy & Compliance Unit. If you are interested in a challenging and exciting career in clean ... hearings and civil litigation; and 3. California laws governing regulatory agencies with legislative and regulatory powers...Service: ### (TTY), ### (Voice) TTY is a Telecommunications Device for the Deaf, and is reachable only from… more
- VTI Life Sciences (San Diego, CA)
- …engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support ... Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training,… more