- Gilead Sciences, Inc. (Foster City, CA)
- …create possible, together. **Job Description** This position is a member of the Medical Affairs Research (MAR) Leadership Team and will report to the VP, Head of ... career interests + Collaboration with colleagues in Clinical Operations, Medical Affairs , Real World Evidence, Health Economics and Outcomes Research, Project… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- **Job Description Summary** As Staff Specialist Regulatory Affairs , you will have a deep understanding of Risk Based frameworks, Agile SDLC, experience with cross ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...related field. + 3-5 years of practical experience regulatory affairs , with a focus on SaMD. + Comprehensive understanding… more
- Danaher Corporation (Sunnyvale, CA)
- …of our team, you'll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission ... Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Regulatory Affairs Principal is responsible for serving as RA lead… more
- Abbott (Alameda, CA)
- Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... also have access to: + Career development with an international company where you can grow the career you...energy, lose weight or enhance athletic performance. The Clinical Affairs Manager will manage teams within the Medical … more
- Abbott (Alameda, CA)
- Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... also have access to: + Career development with an international company where you can grow the career you...with our new sensing technology. **The Opportunity** This **Regulatory Affairs Manager** will work on-site in Alameda, CA for… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …inputs (including all documents required under risk files). + Knowledge of global Regulatory Affairs requirements, regulations, and standards + Strong ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...and interpreting of current and new regulatory requirements and international standards for US and RoW + Support that… more
- Terumo Neuro (Aliso Viejo, CA)
- **12814BR** **Title:** Sr. Specialist, Regulatory Affairs **Job Description:** Responsible for preparing strategy for worldwide product approval submission ... activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requirements for Neurovascular and Peripheral devices. Job… more
- Abbott (Alameda, CA)
- Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of ... also have access to: . Career development with an international company where you can grow the career you...The individual has department level influence with experience in global regulatory submissions and on-market changes, and is generally… more
- Edwards Lifesciences (Irvine, CA)
- …difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and ... international regulatory environments. Working in partnership with external government...provide direction and oversee documentation packages for submission to global regulatory agencies. Prepare GUIDID submission data. Track timelines… more
- Edwards Lifesciences (Irvine, CA)
- …difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and ... international regulatory environments. Working in partnership with external government...+ Prepare and oversee documentation packages for submission to global regulatory agencies. Assist with GUDID submissions. Track timelines… more