Principal Clinical Advisor, Clinical Engineering
$99.3k - $198.7kAbbott
Job ID: 31163870Posted: Posted TodayStart Date: 2026-10-07Location: United States - California - Temecula, United States of AmericaTime Type: Full timeAbbott 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 healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:Job TitlePrincipal Clinical Advisor, Clinical EngineeringWorking at AbbottAt Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:Career development with an international company where you can grow the career of which you dream.Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.An excellent retirement savings plan with high employer contributionTuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.THE OPPORTUNITY We are seeking a Principal Clinical Advisor, Clinical Engineering to work in one of the following Abbott locations: St Paul, MN, Santa Clara, CA or Temecula CA. The Principal Clinical Advisor, Clinical Engineering will provide clinical knowledge, expertise and direction relevant to manufacturing, quality, performance and patient safety during all phases of development of a product or concepts to assure informed decisions are made. Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.WHAT YOU’LL DOSupport product development by contributing clinical knowledge to bench testing, performing in-vitro and /or in-vivo device evaluations and assisting in the development of new test methods to provide a better understanding of device performance.Create clinical performance evaluation plans to assess physician acceptance and the expected performance of new products by interacting with appropriate personnel, (e.g., physicians, engineers, other clinical coordinators, regulatory affairs).Write device Instructions For Use (IFU).Participate in the Risk Analysis process for new or improved devices to ensure that potential risks to patients associated with use of the device are identified and appropriately analyzed.Participates in the Product Action process by performing and documenting a Health Hazard Assessment and communicating the assessment to Quality Assurance.Contribute clinical perspective to the decision making process regarding product recall or field action by attending meetings with the Product Action committee, summarizing clinical feedback, performing product testing as needed and providing general clinical knowledge and expertise.Establish and cultivate an extensive network of support to facilitate completion of assignments.Participate in the development of less experienced staff by setting an example, providing guidance, and offering counsel.Participate in determining goals and objectives for projects.Influence middle management on technical or business solutions.Exercise judgment in selecting innovative, practical methods to achieve problem resolution.EDUCATION AND EXPERIENCE YOU’LL BRINGRequiredBachelor's degree plus 7+ years of related work experience with a strong understanding of specified functional area, or an equivalent combination of education and work experience preferred. Will consider certification in related field or health industry with combined work experience. RT, RN, or RCIS certification or degree4-5 year recent catheter lab experience (coronary + endovascular ideal)Solid understanding and application of business concepts, procedures and practices. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.Willingness to travel up to 30-50% (including international)PreferredWillingness to train to on-the-job skill sets:Simulated catheter lab product testing during product developmentStrong writing skills (protocols/reports)Strong verbal communication skillsInterpersonal skill set interfacing with physiciansFamiliarity operating fluoroscopy unit and operating in fluoroscopy/sterile environmentExperience as a scrub technician during proceduresExperience working with medical device Quality systems and/or regulatory product approval processesExperience with Microsoft Office products, including Powerpoint for presentations and Excel for data analysisWHAT WE OFFERAt Abbott, you can have a good job that can grow into a great career. We offer:A fast-paced work environment where your safety is our priorityTraining and career development, with onboarding programs for new employees and tuition assistanceFinancial security through competitive compensation, incentives and retirement plansHealth care and well-being programs including medical, dental, vision, wellness and occupational health programsPaid time off401(k) retirement savings with a generous company matchThe stability of a company with a record of strong financial performance and history of being actively involved in local communitiesLearn more about our benefits that add real value to your life to help you live fully: Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future.Abbott is an Equal Opportunity Employer, committed to employee diversity.Connect with us at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.The base pay for this position is $99,300.00 – $198,700.00In specific locations, the pay range may vary from the range posted.JOB FAMILY:Clinical Affairs / StatisticsDIVISION:AVD VascularLOCATION:United States > Temecula : Building E - TEADDITIONAL LOCATIONS:United States > Minnesota > St. Paul : 1225 Old Highway 8 NWWORK SHIFT:StandardTRAVEL:Yes, 50 % of the TimeMEDICAL SURVEILLANCE:NoSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: is the Law link - Espanol:
$99.3k - $198.7k
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$78k - $156k
...Premarket: Assess the acceptability of quality, preclinical and clinical documentation for submission filing. Compile, prepare,... ...Qualifications Bachelor's degree in science/technical discipline (engineering, life sciences). Master’s degree. Experience with US (51...Work experience placementWorldwide- ...Abbott is seeking a Principal Regulatory Affairs Specialist for its Vascular Division, on-site in Santa Clara, CA or Temecula, CA. You... ...manage global submissions, and partner with Regulatory, Quality, Clinical, R&D, Manufacturing and others to ensure lifecycle regulatory...
$150k - $200k
...Nurse Practitioner to join its growing team. This is an excellent opportunity for a seasoned dermatology PA or NP who enjoys a busy clinical environment and is looking for strong earning potential, comprehensive benefits, and long-term stability. Position Highlights:...- ...Overview Primary contact for engineering support of In-Process Inspectors. Support production efforts and process improvements (trend analysis, process validation, SPC). Coordinate In-Process MRB activities. Support Quality Systems (perform audits, SOP improvement,...
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