Senior Specialist, Product Performance, Medical Affairs

Job ID: 31150930Posted: Posted 21 Days AgoStart Date: 2026-07-10Location: 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 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:Job TitleSr. Specialist Clinical Product PerformanceWorking 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 OpportunityWe are seeking a Sr. Specialist Clinical Product Performance to work out our Temecula, CA or Santa Clara, CA location for our Abbott Vascular division.This is a fully onsite role.Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.Specialist professional individual contributor with comprehensive knowledge in the area of medical or clinical interventional therapies.Provides daily business operations support to cross-functional teams as part of the Clinical Product Performance. Ability to execute highly complex or specialized projects.Provide assistance to ensure development of a strategy for the division's medical oversight product performance function. What You’ll Work OnDaily responsibility/scope for on-market product and clinical study product performance, including post-market clinical data from commercial use of products.As the Clinical Specialist in the Quality and Product Performance sub-function, considered as highly experienced and knowledgeable resource within the organization in overseeing the direction, planning, execution, clinical trials/research and product quality/safety activities.Reports to Associate Medical Director. Provides oversight for on-market product and product performance functions, including monitoring of product safety related items (i.e. complaints, MDRs), reporting, evaluation, and safety in post-market and clinical trials.Reviews and evaluates product performance data and trends to provide early identification of issues related to product performance or usage concerns in order to minimize clinical safety risk. This includes designing changes to product performance assessment and management to improve ongoing monitoring and risk assessmentAnalyzes customer complaints and coordinates with PPG to determine which are regulatory reportable and is a key contact for activities with internal, field, and end use customers.Coordinates and provides reporting information for reports submitted to the regulatory agencies as applicable.Review complaint communications and assess for regulatory compliance, reportability, and potential impact to patient safety and business operations.Investigates complaints by gathering sufficient data from clinical staff, field representatives, internal employees, and laboratory analysis.Serve as key resource in areas of MDR reporting, post-market product experience, and risk management.Accountable for understanding compliance requirements, risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls.Recognizes and reports adverse events and product complaints according to established regulations, DOP's and guidelines.Complies medical and scientific information for Abbott products and products in development and ensure that clinical information is of high quality and communicated in an accurate, balanced, timely and compliant way.Maintains thorough knowledge of assigned devices, drugs, history, and disease states treated to provide scientifically balanced medical devices and drug information to inquiries on Abbott Vascular products and associated disease states from multiple sources, including telephones, letters, faxes, business reply cards and e-mail from internal and external customers.Works cross functionally with division Compliance, Clinical Science, Regulatory Affairs, Medical Affairs and Commercial organizations, as required. Requires involvement with all on-market product performance, product performance, quality compliance, clinical science, medical information, scientific, and regulatory groups within Abbott.Required QualificationsBachelors Degree in Pharmacy, Nursing, RT, Life Science, or other health-related field, or equivalent qualification5+ years of relevant experienceA background in cardiology, cardiac surgery or vascular medicine/surgery is preferred.Experience working in a quality related role, or equivalent time in clinical laboratory, medical clinic, or nursing experience.Preferred QualificationsHighly prefer MD,RN or RT with Cath Lab experienceStrong ability to work cross functionally, understand various needs across diverse functions, and prioritize work according to business unit needs.Experience prioritizing and managing project initiatives across multiple functions and/or business units. Experience working in a broader enterprise/cross division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business modelAbility to work effectively within a team and as an individual contributor in a fast-paced changing environment -- multi-tasks, prioritizes and meets deadlines in timely manner. Strong project management, team skills, and influential managementStrong verbal and written communications with ability to effectively communicate at multiple levels in the organizationAdept at handling multiple assignments in a timely manner and meeting assigned deadlinesAbility to travel, potentially approximately 10%, including internationallyApply NowLearn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. 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:Medical & Scientific AffairsDIVISION:AVD VascularLOCATION:United States > Temecula : Building D - TDADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 10 % 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: