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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 healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Working at Abbott At 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 you dream of., • 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 contribution., • Tuition reimbursement, the ___ student debt program and ___ 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 Our location in Temecula, CA currently has an opportunity for a QC Chemist. THIS IS AN ON-SITE DAILY POSITION The Opportunity This position works out of our Temecula, CA location in the Abbott Vascular Division. Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease. What You’ll Work On Support raw material, in-process material, and finished product lot release, stability studies, engineering evaluations, and any relevant investigation by performing required analytical testing under the GMP environment. MAIN RESPONSIBILITIES • Performs routine analysis using approved test methods in a timely manner., • Prioritizes assigned workload to meet the customer’s needs., • Maintains current status on all training requirements and supports training activities for other laboratory personnel., • Understands and follows GMP requirements with respect to laboratory operation, testing, results generation, and documentation., • Carries out change requests/change controls as needed and be able to provide necessary explanations or justifications to the change., • Recognizes OOS, OOT, and exception events., • Initiates and conducts investigation under the supervision of senior laboratory staff., • Carries out method development, validation, verification, and transfer by following established protocols whenever required., • Prepares technical protocols and reports as needed under general supervision., • Maintains a safe working environment in accordance with established procedures and requirements., • Cultivates a wide range of internal networks and begins to develop an extensive external network of resources to facilitate completion of tasks., • May lead a project team of moderate scope., • Provides guidance to less experienced staff., • Acts as a mentor to lower level individual contributors., • Influence exerted at peer level and occasionally at first levels of management., • Plans, organizes, and prioritizes own daily work routine to meet established schedule., • Exercises authority and judgment within defined limits to determine appropriate action., • Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules and may result in the allocation of additional resources. Required Qualifications Education • Bachelors Degree or Masters Degree OR an equivalent combination of education and work experience, • 2-5+ years of related work experience with a good understanding of specified functional area., • Working technical knowledge and application of concepts, practices and procedures. Preferred Qualifications • Basic knowledge of cGMP and quality system environment, • Experience with wet chemistry, ICP-OES or chromatography (HPLC, GC or GPC), • Familiar with LIMS Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn 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. The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

Senior Director of Regulatory Affairs.Hybrid working - some travel to Bay Area.Competitive compensation + strong benefits.Director of Regulatory Affairs.US and a passion for mentorship, cross-functional collaboration, and innovation in a fast-paced, mission-driven environment.Lead a talented regulat

Senior Director of Regulatory Affairs.Hybrid working - some travel to Bay Area.Competitive compensation + strong benefits.Director of Regulatory Affairs.US and a passion for mentorship, cross-functional collaboration, and innovation in a fast-paced, mission-driven environment.Lead a talented regulat

Senior Director of Regulatory Affairs.Hybrid working - some travel to Bay Area.Competitive compensation + strong benefits.Director of Regulatory Affairs.US and a passion for mentorship, cross-functional collaboration, and innovation in a fast-paced, mission-driven environment.Lead a talented regulat