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["Quality Assurance Specialist","Quality Assurance Specialist"]

Abbott

  • Pomona
  • 6 days ago

    Highlights

    Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities. Title: Quality Assurance SpecialistLocation: Pomona, CaliforniaDuration: 7 Months100% OnsiteResponsibilitiesDemonstrated ability to carry out assignments in a timely, accurate manner and accomplishing tasks as required with little or no supervision.

    Numbers & Facts

    LocationPomona
    IndustryHealthcare Services
    Company Size10,000 employees or more
    Year Founded1910
    Websitehttp://www.abbott.com/

    Description

    Title: Quality Assurance SpecialistLocation: Pomona, CaliforniaDuration: 7 Months100% OnsiteResponsibilitiesDemonstrated ability to carry out assignments in a timely, accurate manner and accomplishing tasks as required with little or no supervision.Ability to interact effectively with all levels of the organization and perform multiple tasks in a fast‑paced environment.Proficient in one or more Quality processes such as incoming inspection, and/or change management, and/or records (including batch release). May also support some record administration and batch record review duties, including Certificate of Analysis / Certificate of Conformance creation and/or review for material lot release.Work with groups within the organization to get corrections and clarifications to Device History Records.Facilitates the Change Control process in the electronic change control system and tracks the change process through development, approval, and implementation.Able to assist others with Change Control process and offer guidance and best practices.May prepare labeling for all finished product and perform labeling of product.Analyzes and interprets the significance of the proposed changes using independent judgment to guide change initiators in the development of accurate change requests.Reviews standard operating procedures, logs, forms, manufacturing records, work instructions and all other Quality records for adherence to established templates, good documentation practices and adequacy of referenced procedures and part numbers.Utilize database to perform transactions and verify product information.Generate and/or review Certificate of Conformance / Certificates of Analysis for Final Product.Filing of records.Communicates issues effectively and partners with cross‑functional associates to meet compliance requirements.Is able to leverage collaboration and helps to drive organizational improvements with compliance issues.Able to troubleshoot issues and improve systems as needed.Is able to coach staff, in real‑time, to resolve issues and improve future outcomes.Works on assignments that are complex in nature where considerable judgment and initiative are required in resolving problems and making recommendations.Knowledgeable of federal and other regulations, e.g. QSRs, ISO 13485, CMDR, etc.Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices; build productive internal/external working relationships.Carries out duties in compliance with established business policies.Other duties as assigned, according to the changing needs of the business.Minimum Qualifications | Education/ExperienceHigh School Diploma or GED.3‑5 years of related experience.Experience with MS Office.Able to work on multiple tasks as a team member and/or ability to operate as an individual contributor.Must be detail‑oriented, self‑motivated and available for flexible scheduling.Strong communication, problem solving and motivational skills.Preferred QualificationsBachelor's Degree.Working knowledge of Quality Assurance in a medical device manufacturing environment, preferably in‑vitro diagnostic.Knowledge of Quality System Regulations.CompetenciesHigh level of attention to detailTeamworkCommunicationStrong organizational skillsInitiativeAdaptabilityConsultants Eligible Benefits Upon Waiting PeriodMedical and Prescription Drug PlansDental PlanVision PlanHealth Savings Account (for High‑Deductible Health Plans)Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)Supplemental Life InsuranceShort Term Disability (coverage varies by state)Long Term DisabilityCritical Illness, Hospital coverage, Accident InsuranceMetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance401(k)#J-18808-Ljbffr

    About Company

    At Abbott, we are enthusiastic, energetic and committed to doing great work every day. Our employees are passionate about helping to translate science into lasting contributions to health care and the health of people worldwide. At the heart of our organization is our "Promise for Life"—a statement that embodies our company's commitment to employees, shareholders, local communities and the people who depend on our company and products to live healthier lives.

    Vital to our promise is the speed in which we act, respond and deliver. As Abbott employees, we are ready to meet change and challenges head-on. As a result, we are a company that adapts quickly, and through our passion for innovation we are able to continually create a pipeline of products that help improve the length and quality of life around the world.

    We are proud of our rich, more than 120-year history. We continue to be driven to advance leading-edge science and technologies, support diversity, focus on exceptional performance and earn the trust of those we serve.

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