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Senior Automation Engineer, R&D

Abbott

  • La Jolla, California
  • 8 days ago

    Highlights

    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), Keyboard use (greater or equal to 50% of the workday), Routine work with chemicals, Work with human blood or other potentially infectious materials . The successful candidate has experience working in a collaborative, fast-paced team to build scalable, highly integrated automation platforms which enable users to reliably and efficiently deliver timely, high-quality results in a regulated environment.

    Numbers & Facts

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

    Description

    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 115,000 colleagues serve people in more than 160 countries.

         

    JOB DESCRIPTION:

    Position Overview
    The Senior Automation Engineer, R&D is a key problem solving, individual contributor that uses in-depth conceptual and practical knowledge to achieve project goals. This position will leverage understanding of engineering principles, methods, data, and judgment to influence the course of product development activities.

    The Senior Automation Engineer, R&D will develop and deploy robust laboratory automation solutions for Next-Generation Sequencing based assays in support of high complexity laboratory developed tests.  This position will utilize technical skills, with oversight, to participate in conceiving, planning, and executing research and development activities to achieve project goals. The successful candidate has experience working in a collaborative, fast-paced team to build scalable, highly integrated automation platforms which enable users to reliably and efficiently deliver timely, high-quality results in a regulated environment.

    Essential Duties
    Included, but are not limited to, the following:

    • Develop automated laboratory solutions to meet the requirements of existing or new assay workflows.
    • Iteratively design, develop, and implement automated liquid handler methods for use in a high throughout environment, improve methods based on feedback from experimental data and user feedback.
    • Support accurate and robust automation software integration with external systems (LIMS, integrated hardware, etc.).
    • Support design transfer and deployment of automation solutions across multiple sites which meet product requirements and are fully integrated with clinical laboratory workflows.
    • Support process development needs such as automated Operational Qualification procedures.
    • Mentor junior level engineers.
    • Assist and train laboratory personnel on the use of automated systems.
    • Maintain and troubleshoot automated systems and processes.
    • Participate in new product design and design improvements to existing products.
    • Collaborate with cross-functional teams to ensure all development activities are conducted in adherence to applicable national/international regulations, guidelines, company policies, SOPs, and industry standards.
    • Lead Human Factors Engineering/Usability Engineering tasks and activities.
    • Lead product risk management activities involving system Hazard Analysis (HA) Failure Modes and Effects Analysis (FMEA).
    • Collaborate with Quality team to establish templates and processes for the documentation of systems engineering tasks and activities.
    • Participate in the definition of key development deliverables, milestones, dependencies, risks, and mitigations as part of the Integrated Program Plan.
    • Establish interfaces across other organizational groups.
    • Apply strong analytical and problem-solving skills.
    • Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
    • Support and comply with the company’s Quality Management System policies and procedures.
    • Maintain regular and reliable attendance.
    • Ability to act with an inclusion mindset and model these behaviors for the organization.
    • Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
    • Ability to lift up to 20 pounds for approximately 5% of a typical working day
    • Ability to comply with any applicable personal protective equipment requirements.
    • May perform repetitious actions using lab tools.
    • Ability to travel 10% of working time away from work location, may include overnight/weekend travel.


    Minimum Qualifications

    • Bachelor’s Degree in Engineering, Biological Sciences or field as outlined in the essential duties.
    • 5+ years of relevant experience in product development.
    • Demonstrated ability to perform the essential duties of the position with or without accommodation.
    • Legal authorization to work in the country of employment without current or future sponsorship.


    Preferred Qualifications

    • Extensive Hamilton Venus programming experience
    • HSL code programming experience
    • Integration experience with workcells/end-to-end platforms

         

    The base pay for this position is

    $78,000.00 – $156,000.00

    In specific locations, the pay range may vary from the range posted.

         

    JOB FAMILY:

    Engineering

         

    DIVISION:

    ONCO Cancer Diagnostics

            

    LOCATION:

    United States > La Jolla : Torrey Pines Science Park

         

    ADDITIONAL LOCATIONS:

         

    WORK SHIFT:

    Standard

         

    TRAVEL:

    Yes, 10 % of the Time

         

    MEDICAL SURVEILLANCE:

    No

         

    SIGNIFICANT 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), Keyboard use (greater or equal to 50% of the workday), Routine work with chemicals, Work with human blood or other potentially infectious materials

         

    Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.

         

    EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf

         

    EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

    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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