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Sr. Mechanical Engineer

Abbott

  • California
  • 30+ days ago

    Highlights

    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. Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

    Numbers & Facts

    LocationCalifornia
    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:

    A healthy heart is essential to good health. That's why we're committed to advancing treatments for people with cardiovascular disease. As a global leader in Cardiac Rhythm Technologies, our breakthrough medical technologies help restore people's health so they can get back to living their best lives, faster. We focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

    Our location in Sylmar, CA, currently has an opportunity for a Sr. Mechanical Engineer.  

    Sr. Mechanical Engineer will design and develop innovative medical devices or components/subsystems in support of company's strategic plan.

    WHAT YOU’LL DO

    • Design medical devices to meet user needs.

    • Establish requirements and specifications for these devices (including justification and supportive testing).

    • Use experimental, empirical and numerical analysis to evaluate designs. Lead test method and model development. Create and own mechanical design drawings and models.

    • Identify and mitigate project risks.

    • Work with internal departments and external vendors to obtain prototype parts and to expand these groups’ capabilities.

    • Lead pre-clinical and support clinical testing of devices.

    • Lead design reviews and support physician visits.

    • Maintains a detailed understanding of the developing clinical environment (i.e. current treatment methods, evolving clinical needs etc.).

    • Maintain a detailed understanding of division, FDA and ISO regulation. Provide input into shaping division quality and regulatory requirements.

    • Work with project management to develop overall schedule. Manage time and tasks within schedule.

    • Make decisions on material usage including implant grade metals and polymers

    • Work closely with outside vendors and manage complex projects with them

    • Document and run design verification and validation testing which will be submitted to the FDA and other regulatory bodies

    • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

    • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

    • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

    • Mentor junior engineering team members providing engineering and technical leadership.

    EDUCATION AND EXPERIENCE YOU’LL BRING

    Required

    • Bachelors Degree in Mechanical Engineering or related or an equivalent combination of education and work experience.

    • Minimum 5 years of experience designing and testing.

    • Experience with a variety of manufacturing processes and designing for manufacturability.

    • Ability to lead small teams and to work within large multi-discipline teams as an individual contributor in a fast-paced, changing environment.

    • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.

    • Multitasks, prioritizes and meets deadlines in timely manner.

    • Exposure to latest design tools and techniques (six sigma, DFM, analytical design).

    • Ability to work in a highly matrixed and geographically diverse business environment.

    • Ability to leverage and/or engage others to accomplish projects.

    Preferred

    • Masters Degree in Mechanical Engineering or related field.

    • Class III medical device R&D experience

    • Cross functional team experience

    • Experience designing and testing electromechanical medical devices.

    • Proficient and experienced in medical device design controls, CAPA, production and process controls and risk management.

    • Wide variety of manufacturing processes and DFM experience

    • Solidworks/Creo or other CAD experience

    • Analytical design, Design for Six Sigma, or similar tool set experience

    WHAT WE OFFER

    At Abbott, you can have a good job that can grow into a great career. We offer:

    • Training and career development, with onboarding programs for new employees and tuition assistance
    • Financial security through competitive compensation, incentives and retirement plans
    • Health care and well-being programs including medical, dental, vision, wellness and occupational health programs
    • Paid time off
    • 401(k) retirement savings with a generous company match
    • The stability of a company with a record of strong financial performance and history of being actively involved in local communities

    Learn more about our benefits that add real value to your life to help you live fully:  www.abbottbenefits.com

    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 www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

         

    The base pay for this position is

    $90,000.00 – $180,000.00

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

         

    JOB FAMILY:

    Product Development

         

    DIVISION:

    CRM Cardiac Rhythm Management

            

    LOCATION:

    United States > Sylmar : 15900 Valley View Court

         

    ADDITIONAL LOCATIONS:

         

    WORK SHIFT:

    Standard

         

    TRAVEL:

    Yes, 5 % of the Time

         

    MEDICAL SURVEILLANCE:

    No

         

    SIGNIFICANT WORK ACTIVITIES:

    Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Work in a clean room environment

         

    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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