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Staff Clinical Product Engineer at Abbott, United States - California - Sylmar

Staff Clinical Product Engineer at Abbott in United States - California - Sylmar. Full-time. $114,000 to $228,000 a year. Apply with swipeandhired.

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:
Job Description

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 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 Opportunity

This position works out of our Sylmar, CA location in the Cardiac Rhythm Management Division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

What You’ll Work On

Lead large group of engineers and scientists and manage the clinical development work for multiple projects within a function, program or therapeutic area and able to meet detailed project timeline and milestones

Plan and implement product development projects, and provide technical leadership and supervision to others

Ensure program objectives are determined and met, logistics are effectively coordinated, and budgets are adhered to. Act as cross-functional liaison to ensure designs and products are meeting customer needs and regulatory requirements.

Understands the business units products and related clinical workflows and know or able to learn about competitive product offering in different geographies

Engages with customers throughout product development cycle, defines clinical and workflow requirements for new product/feature development and represent the Voice of Customer in product development cycle, and drives the translation into new projects through clinical review and evaluation.

Lead the work with field and medical personnel to define the benchmarks for evaluating the clinical performance of these products/features.

Able to interpret data from customers, provide insights and recommendations, and assist the team to identify future product opportunities

Can drive and lead clinical design documentation such as user needs, feature definition, and design validation, and drives them to on-time and high quality completion.

Drives, Develops and directs pre-clinical evaluation protocols, data analysis, and reports

Reports significant progress and final findings of projects to management and product development staff in the company.

Simulates or tests aspects of new projects to evaluate prototypes and validate output as meeting customers’ intended use requirements; analyzes electrograms, diagnostic or programming data collected from the field or from research studies.

Provides input to the risk management file and Clinical Evaluation Reports in support of the product throughout its lifecycle.

Ability to supervise and train junior engineers on completing assigned work.

Help along the entire R&D value chain during ideation, research, product design & development to create smart and connected medical devices with intuitive workflows

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.

Performs other related duties and responsibilities, on occasion, as assigned.

Required Qualifications

Bachelors Degree in biomedical, mechanical, electrical, or similar engineering field, or an equivalent combination of education and work experience

Minimum 7 years of progressively more responsible work experience in medical device industry or equivalent

Demonstrated ability to apply understanding of clinical application to issues in order to bring tasks to resolution within assigned projects.

Strong analytical, problem solving skills

Requires comprehensive written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, and follow-up skills, the ability to meet deadlines on multiple projects as well as the ability to converse effectively with all levels of employees.

Ability to travel approximately 20%, including internationally.

Preferred Qualifications

Master’s or Doctoral Degree in biomedical, mechanical or electrical engineering, or a biological or physical science or medicine

Advanced credential in a relevant discipline/concentration, including Biomedical Engineering, preferred.

Fluent in medical procedure terminology and sound knowledge of cardiac anatomy

Demonstrated experience in authoring or co-authoring peer-reviewed scientific publications

Medical device experience in the cardiac space preferred

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
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 www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.

The base pay for this position is
$114,000.00 – $228,000.00 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:
No
MEDICAL SURVEILLANCE:
Yes
SIGNIFICANT WORK ACTIVITIES:
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), 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