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Abbott

Makes heart devices, glucose sensors and lab tests

Electrical Development Quality Engineer 2

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeSylmar, Los Angeles, CA, USA$81.5k - $141.3k

About the Job

Requirements

  • A bachelor's degree in Engineering or a Technical Field, or an equivalent combination of education and work experience.
  • Two years of quality engineering experience and demonstrated use of Quality tools and methodologies.
  • Ability to work in a highly matrixed and geographically diverse business environment.
  • Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
  • Ability to leverage or engage others to accomplish projects.
  • Strong verbal and written communication skills, with the ability to communicate effectively at multiple organizational levels.
  • Ability to multitask, prioritize, and meet deadlines in a timely manner.
  • Strong organizational and follow-up skills, and attention to detail.
  • Ability to travel approximately 10%, including internationally.

Responsibilities

  • Execute and support on-time completion of Design Control Deliverables.
  • Be accountable for Electrical Design Verification and Validation planning and execution, including active cross-functional root-cause analysis investigation and resolution activities.
  • Lead or support Risk Management activities from product Concept through Commercialization.
  • Support electrical design test and inspection method development, and lead method validation activities.
  • Ensure Design History File (DHF) content completion, integrity, and regulatory and standards compliance; communicate and resolve gaps collaboratively.
  • Support manufacturing process development and qualification for new product commercialization and product changes.
  • Support internal and external audits and audit responses.
  • Support product re-certifications.
  • Support the establishment of objective, measurable, discrete, and verifiable customer and product requirements.
  • Support objective component specification definitions, supplied component sampling plan development, and vendor qualifications.
  • Complete Document Change Request Reviews in a timely and objective manner.
  • Support company initiatives and Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
  • Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments.
  • Maintain positive and cooperative communication and collaboration with employees at all levels, customers, contractors, and vendors.

Desired Qualifications

  • Experience working in a broader enterprise or cross-division business unit model.
  • A master's degree.

About the Company

Abbott

Makes heart devices, glucose sensors and lab tests

Abbott makes medical devices, diagnostic tests, nutrition products and branded generic drugs for hospitals, laboratories, pharmacies and patients. Its best-known product is the FreeStyle Libre, a coin-sized sensor worn on the upper arm that tracks blood sugar around the clock without routine finger pricks. Its other lines run from heart valves, pacemakers and brain stimulators to lab analyzers, rapid tests and mail-in colon cancer screening kits, and Abbott earns money by selling these products to health systems, labs, retailers and consumers. The company was founded in 1888 by Chicago physician Wallace Abbott and is based in Abbott Park, Illinois.

Company size
10,001+
Company stage
IPO
Headquarters
Abbott Park, IL
Founded
1888

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