Engineer

Abbott

Burlington (MA)

On-site

USD 55,104 - 82,656

Full time

14 days+

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Benefits offered by this job

Medical and Prescription Drug Plans
Dental Plan
Vision Plan
Health Savings Account (for High‑Deduc
Flexible Spending Accounts
Supplemental Life Insurance
Short Term Disability
Long Term Disability
Critical Illness, Hospital coverage, 

MetLife Legal, MetLife ID Fraud, and 

401(k)

Job summary

Abbott in Burlington, MA is seeking an Engineer to perform failure analysis on explanted long-term biomedical implant products. The role requires applying theoretical principles, evaluation, and analytical techniques to identify root causes and support quality systems.

You will collaborate with Product Development, Engineering, Manufacturing, and Product Surveillance, mentor junior staff, and help define test equipment.

Qualifications

  • Bachelor’s Degree in Engineering is required; Electrical or Biomedical Engineering preferred.
  • Engineering work experience is preferred.
  • Knowledge of global medical device reporting regulations and medical terminology preferred.
  • Strong written and verbal communication, interpersonal, facilitation, and presentation skills required.
  • Ability to manage multiple assignments, prioritize effectively, and meet deadlines in a fast-paced environment.
  • Ability to work independently and collaboratively across teams and communicate effectively with all levels of employees.
  • Demonstrated record of delivering reliability engineering insights that support management decision‑making.
  • Proficiency with personal computer applications, including spreadsheets, word processing, databases, and specialized software.

Responsibilities

  • Perform failure analysis on explanted long term biomedical implant product.
  • Apply theoretical principals, evaluation, ingenuity, and analytical techniques to identify root cause failure mechanisms.
  • Meet deadlines on multiple assignments and operate in a diverse cross‑functional team environment.
  • Proactive in finding quality improvements related to Failure Analysis.
  • May serve as lead and mentor less experienced lab staff.
  • Work cross functionally with Product Development, Engineering, Manufacturing, and Product Surveillance.
  • Aid in defining test equipment to accomplish quality responsibilities.
  • Support Company initiatives in QMS, EMS, and regulatory requirements.
  • Comply with FDA regulations, other regulatory requirements, and company policies.
  • Maintain positive communications with all levels of employees, customers, contractors, and vendors.

Skills

Root cause analysis
Cross-functional collaboration
Analytical thinking
Project management
Effective communication

Education

Bachelor’s Degree in Engineering

Job description

Title: Engineer

Location: Burlington, MA

Duration: 7 Months

100% Onsite

Main Responsibilities
  • Perform failure analysis on explanted long term biomedical implant product.
  • Work requires the application of theoretical principals, evaluation, ingenuity, and creative/analytical techniques to identify root cause failure mechanisms.
  • Must be able to meet deadlines on multiple assignments and be able to operate in a diverse cross‑functional team environment.
  • Proactive in finding quality improvements related to Failure Analysis
  • May serve as lead and assign work to less experienced personnel and serves as a mentor when assisting less experienced lab staff in solving more complex problems.
  • Works cross functionally and collaboratively with Product Development, Engineering, Manufacturing, and Product Surveillance.
  • Aides in definition of test equipment as required to accomplish quality responsibilities.
  • 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.
Qualifications
  • Bachelor’s Degree in Engineering required; Electrical or Biomedical Engineering preferred
  • Engineering work experience preferred
  • Knowledge of global medical device reporting regulations and medical terminology preferred
  • Strong written and verbal communication, interpersonal, facilitation, and presentation skills required
  • Strong analytical, quantitative, organizational, follow‑up, and attention‑to‑detail skills
  • Ability to manage multiple assignments, prioritize effectively, and meet deadlines in a fast‑paced environment
  • Ability to work independently and collaboratively across teams and communicate effectively with all levels of employees
  • Demonstrated record of delivering reliability engineering insights that support management decision‑making
  • Proficiency with personal computer applications, including spreadsheets, word processing, databases, and specialized software
Consultants Eligible Benefits Upon Waiting Period
  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High‑Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)
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