Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Dexian DISYS

Associate Failure Analysis Engineer

Career Insights for Product Quality Engineer

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Massachusetts data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Product Quality Engineer evaluates and tests products and manufacturing systems, to ensure that products are produced that meet quality and performance standards as well as safety and regulatory requirements. Develops product quality standards and monitors production and product testing.

$97,977 / year median in Massachusetts

+2% projected growth

Explore Career

Job Description

Associate Failure Analysis Engineer Dexian DISYS United States, Massachusetts, Acton Jul 14, 2026 Associate Failure Analysis Engineer Job details Posted 14 July 2026 Location Acton, MA Reference 1011180 Job description
Job Title:
Associate Failure Analysis Engineer
Location:
Acton, MA United States
Duration :
3 + Months
Department:
Pharmaceuticals
Pay Range:
$48 - $50/hr On W2
Job Responsibilities:
  • Perform moderately complex tasks to ensure compliance with quality standards.
  • Partner with quality assurance engineers and other team members to ensure effective inspection and testing procedures are implemented and maintained.
  • Generate, review and maintain Quality records in support of the Quality System, e.g., training, internal audits, NCR, and CAPA.
  • Perform product testing and failure analysis.
  • Review Lot Acceptance records and DHRs, create trend charts.
  • Perform investigation triage and deep dive investigations to develop hypothesis for failure.
  • Collect log quality data and trend results.
  • Accountability for quality investigation and root cause analysis.
  • Assist in gathering information during FDA and
ISO 13485
inspections.
  • Evaluate process flow by applying Lean Six Sigma methodology to streamline.
  • Trouble shoot new failure modes.
  • Evaluate process and engineering controls to improve safety and efficiency.
  • Perform other duties as assigned.
Education and Experience:
Minimum Requirements:
  • Bachelors Degree in an engineering or scientific discipline , or equivalent experience.
Preferred Skills and Competencies:
  • Computer proficiency in MS office (specifically Excel)
  • Electrical and mechanical background strongly preferred
  • Experience creating and analyzing charts in MS Excel a plus
  • Knowledge of Six Sigma, Lean, SPC, ASQ and/or ISO process controls a plus
  • Prior experience working in a regulated industry (medical device) and/or experience working in a bio-hazard/lab environment preferred
  • Preferred 2 years in a Quality related function, working with QSR and/or
ISO 13485.
  • Effective verbal and excellent technical writing skills.
  • Excels at generating and maintaining organized and accurate records. Physical Requirements (if applicable):
  • Sitting 70%, Standing 30%
  • Frequent lifting