Quality Data & Trending Analyst (Medical Devices)

Abbott

Alameda (CA)

On-site

USD 90,000 - 120,000

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
Flexible Spending Accounts
Life Insurance
Short Term Disability
Long Term Disability
401(k)

Job summary

Abbott in Alameda, CA is seeking a Quality Engineering Analyst (Tracking & Trending) to support complaint and quality data analysis in a regulated medical device environment. You will perform trending investigations, analyze complaint data, and support root cause investigations while driving continuous improvement.

This on-site role collaborates with Quality, Operations, Manufacturing and R&D to ensure FDA/ISO compliance.

Qualifications

  • Bachelor's degree in Biomedical Engineering or related engineering discipline.
  • 2–3 years of experience in medical device or pharmaceutical industries.
  • Experience in FDA/ISO regulated environments.

Responsibilities

  • Perform complaint tracking and trending activities using quality databases and analytical tools.
  • Analyze complaint, CAPA, and quality system data to identify trends and risks.
  • Support root cause investigations and CAPA activities.
  • Create dashboards and reports using Excel, Power BI, JMP, SQL, and Python.
  • Collaborate with Quality, Operations, Manufacturing, and R&D teams.
  • Document investigative findings and support regulatory compliance requirements.

Skills

Quality data analysis
CAPA investigations
Excel analytics
Power BI
SQL querying
Python basics
Dashboard development

Education

Bachelor's in Biomedical Engineering
Related Engineering Discipline

Tools

JMP
Excel
Power BI
SQL
Python

Job description

Abbott in Alameda, CA is seeking a Quality Engineering Analyst (Tracking & Trending) to support complaint and quality data analysis in a regulated medical device environment. You will perform trending investigations, analyze complaint data, and support root cause investigations while driving continuous improvement.

This on-site role collaborates with Quality, Operations, Manufacturing and R&D to ensure FDA/ISO compliance.

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