Data Analyst II: Requirements & Analysis for Healthcare Tech

Thornton Tomasetti

Saint Paul (MN)

On-site

USD 61,000 - 123,000

Full time

6 days ago
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Benefits offered by this job

Health insurance options
Tuition reimbursement
Retirement savings plan

Job summary

Abbott is seeking a Data Analyst II to support requirements and data workflows across the Medical Writing division in Minnesota. The role emphasizes documenting requirements, RTMs, and design/verification materials for medical devices and diagnostics.

You will collaborate with Systems Engineering, Quality/Regulatory, Risk, and Software teams; participate in backlog refinement, sprint planning, and cross‑functional reviews to resolve ambiguity quickly and decisively.

Qualifications

  • Bachelor’s degree in a relevant field; knowledge of software development processes (SDLC).
  • Excellent written and oral communication skills; ability to document clearly.
  • Willing to learn medical device regulations and quality processes.
  • Proactive, independent work style and ability to work with cross‑functional teams.
  • Experience with requirements tools: DOORS, CodeBeamer, JAMA.

Responsibilities

  • Support development of functional and non‑functional requirements; manage documentation across releases.
  • Facilitate technical reviews and workshops with Systems and Software engineers.
  • Maintain single source of truth for requirements; manage baselines and versioning.
  • Assist in tools development like glossaries, style guides, knowledge bases, and data views.
  • Publish requirement specs, design and verification docs.

Skills

Technical communication
Documentation
Analytical thinking
Independent worker

Education

Bachelor's degree or equivalent

Tools

DOORS
Codebeamer
JAMA
SharePoint
Confluence
JIRA
MS Office

Job description

Abbott is seeking a Data Analyst II to support requirements and data workflows across the Medical Writing division in Minnesota. The role emphasizes documenting requirements, RTMs, and design/verification materials for medical devices and diagnostics.

You will collaborate with Systems Engineering, Quality/Regulatory, Risk, and Software teams; participate in backlog refinement, sprint planning, and cross‑functional reviews to resolve ambiguity quickly and decisively.

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