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# Data Analyst II

- **Company:** Abbott Laboratories
- **Location:** Saint Paul, MN, United States
- **Salary:** $61,300.0 - $122,700.0
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Data Analysis, Systems Engineering, Confluence, JIRA, Microsoft Office, Microsoft Visio, Microsoft PowerPoint, Scrum Methodology, Systems Development Life Cycle, Requirements Traceability, Microsoft SharePoint, Software Engineering, Software Project Management, Software Systems, Management of Software Versions, Jama (Software), CodeBeamer, DOORS (Software), Information Technology
- **Published:** October 1, 2026
- **Apply:** https://abbott.wd5.myworkdayjobs.com/abbottcareers/job/United-States---Minnesota---St-Paul/Data-Analyst-II_31163013-1

## About the Role

* Service-oriented
 * Curiosity and willingness to learn
 * Attention to detail
 * Critical and analytical thinking
 * Ability to understand and summarize advanced technical concepts
 * Excellent organizational skills
 * Strong content management skills, * Bachelor's degree in Technical Communication, Engineering, Computer Science, Biomedical Engineering, Systems Engineering, or relevant field;
 * Clear understanding of software development processes (SDLC).
 * Excellent communication and documentation skills.
 * Willing to learn medical device regulations and quality processes.
 * Demonstrated ability to work proactively and independently.
 * Experience with requirements tools: DOORS, Codebeamer, JAMA
 * Experience with the software development process and deliverables.
 * Experience with SharePoint, Confluence, JIRA
 * Advanced skills in the MS Office suite: Word, Excel, PowerPoint, Visio.

## Description

* Support development of functional and non-functional requirements; provide change management of requirement documentation and a variety of software project deliverables.
 * Facilitate technical review and workshop sessions with Systems and Software Systems engineers.
 * Ensure requirements are well-written, feasible, testable, and aligned to ISO/IEC/IEEE 29148:2018
 * Maintain a single source of truth for requirements; managing baselines and versioning across releases.
 * Assist in the development of tools such as glossaries, style guides, knowledge bases, data views, and workflows that support engineering business functions and data analysis.
 * Edit and publish requirement specifications, software design and verification documentation for design control environments.
 * Support creation and maintenance of requirements traceability matrices (RTMs) linking requirements to design, risk controls, and verification activities.
 * Pilot and document workflows, requirement writing best practices, and guidance for larger team use and cross-functional alignment.

Cross-Functional Collaboration-

 * Collaborate with Systems Engineering, Quality/Regulatory, Risk Management, and Software teams.
 * Coordinate technical review meetings; moderating and recording action items and resolutions.
 * Champion and support continuous improvement of requirements and documentation processes, tools, and metrics.
 * Participate in backlog refinement, sprint planning, reviews, and grooming to clarify scope and acceptance criteria.
 * Serve as a bridge between business, engineering, and QA-resolving ambiguity quickly and decisively.