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Business Analyst III

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Thermo Fisher Scientific

2021-12-03 07:50:53

Job location Sacramento, California, United States

Job type: fulltime

Job industry: Consulting & Corporate Strategy

Job description

**Position Summary:**

The Business Analyst III plays a key role in defining the requirements for software platform products in the Genetic Sciences Division to develop software applications for our world class qPCR, Capillary Electrophoresis, Rapid DNA, and Microarray platforms in both RUO and IVD markets.

**Key Responsibilities:**

+ Partner with our Product Management teams to define requirements for software platform design, development and usability testing.

+ Understand clinical customers and effectively translate their needs to product requirements.

+ Act as a liaison between technical teams, senior management, and the business community, including managing communications between business stakeholders and technical teams

+ Apply best practice methodologies in developing and maintaining requirements deliverables, including user stories, use cases, functional requirements, non-functional and performance requirements, and business rules.

+ Facilitate requirements workshops and hazard analysis activities with cross-functional science, engineering, and product management teams to elicit and review technical requirements and risk controls for new and sustaining software products.

+ Manage requirements, prepare analysis models and diagrams, and generate reports using IBM DOORS Next Generation (DNG), Excel, and Visio or similar.

+ Collaborate with test team to ensure requirements and specifications are concise, accurate, measurable, and testable.

+ Establish traceability between product requirements, specifications, and test cases/results. Prepare trace matrix reports.

+ Manage user change requests and change process

+ Experience with IVD (CE or FDA) regulated markets is a plus.

**Minimum Requirements/Qualifications:**

+ Bachelor's or Master's degree in biological science or software with scientific discipline is a plus.

**Personal attributes:**

+ Experience in developing and delivering requirements for multiple IVD/ Clinical software development programs

+ Experience with requirements gathering and workshop facilitation

+ Experience conducting UX/usability testing with end users

+ Experience interviewing customers to gather user needs

+ Well-versed in QSR design controls (21 CFR 820), ISO 13485, IEC 62304, ISO 14971 and IVD product development experience

+ Experience with Agile software development process

+ An understanding of genetic analysis tools, workflows, and chemistry in at least one of these areas: CE Sanger sequencing, qPCR or microarray is a plus

+ Excellent organizational skills, including the ability to efficiently evaluate, prioritize and handle multiple and changing programs/projects and priorities

+ Ability to think critically and desire to drive constant improvement

+ Excellent communication skills both written and verbal

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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