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Senior Software Business Analyst — Medical Device (Hybrid — Maple Grove, MN) - Contract

Pharmavise Corporation

Maple Grove, Minnesota

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JOB DETAILS
SKILLS
Agile Programming Methodologies, Analysis Skills, Atlassian JIRA, Biomedical Engineering, Business Analysis, Change Management, Code of Federal Regulations, Communication Skills, Computer Science, Continuous Improvement, Cross-Functional, Detail Oriented, DevOps, Digital Imaging and Communications in Medicine (DICOM), Embedded Systems, FDA (Food and Drug Administration), Fortune 500 Customers, HL7 (Health Level 7), Healthcare, Healthcare Software, ISO (International Organization for Standardization), Industry Standards, International Electro-Technical Commission (IEC), Interoperability, Leading Edge Technology, Maple, Medical Equipment, Medical Products, Microsoft Windows Azure, Patient Care, Process Analysis, Process Flow, Product Engineering, Product Lifecycle, Quality Assurance, Regulations, Regulatory Compliance, Regulatory Submissions, Requirements Management, Requirements Management Software, Risk Management, Scrum Project Management and Software Development, Software Administration, Software Development, Software Validation, Testing, Traceability, Usability Engineering, Use Cases, Validation Testing, Waterfall Model of Software Development
LOCATION
Maple Grove, Minnesota
POSTED
5 days ago
Our Fortune 500 Medical Device client has an exciting opportunity for a Senior Software Business Analyst. <\/span>
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Job Summary:<\/span>
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We are seeking an experienced Senior Software Business Analyst to join our dynamic team in the medical device industry. This role is critical to bridging the gap between clinical users, business stakeholders, and software development teams. The ideal candidate will possess strong analytical skills, in -depth knowledge of software development practices, and a deep understanding of regulatory and compliance requirements specific to healthcare and medical device software (e.g., FDA, ISO 13485, IEC 62304).<\/span>
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Responsibilities:<\/span>
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• Collaborate with cross -functional teams including product managers, engineers, QA, regulatory, and clinical experts to define software requirements for medical device products.<\/span>
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• Elicit, document, and manage business and functional requirements using industry -standard techniques (e.g., user stories, use cases, process flows).<\/span>
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• Translate complex clinical and business needs into detailed software requirements specifications (SRS).<\/span>
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• Act as the primary liaison between business stakeholders and development teams throughout the product lifecycle.<\/span>
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• Ensure software solutions align with regulatory standards and risk management processes (e.g., design control, traceability, usability).<\/span>
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• Support software validation and verification efforts by reviewing test plans and ensuring requirements coverage.<\/span>
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• Contribute to continuous improvement initiatives within the software development and requirements management processes.<\/span>
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• Facilitate requirement change management processes and impact analysis.<\/span>
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• Participate in audits and regulatory submissions as needed.<\/span>
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Qualifications:<\/span>
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• Bachelor's or Master’s degree in Business, Engineering, Computer Science, Biomedical Engineering, or related field.<\/span>
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• 5+ years of experience as a Business Analyst, including at least 2 years in a senior or lead role.<\/span>
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• Proven experience in the medical device industry or regulated healthcare software environment.<\/span>
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• Strong knowledge of IEC 62304, ISO 13485, 21 CFR Part 11, and FDA Design Controls.<\/span>
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• Solid understanding of Agile, Scrum, and/or Waterfall methodologies.<\/span>
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• Proficiency with tools such as Jira, Confluence, Azure DevOps, and requirements management software such as Jama (highly preferred)<\/span>
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• Exceptional communication skills with the ability to convey technical concepts to non -technical stakeholders.<\/span>
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• Strong analytical mindset and attention to detail.<\/span>
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Preferred Qualifications<\/span>
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• Experience with SaMD (Software as a Medical Device) or embedded systems.<\/span>
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• Familiarity with HL7, FHIR, DICOM, or other healthcare interoperability standards.<\/span>
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• Certification such as CBAP, PMI -PBA, or similar is a plus.<\/span>
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Why Join Us?<\/span>
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Work with cutting -edge medical technologies that improve patient outcomes. Collaborate with world -class professionals in a mission -driven organization focused on innovation, compliance, and quality.<\/span>
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Other Details:<\/span>
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• Schedule: 08:00:AM - 04:30:PM CST<\/span>
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• Work Setup: Hybrid at Maple Grove, MN<\/span>
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• Contract Length: 6 Months<\/span>
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• Start Date:  9/2/2025<\/span>
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About the Company

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Pharmavise Corporation