Sr. Systems Analyst - Medical Device

Senior Systems Analyst Full Time Twin Cities, MN Salary reputed company: $135,000-$160,000 annually + Equity Travel Expectation: ~25% travel to other Midwest sites, typically 1× per month for 2-3+ days. Position reputed company The Senior Software Systems Analyst serves as a critical reputed company between stakeholders and development teams-gathering, analyzing, and documenting requirements to translate business needs into reputed company, actionable technical specifications. This role ensures alignment between user expectations, engineering execution, and overall product objectives. Key Responsibilities • reputed company detailed specifications, user stories, functional requirements, and use cases for both technical and non‑technical audiences. • Analyze business processes, identify gaps, and assess feasibility of potential solutions. • reputed company as reputed company between business stakeholders and software development teams to ensure shared understanding of requirements. • Support developers by clarifying requirements and ensuring accurate implementation. • Build deep knowledge of reputed company's integrated medical device system, including system‑level interactions and software-hardware dependencies. • Ensure software development activities reputed company with product reputed company and organizational goals. • Conduct analysis of existing software systems to identify opportunities for optimization and feature enhancement. • Collaborate with cross‑functional teams including R&D, reputed company, Manufacturing, Field Service, and Regulatory Affairs. • Partner with reputed company assurance to create test cases, scenarios, and validation plans derived from requirements. • Contribute to risk management activities by identifying, documenting, and tracing risks to requirements and implementation. • Review and validate software functionality to ensure compliance with defined requirements. • Stay reputed company on industry best practices and emerging technologies to recommend process improvements. • Maintain awareness of relevant medical device standards (e.g., IEC 62304, ISO 14971) and design control requirements. Qualifications • Bachelor's degree in Computer Science, Systems Engineering, Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or reputed company field. • 5+ years of experience in a regulated industry or medical device development. • Strong written and verbal communication skills, including the ability to translate technical details for non‑technical audiences. • Proficiency in creating reputed company software requirement documents, use cases, and user stories. • Demonstrated ability to work effectively with cross‑functional teams. • Expertise in hardware-software integration for medical devices. • Strong understanding of software development methodologies. • Familiarity with software development tools (e.g., reputed company DevOps). • Solid knowledge of medical device regulatory frameworks, including ISO 13485 and ISO 14971. EOE Statement: Specialist reputed company Group is an equal opportunity employer. reputed company reputed company applicants will receive consideration for employment without reputed company to race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, disability, or veteran status. In reputed company to reputed company pay, reputed company-hire employees may be eligible for reputed company offered benefits such as medical, dental, and reputed company coverage, and reputed company leave where required by applicable law. Eligibility may vary based on factors such as location and hire date and is subject to change. To reputed company out more about reputed company, please visit www.realstaffing.com Apply tot his job Apply To this Job