Business Analyst -5
Spotted 1h agoFull-time
Job details
- Work mode
- On-site
- Employment
- Full-time
- Level
- Mid level
- Experience
- 3+ years
- Posted
- Oct 19, 2026
- Last confirmed open
- Oct 19, 2026
Job description
About this role
Santa Clara, California 95050 Posted October 19th, 2026
Job Type: Full Time
Job Category
IT
Job Description
Role: Business Analyst - Regulatory & Clinical Affairs
Location: Santa Clara, CA – Onsite
Fulltime – Permanent
Job Description
Must Have Technical/Functional Skills
- 3-5 years of relevant Business Analyst experience, with a target of approximately 5 years.
- Minimum 2 years of experience in the medical device/MedTech sector, specifically supporting Regulatory Affairs and/or Clinical Affairs processes.
- Strong understanding of regulated medical device business processes, quality systems, documentation controls, and applicable regulatory expectations.
- Ability to independently assess current-state workflows, identify pain points, control gaps, manual effort, and opportunities for AI-enabled automation.
- Experience translating business needs into clear problem statements, business requirements, functional requirements, user stories, acceptance criteria, and process maps.
- Working knowledge of AI, intelligent automation, workflow automation, analytics, and digital transformation concepts, including identification of appropriate use cases and business value.
- Ability to evaluate proposed solutions for regulatory, clinical, data privacy, quality, validation, traceability, and change-management considerations.
- Experience facilitating discovery workshops, stakeholder interviews, requirements reviews, and prioritization sessions.
- Strong analytical skills with proficiency in process mapping, gap analysis, root cause analysis, data analysis, and KPI definition.
- Proficiency with Microsoft Office tools, including Excel, PowerPoint, Word, Visio or equivalent process-mapping tools; experience with requirements or agile tools is preferred.
- Excellent written and verbal communication skills, with the ability to engage stakeholders from individual contributors through VP-level leadership.
Roles & Responsibilities
- Independently assess Regulatory Affairs and Clinical Affairs business processes to understand objectives, workflows, systems, data, controls, pain points, and dependencies.
- Identify and evaluate AI, automation, analytics, and workflow-improvement opportunities based on business value, feasibility, risk, and regulatory impact.
- Develop concise opportunity statements, problem statements, business cases, process maps, requirements, user stories, acceptance criteria, and traceability documentation.
- Partner with Regulatory Affairs, Clinical Affairs, Quality, IT, Data/AI, Privacy, Security, and other cross-functional stakeholders to validate needs and align on solution scope.
- Facilitate workshops and interviews with stakeholders at all levels, from individual contributors to VP leadership, and communicate findings in a clear, decision-oriented format.
- Document current-state and future-state processes, business rules, data flows, roles, handoffs, risks, assumptions, and success measures.
- Prioritize use cases and requirements; support solution evaluation, backlog refinement, testing/UAT readiness, implementation planning, and change adoption.
- Ensure proposed solutions maintain appropriate regulatory, clinical, quality, privacy, validation, documentation, and audit-trail considerations.
- Prepare executive-ready summaries, presentations, dashboards, and recommendations that enable timely decisions.
- Drive assigned work independently within the short-term contract timeline and escalate decisions, risks, and dependencies promptly.
Required Skills
Data Analyst
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