Medical Device Workflow & Validation Lead (Remote, Continental United States)

We are looking for a Medical Device Workflow & Validation Lead to join our growing team! ABOUT THE ROLE: We are hiring a Medical Device Workflow & Validation Lead that helps to represent the reviewer's perspective across our document intelligence platform, including product development and client delivery. You will help us understand how reviewers work, translate their needs into clear requirements, validate features from a domain perspective, and lead client demonstrations and user acceptance. This role is responsible for ensuring that alerts, evidence, and workflows provide genuine value without creating unnecessary reviewer burden or presenting automated findings as regulatory conclusions KEY RESPONSIBILITIES: • Build strong working relationships with client reviewers and establish a regular, structured feedback process. • Lead discovery and validation sessions using prototypes and working software. • Translate reviewer needs into workflows, business rules, user stories, and measurable acceptance criteria. • Validate proposed requirements and workflows before development begins. • Partner with the Senior Product Manager to ensure requirements are accurate from a medical-device review perspective. • Define meaningful alert categories, priorities, reviewer actions, and escalation paths. • Evaluate alert relevance, false positives, false negatives, evidence quality, usability, and reviewer effort. • Test completed capabilities from a reviewer's perspective and identify missing requirements, confusing behavior, unsupported conclusions, and workflow gaps. • Lead client demonstrations, user acceptance testing, feedback capture, and acceptance or signoff. • Maintain traceability from the original client's needs through requirements, validation, and approval. • Improve domain understanding across product, engineering, data science, and leadership teams. REQUIRED QUALIFICATIONS: • Previous experience as a medical-device reviewer with experience in medical-device regulatory review, regulatory affairs, quality assurance, clinical review, or related regulated-document field. • Strong understanding of medical-device submission documentation and review processes. • Experience gathering requirements and working directly with clients, reviewers, or other domain stakeholders. • Ability to translate complex domain needs into clear, testable product requirements. • Experience conducting user acceptance testing or structured software validation. • Ability to identify missing evidence, unsupported conclusions, workflow gaps, and unintended consequences. • Strong analytical, facilitation, documentation, and communication skills. • Credibility and confidence when working with client domain experts. • Comfort collaborating with product managers, engineers, data scientists, and UX teams. • Must be authorized to work in the United States and have lived in the US for 3 or more consecutive years. • Must be able and willing to obtain a Public Trust Clearance USE OF AI ASSITIVE TECHNOLOGY All application materials must be your own original work, and interviews must be completed independently. Use of AI-generated content in applications or AI assistance during interviews will result in disqualification. BENEFITS: We invest in our team members so you can live your best life professionally and personally, offering a competitive salary and benefits. • Health Insurance -100% employer-paid premiums - ICA covers the full cost of one of three offered medical plans • Dental Insurance • Vision insurance • Health Spending Account • Flexible Spending Account • Life and Disability insurance • 401(k) plan with company match • Paid Time Off (Vacation, Sick Leave and Holidays) • Education and Professional Development Assistance • Remote work from anywhere within the continental United States LOCATION & TELEWORK This is a remote position following Eastern Standard Time (EST). Candidates residing in the DMV area preferred.