BryceTech is seeking a Product Management Support – Blood Subject Matter Expert to provide specialized medical and technical expertise to the Defense Health Agency (DHA), Warfighter Protection and Acute Care (WPAC) portfolio. This position will support the development and management of blood and blood products, blood research and operations, and combat casualty care products and devices, applying subject matter expertise across the medical product development lifecycleResponsibilitiesServe as a subject matter expert in blood and blood products, blood research, and blood product operationsProvide technical expertise related to traumatic hemorrhage, hematology, transfusion medicine, and combat casualty care products and devicesProvide senior technical input to Product Managers and PMO leadershipSupport advanced development requirements for medical products and related initiativesIndependently manage multiple technical efforts, priorities, and projectsParticipate as a substantive member of Integrated Product Teams, working groups, committees, and other technical forumsSupport product development design sessions and technical discussions throughout the product lifecycleConduct market research and monitor relevant technology and industry developmentsEngage with Government, industry, academic, clinical, technical, and other stakeholdersAssess and monitor technical risks and stakeholder positions and communicate findings to Product Managers and PMO leadershipSupport Product Managers with acquisition documentation throughout the DoD Acquisition LifecycleProvide technical input to Acquisition Strategies, Acquisition Decision Memoranda, Acquisition Program Baselines, Analysis of Alternatives, Requirements Documents, Concepts of Operations, Life Cycle Sustainment Plans, LCCEs, RFIs/RFPs, Systems Engineering Plans, and TEMPsPrepare or contribute to white papers, RFI responses, technical guides, executive summaries, situational reports, data summaries, market research reports, risk assessments, protocols, decision logs, and briefingsReview program documentation for technical accuracy and provide expert analysisProvide technical input related to non-clinical studies and clinical trial design and executionReview non-clinical study reports, clinical protocols, regulatory applications, and related communicationsProvide technical input concerning chemistry, manufacturing, and controls for applicable biologics, drugs, and devicesSupport development of plans for testing, fielding, delivery, and training of assigned productsSupport development and implementation of policies, regulations, and documentation governing blood products and combat casualty care productsReview FDA recommendations and applicable clinical and regulatory documentationCommunicate complex technical information effectively to personnel at multiple organizational levels
