Product Management Support - Blood Subject Matter Expert

BryceTech•Frederick, MD

1d•$150,000 - $190,000

About The Position

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 lifecycle.

Requirements

10+ years of related experience in medical product development
Demonstrated subject matter expertise in blood and blood products, hematology, transfusion medicine, blood product operations, traumatic hemorrhage, or closely related combat casualty care disciplines
Experience supporting medical product development, research, clinical programs, or related medical technology activities
Ability to analyze and communicate complex scientific and technical information
Strong written and verbal communication skills
Ability to work independently and manage multiple concurrent technical efforts
Ability to participate effectively in IPTs and cross-functional teams
Working knowledge of DoD acquisition processes applicable to medical product development is required

Nice To Haves

Active DoW secret clearance preferred

Responsibilities

Serve as a subject matter expert in blood and blood products, blood research, and blood product operations
Provide technical expertise related to traumatic hemorrhage, hematology, transfusion medicine, and combat casualty care products and devices
Provide senior technical input to Product Managers and PMO leadership
Support advanced development requirements for medical products and related initiatives
Independently manage multiple technical efforts, priorities, and projects
Participate as a substantive member of Integrated Product Teams, working groups, committees, and other technical forums
Support product development design sessions and technical discussions throughout the product lifecycle
Conduct market research and monitor relevant technology and industry developments
Engage with Government, industry, academic, clinical, technical, and other stakeholders
Assess and monitor technical risks and stakeholder positions and communicate findings to Product Managers and PMO leadership
Support Product Managers with acquisition documentation throughout the DoD Acquisition Lifecycle
Provide 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 TEMPs
Prepare or contribute to white papers, RFI responses, technical guides, executive summaries, situational reports, data summaries, market research reports, risk assessments, protocols, decision logs, and briefings
Review program documentation for technical accuracy and provide expert analysis
Provide technical input related to non-clinical studies and clinical trial design and execution
Review non-clinical study reports, clinical protocols, regulatory applications, and related communications
Provide technical input concerning chemistry, manufacturing, and controls for applicable biologics, drugs, and devices
Support development of plans for testing, fielding, delivery, and training of assigned products
Support development and implementation of policies, regulations, and documentation governing blood products and combat casualty care products
Review FDA recommendations and applicable clinical and regulatory documentation
Communicate complex technical information effectively to personnel at multiple organizational levels