Senior Scientist / Engineer – Transplantation, Biopreservation, Bioengineering

Posted Sep 10

This is a fully remote position, open to applicants in South Carolina.

πŸ“‹ Description

β€’ Provide support to the Advanced Research Projects Agency for Health (ARPA-H) in areas such as transplantation, organ and tissue preservation, engineered tissues, organoids, microphysiological systems, and advanced therapeutic manufacturing.

β€’ Work in collaboration with the ARPA-H Program Manager and team to create, fund, and oversee R&D programs.

β€’ Deliver direct technical assistance to R&D performer teams, Government Program Managers, and stakeholders in health innovation.

β€’ Leverage expertise in transplantation and regenerative medicine to inform emerging technologies, clinical workflows, manufacturability, regulatory considerations, and implementation strategies.

β€’ Offer technical and strategic guidance for tissue and organoid manufacturing, organ-on-chip platforms, biopreservation, ex vivo organ perfusion, diagnostics, and translational technologies.

β€’ Assess technologies in light of clinical and operational realities, including organ recovery, preservation logistics, cold-chain issues, perfusion evaluation, and transplant-center workflows.

β€’ Perform landscape analyses and technical evaluations on emerging capabilities, vendors, performers, and scientific trends.

β€’ Evaluate commercialization pathways, scale-up processes, manufacturability, quality systems, GMP, regulatory strategies, reimbursement challenges, supply chain issues, and barriers to clinical adoption.

β€’ Review technical proposals, performer submissions, milestones, deliverables, and program risks.

β€’ Compile reviewer feedback and draft recommendations, project summaries, and presentation materials.

β€’ Identify subject-matter experts, potential performers, testing and evaluation partners, and transition stakeholders.

β€’ Assist with program management tasks, technical meetings, site visits, performer progress tracking, schedule risk identification, and briefing material preparation.

β€’ Stay informed of scientific, clinical, regulatory, and market developments.

β€’ Engage directly with the Government Program Manager, Mission Office leadership, performer teams, and external stakeholders.


⛳️ Requirements

β€’ PhD in physiology, systems biology, bioengineering, tissue engineering, regenerative medicine, or a related field; or an MD with substantial experience in transplantation, organ preservation, transplant surgery, transplant medicine, or a closely related discipline.

β€’ Proven subject-matter expertise in organ preservation, ex vivo organ perfusion and diagnostics, transplant biology, regenerative medicine, or translational bioengineering.

β€’ Proficient in critically evaluating technical data, experimental designs, and development pathways.

β€’ Experience in condensing complex scientific information into clear written and visual communications.

β€’ Background in supporting intricate R&D initiatives involving academic, clinical, and/or industrial stakeholders.

β€’ Capability to bridge the gap between basic science, engineering development, and clinical or transplant operational realities.

β€’ Excellent interpersonal, written, and verbal communication skills.

β€’ Ability to work autonomously and collaboratively, manage priorities effectively, and maintain a high level of attention to detail, organization, and proactivity.

β€’ U.S. citizenship or lawful permanent residency is required.

β€’ Active federal government Public Trust, or the ability to obtain one.

β€’ A minimum of one year of experience supporting DARPA or similar federal ARPA agencies.

β€’ Experience in supporting a federal or commercial health agency or organization.

β€’ Familiarity with the biomedical research landscape.

β€’ At least two years of experience in federal healthcare and/or scientific consulting.

β€’ Additional experience in transplantation, organ perfusion, biopreservation, engineered tissues, organoids, organ-on-chip/MPS, biofabrication, advanced therapeutic manufacturing, translational commercialization, regulatory strategy, quality systems, reimbursement, and barriers to clinical adoption.


🏝️ Benefits

β€’ Discretionary bonuses.

β€’ Signing or retention incentives.

β€’ Competitive compensation package.

β€’ Remote work arrangement.

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