Scientific and Technical Advisor: Biopharmaceutical​/Nucleic Acid Manufacturing Specialist

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Work in a dynamic, fast‑paced environment as a scientific and technical advisor supporting advanced research and development in biomedical engineering and life sciences. Leverage a breadth of expertise in cell and molecular biology, genetic engineering, QC analytical techniques, and assay development to evaluate and shape programs that address critical healthcare, public health, and operational challenges, such as DNA, RNA, and viral vector manufacturing for therapeutic applications.

Collaborate with world‑class scientists, engineers, and clinicians to assess emerging technologies, identify high‑impact opportunities, and drive development in areas such as implantable and wearable devices, regenerative medicine, advanced diagnostics, and integrated biomedical platforms. Provide strategic assessments, create technical reports, develop program plans, track technological progress, and perform related tasks to advance client R&D objectives. Support program management and development, prepare high‑quality briefing materials, and engage regularly with stakeholders.

Operate with minimal guidance, balancing multiple priorities while delivering high‑value results.

• Ideal candidates are collaborative, will have ARPA‑H and/or broader‑ARPA experience, and have a PhD in cell or molecular biology (or a closely related discipline) and a minimum of five (5) years of industry experience in the biopharmaceutical and/or biomanufacturing sector, with demonstrated hands‑on expertise supporting cell and gene therapy–relevant development and manufacturing efforts (DNA, RNA, and viral vectors).
• Demonstrated proficiency in cell and molecular biology laboratory techniques, including experience with: (1) QC analytical methods and assay development for cell and gene therapy products, (2) genetic engineering of mammalian cells, and (3) stem cell differentiation workflows.
• Demonstrated record of authoring technical papers, reports, or program plans for both technical and non‑technical audiences.
• Ability to develop pitches and present complex engineering and biomedical concepts to multidisciplinary audiences.
• Must have strong PowerPoint and Excel skills, which include proficiency with keyboard shortcuts and ability to create PPT slides and Excel files on the fly during a meeting in a high‑pressure environment.
• Must be able to obtain a federal government Public Trust clearance.

• Advise on new and existing initiatives, including program planning and execution support.
• Conduct technical due diligence and literature reviews across DNA, RNA, and viral vector product development and manufacturing for therapies.
• Evaluate technical, scientific, regulatory, and technoeconomic data for novelty, rigor, robustness, and feasibility; synthesize clear takeaways.
• Draft and review technical materials including program plans, solicitations, internal reports, and briefing products for technical and non‑technical audiences.
• Assess the R&D landscape to identify portfolio gaps and priority needs aligned with mission objectives.
• Monitor technical progress against defined metrics and support course‑correction, risk identification, and milestone tracking.
• Operate effectively within a team and independently, contributing critical thinking and cross‑functional collaboration to technical R&D efforts.
• Travel as required to support mission requirements (approximately 10‑20% as needed)

• Knowledge of current FDA regulatory frameworks and their application to product development and manufacturing is a plus.
• Experience…