Senior Director, LNP Formulation & Process Development

miraibio

Cambridge (MA)

On-site

USD 210,000 - 270,000

Full time

6 days ago
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Job summary

Mirai Bio in Cambridge, MA seeks a Senior Director of Lipid Nanoparticle (LNP) Formulation & Process Development to lead the LNP formulation, process development, and small-scale production. You will guide scientific and operational strategy across programs, develop scalable capabilities, and mentor a growing team of scientists while partnering with clients.

The role requires deep LNP expertise, strong leadership, and client-facing skills to drive program success and transfer knowledge to

Qualifications

  • Ph.D. in Pharmaceutical Sciences, Chemical Engineering, Bioengineering, Chemistry, Biochemistry, or related field with 12+ years of industry experience; M.S. with 14+ years; or B.S. with 16+ years.
  • Extensive hands-on experience in LNP formulation and process development.
  • Deep understanding of LNP composition, formation, purification, characterization, and relationships between process parameters and product attributes.
  • Demonstrated ability to lead complex technical programs, interpret data, troubleshoot problems, and establish development strategies.

Responsibilities

  • Lead the LNP formulation, process development, and small-scale production function supporting partner and internal programs.
  • Establish technical strategy and best practices for LNP formulation, process development, characterization, and production across multiple payloads and applications.
  • Provide senior technical leadership across multiple programs, including development strategy, experimental planning, data review, risk mitigation, and technical recommendations.
  • Serve as a senior technical interface with clients and partners and support proposals, project scopes, presentations, and business development activities.
  • Oversee non-GMP production of LNP formulations for in vitro, in vivo, and preclinical studies.
  • Drive technical troubleshooting, process optimization, technology transfer, and continuous improvement of LNP production for mRNA, siRNA, gene-editing components, and other nucleic acid payloads.
  • Establish workflows, documentation, and operational practices that improve quality, reproducibility, efficiency, and scalability.
  • Lead, mentor, and develop the LNP team while managing priorities, resources, capacity, and organizational growth.
  • Collaborate cross-functionally to align LNP development and production with broader program and company objectives.

Skills

LNP formulation
Process development
Team leadership
Client-facing

Education

PhD in Pharmaceutical Sciences or related

Job description

COMPANY DESCRIPTION

Mirai Bio is a privately-held, Flagship-founded biotechnology company that is delivering genetic medicines from promise to performance. Mirai was built to solve one of the field's central challenges: achieving precise, scalable delivery of diverse nucleic acid payloads to specific cells and tissues, particularly beyond the liver. By combining a large and growing proprietary in vivo biodistribution dataset, machine learning-guided lipid nanoparticle optimization, modular targeted particle design, and integrated translation and manufacturing capabilities, Mirai helps partners accelerate development, reduce technical risk, and pursue high-value programs making delivery a strategic advantage. We are seeking collaborative, relentless problem solvers that share our passion for defining the future of genetic medicines together.

THE ROLE

We are seeking an experienced Senior Director of Lipid Nanoparticle (LNP) Formulation & Process Development to lead the company's LNP formulation, process development, and small-scale production organization supporting partner and internal research and preclinical programs.

The Senior Director will provide scientific and operational leadership across multiple programs, establish LNP development and production strategies, and build scalable, reproducible capabilities to support a growing portfolio. This individual will lead and develop a team of scientists, serve as a senior technical interface with clients and partners, and collaborate closely with Analytical Development, Translational Biology, Project Management, and other functions.

The successful candidate will combine deep expertise in LNP formulation and processing with strong organizational leadership, program execution, and client-facing skills.

KEY RESPONSIBILITIES
  • Lead the LNP formulation, process development, and small-scale production function supporting partner and internal programs.
  • Establish technical strategy and best practices for LNP formulation, process development, characterization, and production across multiple payloads and applications.
  • Provide senior technical leadership across multiple programs, including development strategy, experimental planning, data review, risk mitigation, and technical recommendations.
  • Serve as a senior technical interface with clients and partners and support proposals, project scopes, presentations, and business development activities.
  • Oversee non-GMP production of LNP formulations for in vitro, in vivo, and preclinical studies.
  • Drive technical troubleshooting, process optimization, technology transfer, and continuous improvement of LNP production for mRNA, siRNA, gene‑editing components, and other nucleic acid payloads .
  • Establish workflows, documentation, and operational practices that improve quality, reproducibility, efficiency, and scalability.
  • Lead, mentor, and develop the LNP team while managing priorities, resources, capacity, and organizational growth.
  • Collaborate cross‑functionally to align LNP development and production with broader program and company objectives.
PROFESSIONAL EXPERIENCE & QUALIFICATIONS
Required
  • Ph.D. in Pharmaceutical Sciences, Chemical Engineering, Bioengineering, Chemistry, Biochemistry, or related field with 12+ years of relevant industry experience ; M.S. with 14+ years ; or B.S. with 16+ years .
  • Extensive hands‑on experience in LNP formulation and process development .
  • Deep understanding of LNP composition, formation, purification, characterization, and the relationships between process parameters and product attributes.
  • Demonstrated ability to lead complex technical programs, interpret data, troubleshoot problems, and establish development strategies.
  • Proven experience leading and developing scientific teams and managing multiple concurrent programs and resources.
  • Strong written, verbal, presentation, and client‑facing communication skills.
Preferred
  • Experience in a CMO, CDMO, CRO, or other client-service organization .
  • Experience developing LNPs across multiple payloads and therapeutic applications.
  • Experience building or scaling LNP formulation, process development, and production capabilities.
  • Experience with technology transfer or transitioning development processes toward larger‑scale or GMP manufacturing.
  • Experience supporting technical proposals, scopes of work and business development activities.
Leadership Profile

The ideal candidate is a hands‑on scientific and organizational leader who can move between technical problem‑solving, portfolio strategy, team leadership, operational planning, and client engagement. The SeniorDirectorwillbeaccountableforleadingahigh‑performingLNP organization and ensuring the reliable delivery of high-quality formulations and development programs that enablepartnerandinternalprograms to advance.

ABOUT FLAGSHIP PIONEERING:

Flagship Pioneering invents and builds platform companies, each with the potential for multiple products that transform huma

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