At a Glance
- Tasks: Lead the development of innovative lipid nanoparticle processes for gene editing therapies.
- Company: Join Prime Medicine, a pioneering biotech company transforming gene editing.
- Benefits: Enjoy competitive pay, health benefits, equity programs, and generous time off.
- Other info: Collaborative environment with opportunities for professional growth and innovation.
- Why this job: Make a real impact in healthcare by developing cutting-edge genetic therapies.
- Qualifications: Ph.D. in relevant field with extensive experience in LNP process development.
The predicted salary is between 100000 - 120000 £ per year.
Company Overview: Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies.
Position Summary: The Senior Scientist / Senior Engineer, LNP Process Development will provide technical leadership for the development, characterization, and scale-up of robust, scalable lipid nanoparticle (LNP) formulation and drug product manufacturing processes. This individual will be responsible for driving LNP process development — spanning formulation, process optimization and characterization, scale-up, and technology transfer support for key pipeline assets.
Key Responsibilities
- Lead the design, execution, and optimization of LNP processes to accommodate novel formulations and drug product manufacturing processes (LNP mixing and tangential flow filtration [TFF]) from bench through GLP/GMP scale, with emphasis on developing robust and scalable processes.
- Serve as a subject matter expert for LNP process development across programs and therapeutic areas, partnering with Research, Platform, Hematology, and other teams to translate novel modalities into developable drug products.
- Evaluate and implement emerging technologies, novel materials, delivery and process innovations that continuously improve delivery efficiency, drug product quality, manufacturability, and cost of goods.
- Support technology transfer activities to external contract development and manufacturing organizations (CDMOs), including preparation of tech transfer packages, on-site execution support (Person-in-Plant), and process troubleshooting.
- Author and contribute to Chemistry, Manufacturing, and Controls (CMC) sections of regulatory filings, briefing books, and regulatory responses related to LNP drug product.
- Maintain impeccable documentation using electronic lab notebooks (ELNs); generate experimental protocols, development reports, technology transfer packages, SOPs, and technical reports to support clinical development.
- Communicate complex technical information clearly through presentations, written reports, and everyday collaboration to diverse audiences including cross-functional stakeholders and external partners.
Qualifications & Experience
- Ph.D. in Chemical Engineering, Biomedical Engineering, Chemistry, Pharmaceutical Sciences, Materials Science, or a related discipline with 8+ years of relevant industrial experience in LNP process development and formulation development; M.S. with 12+ years.
- Demonstrated expertise in LNP formulation processes, TFF operations, and related characterization methods.
- Hands-on experience with LNP delivery and formulation development, process scale-up from bench to GLP/GMP scale, and technology transfer to GMP facilities and/or CDMOs.
- Strong proficiency in analytical characterization techniques (HPLC/UPLC, DLS/SLS, TEM, DSC, SAXS, UV-Vis, fluorescence spectrophotometry) to support process development.
- Experience with statistical design of experiments (DoE) and knowledge of Quality by Design (QbD) methodologies.
- Hands-on experience with defining and setting up equipment systems for LNP and TFF processes.
- Knowledge of CMC regulatory requirements and experience contributing to IND/CTA submissions.
- Excellent communication skills, with the ability to effectively collaborate cross-functionally, prioritize activities to meet program goals, and present complex technical information to diverse audiences.
- Highly self-motivated with strong organizational skills, the ability to manage competing priorities, and a hands-on approach to problem-solving.
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity). Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.
Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.
Senior Scientist / Senior Engineer, LNP Process Development in Cambridge employer: Prime Medicine
Prime Medicine is an exceptional employer, offering a dynamic work environment where innovation in gene editing thrives. With a strong commitment to employee well-being, we provide comprehensive benefits, including robust health and wellness packages, generous paid time off, and opportunities for professional growth. Located in a vibrant area, our culture fosters collaboration and creativity, empowering you to make a meaningful impact on the future of medicine.