Engineer (0-3 years)
Binding Minds Inc. (Certified Disability Owned Business Enterprise)
This job at a glance
- Who can apply
- New grads and up to 3 years · Bachelor's degree
- Work
- On-site in Boston
- Pay
- Not stated by the employer.
- Listed
- Nov 11, 2026 · still open
About the Role
We are seeking an Engineer to join our Formulation Sciences team focused on lipid nanoparticle (LNP) discovery and development for CRISPR-based gene editing therapies. The successful candidate will be responsible for supporting LNP process development, scale-up, and characterization, working as part of a multidisciplinary, fast-paced team environment. The ideal candidate will have some process development industry experience with a desire to contribute to a team focused on championing nanomedicinal products and developing manufacturing solutions based on strong scientific principles.
Key Responsibilities
- Support the design, manufacturing, and characterization of lipid nanoparticles (LNPs) for screening critical process parameters (CPPs) and critical material attributes (CMAs) that impact critical quality attributes (CQAs).
- Support the design and execution of a wide range of experiments, including DoEs, to advance LNP technology and process development.
- Participate in defining equipment specification/selection, draft procedures, and recommended operating parameters/ranges.
- Write protocols, perform experiments, organize and analyze data, interpret results, record experiments in an electronic lab notebook, and summarize work in presentations and technical reports.
- Assist in ordering supplies, making reagents, and maintaining a safe and high-performing laboratory.
- Multi-task across several projects and manage time effectively to achieve results.
- Collaborate with multiple cross-functional teams and execute other duties as assigned.
Requirements & Tech Stack
- Bachelor’s/Master’s degree in chemical engineering, bioengineering, chemistry, pharmaceutical sciences, or another related field.
- Experience with lipid nanoparticle formulations and analytical characterization methods (Preferred).
- Knowledge of practices and equipment used to run manufacturing processes in a GMP environment, including TFF, sterile filtration, single-use technology, and sterile/aseptic processing (preferred).
- Proficiency in literature search and relevant computer software skills.
Qualifications
- Strong problem-solving skills, and a creative/innovative approach in problem solving.
- Ability to work independently and in very dynamic, interdisciplinary team environments.
- Proven record in working with partners/collaborators (desirable).
- Organized, detail-oriented, and an innovative self-starter who continuously seeks to improve existing laboratory methods and processes.
- Effective verbal and written communication skills.
- Minimum of 2 years of relevant industry experience.