Engineer (0-3 years)

Binding Minds Inc. (Certified Disability Owned Business Enterprise)

Boston, MA0–3 yrs42m agovia LinkedIn

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.

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