CRISPR Therapeutics AG

Research Associate II, CRISPR-X - LNP

CRISPR Therapeutics AG$85K — $92K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS or MS in Chemistry, Chemical Engineering, Biochemistry, or related field.
  • 2-5+ years of relevant experience with a bachelor's degree or 0-2+ years with a master's degree.
  • Hands-on expertise in lipid nanoparticle (LNP) formulation and analytical characterization for nucleic acid delivery.
  • Strong grasp of drug delivery systems and gene editing therapies.
  • Proven ability to work independently within a dynamic team-focused research environment.
  • Highly organized with exceptional attention to detail and problem-solving skills.

Responsibilities

  • Design, optimize, and execute LNP formulations with a variety of lipid compositions and therapeutic payloads individually.
  • Utilize LNP analytical characterization techniques and molecular biology methods effectively.
  • Generate reproducible datasets and maintain thorough records with electronic laboratory notebooks.
  • Conduct mammalian cell culture and support various in vitro studies across cross-functional teams.
  • Investigate LNP mechanisms to enhance delivery efficiency and formulation stability for platform innovation.
  • Communicate experimental results and project updates to cross-functional teams effectively.
  • Manage multiple projects and priorities in a collaborative, fast-paced environment.

Benefits

  • Discretionary bonus and equity participation.
  • Comprehensive health and wellness benefits offered.
  • Professional development opportunities and potential for career progression.
  • Collaborative work environment fostering innovation.
Full Job Description

Job Description:

Position Summary

We are seeking a highly motivated Research Associate II to support the design, development, and optimization of novel lipid nanoparticle (LNP) formulations to advance our non-viral delivery platform for hepatic and extra-hepatic tissues, and enable next-generation genome editing therapies from discovery through clinical translation.

The ideal candidate will bring hands-on expertise in LNP formulation development, scale-up, analytical characterization, chemistry, and process development, with a strong passion for innovation in nucleic acid delivery technologies. This individual will join the dynamic, fast-growing, and highly collaborative CRISPR-X division and contribute to both platform technology innovation and preclinical therapeutic programs.

In this role, the candidate will work cross-functionally to develop and characterize advanced delivery systems for emerging editing modalities, helping drive transformative gene editing therapies toward patients with unmet medical needs.

Responsibilities

  • Design, optimize, characterize, and execute lipid nanoparticle (LNP) formulations across a diverse range of lipid compositions and therapeutic payloads with minimal supervision.
  • Apply hands-on expertise in LNP analytical characterization techniques, including RiboGreen assays, DLS, NanoFCM, NTA, TFF, endotoxin testing, and HPLC, as well as molecular biology methods such as DNA/RNA extraction, ELISA, SDS-PAGE, PCR, and Western blotting.
  • Generate high-quality, reproducible datasets and maintain accurate, detailed experimental documentation in electronic laboratory notebooks (ELNs).
  • Perform mammalian cell culture and support in vitro studies, including transient transfection and electroporation in established cell lines. Collaborate cross-functionally with process development, analytical, and in vivo teams to support reproducible manufacturing processes and advance programs toward clinical development.
  • Contribute to platform innovation by investigating LNP mechanisms of action to improve delivery efficiency, therapeutic potency, and formulation stability.
  • Present experimental results, technical findings, and project updates to cross-functional teams and broader organizational audiences.
  • Effectively manage multiple priorities and projects in a fast-paced, highly collaborative research environment.

Minimum Qualifications

  • BS or MS in Chemistry, Chemical Engineering,  Biochemistry, or a related scientific discipline.
  • Relevant industry or academic research experience:
    • Research Associate II: 2-5+ years with a bachelor’s degree or 0-2+ years of relevant experience with a master’s degree
  • Hands-on experience in lipid nanoparticle (LNP) formulation and analytical characterization for nucleic acid and targeted delivery applications.
  • Strong understanding of drug delivery systems and gene editing therapeutics.
  • Demonstrated ability to work independently while contributing effectively within a fast-paced, results-driven, and collaborative research environment.
  • Highly organized with strong scientific rigor, problem-solving skills, and attention to detail.

Preferred Qualifications

  • Experience with high-throughput formulation screening and knowledge of microfluidic mixing process.
  • Prior experience of ionizable lipid design, bioconjugation, and process development preferred.
  • Prior experience with scale-up and large-scale manufacturability development of LNPs.
  • Understanding of RNA engineering, molecular biology, and hands-on experience of maintaining cells and performing in vitro transfection.

Competencies

  • Collaborative – Openness, One Team
  • Undaunted – Fearless, Can-do attitude
  • Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit – Proactive. Ownership mindset.

Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site. 

Research Associate II: Base pay range of $85,000 to $92,000 + discretionary bonus, equity and benefits.

The range provided is CRISPR Therapeutics’ reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.

About CRISPR Therapeutics AG

CRISPR Therapeutics AG, a gene editing company, focuses on developing transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 gene-editing platform. The company develops its products through in-house research programs and partnerships with biopharmaceutical companies and academic researchers. Its lead product candidate is CTX001, an ex vivo CRISPR gene-edited therapy for treating patients suffering from transfusion-dependent beta thalassemia or severe sickle cell disease in which a patient's hematopoietic stem cells are engineered to produce high levels of fetal hemoglobin in red blood cells. The company was formerly known as Inception Genomics AG and changed its name to CRISPR Therapeutics AG in April 2014. CRISPR Therapeutics AG was founded in 2013 and is headquartered in Zug, Switzerland.
Learn more about CRISPR Therapeutics AG
Size
473 employees
Market Cap
$3.3 billion
Industry
Net Income
-$348.8 million
Founded
2013
5 Year Trend
+181.6%
Revenue
$720,000
NASDAQ

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