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Crispr Jobs (NOW HIRING)

Merck & Co.

$62K - $63K/yr

You will also oversee and directly contribute to the computational analysis of optical CRISPR screens and high throughput imaging datasets, bridging morphological phenotypes with our functional ...

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$35K

$56.1K

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How much do crispr jobs pay per year?

As of Aug 7, 2026, the average yearly pay for crispr in the United States is $56,057.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,500.00 and $47,000.00 per year, depending on experience, location, and employer.

What types of projects or research might I work on as a crispr scientist?

As a CRISPR Scientist, you may contribute to projects ranging from basic research in gene function and disease mechanisms to applied initiatives like crop improvement, gene therapy development, or pharmaceutical innovation. Your day-to-day responsibilities might include designing and executing gene-editing experiments, analyzing genetic data, collaborating with interdisciplinary teams, and documenting results for publication or regulatory submissions. Depending on your employer, you could work in academia, biotechnology, agriculture, or medical research industries. This role offers opportunities to make impactful scientific discoveries and gain exposure to emerging technologies, providing a strong foundation for career advancement within the field.

What are the key skills and qualifications needed to thrive in the crispr position, and why are they important?

To thrive in a CRISPR Scientist role, you need a solid background in molecular biology, genetics, and gene-editing techniques, typically supported by an advanced degree in a life science discipline. Familiarity with laboratory equipment, gene-editing platforms like CRISPR-Cas9, and certifications in genetic engineering or molecular techniques are highly valuable. Attention to detail, critical thinking, and strong teamwork capabilities are key soft skills in this position. These skills are crucial to ensure safe, accurate, and innovative application of gene-editing technologies in research or therapeutics.

What is a crispr?

A CRISPR job typically involves working with CRISPR-Cas9 or related gene-editing technologies in fields such as biomedical research, agriculture, or biotechnology. Professionals in this field may design, execute, and analyze gene-editing experiments to modify DNA for therapeutic, industrial, or scientific purposes. Roles can range from research scientists to bioinformatics specialists and lab technicians. Strong knowledge of molecular biology, genetics, and bioengineering is often required.

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Crispr jobs near you
Infographic showing various Crispr job openings in the United States as of August 2026, with employment types broken down into 68% Full Time, 29% Part Time, and 3% Contract. Highlights an 68% Physical, 1% Hybrid, and 31% Remote job distribution, with an average salary of $56,057 per year, or $27 per hour.

Senior Engineer II, mRNA Process Development

CRISPR Therapeutics, Inc.

South Boston, VA • On-site

$140 - $150/hr

Other

Re-posted 2 days ago

Job description

Company Overview

Founded over a decade ago, CRISPR Therapeutics is a biopharmaceutical company that develops gene-based medicines for serious human diseases. It has advanced from a research-stage organization to a leader in the field, with the first CRISPR-based therapy approved for sickle cell disease and transfusion‑dependent beta thalassemia. The company’s pipeline spans hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. CRISPR Therapeutics is headquartered in Zug, Switzerland, with U.S. operations in Boston and San Francisco.

Position Summary

Senior Engineer II – Non‑viral delivery technical development. Lead the design, optimization, and scale‑up of manufacturing processes for gene editing mRNA therapeutics. Bridge research innovation and clinical development, leveraging expertise in nucleic acid chemistry, enzymatic reactions and purification.

Responsibilities
  • Lead the development, optimization, and scale‑up of upstream and downstream unit operations for mRNA drug substance.
  • Apply Design of Experiments (DoE) and statistical analysis to evaluate process parameters, improve yields and ensure consistent product quality attributes.
  • Drive tech transfer of developed processes to internal clinical manufacturing teams or external CDMOs.
  • Author clear, comprehensive technical reports, SOPs, batch records, and tech transfer documentation.
  • Provide on‑floor technical support and troubleshooting during scale‑up and GMP manufacturing runs.
  • Partner with analytical development to correlate process changes with mRNA quality attributes.
  • Mentor, coach and guide research associates and engineers, fostering a collaborative and high‑performing laboratory culture.
  • Represent the technical development function in cross‑functional project teams and present data to senior leadership.
Minimum Qualifications
  • Ph.D. in Chemical Engineering, Bioengineering, Biochemistry, or a related discipline with 2‑4½+ years of industry experience; or
  • Non‑Ph.D. and 10‑12 years of relevant experience.
  • Core mRNA expertise: hands‑on deep experience in in vitro transcription (IVT) kinetics and plasmid DNA linearization.
  • Downstream purification: extensive experience with Tangential Flow Filtration and chromatography modes (Affinity, IEX, RP‑HPLC).
  • Equipment proficiency: operating automated chromatography systems such as ÄKTA Avant/Pure and filtration skids.
  • Data analysis: proficiency with statistical software (JMP, Minitab) for DoE design and data analysis.
  • Strong collaboration, ownership mindset, results orientation and an entrepreneurial spirit.
Preferred Qualifications
  • Experience with mRNA‑LNP formulation.
  • Familiarity with GMP regulations, Quality by Design principles, and preparing regulatory filing documentation.
  • Prior experience managing or directly mentoring junior researchers.
Compensation

Base pay range of $140,000 to $150,000+; bonus, equity and benefits available. Pay determined by job‑related factors.

Equal Employment Opportunity Statement

CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non‑discrimination for all employees and qualified applicants without regard to race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.

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