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Senior Crispr Jobs (NOW HIRING)

Editas Medicine

Senior QA Specialist

Cambridge, MA · On-site

$110K - $120K/yr

Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR ... As the Senior QA Specialist, you will: * Maintain Quality oversight of GMP operations including ...

Allorion Therapeutics

Senior scientist - biology

Natick, MA · On-site

$94K - $129K/yr

... project and senior leadership teams * Evaluate the anti-proliferation efficacy of cancer drug ... and CRISPR-based gene editing, virus-based gene delivery for stable cell line generation

Danaher

Senior Territory Sales Manager

Baltimore, MD · On-site

$230K - $255K/yr

The Senior T erritory Sales Manager is responsible for promoting and selling IDT's full portfolio ... qPCR, CRISPR, Functional Genomics, Synthetic Biology and Next Generation Sequencing. This role ...

Danaher

Senior Territory Sales Manager, Texas

Dallas, TX · Remote

$140K - $160K/yr

The Senior Territory Sales Manager is responsible for promoting and selling IDT's full portfolio of ... Experience with applications within qPCR, CRISPR, and NGS . Travel, Motor Vehicle Record & Physical ...

Danaher

Senior Territory Sales Manager, Texas

Houston, TX · Remote

$140K - $160K/yr

The Senior Territory Sales Manager is responsible for promoting and selling IDT's full portfolio of ... Experience with applications within qPCR, CRISPR, and NGS . Travel, Motor Vehicle Record & Physical ...

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Senior Crispr information

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$25K

$80.3K

$163.5K

How much do senior crispr jobs pay per year?

As of Aug 7, 2026, the average yearly pay for senior crispr in the United States is $80,287.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What is the difference between Senior Crispr vs CRISPR Research Scientist?

AspectSenior CrisprCRISPR Research Scientist
Required CredentialsBachelor's/Master's in Molecular Biology, Genetics, or related; extensive experience in CRISPR techniquesMaster's or PhD in Genetics, Molecular Biology, or related; strong background in gene editing
Work EnvironmentBiotech labs, research institutions, pharmaceutical companiesAcademic labs, biotech firms, research organizations
Employer & Industry UsageUsed in industry settings for product development and researchPrimarily academic and research-focused roles, but also in industry

Senior Crispr professionals typically have more experience and leadership responsibilities, often overseeing projects and teams. CRISPR Research Scientists focus on conducting experiments and advancing gene editing research. Both roles require strong technical skills, but Senior Crispr roles emphasize project management and strategic planning.

What cities are hiring for Senior Crispr jobs? Cities with the most Senior Crispr job openings:
What are the most commonly searched types of Crispr jobs? The most popular types of Crispr jobs are:
What states have the most Senior Crispr jobs? States with the most job openings for Senior Crispr jobs include:
Senior Crispr jobs near you

Senior QA Specialist

Editas Medicine

Cambridge, MA • On-site

$110K - $120K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago

Job description

At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.
Why Choose Editas?
At Editas Medicine, we're a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what's possible in medicine, come join us and become an Editor!
Decoding The Role:
The primary focus of this role in the next 12 months is to advance our lead in vivo development candidate, EDIT-401, into the clinic to establish human proof of concept by ensuring compliance with FDA, cGMP, and international regulatory requirements across manufacturing, testing, product disposition, and quality event management. This role is part of a small QA team with opportunities for cross training into other areas of Quality. EDIT-401 is a potential best-in-class, one-time therapy designed to significantly reduce LDL cholesterol levels. The company is very excited by the potential of this experimental treatment which has demonstrated the ability to reduce mean LDL cholesterol levels by over 90 percent in non-human primates.
Characterizing Your Impact:
As the Senior QA Specialist, you will:
  • Maintain Quality oversight of GMP operations including batch record review, analytical results, certificates of analysis, and Quality Events (e.g. deviations and change controls).
  • Disposition lots.
  • Provide Quality review of assay validation, test method development, and other technical documents.
  • Collaborate with, oversee, and support partner CDMOs/CTOs.
  • Develop comprehensive understanding of the manufacturing processes for Editas products and the associated risk management control strategy to identify process risks and critical controls around processing steps.
  • Author, review, and approve GMP documentation (SOPs, batch records, protocols, technical reports, test methods, specifications, and summary reports) supporting GMP manufacturing.
  • Establish, implement, maintain, improve, monitor, and report on quality and compliance systems.
  • Assist in Quality System and Vendor Management acvitivies

Requirements
The Ideal Transcript:
To thrive in this role, you'll need:
  • Proven ability to work independently, collaborate with peers, and work effectively in a team environment, all while being highly organized.
  • Experience supporting early phas Quality and working with CDMOs/CTOs.
  • Experience with batch record review and lot release.
  • Working knowledge of GMP requirements for Clinical Trial Material in global markets, including understanding of regulatory guidance on gene therapy products.
  • Experience with biologics, protein, RNA, cell/gene therapy, and/or viral products.
  • Expertise working within cGMP compliance and providing GMP documentation.
  • Strong communication and collaboration.
  • Strong problem solving and critical thinking ability and accustomed to risk-based decision making.
  • B.S. in a scientific discipline with 4+ years experience within Quality roles in the biopharmaceutical industry.

Fundamentals That Set You Apart
  • Experience with QC and/or analytical development.
  • Experience managing quality systems, vendors, and supporting audit management.

Benefits
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
Salary Range:
$110,000 - $120,000
Pay Transparency
Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices.
Aspire to be an Editor? We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.

Apply