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Ngs Variant Interpretation Jobs (NOW HIRING)

Provide bioinformatics support to include somatic and germline variant calling and analysis, single ... NGS analysis (whole-exome, whole-genome, RNA-seq, ChIP-Seq, both long- and short-read technologies ...

Provide bioinformatics support to include somatic and germline variant calling and analysis, single ... NGS analysis (whole-exome, whole-genome, RNA-seq, ChIP-Seq, both long- and short-read technologies ...

Provide bioinformatics support to include somatic and germline variant calling and analysis, single ... NGS analysis (whole-exome, whole-genome, RNA-seq, ChIP-Seq, both long- and short-read technologies ...

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Ngs Variant Interpretation information

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$20.5K

$83.3K

$147K

How much do ngs variant interpretation jobs pay per year?

As of Jun 9, 2026, the average yearly pay for ngs variant interpretation in the United States is $83,348.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,000.00 and $111,000.00 per year, depending on experience, location, and employer.

What is NGS variant interpretation?

NGS variant interpretation is the process of analyzing genetic variants identified through Next-Generation Sequencing (NGS) technology to determine their potential impact on health, disease, or traits. This involves filtering, annotating, and classifying variants according to established guidelines, such as those from the American College of Medical Genetics and Genomics (ACMG). Professionals in this field use bioinformatics tools and databases to interpret the clinical significance of genetic changes and often communicate their findings to clinicians or researchers for decision-making in healthcare or research settings.

What is the difference between Ngs Variant Interpretation vs Genetic Counselor?

AspectNgs Variant InterpretationGenetic Counselor
Required CredentialsCertification in genetics or molecular diagnostics, often a laboratory certificationMaster's degree in genetics, counseling, or related field; certification (ABGC, NSGC)
Work EnvironmentLaboratory setting, analyzing genetic data and variantsClinical setting, providing patient counseling and education
Industry UsageUsed primarily in diagnostic labs and research institutionsUsed in hospitals, clinics, and healthcare facilities
Primary FocusInterpreting genetic variants from NGS dataCommunicating genetic information and implications to patients

While Ngs Variant Interpretation specialists focus on analyzing and interpreting genetic data within laboratories, Genetic Counselors work directly with patients to explain genetic information and its health implications. Both roles require a strong understanding of genetics but serve different functions within the healthcare and diagnostics industry.

What are some of the main challenges faced when interpreting NGS variants, and how can professionals address them?

One of the main challenges in NGS variant interpretation is distinguishing between benign and pathogenic variants, especially when dealing with variants of uncertain significance (VUS). Professionals must stay updated with the latest research, utilize comprehensive databases, and collaborate closely with geneticists, clinicians, and bioinformaticians to ensure accurate interpretation. Regular participation in multidisciplinary team meetings and continuous professional development are essential for overcoming these challenges and delivering clinically actionable insights.

What are the key skills and qualifications needed to thrive as an NGS Variant Interpretation Specialist, and why are they important?

To thrive as an NGS Variant Interpretation Specialist, you need a solid background in genetics, molecular biology, and bioinformatics, often supported by an advanced degree in a life science field. Familiarity with next-generation sequencing (NGS) platforms, databases like ClinVar and HGMD, and analysis tools such as GATK and ANNOVAR is typically required. Strong analytical thinking, attention to detail, and effective communication skills help in interpreting complex genomic data and conveying findings to clinicians or researchers. These skills are crucial for ensuring accurate variant classification, supporting clinical decision-making, and advancing personalized medicine.
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What states have the most Ngs Variant Interpretation jobs? States with the most job openings for Ngs Variant Interpretation jobs include:
Senior Scientist, Molecular Biology

Senior Scientist, Molecular Biology

Flagship Pioneering, Inc.

Cambridge, MA

$100K - $136K/yr

Other

Medical, Retirement

Posted 9 days ago


Job description

Company Summary:

Serif Biomedicines, Inc. is a privately held, early-stage biotechnology company developing a novel approach to gene therapy that can address currently untreatable diseases.

Serif Biomedicines was founded by Flagship Pioneering, an innovation enterprise that conceives, creates, resources, and grows first-in-category life sciences companies.

Flagship Pioneering has created over 100 groundbreaking companies over the past twenty years, all of which are pioneering novel and proprietary biological, industrial, and engineering approaches to solve major needs in human health and sustainability. These companies include Moderna (MRNA), Syros Pharmaceuticals (SYRS), Seres Therapeutics (NASDAQ:MCRB), Generate Biomedicines, Tessera Tx, Evelo Biosciences (EVLO), and Indigo Agriculture.

The role

We are looking for a Senior Scientist, Molecular Biology with experience in protein engineering, complex DNA library design, and pooled screening to help build next-generation DNA constructs for programmable medicines. This role is a good fit for someone who has worked on CAR/binder design and is comfortable designing and testing large libraries to support discovery and optimization of engineered proteins.

You will help build and scale platforms for plasmid DNA design, construction, and optimization, with a focus on practical, high-throughput workflows and data-driven decision making. We are looking for someone who brings strong technical skills, thinks critically about experimental design, and is comfortable working in a fast-paced, collaborative environment.

This role reports to the Director of Molecular Biology and includes management of one direct report. You will work closely with other scientists and group leads across the R&D team.

Key responsibilities

  • Using protein prediction models and ab initio modeling to develop proteins of novel function in silico and drive their selection and validation on wet bench
  • Deep expertise characterizing protein structure and function including affinity, stability, etc.
  • Design and build complex DNA libraries, including barcoding strategies, to enable pooled screening and variant tracking.
  • Automation experience for arrayed screening and other biochemical assays
  • Help build and scale high-throughput workflows for DNA and RNA production, screening, and data analysis.
  • Track record of demonstration execution of large-scale library screens to support protein engineering and CAR optimization or binder identification and characterization
  • Protein production and characterization in both bacteria and mammalian cells
  • Contribute to plasmid and construct design for engineered proteins and cell-based systems.
  • Own construct QC, sequence analysis, and tracking of variants, including NGS-based workflows.
  • Work with external vendors as needed, balancing internal builds and outsourcing to meet timelines.
  • Partner closely with other teams, including CMC, to provide designs, materials, and timelines.
  • Mentor junior scientists and support strong practices in experimental design and data quality.
  • Maintain clear and reproducible records (ELN, sequence tracking, sample management).
  • Communicate results clearly to cross-functional teams and leadership.

Who you are

We encourage all candidates with exemplary experience in related fields to apply.

Technical Expertise

  • BS with 14+ years, MS with 12+ years, or PhD with 5+ years of relevant industry experience in molecular biology, bioengineering, or a related field.
  • Deep expertise in protein engineering and CAR
  • Proven track record designing and building complex DNA libraries, including barcoding strategies for pooled screening.
  • Strong command of molecular cloning and plasmid design in high-throughput settings.
  • Demonstrated ownership of large-scale library screens, from design through execution and data interpretation.
  • Expert-level experience with NGS-based library analysis, variant tracking, and sequence QC.
  • Ability to operate effectively in cross-functional teams and drive work forward in a fast-paced environment.
  • Experience mentoring or managing junior scientists.

Leadership & Collaboration

  • Proven ability to lead complex projects and influence cross-functional teams.
  • Strong mentorship skills with commitment to developing others. Previous technical or professional management experience.
  • Excellent communication skills, with the ability to translate complex ideas across disciplines.

Values and Behaviors:

Flagship is an experiment in institutional, entrepreneurial, and innovation practiced in the context of a small company with an insurgent mindset. We are seeking individuals with an entrepreneurial spirit, strong communication skills, and comfort in working in and contributing to a dynamic and cross-functional team environment.

At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, we encourage you to apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background. The level of the role will be commensurate with the education and years of experience of the identified candidates.

Flagship Pioneering and our ecosystem companies are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.

Recruitment & Staffing Agencies: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, "FSP") do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.

Privacy Notice for Applicants: When you apply for a role at Flagship Pioneering or one of its portfolio companies, we collect and use personal information you provide (such as your name, contact details, work history, and application materials) to evaluate your application, communicate with you, and comply with legal obligations. Your application data is processed through Greenhouse, our applicant tracking system, and may also be reviewed using AI-assisted screening tools. We do not sell your personal information. California residents have rights under the CCPA/CPRA including to know, delete, and opt out of the sharing of their personal information. If you are located in the EU or UK, we process your data under GDPR and you have rights to access, rectify, and erase your data. To exercise your rights or for questions, contact privacy@flagshippioneering.com. 

The salary range for this role is $126,000 - $181,500. Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Serif Biomedicines currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Serif Biomedicines's good faith estimate as of the date of publication and may be modified in the future.