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Bioinformatics Programmer Jobs in Dallas, TX (NOW HIRING)

Vytwo

Bioinformatics Pipeline Test Engineer

Prosper, TX · On-site

Bioinformatics Pipeline Test Engineer Domain EXP : (Healthcare Domain) Experience: 2+ Years of exp Location: San Diego CA "Onsite client office" Duration: 6 Months JD in brief: For these candidates ...

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Bioinformatics Programmer information

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$70.3K

$142.3K

$253.1K

How much do bioinformatics programmer jobs pay per year?

As of Jul 26, 2026, the average yearly pay for bioinformatics programmer in Dallas, TX is $142,343.00, according to ZipRecruiter salary data. Most workers in this role earn between $96,200.00 and $174,400.00 per year, depending on experience, location, and employer.

What is a Bioinformatics Programmer job?

A Bioinformatics Programmer is a professional who develops and maintains software tools to analyze biological data, such as DNA sequences, protein structures, and genomic variations. They work at the intersection of computer science and biology, using programming languages like Python, R, and Java to process and visualize complex biological datasets. Their role is crucial in fields like genomics, drug discovery, and biomedical research, where they help automate data analysis and support scientific investigations.

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

To thrive as a Bioinformatics Programmer, you need strong programming skills (often in Python, R, or Java), a solid background in biology or life sciences, and experience working with large-scale biological data. Commonly used tools and systems include bioinformatics software like BLAST, Bioconductor, cloud computing platforms, and version control systems such as Git, and certifications in relevant domains can be advantageous. Critical thinking, problem-solving, and effective communication are essential soft skills for integrating research findings and collaborating with interdisciplinary teams. These skills ensure you can develop robust, accurate computational solutions that drive advances in biological research and healthcare applications.

What does a typical day look like for a Bioinformatics Programmer?

A typical day for a Bioinformatics Programmer involves writing and optimizing code to analyze large datasets, commonly derived from genomics, proteomics, or clinical studies. You'll spend time collaborating with biologists, statisticians, and other programmers to design experiments, validate results, and interpret findings. Most roles also include maintaining data pipelines, troubleshooting software issues, and staying updated with the latest bioinformatics tools and research. The work environment often blends independent coding with regular team meetings and project updates, offering both technical and interdisciplinary challenges. This dynamic workflow makes the role both intellectually stimulating and impactful in advancing scientific discoveries.

What are popular job titles related to Bioinformatics Programmer jobs in Dallas, TX? For Bioinformatics Programmer jobs in Dallas, TX, the most frequently searched job titles are:
What job categories do people searching Bioinformatics Programmer jobs in Dallas, TX look for? The top searched job categories for Bioinformatics Programmer jobs in Dallas, TX are:
What cities near Dallas, TX are hiring for Bioinformatics Programmer jobs? Cities near Dallas, TX with the most Bioinformatics Programmer job openings:
Bioinformatics Programmer jobs near you
Infographic showing various Bioinformatics Programmer job openings in Dallas, TX as of July 2026, with employment types broken down into 87% Full Time, 9% Part Time, 1% Temporary, 1% Contract, and 2% Nights. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $142,343 per year, or $68.4 per hour.

Bioinformatics Pipeline Test Engineer

Vytwo

Prosper, TX • On-site

Full-time

Posted 26 days ago

Job description

Position Title: Bioinformatics Pipeline Test Engineer
 Domain EXP: (Healthcare Domain)
Experience: 2+ Years of exp
 Location: San Diego CA “Onsite client office”
Duration: 6 Months
JD in brief:
For these candidates, it’s imperative to have NGS pipeline experience or education. Working with Illumina sequencing data, AWS healthomics, Nextflo Type experience working on secondary analysis pipelines
Essential Duties:
  • VERIFICATION AND VALIDATION
    •  With direction and guidance from the team lead, help with verification and validation protocols and generate test reports for multiple software solutions used in medical devices and LDT products. 
    • Aid in translation of user and software requirements into executable software verification and validation protocols focusing on various aspects of the software lifecycle.
    • Collaborate with bioinformatics scientists and operations to identify test inputs and understand the development of algorithmic test strategy, testing tools, and testing methodology.
    • Test product functionality and/or confirm product capabilities. 
  • DESIGN CONTROLS 
    1. With direction and guidance from the team lead, help with design controls and appropriate software documentation (e.g. software requirements and/or specifications, architecture documents, software design details doc) for medical device software lifecycle. 
    2. Learn and apply best practices for LDT software and create and manage all applicable documentation. 
    3. Participate in risk assessments for software products, including identification of potential risk mitigations and traceability to software requirements. 
    4. Help with the creation of software documentation, compatible with regulatory requirements. 
  • Utilizing standardized procedures and practices, work on assignments individually and with project team members to achieve department and project objectives and meet deadlines.
  • Exercise excellent verbal and written communication skills with the ability to communicate basic technical information.
  • Work towards challenging goals in a fast-moving environment.
  • Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.
  • Support and comply with the company’s Quality Management System policies and procedures.
  • Maintain regular and reliable attendance.
  • Ability to act with an inclusion mindset and model these behaviors for the organization.
  • Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.
  • Ability and means to travel 10% between local Exact Sciences locations. 
  • Ability to travel 5% of working time away from work location, may include overnight/weekend/international travel. 
 Minimum Qualifications
  • B.S. Degree in Computational Biology, Computer Science, or field as outlined in the essential duties. 
  • Familiarity with the development of bioinformatics pipelines within Next Generation Sequencing and PCR applications.
  • Familiarity with production software development lifecycle.
  • Familiarity with best practices for software development (such as Git, agile, code reviews, CI/CD). 
  • Ability to effectively communicate software system designs. 
  • Excellent communication skills (both written and oral) with the ability to communicate complicated ideas and information effectively at all levels. 
  • Demonstrated ability to perform the essential duties of the position with or without accommodation.
 Preferred Qualifications
  • Experience with programming languages, ideally Python. 
  • Familiar with automated software testing, preferably in the context of medical devices software such as bioinformatics analysis pipelines. 
  • Familiarity with container orchestration concepts and systems, e.g. Docker, Kubernetes, etc. 
  • Familiar working with cloud platforms (AWS, GCP, Azure).
  • Familiarity within an FDA-Regulated, Medical Device, Pharmaceutical, Biotech, or other regulated industry, developing CFR 21 Part 11 and IEC 62304 compliant software. 
  • Familiarity with medical device requirements such as Quality System Regulation (21 CFR part 820) ISO 14971 Medical Device Risk Management, ISO 13485, etc. Work experience is strongly preferred. 
  • Familiarity with bioinformatics analysis pipeline frameworks. 
  • Familiarity with software related Cybersecurity risk management such as FDA Cybersecurity guidance, IEC27000 series, IEC 15408, etc. as well as software audits is a plus.
Familiar with managing requirements in a validated RM tool such as JAMA, DOORS, etc.