Bioinformatics Pipeline Test Engineer

Vytwo; Prosper (TX); On-site; USD 80,000 - 100,000; Full time

Job summary

Vytwo is seeking a Bioinformatics Pipeline Test Engineer in Prosper, Texas, to support validation and testing for bioinformatics software. The ideal candidate will have 2+ years of relevant experience, particularly in NGS pipeline management and familiarity with bioinformatics workflows. Key responsibilities include collaborating with bioinformatics teams for software validation and writing documentation aligned with regulatory requirements. This role offers opportunities for growth in a fast-paced environment focused on innovation and quality.

Qualifications

• Minimum of 2+ years of experience in bioinformatics or related fields.
• Ability to communicate effectively at all levels.
• Experience working in FDA-regulated environments is preferred.

Responsibilities

• Assist in verification and validation protocols for software solutions.
• Collaborate with teams to identify testing methodology.
• Maintain software documentation compliant with regulations.

Skills

NGS pipeline experience

Effective communication

Familiarity with programming languages (Python)

Knowledge of software development best practices

Collaboration with bioinformatics scientists

Education

B.S. Degree in Computational Biology or Computer Science

Tools

Git

Docker

Kubernetes

AWS

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

Job Description 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

• 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.
• Learn and apply best practices for LDT software and create and manage all applicable documentation.
• Participate in risk assessments for software products, including identification of potential risk mitigations and traceability to software requirements.
• Help with the creation of software documentation, compatible with regulatory requirements.
• Utilize 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, IEC 27000 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.