Bioinformatician 1 This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.Your RoleBased in our Rockville, MD facility, the Bioinformatician I designs, develops, and deploys scalable data analysis pipelines to support our expanding genomics and next-generation sequencing (NGS) services in product biosafety and pharmacogenomics. Working closely with cross-functional teams, management, and end-users, you will transform user requirements into robust computational solutions while helping advance NGS applications in biosafety testing.

Responsibilities include:

• Design, build, and troubleshoot bioinformatics pipelines, algorithms, and data analysis strategies for genomics services under the direction of the technical lead
• Analyze and interpret complex experimental data, verify results alongside Study Management, and maintain detailed documentation for study integrity and peer review
• Proactively update Management, Study Directors, and interdepartmental teams on project progress, timelines, and technical bottlenecks
• Draft SOPs, manage change control for validated systems, and explore new technologies to optimize protocols while adhering to safety standards Who You Are

Minimum Qualifications:

• Bachelor's degree with 2+ years in information technologies, computational sciences/programming, bioinformatics, or other scientific discipline OR
• Master's degree with 1+ years of experience in information technologies, computational sciences/ programming, bioinformatics, or other scientific discipline OR
• Ph.

D. in information technologies, computational sciences/ programming, bioinformatics, or other scientific discipline

Preferred Qualifications:

• High proficiency in Linux/UNIX environments, relevant coding languages (e.g., Python, Perl, shell scripting), version control (Git), and software testing frameworks
• Hands-on experience analyzing high-throughput NGS/genomics data using command-line tools, workflow automation (e.g., Galaxy, cloud services), and cluster resource managers (e.g., Torque/Maui)
• Background in wet lab techniques (PCR, qPCR, Sanger/NGS sequencing) and familiarity with GLP/GMP regulations, safety standards, and document control
• Proven ability to draft technical software documentation, SOPs, and user requirement specifications while performing peer reviews and quality audits
• Excellent technical writing, cross-functional communication, and project management skills to lead multiple complex initiatives independently with minimal supervision RSREMD Salary Range for this position - $88,300 - $132,500 annually The offer range represents the anticipated low and high end of the base pay compensation for this position.

The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click . What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!...Visit the Employer site for more details