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704 Quince Orchard Rd, Suite 250, Gaithersburg, MD 20878

Phone: +1 301 798 9222, Fax: +1 301 798 9223, Email:

Bioinformatics Analyst

The key areas of responsibilities of this job include, but are not limited to:

  • Work with EzBiome’s internal microbiome bioinformatics tools and EzBioCloud platform for delivering results to clients
  • Next-Gen Sequencing data processing, QC, genome assembly, annotation, phylogenetic analysis, metagenomic taxonomic and functional classification, comparative metagenomic and statistical analysis, interactive visualizations, data sharing, and storage.
  • Contribute to a team effort in designing, developing and deploying robust workflows, as well as custom scripts, to support the analysis of high-throughput data
  • Write custom scripts to access databases, perform and evaluate quality control and analyze NGS data.
  • Work with internal and external teams to apply appropriate statistical methodologies for analysis of processed microbiome data and interpretation of results.
  • Presenting analysis results, in a clear and concise manner, to an audience not familiar with bioinformatics

Minimum education and professional requirements include, but are not limited to:

  • Bachelor’s degree or higher (Biology/Chemistry/Microbiology/ or related field)
  • Minimum of 1 year of experience in bioinformatics, epidemiology, statistics or related field
  • Experience in processing, data management and analysis of microbiome and isolate whole genome sequencing data, or high-volume biological data management and analysis.
  • Experience in statistical analyses, data display and graphics
  • Skilled at conducting bioinformatics analysis of amplicon (16S rRNA, ITS), shotgun metagenome and isolate whole genome sequencing data
  • Strong skills in R, Unix, and/or other languages commonly used for bioinformatics analysis.
  • Familiarity with publicly available Bioinformatics tools, algorithms and databases
  • Experience with high-performance computing cluster environments, multi-omics analysis, pipeline development, familiarity with sequencing and library preparation for 16S rRNA and whole metagenomic shotgun sequencing. (Preferred)

Laboratory Technician

The key areas of responsibilities of this job include, but are not limited to:

  • Follow established procedures or protocols to perform laboratory tests and/or experiments which may include, but are not limited to: DNA isolation, DNA purification, DNA sequencing.
  • Operate and maintain sanger sequencer and other process equipment
  • Perform instrument qualification and validation
  • Maintain detailed records of experiments through laboratory management systems
  • Perform laboratory related administrative tasks including sample accessioning and database entry
  • Create and revise CGMP protocols/documents and participate in the editing and revision of SOPs
  • Ensure test validity and alert the Supervisor and/or Director of any unusual or abnormal test results prior to reporting results to the customers
  • Perform or support special projects in the lab when needed, and perform all other related duties as assigned.

Education and professional requirements include, but are not limited to:

  • Minimum of Bachelor degree in Biology/Chemistry/Microbiology/ or related field
  • Minimum of 1 years of experience working in a GMP environment.
  • Experience utilizing scientific methods, procedures and techniques, including mass spectrometry, DNA extraction, and sanger and/or next-gen sequencing

Quality Assurance Specialist

The key areas of responsibilities of this job include, but are not limited to:

  • Structure, establish and implement a fully functioning cGMP-based quality system
  • Daily QA activities and related cGMP compliance
  • Manage deviations, investigations, OOS and CAPA
  • Lead the internal and external audits of the various quality elements.
  • Author, or revise SOPs that are technically sound, provide clear instructions to align with cGMP requirements, and support efficient procedures and operations.
  • Support and monitor quality management systems including document control, supplier Quality management, calibration program, equipment management, complaint handling, production control, data analysis.
  • Handle non-routine situations for review and approval by senior staff.
  • Participates in the development, implementation, and monitoring of training programs.
  • Conduct the initial GMP employee training with new hires.
  • Assists with the process to investigate (Root cause analysis), document, review, approve and communicate the status of deviations for internal and outsourced activities.
  • Write, review, and approve deviations in the electronic quality management system. Analyzes the cause, the solution, and preventive measures in case of any incidence.Maintain a high standard of ethics, honesty, and urgency required to meet the quality standards, objectives and goals.

Minimum education and professional requirements include:

  • Bachelor’s degree or higher (Biology/Chemistry/Microbiology/ or related field)
  • 2-3 years (MS with 1 year) of experience in the Pharmaceutical or biotechnology industry with Quality Assurance or a GMP related field
  • Familiar with cGMP/GLP practices, and FDA Guidelines (Preferred)
  • Extensive knowledge of GMP, SOPs and quality systems and regulatory requirements
  • Excellent understanding of validation and Quality Assurance systems
  • Experience with internal and external audit principals
  • Ability to approve test method validation protocols and reports
  • Ability to communicate and work independently with minimal supervision
  • Strong verbal/written and interpersonal communication skills in English
  • The ability to produce high-quality work on complex problems with cross-functional involvement; to anticipate and proactively prevent risks and compromises to quality


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EzBiome is a fast growing company so join