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HomeCompaniesOmgtechBioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote -US)

Bioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote -US)

Omgtech · Remote · Active · BambooHR

Job facts

FieldValue
CompanyOmgtech
TitleBioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote -US)
Normalized title-
Department / team-
LocationNew Jersey, NJ, United States
Work modelRemote / Remote
Employment typeContract
Salary-
Statusactive
ATS providerBambooHR
Posted / first seen2026-03-10 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-04

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PageWhat it containsOpen
Company jobsActive postings from Omgtech.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through BambooHR.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in New Jersey.Open
Work model jobsActive Remote postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyOmgtech
Sourcec4dbb2aa-e9fe-4c96-acfb-0428b73e41c6
ATS providerBambooHR

Description

Bioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote -US) We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the life science Industry. Location:  Flexible (Remote) – Must overlap  at least 5 hours with EST  daily Job summary We are seeking an experienced Bioinformatics Pipeline Validation Manager to lead validation efforts for bioinformatics pipelines. This individual will manage a team responsible for ensuring that computational pipelines used in genomics and clinical research meet regulatory, quality, and performance standards. This role is within a  life sciences organization  focused on advancing molecular diagnostics and genomic technologies. The ideal candidate will bring strong  bioinformatics, NGS pipeline validation, Cancer genomics and clinical diagnosis experience and leadership experience , along with a deep understanding of regulated environments such as  GxP, CLIA, or CAP . Key Responsibilities Leadership & Team Management Lead, mentor, and develop a team of bioinformatics validation scientists and analysts. Oversee workload planning, project assignments, and team performance tracking. Foster a collaborative, high-performing team culture focused on quality, efficiency, and innovation. Pipeline Validation & Quality Assurance Own end-to-end validation of bioinformatics pipelines, including NGS, WGS/WES, RNA-seq, variant calling, annotation, and QC workflows. Develop and execute validation plans, protocols, test cases, and acceptance criteria. Ensure pipelines meet applicable regulatory requirements (e.g., CLIA, CAP, FDA). Perform software verification and validation (SV&V) and document results thoroughly. Technical Expertise & Execution Collaborate with bioinformatics engineers, data scientists, and software developers to optimize pipeline design and performance. Evaluate new tools, algorithms, and software for integration into analytical workflows. Troubleshoot pipeline issues and lead root-cause analysis efforts. Ensure reproducibility, scalability, and robustness of computational workflows. Cross-Functional Collaboration Partner with wet lab teams, QA, clinical operations, and product management to align validation objectives with timelines and business goals. Represent the validation team in client meetings, audits, and technical reviews. Documentation & Compliance Maintain detailed documentation of validation activities, including version control and release notes. Prepare documentation for regulatory submissions and internal audits. Establish and enforce validation standards, SOPs, and best practices. Required Qualifications 10+ years of experience in bioinformatics, genomics data analysis, cancer genomics and clinical diagnosis exp pipeline validation. 4+ years of leadership or management experience leading technical teams. Strong experience with NGS data processing pipelines, including quality control, alignment, variant calling, annotation, and interpretation. Hands-on experience with bioinformatics workflow management tools such as Nextflow, Snakemake, WDL, Cromwell, or Galaxy. Experience with common NGS analysis tools such as BWA, Bowtie2, GATK, SAMtools, Picard, FastQC, MultiQC, and VEP/ANNOVAR. Experience with containerization and reproducibility tools such as Docker, Singularity/Apptainer, and workflow environment management tools like Conda or Bioconda to ensure reproducible bioinformatics pipelines. Proficiency in scripting or programming languages such as Python, R, or Bash. Experience working in regulated environments (GxP, CLIA, CAP, or similar). Familiarity with software validation lifecycle, automated testing, and documentation practices. Bachelor’s or master’s degree in bioinformatics, Computational Biology, Genomics, Computer Science, or related field. Preferred Qualifications Experience supporting clinical genomics or diagnostic pipelines. Knowledge of cloud platforms such as AWS, Google Cloud Platform, or Azure used for scalable bioinformatics workflows. Experience with CI/CD tools such as Jenkins, GitLab CI, or GitHub Actions. Experience managing large-scale genomic datasets and distributed computing environments. Other Job Details: Location:  Remote Candidate rate: : $65 on C2C and $60 on W2 Docs required: ID proof will be required.

Full job record

Job IDd2cfe66454a4e2cd55394636198ff7af3b70276b
Org ID0e893203-050a-4412-a944-b6dcfe54384e
Source IDc4dbb2aa-e9fe-4c96-acfb-0428b73e41c6
Board IDc4dbb2aa-e9fe-4c96-acfb-0428b73e41c6
Providerbamboohr
Provider Job Key294
TitleBioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote -US)
Normalized Title
Statusactive
Activeyes
Location Text
Department
Team
Employment Typecontract
Workplace Typeremote
Remote Policyremote
CountryUnited States
RegionNJ
CityNew Jersey
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://omgtech.bamboohr.com/careers/294
Apply URLhttps://omgtech.bamboohr.com/careers/294
First Seen At2026-05-30 06:04:53Z
Last Seen At2026-06-04 11:44:39Z
Last Checked At2026-06-04 11:44:39Z
Last Changed At2026-05-30 06:04:53Z
Inactive At
Source Posted At2026-03-10 00:00:00Z
Source Updated At
Raw Payload Uris3://bluework-jobs-prod-raw-590183727216/raw/provider=bamboohr/board=omgtech/date=2026-06-04/2026-06-04T11-44-39-121Z-a0da9594ec36def9c71f7ea9d21d4f550c0834366ce4d2cb26d689449958b658.json
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    "description": "<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; text-decoration: underline\"><span style=\"font-weight: bold\">Bioinformatics Pipeline Validation Manager with Cancer genomics exp (Remote -US)</span></span><br><br><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">We are looking to hire a candidate with the skills sets mentioned and experience for one of our clients within the life science Industry.  </span><br></p>\n<p><br><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"><span style=\"font-weight: bold\">Location:</span> Flexible (Remote) – Must overlap <span style=\"font-weight: bold\">at least 5 hours with EST</span> daily</span><br><br></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Job summary<br></span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">We are seeking an experienced Bioinformatics Pipeline Validation Manager to lead validation efforts for bioinformatics pipelines. This individual will manage a team responsible for ensuring that computational pipelines used in genomics and clinical research meet regulatory, quality, and performance standards. This role is within a <span style=\"font-weight: bold\">life sciences organization</span> focused on advancing molecular diagnostics and genomic technologies.</span><br><br></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">The ideal candidate will bring strong <span style=\"font-weight: bold\">bioinformatics, NGS pipeline validation, Cancer genomics and clinical diagnosis experience and leadership experience</span>, along with a deep understanding of regulated environments such as <span style=\"font-weight: bold\">GxP, CLIA, or CAP</span>.</span><br><br></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"><span style=\"font-weight: bold\">Key Responsibilities<br><br></span></span></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Leadership &amp; Team Management</span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Lead, mentor, and develop a team of bioinformatics validation scientists and analysts.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Oversee workload planning, project assignments, and team performance tracking.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Foster a collaborative, high-performing team culture focused on quality, efficiency, and innovation.</span></li>\n</ul>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Pipeline Validation &amp; Quality Assurance</span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Own end-to-end validation of bioinformatics pipelines, including NGS, WGS/WES, RNA-seq, variant calling, annotation, and QC workflows.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Develop and execute validation plans, protocols, test cases, and acceptance criteria.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Ensure pipelines meet applicable regulatory requirements (e.g., CLIA, CAP, FDA).</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Perform software verification and validation (SV&amp;V) and document results thoroughly.</span></li>\n</ul>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Technical Expertise &amp; Execution</span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Collaborate with bioinformatics engineers, data scientists, and software developers to optimize pipeline design and performance.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Evaluate new tools, algorithms, and software for integration into analytical workflows.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Troubleshoot pipeline issues and lead root-cause analysis efforts.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Ensure reproducibility, scalability, and robustness of computational workflows.</span></li>\n</ul>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Cross-Functional Collaboration</span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Partner with wet lab teams, QA, clinical operations, and product management to align validation objectives with timelines and business goals.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Represent the validation team in client meetings, audits, and technical reviews.</span></li>\n</ul>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Documentation &amp; Compliance</span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Maintain detailed documentation of validation activities, including version control and release notes.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Prepare documentation for regulatory submissions and internal audits.</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Establish and enforce validation standards, SOPs, and best practices.</span><br><br></li>\n</ul>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"><span style=\"font-weight: bold\"><br></span></span></p>\n<p><span style=\"font-weight: bold\">Required Qualifications</span></p>\n<ul>\n<li>10+ years of experience in bioinformatics, genomics data analysis, cancer genomics and clinical diagnosis exp pipeline validation.</li>\n<li>4+ years of leadership or management experience leading technical teams.</li>\n<li>Strong experience with NGS data processing pipelines, including quality control, alignment, variant calling, annotation, and interpretation.</li>\n<li>Hands-on experience with bioinformatics workflow management tools such as Nextflow, Snakemake, WDL, Cromwell, or Galaxy.</li>\n<li>Experience with common NGS analysis tools such as BWA, Bowtie2, GATK, SAMtools, Picard, FastQC, MultiQC, and VEP/ANNOVAR.</li>\n<li>Experience with containerization and reproducibility tools such as Docker, Singularity/Apptainer, and workflow environment management tools like Conda or Bioconda to ensure reproducible bioinformatics pipelines.</li>\n<li>Proficiency in scripting or programming languages such as Python, R, or Bash.</li>\n<li>Experience working in regulated environments (GxP, CLIA, CAP, or similar).</li>\n<li>Familiarity with software validation lifecycle, automated testing, and documentation practices.</li>\n<li>Bachelor’s or master’s degree in bioinformatics, Computational Biology, Genomics, Computer Science, or related field.<br><br></li>\n</ul>\n<p><span style=\"font-weight: bold\">Preferred Qualifications</span></p>\n<ul>\n<li>Experience supporting clinical genomics or diagnostic pipelines.</li>\n<li>Knowledge of cloud platforms such as AWS, Google Cloud Platform, or Azure used for scalable bioinformatics workflows.</li>\n<li>Experience with CI/CD tools such as Jenkins, GitLab CI, or GitHub Actions.</li>\n<li>Experience managing large-scale genomic datasets and distributed computing environments.</li>\n</ul>\n<p> <span style=\"font-family: Inter, sans-serif; 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