US Tech Solutions, Inc.Bioinformatics Analyst III US Tech Solutions, Inc.Bioinformatics Analyst IIINorth Chicago, IL$60–$63 / hourTemporaryContractorFull timeThe successful candidate will work closely with stakeholders in the Quantitative Insights Lab (QuIL) organization to support cross-project data science efforts spanning in silico perturbation analysis, toxicogenomics, and mechanistic profiling. Education:MS degree with 5+ years of experience or PhD with 0+ years of experience in a quantitative field such as Bioinformatics, Computer Science, Computational Genetics, Biostatistics, AI/ML, or a related discipline with strong computational training.
Executive Directions & Pinnacle Int'lNewDirector of Bio-Innovation Executive Directions & Pinnacle Int'lDirector of Bio-InnovationChicago, IL$150,000–$225,000 / yearThe position entails leading the departments of Bioengineering, Cell Biology, and Bioinformatics (including 3 Department Leads and a staff of 11) ensuring the discovery team consistently and rapidly produces innovative, market-ready traits for their global plant breeders. D. in Molecular Biology, Plant Biotechnology, Bioengineering, or a related field preferred with 10+ years of experience in biotech or agricultural R&D, with at least 5 years in a senior leadership role managing technical teams.
BiomeSenseSenior Bioinformatics Engineer BiomeSenseSenior Bioinformatics EngineerChicago, ILFull timeFrontend / Backend Development – design, implement, and maintain robust data ingestion interfaces leveraging external APIs and clinical ontologies such as SNOMED, MedDRA, and ICD-10, adhering to software engineering best practices including wireframe design, unit testing, version control, code review, and security and compliance. You’ll join near the ground floor of development, getting hands-on experience building the infrastructure, pipelines, and novel analytical workflows to turn raw microbiome data into actionable and high-integrity microbiome intelligence.
Northwestern UniversityProstate Cancer Biology, Cancer Epigenetics and Bioinformatics Northwestern UniversityProstate Cancer Biology, Cancer Epigenetics and BioinformaticsChicago, ILThe Department of Urology at Northwestern University Feinberg School of Medicine seeks a full-time tenure track Investigator at the rank of Assistant Professor in the areas of prostate cancer biology, cancer epigenetics and bioinformatics. Please prepare all documents in advance as Adobe PDF files, and please be sure all information is entered correctly and accurately (especially names and email addresses), as there will be no opportunity for online revision after your application has been submitted.
University of ChicagoNewComputational Biologist University of ChicagoComputational BiologistChicago, IL$60,000–$80,000 / yearThe Computational Biologist will contribute to the development and application of statistical and computational tools across NIH-funded projects, integrating large-scale GWAS with metabolomics data to uncover mechanisms underlying complex diseases and developing polygenic risk scores that transfer genetic signals across human populations and model organisms to study addiction-related traits, COPD, type 2 diabetes, and other common diseases. The Section of Genetic Medicine conducts impactful investigations focused on quantitative genetics, systems biology and genomics, bioinformatics and computational biology as well as through extensive collaborations of the faculty throughout the Department of Medicine, Biological Sciences Division and the University of Chicago.
TempusNewSenior Software Engineer II, Data Products TempusSenior Software Engineer II, Data ProductsChicago, IL$150,000–$190,000 / yearData & Database Expertise: Strong familiarity with distributed, relational database design (GCP Cloud Spanner) and data modeling (JSON Schema, Avro, or similar), including schema migrations and enforcing data contracts. You will play a pivotal role in architecting and driving technical strategy for services and APIs that allow bioinformatics scientists, ML and Agent developers to rapidly develop, deploy, and operate their solutions in a highly regulated, secure, and scalable environment.
Masco CorporationData Scientist Masco CorporationData ScientistNorth Chicago, ILRemoteWe’re a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. • Extensive experience searching scientific literature and constructing complex search strategies in databases such as MEDLINE, Embase, Derwent Drug File, or BIOSIS.
Tempus AI IncManager, Regulatory Submissions Tempus AI IncManager, Regulatory SubmissionsChicago, IL$110,000–$150,000 / yearExperience with: • Premarket Approval (PMA) applications, de novo Requests for Reclassification, 510(k)s, Investigational Device Exemption (IDE) requirements • Ex-US, CE Marking, UKCA registration, performance studies as required under IVDR and MDR • Software validation and risk management • Cybersecurity in medical devices • Machine learning validation requirements • Lifecycle management of medical devices/IVDs • Changes to medical devices or IVDs, including those that trigger reporting or regulatory submissions • Relevant sections of 21 CFR 820/ISO 13485, 21 CFR 812, CAP/CLIA • Strong communication, presentation, and interpersonal skills • Experience guiding cross-functional teams of subject matter experts • Experience working in a startup-like environment • Experience interacting with regulators • Ability to work well with quality, clinical, medical, bioinformatics, and laboratory teams across a variety of therapeutic areas • Responsive to feedback, willing to change direction, and able to identify creative solutions to meet business and regulatory needs • Excellent attention to detail • Strong project management skills and the ability to execute on project plans in a fast-paced environment • Scientific background • PhD preferred • Minimum of 5+ years of experience in Regulatory Affairs experience related to medical devices • Knowledge of engineering concepts and biology with ability to evaluate device performance data and develop testing plans. • Establishing processes for efficiently addressing the requirements of multiple regulatory frameworks at scale • Developing and executing premarket and postmarket regulatory project plans and strategies, including assessments of change controls • Working closely with cross-departmental subject matter experts to guide the creation of documentation needed for regulatory applications and internal records • Working closely with business leadership to ensure regulatory strategy aligns with commercial goals • Making regular reports to our executive team, operationalizing leadership direction quickly and efficiently.