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Devops Engineer Business Development

Ashburn,VA

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961 Devops Engineer Business Development jobs in Ashburn,VA

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Release Manager, Design Engineering

Amazon Data Services

Herndon, VA 20170

Urgently Hiring
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Kubernetes Platform Engineer / Development Operations (TS/SCI with Poly Required)

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Chantilly, VA 20152

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DevOps Software Engineer - TS/SCI Cleared

Leidos

Rockville, MD 20850

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GIS DevOps Engineer

Vantor

Herndon, VA 20170

~ 16 min OnsiteEducation AssistanceHealth InsuranceRetirement Benefit

  • Must be a U.S. Citizen with an active TS/SCI with CI poly (or willingness to obtain a CI poly)
  • This position requires an active U.S. Government Security Clearance at the TS/SCI with CI poly level.
  • Export Control/ITAR: Certain roles may be subject to U.S. export control laws, requiring U.S. person status as defined by 8 U.S.C. 1324b(a)(3).
  • Minimum of 14 years of total professional experience in a technical support role
  • Demonstrated technical experience with DevSecOps
  • Demonstrated experience working with Kubernetes in production environments
  • Demonstrated experience with Red Hat OpenShift
  • Proficiency in container technologies such as Docker or CRI-O
  • Experience with CI/CD tools (e.g., Jenkins, GitHub Actions, GitLab CI)
  • Open source and custom application deployments and maintenance experience.
  • Capable of working effectively with a geographically distributed ops & development team
  • Demonstrated ability to communicate effectively with customers and team in written and oral forums
  • Willingness to work 90% or as needed in a SCIF environment with some on-call or after-hours onsite support for customer's mission in either Herndon, VA; Westminster, CO; or St. Louis, MO
  • Degree or equivalent demonstrated experience in a technical field.
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Manassas, VA 20110

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Cyber Security Subject Matter Expert

GovCIO LLC

Washington, DC 20510

$200,000/yr
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GBS Marketing Business Development Executive, LE

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Arlington, VA 22209

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Herndon, VA 20171

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Senior Engineer I/II, Mechanical

MaxCyte

Rockville, MD 20850

~ 45 min OnsiteHealth InsurancePaid Time Off

  • B.S. in Mechanical Engineering required
  • M.S. preferred
  • 5+ years of relevant experience in mechanical design in life science consumable, medical device, pharma, bioprocess components, or other regulated product development environments
  • 10+ years for Level II
  • Direct experience designing single-use consumables and fluid control assemblies for cell therapy, gene therapy, bioprocessing, or sterile fluid handling systems
  • Experience with scaling up and high-volume manufacturing
  • Experience designing bioprocessing technologies such bioreactors, gas exchange, filtration, centrifugation, cell isolation, purification, process analytics, etc.
  • Strong understanding of fluid handling and fluid control systems, including tubing-based flow paths, pressure-driven flow, pumping, valving, and manifolds
  • Experience integrating fluid sensing including bubble detection, pressure & liquid sensing, etc.
  • Experience with FEA preferred (e.g., COMSOL)
  • Experience designing for GMP manufacturing environments, including cleanroom-compatible use, contamination control, and sterile closed-system processing
  • Strong knowledge of materials used in GMP manufacturing systems
  • Experience designing complex mechanical systems, subsystems, and components
  • Experience designing fluid interfaces and sealing solutions including rotating fluid connections, dynamic seals, face seals, gaskets, and disposable-to-instrument mating mechanisms
  • Experience with DFx including manufacturing, assembly, reliability, usability, cost, etc.
  • Experience with tolerance analysis
  • Proficient in SolidWorks
  • SolidWorks PDM preferred
  • Experience with QbD principles, Design for Six Sigma (DFSS), Critical Parameters Design and Management (CPD&M) or similar
  • Working knowledge of Minitab for statistical analysis and Design of Experiments (DOE) preferred
  • Skilled in prototyping
  • Working knowledge of fabrication and assembly methods such as plastic injection molding, 3D printing, CNC machining, sheet metal forming, semi-automated & automated assembly, adhesives, conversion of films and foils, etc.
  • Working knowledge of metrology tools
  • Strong knowledge of Design Control (ISO 13485) and GMP compliance for cell therapy manufacturing environments
  • Familiar with ISO 9001, ISO 10993, ISO14971 and other relevant international safety and quality standards
  • Experience writing protocols, executing tests, overseeing outsourced testing, and writing reports
  • Knowledge of extractables/leachable, sterilization methods, particulate control preferred
  • Strong interpersonal skills with a track record of cross-functional collaboration, problem solving, and driving technical alignment
  • Excellent written and verbal communication skills
  • Travel 10-15% domestically
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