566 Senior Full Stack Developer jobs in Clifton,VA

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Senior Real Estate Development Manager, AWS Infrastructure Services

Amazon Data Services

Arlington, VA 22203

~ 35 min OnsiteHealth InsurancePaid Time OffRetirement Benefit

8+ years of experience in large-scale site selection, real estate land acquisitions and lease negotiations
5+ years experience performing the full range of land entitlement functions leveraging a combination of internal and external resources
5+ years experience in site due diligence, site development, and negotiation of entitlement agreements for large complex projects.
Bachelor's Degree in Urban Planning, Architecture, Civil Engineering, Real Estate or related fields.

SmartExplore AI is experimental.

New, Posted 13 hours ago

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Senior Strategy Learning Evaluation Officer Education

Confidential

Washington, DC 20001

~ 40 min OnsiteUrgently Hiring

New, Posted 11 hours ago

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Senior Manager, AI Engineering (People Leader) (Gen AI Platform Services)

Capital One

Mc Lean, VA 22101

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Senior Linux System Administrator

Leidos

Fairfax, VA 22030

~ 21 min OnsitePaid Time OffRetirement Benefit

US Citizen with at least an active Secret clearance.
Bachelor's degree with 8+ years of experience
Master's degree with 6+ years of experience
Additional experience may be considered in lieu of a degree.
5+ years of experience providing System Administration to DoD IT systems.
DoD 8570 IAT level I compliant.

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Senior GEOINT Analyst

ManTech

Springfield, VA 22150

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Senior Linux System Administrator

Leidos

Springfield, VA 22153

~ 29 min OnsitePaid Time OffRetirement Benefit

US Citizen with at least an active Secret clearance.
Bachelor's degree with 8+ years of experience
Master's degree with 6+ years of experience
Additional experience may be considered in lieu of a degree.
5+ years of experience providing System Administration to DoD IT systems.
DoD 8570 IAT level I compliant.

SmartExplore AI is experimental.

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Senior Manager, Machine Learning Engineering

Capital One

Mc Lean, VA 22101

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Senior Engineer I/II, Mechanical

MaxCyte

Rockville, MD 20850

~ 46 min OnsiteHealth InsurancePaid Time Off

B.S. in Mechanical Engineering required
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 Design for Six Sigma (DFSS), Quality by Design (QbD) components or similar; Working knowledge of Minitab for statistical analysis and 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 ability: 10-15% domestically