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Scientist Process Development

Washington,DC

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543 Scientist Process Development jobs in Washington,DC

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Quantum Error Correction Scientist

Johns Hopkins Applied Physics Laboratory (APL)

Laurel, MD 20723

$105,000/yr
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Scientist, Software Engineer

L3Harris Technologies

Chantilly, VA 20151

Bilingual Preferred
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Director, Data Science

Gartner

Arlington, VA 22209

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Director - Life Sciences Advisory - Commercial

Guidehouse Careers

Arlington, VA 22204

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Open-Rank, Term Information Sciences and Technology Faculty

George Mason University

Fairfax, VA 22030

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Associate Director - Life Sciences Advisory - Medical Affairs/Real World Evidence (RWE)

Guidehouse Careers

Arlington, VA 22204

Recommended
Scientist, Software Engineer

L3Harris Technologies Careers

Chantilly, VA 20152

Bilingual Preferred
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Electro-Optical Systems Engineer

Fibertek

Herndon, VA 20171

~ 34 min Onsite

  • A bachelor's degree in engineering, system engineering or optics
  • A minimum of 10 to 15 years of relevant experience
  • Experience in Systems Engineering with an emphasis in requirements development, test planning, test documentation, and systems integration, verification, and validation
  • Experience developing and managing system and subsystem requirements flow down
  • Demonstrated ability to lead and implement systems engineering best practices and tools from the ground up
  • Experience with systems engineering and requirements management software tools and model-based systems engineering (MBSE)
  • Ability to effectively communicate technical results and report problems through written and/or graphical formats
  • U.S. citizenship is required
  • Secret or Top Secret Clearance preferred
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AI Platform and DevSecOps Engineer

Johns Hopkins Applied Physics Laboratory (APL)

Laurel, MD 20723

$100,000/yr
Easy Apply
Senior Engineer I/II, Mechanical

MaxCyte

Rockville, MD 20850

~ 36 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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