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Roche

Global pharmaceuticals and diagnostics company

Staff Process Development Engineer

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeCarlsbad, CA, USA

About the Job

Requirements

  • A bachelor's degree or foreign equivalent in Engineering or a related field is required.
  • Eight years of progressive, post-baccalaureate experience as an Engineer or in a related position in the pharmaceutical, biotechnology, or medical industry is required.
  • At least two years of experience must include using Computational Fluid Dynamics (CFD) or flow-simulation software to model nanoliter- or microliter-scale fluid dispensing processes.
  • At least two years of experience must include developing, characterizing, or validating automated manufacturing vision systems or optical inspection hardware for defect detection.
  • At least two years of experience must include designing or characterizing surface treatment processes, including plasma cleaning or chemical vapor deposition, using surface analysis techniques to ensure robust material adhesion.
  • At least two years of experience must include applying Design for Six Sigma methodologies and using JMP or Minitab to plan and perform Design of Experiments and process capability analysis.
  • At least two years of experience must include leading design transfer of electromechanical and microfluidic devices, including planning and generating IQ/OQ/PQ protocols compliant with ISO 13485 and FDA 21 CFR Part 820.
  • At least two years of experience must include performing complex root cause analysis on manufacturing non-conformances by correlating production data with theoretical engineering models, such as thermal, fluidic, or optical models.

Responsibilities

  • Drive stable and reliable production for newly transferred manufacturing processes.
  • Develop and characterize manufacturing processes, including plasma or carbon dioxide surface treatment and precision dispensing of fluids and adhesives.
  • Create and maintain process input and output specifications; perform capacity analyses, troubleshooting, testing, and support for existing products and new product lines.
  • Drive process development, characterization, and improvement activities for new and existing product lines.
  • Lead project teams working on product improvements, automation, and quality improvements.
  • Apply statistical methods to production performance datasets to monitor, track, and trend performance, and assess opportunities to improve capacity, yield, or utilization.
  • Troubleshoot and investigate manufacturing-process issues and communicate findings.
  • Perform complex root cause analysis on manufacturing non-conformances by correlating production data with theoretical engineering models to implement sustainable countermeasures for micro-fabrication and device-assembly issues.
  • Develop and characterize precision nanoliter-scale dispensing processes for reagents and adhesives using Computational Fluid Dynamics and flow-simulation modeling to predict fluid behavior and optimize deposition accuracy in high-throughput manufacturing environments.
  • Design and validate plasma and carbon dioxide cleaning processes using surface analysis data, such as contact angle measurements or Scanning Electron Microscopy, to ensure robust adhesion for laser bonding and micro-assembly applications.
  • Develop and qualify automated manufacturing vision systems for defect detection using optics fundamentals, image-processing algorithms, and hardware limitations to support in-line quality inspection of medical-device assemblies.
  • Improve process stability and capability by applying Design for Six Sigma methods and advanced statistical analysis, including Design of Experiments and Gauge R&R, using JMP or Minitab to model process windows for critical-to-quality parameters.
  • Lead design transfer of complex electromechanical and microfluidic devices from research and development to production, including generating Installation, Operational, and Performance Qualification protocols compliant with ISO 13485 and FDA 21 CFR Part 820.

About the Company

Roche

Global pharmaceuticals and diagnostics company

Roche is a global leader in pharmaceuticals and diagnostics. It develops medicines and diagnostic tools that help detect, monitor, and treat diseases, using research and biotechnology to drive new therapies and tests. Roche combines drug development with in-house diagnostic products to support personalized medicine, where treatments are tailored to individual patients based on test results. Its approach differs from many peers by integrating drug discovery with diagnostic capabilities and by expanding its research through strategic acquisitions (like Genentech) to strengthen its biotechnology and R&D capabilities. The company’s goal is to improve patient outcomes and healthcare worldwide by delivering reliable medicines, accurate diagnostic tests, and data-driven care.

Company size
1-10
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1896

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