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Design Engineer - Bioprocess Components

Job in Rohnert Park, Sonoma County, California, 94928, USA
Listing for: IDEX Corporation
Full Time position
Listed on 2026-07-18
Job specializations:
  • Engineering
    Manufacturing Engineer, Biomedical Engineer, Process Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 109800 - 164600 USD Yearly USD 109800.00 164600.00 YEAR
Job Description & How to Apply Below

If you’re looking for a special place to build or grow your career, you’ve found it. Whether you’re an experienced professional, a recent college graduate or somewhere in between, IDEX is a place where you can apply your existing skills and learn new ones in an environment where you can make an impact.

With interesting opportunities in engineering, marketing, sales, supply chain, operations, HR, finance, and more across more than 40 diverse businesses () around the globe, chances are, we have something special for you.

Who is IDEX Health & Science (IH&S)?

As a business unit of IDEX Corporation, IH&S has a long history of driving growth in life sciences and healthcare by embracing innovation and redefining the supplier-customer relationship. The work we do every day allows us to discover key insights and break new ground to create some of the most meaningful technologies that have a lasting impact on companies, industries, and society.

IDEX

HEALTH & SCIENCE, LLC

IDEX Health & Science is the global leader in life science fluidics, microfluidics, and optics, offering a three-fold advantage to customers by bringing optofluidic paths to life with strategic partnerships, solutions, and expertise. As one of the few companies in the world with component, sub-system, and application-level experts, IDEX Health & Science helps instrument developers solve the most demanding fluidic and optical challenges in a wide array of applications.

With over 1,000 employees around the world, we believe partnership will change the way the world innovates, leading to new technologies that improve our health, protect our planet, and enrich our lives. For more information visit:

Our formula for success is simple. We work hard to maintain a culture where you can own your work; you are encouraged to try new ideas in a collaborative environment; and you can apply your skillset to enable our clients to gain a competitive advantage in their own market. At IDEX Health & Science, you have the opportunity to work with a great group of people, mentor others, and build a great future.

Position

Summary

The Bioproduction Design Engineer is responsible for the design, development, and optimization of components and subsystems used in upstream and downstream biopharmaceutical manufacturing, including fluidic systems, single-use assemblies, and process instrumentation. This role bridges product development and bioprocess application, ensuring designs meet performance, regulatory, and manufacturability requirements for use in GMP environments.

The position requires strong cross-functional collaboration with R&D, quality, manufacturing, and customers to translate process requirements into robust and scalable hardware solutions.

Key Responsibilities Product Design & Development
  • Design and develop bioproduction components such as sensors, tubing assemblies, connectors, manifolds, filters, and related flow-path devices
  • Create detailed CAD models, drawings, and specifications for new products and revisions
  • Optimize designs for performance, manufacturability, cost, and scalability
  • Apply engineering principles to optimize fluid control, mass transfer, and material compatibility in bioproduction systems
System Integration & Application Engineering
  • Translate bioprocess requirements (e.g., sterility, flow rates, shear sensitivity, extractables/leachables) into component designs
  • Integrate components into larger systems such as single-use assemblies, bioreactors, or downstream skids
  • Support customer-specific design adaptations and custom configurations
Testing, Validation & Analysis
  • Collaboratively develop test plans for performance validation (e.g., flow, pressure, integrity, sterility assurance)
  • Analyze data to validate designs and identify opportunities for improvement
  • Perform root cause analysis and troubleshooting of design and field issues
Regulatory & Quality Compliance
  • Ensure designs comply with biopharma standards (e.g., GMP, FDA, ISO, USP guidelines)
  • Support documentation for design controls, risk assessments (FMEA), and validation protocols
  • Contribute to quality systems including change control and CAPA
Cross-Functional Collaboration
  • Work closely with…
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