Design Engineer - Bioprocess Components
Job in
Rohnert Park, Sonoma County, California, 94928, USA
Listed on 2026-07-13
Listing for:
IDEX
Full Time
position Listed on 2026-07-13
Job specializations:
-
Engineering
Manufacturing Engineer, Biomedical Engineer, Process Engineer, Quality Engineering
Job Description & How to Apply Below
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 bioprocess engineers, scientists, and manufacturing teams to support product design and introduction
+ Collaborate with Supply Chain on materials, components, and vendor requirements
+ Participate in design reviews and technical risk assessments
** Required Qualifications*
* + Bachelor's or Master's degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or related field
+ 3-8+ years in product design, preferably in bioprocessing, medical devices, or fluidics
+ Proficiency in CAD tools (e.g., Solid Works)
+ Understanding of fluid systems, sensors, materials, and sterilization methods
** Preferred Experience*
* +
Experience with single-use technologies, sterile fluid paths, or bioprocess equipment
+ Familiarity with…
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