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IDEX

Precision engineering for health and safety

Design Engineer - Bioprocess Components

Biomedical Engineering & Medical DevicesConfirmed live in the last 24 hours
Full-timeRohnert Park, CA, USAIn-person

About the Job

Requirements

  • A Bachelor's or Master's degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or a related field.
  • Three to eight or more years of experience in product design, preferably in bioprocessing, medical devices, or fluidics.
  • Proficiency with computer-aided design tools such as SolidWorks.
  • Understanding of fluid systems, sensors, materials, and sterilization methods.
  • Strong analytical and problem-solving skills for design validation and data interpretation.
  • Ability to design for reliability, sterility, and regulatory compliance.
  • Cross-functional communication and customer-facing technical skills.
  • Systems-level thinking for component-to-system integration.
  • Attention to detail and documentation rigor.

Responsibilities

  • Design and develop bioproduction components such as sensors, tubing assemblies, connectors, manifolds, filters, and related flow-path devices.
  • Create detailed computer-aided design 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.
  • Translate bioprocess requirements, including sterility, flow rates, shear sensitivity, and extractables and 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.
  • Collaboratively develop test plans for performance validation, including flow, pressure, integrity, and sterility assurance.
  • Analyze data to validate designs and identify opportunities for improvement.
  • Perform root cause analysis and troubleshoot design and field issues.
  • Ensure designs comply with biopharma standards, including Good Manufacturing Practice, Food and Drug Administration, International Organization for Standardization, and United States Pharmacopeia guidelines.
  • Support documentation for design controls, risk assessments using Failure Mode and Effects Analysis, and validation protocols.
  • Contribute to quality systems, including change control and corrective and preventive actions.
  • Work 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.

Desired Qualifications

  • Experience with single-use technologies, sterile fluid paths, or bioprocess equipment.
  • Familiarity with extractables and leachables, biocompatibility, and material selection.
  • Knowledge of manufacturing processes such as injection molding, extrusion, and assembly.
  • Experience with sensor integration, including pressure, flow, pH, and conductivity.

About the Company

IDEX

Precision engineering for health and safety

IDEX is a global provider of engineered, high-precision components and systems for specialized markets, with two main segments: Health Sciences Technologies and Fire Safety Diversified Products. In Health Sciences, it designs liquid subassemblies and precision parts for research and diagnostics; in Fire Safety, it makes pumps, controls, valves, nozzles, and rescue tools for firefighting. It also offers stainless steel banding and clamping devices and metering, dispensing, and mixing equipment for paints and colorants. The company aims to create value by delivering dependable, precisely engineered solutions tailored to exact customer needs in health science, fire safety, and industrial dispensing and joining applications.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Northbrook, IL
Founded
1987

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