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Senior Mechanical Engineer - Consumables Design

Job in San Diego, San Diego County, California, 92189, USA
Listing for: Burke Porter, an Ascential Technologies Brand
Full Time position
Listed on 2026-10-17
Job specializations:
  • Engineering
    Manufacturing Engineer, Mechanical Engineer, Biomedical Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 150000 - 185000 USD Yearly USD 150000.00 185000.00 YEAR
Job Description & How to Apply Below

Position Summary for Senior Mechanical Engineer

The Senior Mechanical Engineer leads mechanical design of disposable and consumable components for life-science instruments and medical devices. This role brings deep, hands-on expertise in plastics design, injection molding, and plastics joining/welding for IVD and human-use medical device consumables, along with a strong command of design for user experience, human factors, and bioburden/sterility control. The skill set is intended to support an ongoing portfolio of related development programs (for example, dialysis and other extracorporeal consumables, diagnostic cartridges or cassettes, drug-delivery consumables, and other single-use fluidic or reagent-handling components).

The Senior Mechanical Engineer partners closely with chemical, systems, electrical, software, and human factors engineering to integrate fluidic, chemistry, controls, and usability requirements into manufacturable, reliable, and user-friendly consumable designs, while providing technical leadership and credible client interface throughout each program.

Key Responsibilities Consumable & Plastics Design
  • Lead mechanical design of consumable/disposable components (e.g., cartridges, cassettes, fluid-path sets, connectors, filters) for life-science instruments and medical devices.
  • Apply best-practice plastics design principles (wall thickness, draft angles, ribs/bosses, gate and parting-line placement) to ensure part manufacturability and performance.
  • Specify and validate plastics joining and welding methods (ultrasonic welding, heat staking, solvent bonding, laser welding) appropriate for fluid-path integrity and biocompatibility.
  • Evaluate materials for chemical compatibility and biocompatibility, partnering with Quality and Regulatory as needed.
  • Design sterile barrier packaging systems (e.g., pouches, trays, seals) suited to the target sterilization modality and shelf-life requirements.
  • Apply design-for-user-experience and human factors principles (IEC 62366) to consumable design, including error-proofing, tactile/visual feedback, and ease of loading for both clinical and home-use operators.
  • Design consumables for bioburden control and sterility assurance, including material selection and compatibility with sterilization modalities (EtO, gamma, e-beam).
  • Lead design-for-manufacture (DFM) and design-for-assembly (DFA) reviews with internal manufacturing/operations teams as well as external tooling vendors and contract manufacturing partners, including tolerance stack-up and GD&T analysis.
  • Lead verification testing of consumables (e.g., burst/leak testing, drop/shock, fatigue, shelf-life) to support design verification and validation. Lead process validation efforts for consumables.
  • Support pilot builds and design-transfer activities, ensuring consumable designs are robust for high-volume manufacturing.
Technical Leadership & Client Interface
  • Serve as the technical authority on consumables design, manufacturability, and human factors across the program portfolio.
  • Present mechanical design status, risk assessments, and manufacturability trade-offs at design reviews and client meetings.
  • Mentor mechanical engineers on plastics design, DFM/DFA for both internal and external manufacturing, and sterility/bioburden best practices.
  • Represent the mechanical/consumables workstream credibly to clients, balancing innovation, manufacturability, and program constraints.
Cross-Functional Collaboration
  • Partner with process- and materials-focused engineering colleagues to ensure fluid-path materials and geometries meet chemical compatibility, biocompatibility, and performance requirements.
  • Partner with Systems Engineering to ensure consumable-level requirements are captured, traced, and verified within the system design-control framework.
  • Coordinate with Quality and Regulatory on biocompatibility (ISO 10993), sterilization validation, and design-history-file documentation.
  • Collaborate with Operations and Supply Chain on tooling strategy, supplier qualification, and scale-up planning.
Qualifications

Required

  • BS in Mechanical Engineering; MS preferred.
  • 7+ years of mechanical design experience, with significant focus on disposable/consumable components for IVD or human-use medical devices.
  • Deep, hands-on expertise in plastics design and injection molding, including resin selection, tooling considerations and DFM/DFA practices for both internal and external manufacturing.
  • Experience with die cutting, coating, converting and associated processes…
Position Requirements
10+ Years work experience
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