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Confluent Medical Technologies

Contract manufacturer of Nitinol medical devices

Manufacturing Lead

Manufacturing & Production OperationsConfirmed live in the last 24 hours
Full-timeAlajuela Province, Alajuela, Costa RicaNo salary listedIn-person

About the Job

Requirements

  • High school degree and 6–7 years of related experience.
  • Basic personal computer skills, including electronic mail, word processing, spreadsheet, and graphics software.
  • Ability to work varying shifts and overtime as required.
  • Ability to read, write, and understand English.
  • Ability to complete company- and department-required training courses.
  • Ability to work in a team environment.
  • Ability to read and interpret complex engineering drawings and other technical documentation associated with production.
  • Ability to read and interpret machine performance test results.
  • Ability to interpret Material Safety Data Sheets.
  • Ability to use optical comparators, video systems, and other magnification systems to perform assembly and inspection processes.
  • Ability to use and read measuring devices, including rulers, calipers, micrometers, reticules, pull-testers, thermometers, and gauges.
  • Ability to distribute work and effectively convey instructions to others.
  • Ability to follow complex verbal instructions and understand and apply regulatory requirements, including Quality System Regulation and International Organization for Standardization requirements, in everyday activities.
  • Ability to use personal computers and associated software.
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
  • Ability to add, subtract, multiply, and divide using whole numbers, common fractions, and decimals.
  • Manual dexterity sufficient to reach and handle items, work with the fingers, and perceive attributes of objects and materials.
  • Ability to adjust focus and meet visual work standards, with annual testing.

Responsibilities

  • Perform complex tasks in the Costa Rica manufacturing area.
  • Maintain certification on critical process steps, including Af Go/No Go testing, diameter measurement using a laser micrometer, visual inspection, SmartScope, Af testing, and lot closure.
  • Coordinate, support, and follow production activities hands-on and technically in medical-device manufacturing in accordance with written documentation and approved operating procedures, including Work Instructions, Operating Procedures, and Engineering Operating Procedures.
  • Manage a team of operators by generating daily job assignment schedules, overseeing execution of their responsibilities, resolving minor team conflicts, and training and coaching less experienced operators to gain additional process certifications.
  • Reassign associates to appropriate workstations to balance the production line while meeting productivity and quality goals, and assist less experienced associates with Bump-n-Slide procedures.
  • Manage training needs to maintain a pool of certified operators, with primary and backup coverage for every process step on the line.
  • Communicate with teammates, Leads, Supervisors, or Maintenance to resolve process or basic tool issues, including repeated defects, equipment that is not functioning as expected, or rebooting a computer.
  • Accurately record and complete manufacturing documentation, including logbooks, travelers, log sheets, and production records, with minimal supervision, and mentor less experienced personnel on these procedures.
  • Read and follow Work Instructions, Engineering Operating Procedures, and other documents for process information such as tool size and process equipment settings, and mentor less experienced operators on these documents.
  • Collect data using hand-held or equipment-based measuring devices and transfer data into a computer database.
  • Conduct basic to complex visual quality inspections of parts in accordance with process or other control procedures, such as Work Standards.
  • Maintain a clean and orderly workstation, supply racks, and parts storage bins.
  • Obtain supplies from the warehouse.
  • Report Servoy, IT, and Epicor issues to the Supervisor and appropriate support group.
  • Use the C-Pro software module to check and print training certification status for oneself and others.
  • Participate in process- or safety-related improvement activities.
  • Use in-depth knowledge of Servoy to resolve basic issues.
  • Write emails to keep Supervisors, Leads, and Engineering informed of issues or updates.
  • Complete basic production, health, safety, and environmental hazard communication training.
  • Follow corporate, safety, and production standard operating procedures.
  • Ensure personal and company compliance with applicable federal, state, local, and company regulations, policies, and procedures for health, safety, and environmental compliance.
  • Supervise Production Associates through planning and scheduling work and reviewing and approving tasks.

About the Company

Confluent Medical Technologies

Contract manufacturer of Nitinol medical devices

Confluent Medical Technologies provides contract manufacturing and materials science services to medical device OEMs, supporting projects from early design and prototyping through full-scale production and commercialization. Its offerings span Nitinol components, high-precision polymer tubing, biomedical textiles, and complex catheter systems, all produced through a vertically integrated process that covers raw materials to finished devices. The company differentiates itself by owning the entire supply chain from Nitinol alloy to the final product and by expanding capabilities through acquisitions in catheters, textiles, and polymer components. Its goal is to help OEMs bring safe, high-quality interventional devices to market faster by delivering end-to-end manufacturing and materials science support.

Company size
1,001-5,000
Company stage
Debt Financing
Total funding
$590M
Headquarters
Scottsdale, AZ
Founded
1991

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