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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 listedHybrid

About the Job

Requirements

  • A high school degree and 6–7 years of related experience are required.
  • Basic personal computer skills, including electronic mail, word processing, spreadsheets, and graphics, are required.
  • The ability to work varying shifts and overtime as required is necessary.
  • The ability to read, write, and understand English is required.
  • The ability to complete company- and department-required training courses is necessary.
  • The ability to read and interpret complex engineering drawings and other technical production documentation is required.
  • The ability to read and interpret machine performance test results is required.
  • The ability to interpret Material Safety Data Sheets is required.
  • The ability to use optical comparators, video systems, and other magnification systems for assembly and inspection processes is required.
  • The ability to use and read measuring devices, including rulers, calipers, micrometers, reticules, pull-testers, thermometers, and gauges, is required.
  • The ability to distribute work and effectively convey instructions to others is required.
  • The ability to follow complex verbal instructions and apply regulatory requirements, including Quality System Regulations and International Organization for Standardization requirements, in daily activities is required.
  • The ability to use personal computers and associated software is required.
  • The ability to read and interpret safety rules, operating and maintenance instructions, and procedure manuals is required.
  • The ability to perform basic arithmetic using whole numbers, common fractions, and decimals is required.
  • Sufficient manual dexterity to reach and handle items, work with the fingers, and perceive attributes of objects and materials is required.
  • The ability to adjust focus and meet visual work standards, including annual testing, is required.
  • The employee must wear special garments while working in a clean-room environment.
  • The employee must comply with applicable federal, state, local, and company health, safety, and environmental regulations, policies, and procedures.
  • The employee must complete basic production, health, safety, and environmental hazard communication training.

Responsibilities

  • Perform complex tasks in the Costa Rica manufacturing area.
  • Maintain certification on critical process steps, including Go/No-Go testing, diameter measurement using a laser micrometer, visual inspection, SmartScope, testing, and lot closure.
  • Coordinate, support, and follow production activities, both hands-on and technically, while manufacturing medical devices according to written documentation and approved operating procedures.
  • Manage a team of operators to meet productivity and quality goals by generating daily job assignment schedules, overseeing execution of job responsibilities, resolving minor team conflicts, and training and coaching less experienced operators toward 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 each process step on the line.
  • Communicate with teammates, leads, supervisors, or maintenance personnel to resolve process or basic tool issues, including repeated defects, equipment that is not functioning normally, and computer reboots.
  • Accurately complete manufacturing documentation, including logbooks, travelers, log sheets, and production records, and mentor less experienced personnel on these procedures.
  • Read and follow work instructions, EOPs, and other documents for process information such as tool sizes and equipment settings, and mentor less experienced operators in using these documents.
  • Collect data using hand-held or equipment-based measuring devices and enter it into a computer database.
  • Conduct basic to complex visual quality inspections of parts in accordance with process or other control procedures, including work standards.
  • Maintain clean and orderly workstations, supply racks, and parts storage bins.
  • Obtain supplies from the warehouse.
  • Report Servoy, information technology, 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 other employees.
  • Participate in process- or safety-related improvement activities.
  • Use in-depth knowledge of Servoy to resolve basic issues encountered.
  • Write emails to keep supervision, leads, and engineering informed of issues or updates.
  • Follow corporate, safety, and production standard operating procedures.
  • 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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