October 2, 2024

Confluent Medical Technologies

OTHER

Manufacturing Lead

Job Description:

Job Description

Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production. Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing. Our primary capabilities include: Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires. We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.

At Confluent, we are committed to our values of teamwork, innovation, accountability, integrity, leadership, and customer focus, and we invest in a team who represents these values. Every member of our team plays a critical role in delivering life-saving medical devices through innovative materials science, engineering, and manufacturing. We are the medical device industry's most trusted partner, and we accomplish this with an organization focused on safety, efficiency, and customer satisfaction.

We are looking for a Manufacturing Lead to join our team in Costa Rica. If you enjoy working in a fast-paced environment and making an impact on our life-saving work, this may be a good fit for you! As a uniquely qualified candidate, you will:

SUMMARY: Working under little to no supervision and following detailed verbal, written, and hands-on instructions. Manage a team of operators to meet productivity and quality goals by performing the following duties.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

Perform complex tasks in the Costa Rica manufacturing area.
Certified on critical process steps such as Af Go/No Go testing, Diameter Measurement using Laser Micrometer, Visual Inspection, Smart Scope, Af Testing, and Lot Closure but not limited to just these steps.
Coordinate, support and follow production activities, both hands-on and technically, in manufacturing medical devices per written documentation and approved operating procedures (WIs, OPs, EOPs).
Be able to manage a team of operators by generating daily job assignment schedules, overseeing the execution of their job responsibilities, resolving minor team conflicts, and training/coaching less experienced operators in their quest to gain more processing certifications.
Effectively re-assign associates to appropriate workstations to keep the line balanced while meeting productivity and quality goals. Be able to assist less experienced associates with Bump-n-Slide procedures.
Manage training needs to maintain a pool of certified operators so there is a minimum of a primary and back-up coverage for every process step in the line.
Effectively communicate with teammates, Leads, Supervisor or maintenance in resolving process or basic tool issues. Examples include: finding multiple quantities of the same defect, equipment not functioning as normally expected, or re-booting a computer.
Accurately record and complete manufacturing documentation, i.e., logbooks, travelers, log sheets, production records with minimal supervision. Be able to mentor less experienced personnel on these procedures.
Read and follow Work Instructions, EOPs or necessary documents for process information such as tool size and/or process equipment settings. Be able to mentor less experienced operators on these same documents.
Perform data collection using hand or equipment measuring devices and transfer data into a computer database.
Able to conduct basic to complex quality visual inspection of parts in accordance with process or other control procedures such as Work Standards.
Maintain clean and orderly workstation, supply racks, and parts storage bins.
Able to obtain supplies from the warehouse.
Communicate and report Servoy, IT, and Epicor issues to supervisor and appropriate support group.
Knowledge of C-Pro software module to check and print training certification status of your own and that of others.
Participate in improvement activities related to process or safety.
Have in-depth knowledge of Servoy and be able to resolve basic issues encountered.
Write email system to keep supervision, Leads, and engineering informed of issues or updates.
Completed basic production, health, safety, and environmental hazard communication training.
Follow all corporate, safety and production standard operating procedures.
Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.

EDUCATION and/or EXPERIENCE:

High school degree
2-3 years of related experience.
Basic personal computer skills including electronic mail, word processing, spreadsheet and graphics.

COMMENTS: This job description is an outline of the major recurring responsibilities of the job. It is not intended to be all‑inclusive of the work to be performed. Other related job objectives, special assignments, and less significant responsibilities will typically be performed by the incumbent(s).