Transfer Engineer, Staff

Posted 16 Days Ago
Be an Early Applicant
Alajuela, Alajuela, CRI
In-Office
Mid level
Healthtech
The Role
Provides technical leadership for manufacturing process transfers into commercial production. Leads line setup, validation, startup, tooling and fixture implementation, process testing, data analysis, root-cause investigations, release testing, documentation, and cross-functional coordination. Drives continuous improvement, process optimization, capacity enhancement, and compliance with quality, safety, and regulatory requirements for medical device manufacturing.
Summary Generated by Built In

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. 


We are looking for a Staff Transfer Engineer to join our team. In this role, you will provide technical leadership for manufacturing process transfer projects, supporting the successful transition of products and processes into commercial manufacturing. You will be responsible for analyzing complex situations, organizing and prioritizing activities, and coordinating cross-functional efforts to ensure projects are executed efficiently, on schedule, and in alignment with quality and operational requirements.


The Staff Transfer Engineer will play a key role in driving continuous improvement, manufacturing process optimization, product flow, and capacity enhancement, with the goal of improving overall manufacturing efficiency and achieving established service level and performance targets.

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

  • Independently plan and execute engineering assignments, applying sound judgment to evaluate, adapt, and improve standard techniques, procedures, and criteria.
  • Lead and support manufacturing process transfer activities, including production line setup, validation, and startup at the receiving site.
  • Participate in the design, testing, and implementation of manufacturing tooling and fixtures.
  • Coordinate daily activities of operators during manufacturing transfers, ensuring training and project activities are completed according to schedule.
  • Analyze process data, identify root causes, and recommend solutions to resolve manufacturing and process issues.
  • Conduct manufacturing reviews, pre-validation assessments, experiments, and testing to support the safe, compliant, and effective implementation of new processes.
  • Define, execute, and document in-process and product release testing, including test procedures, data collection, and results.
  • Prepare technical reports and maintain accurate engineering documentation in accordance with company procedures, regulatory requirements, and engineering best practices.
  • Ensure project resources follow applicable company safety, quality, environmental, and operational policies.
  • Set up, adjust, and operate basic R&D, laboratory, and manufacturing equipment as required.
  • Collaborate with cross-functional teams, applying broad knowledge of engineering principles and related disciplines to develop solutions and improve manufacturing processes.

EDUCATION AND/OR EXPERIENCE:

  • Bachelor’s degree in Engineering or a related technical discipline.
  • Strong understanding of medical device manufacturing processes, quality systems, and industry requirements.
  • Hands-on experience with catheter manufacturing
  • 4+ years of relevant engineering experience, preferably in roles such as New Product Introduction (NPI), Process Transfer, Manufacturing Engineering, or similar.
  • Fluent in English (B2) both written and verbal, with the ability to effectively communicate technical information in a professional environment.
  • Strong knowledge of statistical methods and process improvement tools, including Capability Analysis, C/R, Gage R&R, and Design of Experiments (DOE).
  • Six Sigma certification is preferred and considered an asset.

OTHER SKILLS AND ABILITIES:


  • Proficient in statistical analysis and data interpretation
  • Demonstrates more than a basic understanding of engineering principles, manufacturing processes, and project management fundamentals.
  • Developing proficiency in structured problem-solving methodologies, including root cause analysis and data-driven decision-making.
  • Ability to provide effective group leadership and cross-functional coordination, particularly when managing complex or competing priorities.
  • Strong organizational and prioritization skills, with the ability to manage multiple tasks and projects simultaneously.
  • Ability to work effectively with cross-functional teams and communicate technical information clearly to diverse stakeholders.
  • Demonstrates sound judgment and the ability to identify and implement practical solutions to engineering and manufacturing challenges.

A valid U.S. visa is preferred for this role.


This position 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. The incumbent(s) will typically perform other related job objectives, special assignments and less significant responsibilities.

Skills Required

  • Bachelor's degree in Engineering or a related technical discipline
  • Strong understanding of medical device manufacturing processes, quality systems, and industry requirements
  • 4+ years of relevant engineering experience, preferably in New Product Introduction, Process Transfer, Manufacturing Engineering, or similar roles
  • Fluent English at B2 level, written and verbal
  • Strong knowledge of statistical methods and process improvement tools, including Capability Analysis, C/R, Gage R&R, and Design of Experiments
  • Six Sigma certification

Confluent Medical Technologies, Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Confluent Medical Technologies, Inc. and has not been reviewed or approved by Confluent Medical Technologies, Inc..

  • Healthcare Strength — Benefits are considered solid, with medical, dental, and vision coverage described positively and HSA-eligible options supported by employer contributions. Feedback suggests core health coverage is a relative bright spot within the total package.
  • Retirement Support — A 401(k) with company match is repeatedly highlighted as a positive element. Feedback suggests retirement provisions add meaningful value to total compensation.
  • Fair & Transparent Compensation — Compensation is considered competitive in several engineering and managerial tracks, with role-specific pay bands viewed as strong in those paths. Feedback suggests certain professional roles receive competitive pay bands.

Confluent Medical Technologies, Inc. Insights

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The Company
HQ: Scottsdale, AZ
1,068 Employees
Year Founded: 1991

What We Do

Confluent Medical Technologies applies materials science to MedTech innovation. Confluent specializes in expert design and development of large-scale manufacturing specializing in interventional catheter-based devices and implants. Our key capabilities include Nitinol components and tubing, balloon and complex catheters, high-precision polymer tubing, and implantable textiles. We operate in 8 state-of-the-art facilities across the United States and Costa Rica and currently employ over 2,000 employees. Confluent has earned the confidence of leaders in the medical device community through a proven track record of innovation, engineering, and manufacturing.

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