Manufacturing Engineer, Staff

hace 23 horas

Alajuela, Alajuela, Costa Rica Confluent Medical Technologies A tiempo completo $60.000 - $120.000 al año

Job Description:

Confluent Medical Technologies is a financially healthy and rapidly growing medical device company 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 and tubing, balloon expandable stents and catheters, complex catheters, biomedical textiles, and high precision polymer tubing. 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 Manufacturing Engineer, Staff to join our team. As a uniquely qualified candidate, you will be responsible for ensuring compliance with company and regulatory standards for Health, Safety, and Environment. Leads continuous improvement initiatives to enhance manufacturing efficiency, quality, and cost-effectiveness.

Key Responsibilities:

  • Ensure adherence to all HSE policies and procedures.
  • Collaborate with R&D, Design, and Transfer teams to understand product and process requirements.
  • Develop and implement standard manufacturing methods and process controls.
  • Conduct time studies, cost analyses, and root cause investigations to drive process optimization and yield improvement.
  • Design and validate production layouts, equipment, and tooling in alignment with safety and environmental standards.
  • Lead product transfers and new product introductions, ensuring smooth and compliant ramp-up.
  • Supervise and coordinate engineering and technical staff.
  • Partner with customers and suppliers to resolve quality issues and support ongoing improvements.

EDUCATION and/or EXPERIENCE:

  • Bachelor´s degree in engineering
  • Strong English communication skills (90%)
  • Minimum of 6 years of experience as an Engineer in the medical device industry.
  • Proven experience in Sustaining Engineering.
  • Experience managing improvement projects, transfers, CIPs, etc.
  • Experience in process validations.
  • Knowledge and experience in regulatory topics such as complaints, NCRs, CAPAs, etc.
  • Extensive experience in root cause analysis.

Qualifications & Skills

  • Team leadership experience.
  • Strong technical expertise in manufacturing processes, tooling, workflow design, and production equipment.
  • Experience applying Operational Excellence and Quality Tools (5S, Kaizen, Pareto, Ishikawa, Control Charts, etc.); Green Belt certification or equivalent preferred.
  • Proven ability to become a Subject Matter Expert (SME) and train or mentor others.
  • Strong leadership, analytical, and problem-solving skills.
  • Highly organized, detail-oriented, and able to manage multiple priorities under pressure with minimal supervision.
  • Demonstrates accountability, structured communication, and sound business vision.

COMMENTS: 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.

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