Manufacturing Engineer

Kalogon•Melbourne, FL

2d•Onsite

About The Position

We are seeking a motivated Manufacturing Engineer to join our team. This role is crucial for improving product manufacturability, optimizing production processes, and ensuring quality assurance and compliance with ISO 13485 standards for Class I Medical Devices. You will work closely with production technicians and engineering teams to implement product changes, reduce rework rates, and enhance efficiency. This is an on-site role at our offices in Melbourne, FL.

Requirements

Bachelor’s degree in Engineering, Manufacturing Engineering, Industrial Engineering, or related field (or equivalent practical experience).
3–7 years of experience in manufacturing engineering, quality engineering, or a related production role.
Strong knowledge of Quality Management Systems, process auditing, and manufacturing quality methodologies.
Experience performing root cause analysis and driving CAPA to resolution.
Familiarity with design for manufacturability (DFM) principles and experience collaborating with engineering on product and process changes.
Experience with Lean and continuous improvement tools.

Responsibilities

Design and implement product changes with a focus on rework rates, cost, and assembly time, utilizing direct feedback from production technicians and field feedback to validate improvements and surface further opportunities.
Lead root cause analysis for defects and non-conformances, driving corrective and preventive actions (CAPA) to resolution and verifying effectiveness.
Manage analysis and disposition of units returned through the Return Authorization (RA) process, ensuring root cause is identified, findings are documented, and systemic corrective actions are driven when required.
Apply Lean and continuous improvement methodologies to evaluate and refine manufacturing processes, building quality into operations rather than inspecting it at the end.
Manage engineering change orders (ECOs) for existing product lines.
Analyze SOPs, assembly workflows and production training to optimize the efficiency of manufacturing processes and ensure consistent quality parts.
Manage facility upgrades for new equipment, including evaluating equipment requirements, assessing current facility utilities, coordinating contractors' quotes, and overseeing installation.
Own and implement manufacturing processes and systems that adhere to ISO 13485 for Class I Medical Devices.
Conduct regular spot checks and audits across the manufacturing line to verify conformance to process documentation, work instructions, and quality standards.