Manufacturing Engineer II – Shift C

About the role

We are seeking a Manufacturing Engineer II to join our production team on Shift C. The role focuses on ensuring product quality, safety, and efficient manufacturing processes within a medical‑device environment.

Key responsibilities

• Maintain compliance with quality policies and procedures that impact patient safety and product quality.
• Monitor and improve product quality indicators, ergonomic safety, and process performance (efficiency, yield).
• Perform data‑driven analysis to support corrective and preventive actions and demonstrate their effectiveness.
• Plan and execute technical projects, coordinating resources, timelines, documentation, and cross‑functional teams.
• Identify root causes and resolve production‑related issues.
• Participate in design, development, installation, validation, and qualification of equipment and processes, including feasibility studies and technical documentation.
• Support continuous‑improvement initiatives and cost‑reduction projects.
• Collaborate on calibration system maintenance, drawing control, and documentation.
• Collect, analyze, and present production data for meetings, business plans, and KPI reporting.
• Plan activities, control expenses, attend meetings, and prepare monthly reports.

Required profile

• Bachelor’s degree in an engineering, scientific, or technical discipline.
• Minimum of two years of experience in an engineering, scientific, or technical role within the medical industry.
• Intermediate proficiency in English.

Required skills