Maintenance Engineer

Job Description Purpose

The Maintenance Engineer supports reliable, predictable performance of manufacturing and facility equipment within a high‑precision dental production environment. The role improves equipment uptime through data‑driven maintenance strategies, hands‑on troubleshooting, and cross‑functional collaboration. The Maintenance Engineer applies sound engineering principles to optimize equipment performance, support continuous improvement, and maintain compliance with regulatory and safety standards.

• Execute preventive and corrective maintenance activities for CNC equipment (Mikron, Willemin), sintering furnaces, dust collection systems, HVAC, chillers, and electrical systems (400/480V).
• Diagnose and resolve mechanical, electrical, hydraulic, pneumatic, and controls issues to restore equipment functionality.
• Support installation, commissioning, and validating activities for new or modified equipment.
• Assist in structured problem‑solving and implement corrective actions to reduce downtime.
• Collaborate with engineering, technicians, and production teams to support Total Productive Maintenance and continuous improvement initiatives.
• Escalate issues appropriately and communicate equipment status clearly and professionally.
• Support maintenance scheduling, work order execution, and documentation using SAP and Falcony.
• Support spare parts inventory tracking and consumable tracking systems and processes.
• Maintain accurate maintenance records aligned with SOPs, GMP, and ISO requirements.
• Follow all safety standards, lockout/tagout procedures, and company policies.
• May provide limited informal guidance to new team members.
• Perform other duties as assigned.
• This is a fully on‑site position.

• Bachelor’s degree in an Engineering / Technical field or 2+ years of equivalent work experience.
• Knowledge of testing methodologies (ex. software testing).
• Ability to troubleshoot applications and identify root causes of defects.
• Comfortable managing priorities and timelines.
• Detail‑oriented with a focus on accuracy and quality.
• Ability to track testing progress and ensure completion.
• Strong understanding of Windows OS environments.

• Experience developing verification test cases, procedures, plans, analyzing test results, and writing reports.
• Experience on setting up computer workstations and deploying software onto target systems and/or virtual machines.
• Experience in system‑level verification testing in a regulated industry; experience in a medical device industry (21 CFR Part 820.30, ISO
  13485) preferred.
• Knowledge of Medical Device/FDA Regulated Industry and compliance with IEC‑60601, 62304, ISO
  14971, IEC 62366, EU MDR preferred.
• Experience with requirements management (including technical content reviews), design reviews, test reviews, and change control activities.
• Experience using Requirements, Test Case and Incident Management tools (e.g. – Jama, DOORS, JIRA).
• Hands‑on experience with designing, building, and maintaining test fixtures and/or working with external laboratories to perform testing.

• Customer Focus
• Drives Results
• Collaborates
• Nimble Learning
• Resourcefulness
• Decision Quality

$80,100 - $97,800

Nobel Biocare

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