Quality Assurance & Change Management Lead

Carl Zeiss X-ray Microscopy, Inc.; Dublin (CA); On-site; USD 84,000 - 104,000; Full time

Benefits offered by this job

Medical

Vision

Dental

401k Matching

EAP

Paid Time Off

Job summary

Carl Zeiss X-ray Microscopy, Inc. in Dublin, CA is seeking a dedicated quality assurance professional to support business operations, ensure adherence to ISO standards, and drive continuous improvement across engineering, production, and supply chains in a fast-paced environment.

You will oversee daily Change Management activities (ECR/ECO/DCO/PCO), audit quality logs, maintain revision-controlled documents, participate in CAPA and 8D activities, and collaborate with global stakeholders to align

Qualifications

• Bachelor's or equivalent in Mechanical, Electrical or Mechatronics Engineering.
• Strong quality assurance background with ISO standards familiarity.
• Experience with change management and documentation control.

Responsibilities

• Oversee daily Change Management operations (ECR/ECO/DCO/PCO) and related activities.
• Audit quality logs and verify procedures compliance.
• Maintain revision-controlled documents and master data in ERP/MRP systems.
• Lead Investigations using CAPA, 8D methodologies and drive corrective actions.
• Collaborate with cross-functional teams and global stakeholders to improve quality performance.

Skills

Quality mindset

Cross-functional collaboration

Analytical thinking

Document control

CAPA/8D problem solving

Independent worker

Time zone coordination

Education

Mechanical, Electrical or Mechatronics Engineering degree

Tools

SolidWorks

PDM/ERP systems

MS Office

MRP system

Job description

Carl Zeiss X-ray Microscopy, Inc. in Dublin, CA is seeking a dedicated quality assurance professional to support business operations, ensure adherence to ISO standards, and drive continuous improvement across engineering, production, and supply chains in a fast-paced environment.

You will oversee daily Change Management activities (ECR/ECO/DCO/PCO), audit quality logs, maintain revision-controlled documents, participate in CAPA and 8D activities, and collaborate with global stakeholders to align