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Duration: Permanent

2-5 years of experience in manufacturing and/or process engineering.

Development of specifications and user requirements for new equipment that support manufacturing operations

Planning, development, and execution of equipment/process qualifications as it relates to CNC machining, manufacturing, inspection, and production readiness

Support development of and author Process Validation/Verification/ Qualification documents, Work Instructions, Manufacturing Specifications, Standard Operation Procedures, etc.

Perform statistical analysis of data to determine process capability

Assess, review, and support the development of product inspection Test Methods and Test Method Validations (TMV’s)

Support cross-functional teams working on equipment/facility commissioning and qualification

Takes ownership of validation/verification deliverables throughout the execution of the Project

Ensures technical deliverables are completed to schedule

May require international travel (up to 10%)

Good to have skills*

Experience working in a regulated industry, such as Medical Device, Pharma or Biotech.

Experience with CMM (Coordinate Measuring Machine) equipment.

Experience in project management.

Experience with machining processes, metal finishing processes, laser processing or production automation.

Knowledge of statistical data analysis and associated tools (e.g. Minitab).

Key responsibilities*

Supports the needs of manufacturing areas in terms of meeting the requirements for quality standards and compliant documentation, capacity, product availability and cost.

Skills:

Worked in Medical Devices, Pharma or Biotech, CMM (Coordinate Measuring Machine) equipment, machining processes, metal finishing processes, laser processing or production automation, statistical data analysis and associated tools (e.g. Minitab).

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Confirmed 7 hours ago. Posted a day ago.

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