Job Description Summary

Engineering associated with the manufacturing process. Impacts departmental operations and responsible for planning/execution. The role has some autonomy but is focused on execution of activities within an operating discipline covered by standard functional practices and procedures. Some judgment may be required but this is typically with guidance.

Job Description

This Job is responsible for:

Design transfer:

• Lead the design transfer activities of product specifications to manufacturing by working with global design owners and local partners.

• Review the design specifications feasibility in terms of assembly and test, make sure that production constrains are respected.

• Define and validate production and test processes including production instructions and reports.

• Coordination of manufacturing releases

• Lead the manufacturing documentation development and release

Manufacturing process set up, validation and continuous improvement:

• Drive improved product quality by identifying manufacturing issues, developing cost-effective solutions, and overseeing successful implementation into production.

• Work with contract manufacturing supplier’s production associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment and product design.

• Monitor and optimize contract manufacturing supplier’s workstations designs and manufacturing cycle time

• Actively support lean, continuous improvement and design for manufacturing initiatives.

• Monitor and improve productivity, while ensuring all customer commitments are met in a timely, quality and cost-conscious manner

• Maintain (calibration and verification support) and troubleshoot production equipment

• Define, validate and control production process including tooling and equipment. Work with local and global suppliers to purchase and maintain them.

• Validate design specifications and shop floor application of new product, tools, or equipment.

• Specify and expedite planned maintenance routines on all production equipment and systems.

• Work closely with regulatory affairs department to support the compliance with all local regulations.

• Define and support local parts purchases and validation process according to GE HealthCare quality procedures.

• Design the production layout and assure the conformity to EHS policy and to local regulations.

• Act as a materials change coordinator or/and manufacturing process leader: be the contact point for design or process change communications and lead the implementation of changes in cooperation with supplier quality engineer (SQE)

• Provide guidance and expertise to manufacturing engineer

Quality control:

• Responsible for determining processes requiring validation, development of plans and analysis criteria, execution and final analysis.

• Ensuring regulatory compliance through Validation & Verification.

• Lead quality metrics follow up and control in production and drives process quality improvements and simplification

• Assure that corrective action is taken to resolve observed safety concerns in all areas.

• Support and follow up contract manufacturing supplier’s CAPA cases management.

• Support SQE & follow up for contract manufacturing supplier’s SCAR’s

• Ensure compliance to GE HealthCare quality procedures and local regulations.

Minimum Requirements:

• B.S. Degree in Mechanical, Electrical, Industrial Engineering or related technical degree

• 7 years of experience in production, engineering

• Good analytical and planning skills

• Excellent English (Writing & Communicating)

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