Manufacturing Engineer

GE Healthcare

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.