Manufacturing Specialist 1 - Prod Process and Equip_HC at GE HealthCare

**Who this is for** This role is for a detail-oriented Manufacturing Specialist who will support product and production processes through system and document co

Work type: unknown

Location: WuXi

Type: Full-time

Summary

**Who this is for** This role is for a detail-oriented Manufacturing Specialist who will support product and production processes through system and document control, tooling design, and continuous improvement initiatives. You will focus on safety, quality, delivery, and cost reduction. **Key highlights** As a Manufacturing Specialist 1 at GE HealthCare, you will play a key role in enhancing product quality and production efficiency. Responsibilities include developing system solutions, managing validation processes, creating standardized documentation, and driving LEAN manufacturing implementation. **You might be a good fit if you...** - Have a B.S. Degree in Mechanical, Electrical, Industrial Engineering or a related technical degree with 3 years of experience in supply chain, engineering, or tooling design. - Demonstrate experience owning production processes, quality systems, audit, and document control. - Possess good data analysis skills and communication abilities with various functional teams. - Are eager to lead digital & automation manufacturing transformation and LEAN initiatives.

Job Description

# Job Description Summary

As this role you will support the the product and production process as system/document controller and tooling design, as well as other process improvement requirements for the product and system. Responsibilities include safety, quality, delivery, cost, and need to use methodology and system thinking to meet tools, documentation, on-site requirements. Lead new processes and tooling design, do a good job in product quality and delivery risk control, and continuously improve production efficiency and reduce product costs.

GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.tex

# Job Description

Role Summary/Purpose

• Provide system/document control support for the production team. Responsibilities include providing documentation and floor support associated with safety, manufacturing and quality methods, tooling, and equipment. Aggressively initiate new processes and methods that will improve safety, productivity, reduce product cost and/or improve product quality.

• Drive improved product quality by identifying manufacturing process issues, developing system solutions with document control, and overseeing successful implementation into production.


• Work with QA\Production\Design and all function team to resolve manufacturing and quality system problems related to methods, processes, tooling, equipment and product design.


• Ensuring regulatory compliance through Validation & Verification. Responsible for determining processes requiring validation, development of plans and analysis criteria, execution and final analysis and acceptance.


• Develop new process and system document to control the risk and standardized document level work by lean.


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


• Co-ordination of manufacturing releases per engineer change request.


• Lead Compliance, as well as Environmental, Health & Safety efforts in support of plant goals


• Driving LEAN manufacturing implementation


• Lead and drive digital & automation manufacturing transformation

• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position


• Complete all planned Quality & Compliance training within the defined deadlines


• Identify and report any quality or compliance concerns and take immediate corrective action as required


• Knowledge and understanding of document control, design transfer, verification, validation, acceptance activity, DMR, DHR and electronic signature requirements to ensure that product, equipment, tools, processes, software, training and documentation meet requirements.

• B.S. Degree in Mechanical, Electrical, Industrial Engineering or related technical degree with 3 years of experience in supply chain or engineering or tooling design.


• Demonstrated experience owning production processes, and quality system, audit and document control.


• Good data analysis skill or A3 report.


• Good communication Skills with different function team including engineer, supply chain.


• Project management experience (acting as leader) is preferred.

• Preferred Qualifications:

Inclusion and Diversity

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