Automation Engineer

Job description

3435420
Additional Cities

Logan
Career Level

Experienced
Relocation Assistance

Yes
Business

GE Healthcare
Business Segment

Healthcare BioPharma
Function

Manufacturing
Country/Territory

United States
Additional States/Provinces

Utah
Postal Code

84321
Role Summary/Purpose

Plan the day to day execution and technical support for the introduction of processes for new product development and existing manufacturing. Support efforts to consistently improve product and process quality. This role is recognized as a key manufacturing technology leader within their organization. Interface with global counter-parts to achieve program goals and integrate global activities when necessary.
Essential Responsibilities

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

·  Work with manufacturing leadership to identify and resolve manufacturing and quality
problems related to methods, processes, tooling, equipment and product design
·  Monitor and
improve productivity through the use of Lean Six Sigma or related tools, while ensuring all
customer commitments are met in a timely, quality and cost-conscious manner

·  Participate in early focus on manufacturability in NPI and/or Advanced Technology programs.
Drive rigor in process capability assessment, process layout, tooling and equipment development
and QMS Design Transfer execution

·  Clearly understand existing processes in order to provide support for manufacturing process
technology roadmap

·  Support and execute AME initiatives with wide business impact and ensure to share best
practices across the Global Supply Chain

·  Drive AME initiatives across sites while providing business-wide impact and enabling sharing
of best practices across the Global Supply Chain

·  Ensure regulatory compliance through Qualification & Validation. Responsible for ensuring
rigor in determining processes requiring validation, development of plans and analysis

·  criteria, execution and final analysis and acceptance

·  Help execute continuous simplification of QMS methods and their applications by working with
cross-functional team including Operations and Quality Assurance. Work with the facilities and
maintenance team to implement change and ensure the required product capacity is in place
before it is required by customer demand 

Quality Specific Goals: 

·  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 
·  Drive continuous improvement on all related processes, work instructions, and procedures to ensure ongoing standardization and simplification of the Quality Management System.

Candidates should note that this role will be in scope for the proposed transition of GE Biopharma to Danaher and will transfer to Danaher at close of this transaction. 

Qualifications/Requirements

·  B.S. Degree in Mechanical, Electrical, Industrial Engineering OR an Associates Degree and a minimum of 3 years experience in production, engineering or troubleshooting of PC/server based systems, OR High School diploma with a minimum of 5 years of experience in production, engineering or troubleshooting of PC/server based systems 
·  Demonstrated troubleshooting, analytical and planning skills 
·  Ability to work independently 
·  Demonstrated strong communication skills (written and verbal)
Desired Characteristics

·  MS/PHD in technical concentration/field

·  Co-op or internship experience in Manufacturing Engineering

·  6-sigma DMAIC & DFSS certified

·  Experiences in Process Intensive manufacturing

·  Product and Process Development experience

·  Solid working knowledge of GEHC QMS procedures for GMP

·  Experienced developing tools and templates

·  Demonstrated program or project management skills

·  Demonstrated experience owning production processes / growing capability in yield and quality

·  Experience working with global teams
About Us

There is no other life sciences company quite like GE Healthcare Life Sciences. A $5 billion business with more than 11,000 individuals in over 100 countries, we are at work enabling a new era in medicine. For more than 60 years, GE Healthcare Life Sciences has globally supported the development and use of new therapies, helping accelerate the journey from biological understanding to clinical therapy. GE Healthcare Life Sciences works with cutting edge technology enabling and advancing the discovery, diagnosis and medical treatments of the present and the future. We are accelerating biology to cell therapy in ways no other company can. 

Follow us on Facebook and Twitter and watch our discoveries in action on our YouTube channel.
Learn More About GE Healthcare – Life
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Learn More About Careers at GE Healthcare – Life
Sciences

GE offers a great work environment, professional development, challenging careers, and competitive compensation. GE is anEqual Opportunity Employer . Employment decisions are made without regard to race, color, religion, national or ethnic origin, gender (including pregnancy), sexual orientation, gender identity or expression, age, disability, veteran status or any other characteristics protected by law.
Additional Eligibility Qualifications

GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
Primary Country

United States
Primary State/Province

Utah
Primary City

Logan