Production Support Specialist 3rd shift Job Otro

de Empresa en Estado de Mexico
Publicado el 11-10-2016 en Otros

Job Number: #

Business: GE Healthcare
Business Segment:
Healthcare Global Supply Chain
About Us: GE is the world’s Digital Industrial Company, transforming industry
with software-defined machines and solutions that are connected, responsive
and predictive. Through our people, leadership development, services,
technology and scale, GE delivers better outcomes for global customers by
speaking the language of industry.
Posted Position Title: Production Support Specialist 3rd shift
Career Level: Experienced
Function Segment:
Shop Operations
State, China or Canada Provinces:
City: Ciudad Juarez
Postal Code: 32575
Relocation Assistance: No
Role Summary/Purpose: Description: Responsible for coordinating with the
Production Team Leader, Engineering Managers, Production Planner and other
departments of the company to assist with quality improvements of the product
and process.
Essential Responsibilities:
– Coordination of new product introduction into the work center and
participation on Pilot Production Teams, including identifying training needs,
developing work process flows, and identifying specialized tooling
– Ensuring a safe, clean and efficient work area for the employees working in
assigned product area
– Monitoring and reporting all resource issues
– Working with the Group Leaders ensuring product and process quality related
to daily production flow
– Monitoring, reporting and investigation of defects attributed to their
areas through direct interface with the MRB
– Implementing process improvements to improve quality and productivity
levels. Uses Lean concepts to improve efficiency.
– Ensuring that QA procedures and policies are followed within his/her
assigned area
– Ensuring manufacturing documentation used during the production process is
of the correct and most current revision
– Comply with EHS regulations and policies
– Other duties as assigned, and may be asked to be included in quality
activities, training sessions, and employee activity teams
Qualifications/Requirements: Quality Specific Goals:
1. Aware of and comply with Stop Order, Concession, Non-Conforming Material,
Material Identification & Segregation, Documentation Configuration Control,
Good Documentation Practices, Approved Supplier/Sourcing & DMR/DHR
requirements as associated with this job type/position.
2. 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
3. Complete all planned Quality & Compliance training within the defined
4. Identify and report any quality or compliance concerns and take immediate
corrective action as required
5. Training: Aware of and comply with GEHC training requirements
– High School Diploma or local equivalent
– 5 or more years of related manufacturing experience
– Ability to communicate, receive and understand instructions regarding
duties to be performed Preferred Qualifications:
– Associates degree or local equivalent and 3 years of related experience or;
– Bachelors degree
– Prior experience working in a medical device manufacturing environment
– experience in GMP work environment
Additional Eligibility Qualifications:
Desired Characteristics: N/A

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