Quality Change Specialist
Indianapolis, IN Indianapolis, IN Contract Contract $25.
97 an hour $25.
97 an hour 11 hours ago 11 hours ago 11 hours ago Title:
Quality Change Specialist Location:
Indianapolis, IN Start date:
ASAP Our client is looking for the following:
Responsibilities:
Responsible for the management and processes of the PLM and MDG-M systems.
Monitors progress of workflows, helps facilitate issues during the workflow, and escalates as needed.
Assumes the role of a Change Coordinator or Content Manager as needed.
Prepares and/or revises departmental procedures within PLM Engineering scope.
Participates on cross-functional project teams to provide documentation and distribution expertise.
Also provides appropriate support to help transfer new products into production.
Collaborates on complex changes and provides guidance and understanding to users to process changes through the system quickly and efficiently.
Reviews and ensures that change requests and change notices move through the system accurately and efficiently.
Acts as liaison between departments and quality assurance, quality systems, etc.
Supports Process Leads on internal project work.
Exercises good time management and project management skills Works with the Global PLM team to ensure system accuracy and completeness of change management, document control, and materials management.
Participates on and leads special projects as assigned.
Supports LCM activities/changes throughout the product lifecycle.
Distributes documentation and software to internal customers, vendors, affiliates, and manufacturing partners.
With the following credentials:
Requirements:
High school diploma.
3 years' related experience.
Strong communication, influence, leadership, conflict management, negotiation, and writing skills.
Proficiency with office software.
Strong communication, customer service, and interpersonal skills.
Ability to work independently, multi-task, and adjust rapidly to new priorities.
Excellent organizational, time management and analytical skills.
Demonstrated competency in taking initiative.
Detail oriented.
Ability to handle multiple functions at one time.
Bachelor's degree preferred.
Previous experience in a regulated industry preferred.
Windchill and SAP experience preferred.
Good understanding of the regulations that govern the medical device industry and the policies needed for effective change control.
Solid understanding of manufacturing and inventory management procedures.
System One offers eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
Title:
Quality Change Specialist Location:
Indianapolis, IN Start date:
ASAP Our client is looking for the following:
Responsibilities:
Responsible for the management and processes of the PLM and MDG-M systems.
Monitors progress of workflows, helps facilitate issues during the workflow, and escalates as needed.
Assumes the role of a Change Coordinator or Content Manager as needed.
Prepares and/or revises departmental procedures within PLM Engineering scope.
Participates on cross-functional project teams to provide documentation and distribution expertise.
Also provides appropriate support to help transfer new products into production.
Collaborates on complex changes and provides guidance and understanding to users to process changes through the system quickly and efficiently.
Reviews and ensures that change requests and change notices move through the system accurately and efficiently.
Acts as liaison between departments and quality assurance, quality systems, etc.
Supports Process Leads on internal project work.
Exercises good time management and project management skills Works with the Global PLM team to ensure system accuracy and completeness of change management, document control, and materials management.
Participates on and leads special projects as assigned.
Supports LCM activities/changes throughout the product lifecycle.
Distributes documentation and software to internal customers, vendors, affiliates, and manufacturing partners.
With the following credentials:
Requirements:
High school diploma.
3 years' related experience.
Strong communication, influence, leadership, conflict management, negotiation, and writing skills.
Proficiency with office software.
Strong communication, customer service, and interpersonal skills.
Ability to work independently, multi-task, and adjust rapidly to new priorities.
Excellent organizational, time management and analytical skills.
Demonstrated competency in taking initiative.
Detail oriented.
Ability to handle multiple functions at one time.
Bachelor's degree preferred.
Previous experience in a regulated industry preferred.
Windchill and SAP experience preferred.
Good understanding of the regulations that govern the medical device industry and the policies needed for effective change control.
Solid understanding of manufacturing and inventory management procedures.
System One offers eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
97 an hour $25.
97 an hour 11 hours ago 11 hours ago 11 hours ago Title:
Quality Change Specialist Location:
Indianapolis, IN Start date:
ASAP Our client is looking for the following:
Responsibilities:
Responsible for the management and processes of the PLM and MDG-M systems.
Monitors progress of workflows, helps facilitate issues during the workflow, and escalates as needed.
Assumes the role of a Change Coordinator or Content Manager as needed.
Prepares and/or revises departmental procedures within PLM Engineering scope.
Participates on cross-functional project teams to provide documentation and distribution expertise.
Also provides appropriate support to help transfer new products into production.
Collaborates on complex changes and provides guidance and understanding to users to process changes through the system quickly and efficiently.
Reviews and ensures that change requests and change notices move through the system accurately and efficiently.
Acts as liaison between departments and quality assurance, quality systems, etc.
Supports Process Leads on internal project work.
Exercises good time management and project management skills Works with the Global PLM team to ensure system accuracy and completeness of change management, document control, and materials management.
Participates on and leads special projects as assigned.
Supports LCM activities/changes throughout the product lifecycle.
Distributes documentation and software to internal customers, vendors, affiliates, and manufacturing partners.
With the following credentials:
Requirements:
High school diploma.
3 years' related experience.
Strong communication, influence, leadership, conflict management, negotiation, and writing skills.
Proficiency with office software.
Strong communication, customer service, and interpersonal skills.
Ability to work independently, multi-task, and adjust rapidly to new priorities.
Excellent organizational, time management and analytical skills.
Demonstrated competency in taking initiative.
Detail oriented.
Ability to handle multiple functions at one time.
Bachelor's degree preferred.
Previous experience in a regulated industry preferred.
Windchill and SAP experience preferred.
Good understanding of the regulations that govern the medical device industry and the policies needed for effective change control.
Solid understanding of manufacturing and inventory management procedures.
System One offers eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
Title:
Quality Change Specialist Location:
Indianapolis, IN Start date:
ASAP Our client is looking for the following:
Responsibilities:
Responsible for the management and processes of the PLM and MDG-M systems.
Monitors progress of workflows, helps facilitate issues during the workflow, and escalates as needed.
Assumes the role of a Change Coordinator or Content Manager as needed.
Prepares and/or revises departmental procedures within PLM Engineering scope.
Participates on cross-functional project teams to provide documentation and distribution expertise.
Also provides appropriate support to help transfer new products into production.
Collaborates on complex changes and provides guidance and understanding to users to process changes through the system quickly and efficiently.
Reviews and ensures that change requests and change notices move through the system accurately and efficiently.
Acts as liaison between departments and quality assurance, quality systems, etc.
Supports Process Leads on internal project work.
Exercises good time management and project management skills Works with the Global PLM team to ensure system accuracy and completeness of change management, document control, and materials management.
Participates on and leads special projects as assigned.
Supports LCM activities/changes throughout the product lifecycle.
Distributes documentation and software to internal customers, vendors, affiliates, and manufacturing partners.
With the following credentials:
Requirements:
High school diploma.
3 years' related experience.
Strong communication, influence, leadership, conflict management, negotiation, and writing skills.
Proficiency with office software.
Strong communication, customer service, and interpersonal skills.
Ability to work independently, multi-task, and adjust rapidly to new priorities.
Excellent organizational, time management and analytical skills.
Demonstrated competency in taking initiative.
Detail oriented.
Ability to handle multiple functions at one time.
Bachelor's degree preferred.
Previous experience in a regulated industry preferred.
Windchill and SAP experience preferred.
Good understanding of the regulations that govern the medical device industry and the policies needed for effective change control.
Solid understanding of manufacturing and inventory management procedures.
System One offers eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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