ZipRecruiter
Overview
Job Title:
Supplier Quality Engineer Duration:
9+ Months (Possible temp to hire) Location:
Arden Hills, MN 55112 Hybrid Role:
3 days a week Responsibilities
The Supplier QA Engineer will play a key part in leading performance improvement of suppliers and increasing the suppliers’ capabilities to consistently meet client's requirements.
Will support Global Sourcing, supplier manufacturing operations, and global quality systems by participating in global communities of practice and value improvement projects
Drives improvement and corrective actions in the quality of components sourced from outside suppliers.
Assess & drive reactive as well as proactive supplier project(s)/investigations partnering with Supplier Engineering, Manufacturing/Test operations, Commercial Sourcing, Design Assurance, R&D
Develops solutions to a variety of complex problems of diverse scope and complexity where analysis of data requires evaluation of identifiable factors.
Plans and organizes non-routine tasks with approval.
Initiates or maintains work schedule and priorities. Plans and organizes project assignments and maintains project schedules
Interprets, executes and recommends modifications to company policies.
Assists in establishing departmental policies and procedures. Work is reviewed upon completion for adequacy in meeting objectives
Establishes and cultivates a wide range of business relationships to facilitate completion of assignments. Interacts with suppliers.
Participates in determining goals and objectives for projects.
Contributes to the completion of specific programs and projects.
Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources
Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the Quality Policy.
Education/Experience
BS degree in an Engineering related field, such as: Mechanical Engineering, Materials Engineering, Chemical Engineering, Electrical Engineering, or similar technical degree with 1-2 years related experience.
Experience in Quality Management Systems, regulatory compliance, and risk management.
People with Med device QMS or experience working with Manufacturing.
Experience with problem solving quality tools,
Corrective/Preventive
Actions (CAPA), Technical Documentation
Qualifications:
Experience with or lead auditor certification to ISO 13485, 9001, TS 16949 standards
Ability to communicate cross functionally with suppliers, team members and leadership
Company Description
Opportunity to work with a large company
#J-18808-Ljbffr
Job Title:
Supplier Quality Engineer Duration:
9+ Months (Possible temp to hire) Location:
Arden Hills, MN 55112 Hybrid Role:
3 days a week Responsibilities
The Supplier QA Engineer will play a key part in leading performance improvement of suppliers and increasing the suppliers’ capabilities to consistently meet client's requirements.
Will support Global Sourcing, supplier manufacturing operations, and global quality systems by participating in global communities of practice and value improvement projects
Drives improvement and corrective actions in the quality of components sourced from outside suppliers.
Assess & drive reactive as well as proactive supplier project(s)/investigations partnering with Supplier Engineering, Manufacturing/Test operations, Commercial Sourcing, Design Assurance, R&D
Develops solutions to a variety of complex problems of diverse scope and complexity where analysis of data requires evaluation of identifiable factors.
Plans and organizes non-routine tasks with approval.
Initiates or maintains work schedule and priorities. Plans and organizes project assignments and maintains project schedules
Interprets, executes and recommends modifications to company policies.
Assists in establishing departmental policies and procedures. Work is reviewed upon completion for adequacy in meeting objectives
Establishes and cultivates a wide range of business relationships to facilitate completion of assignments. Interacts with suppliers.
Participates in determining goals and objectives for projects.
Contributes to the completion of specific programs and projects.
Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources
Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the Quality Policy.
Education/Experience
BS degree in an Engineering related field, such as: Mechanical Engineering, Materials Engineering, Chemical Engineering, Electrical Engineering, or similar technical degree with 1-2 years related experience.
Experience in Quality Management Systems, regulatory compliance, and risk management.
People with Med device QMS or experience working with Manufacturing.
Experience with problem solving quality tools,
Corrective/Preventive
Actions (CAPA), Technical Documentation
Qualifications:
Experience with or lead auditor certification to ISO 13485, 9001, TS 16949 standards
Ability to communicate cross functionally with suppliers, team members and leadership
Company Description
Opportunity to work with a large company
#J-18808-Ljbffr