At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER.
With over 60, diverse, talented and dedicated employees across locations in countries, our vision is to be the most technologically advanced and trusted manufacturing provider.
We combine an unmatched breadth and depth of end-market Importante empresa, technical and design capabilities, manufacturing know-how, supply chain insights and global product management expertise to enable succer the world's leading brands.
We are driven by a common purpose to make a positive impar each other, our communities, and the environment.Works under the direction of the Assurance Organization and is responsibr providing direct support to the QA Team and Operationnctions to achieve, efficiency, and cost targets, while ensuring compliance to all applicable standards.ESSENTIAL DUTIES AND RESPONSIBILITIES Assurance resource supporting activities and initiatives related but not limited to operationnctions and materials contror example, involvement in activities related to rework, in process inspections, document / records reviews and product release.
Support activities, as needed, related to customer complaint investigation and sample / product analysis process.
Support and serve as a resourr issues including but not limited to nonconformanilure investigations, assisting in establishing scope or nt of non-conformances (bounding/bracketing), assist in determination / completion of risk assessment, rework activities and product release.
Work closely with QA Technicians Senior and level II in base business related activities to ensure adequate operations support Provide Assurance suppor EES-Albuquerque operations.
Support QA Team on a daily basis in related activities deliverables.
Works in the different áreas of Assurance based on business needs.
Supports Operationnctions,, Engineering and others to ensure objectives are met.
Supports Operationnctions,, Engineering and others, as needed, in the implementation of corrections / corrective actior identified issues, through the use of principles and data.
Executes protocols as necessary.
Performs tests and data analyses to recommend disposition of material.
Responsibr monitoring and reporting QA holds.
Responsibr the control and monitoring of the QA holdárea.
Completes records of inspection results, acceptance, rejection, and disposition of material.
Interpret and execute statistical analyses, as needed, including but not limited EA and SPC.Support Operationnctions, Assurance among others in continuous improvement activities as they relate to the reduction of product inquiries, efficiencies and or other initiatives.
Maintain knowledge of all procedures, change to specifications (Process, Confidencial Manuals, Material Specifications, etc.), and regulations related to their área of responsibility.
Maintain process knowledr the assigned área of responsibility.
Provide materials/communication or service to customers in a timely manner.
Recommends revisions, corrections, and changes to test equipment, procedures, and methods.
Provide initiative to the QA organization through continuous improvement projects.
Provide necessaedback to customersters collaborative discussions with business partners regarding issues, projects, and activities as required.
Manages varying circumstances and changing conditions as multiple situations may have to be addressed at the same time.
Support / Provide coverar absences as required.
Work cooperatively toward effective outcomes.
Work to resolve differences in a collaborative efforllow all company safety policies and other safety precautions within the work área.
Promote safety to all that enter the work área.
Attend required safety Confidencial Participate in implementation of the EMS management system including continual improvement, pollution prevention, objectives and targets, and regulatory compliance.
Implement allow all applicable EMS procedures.
Adhere to the site's EHS Code of Conduct.
Other responsibilities may be assigned and not all responsibilities listed may be assigned.MANAGEMENT & SUPERVISORY RESPONSIBILITIES Job is NOT directly responsibr managing other employees (e.G., hiring/termination and/or pay decisions, performance management).JOB QUALIFICATIONSKNOWLEDGE REQUIREMENTS Knowledge of product and process specifications.
General knowledge of medical devices preferred.
Knowledge of Good Manufacturing Practices (GMPs) and ISO (International Organizatir Standardization) policy And procedures is preferred.EDUCATION & Importante empresa REQUIREMENTS High school diploma or equivalent required.
Two ur years of Importante empresa within manufacturing operations, preferably in the