At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the worlds top brands offering comprehensive engineering manufacturing and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

JOB SUMMARY
Develops and implements quality plans programs and procedures using quality control statistics lean manufacturing concepts and analyses. Ensures that performance and product quality conforms to established company customer and regulatory requirements. Reviews analyzes and reports on quality discrepancies related to assembly and process. Leads investigation of problems and develops dispositions modifications and corrective actions for recurring or non-recurring discrepancies. Interfaces with manufacturing engineering customer vendor and subcontractor representatives to ensure requirements are met. Has primary responsibility for planning and implementing the positions key responsibilities as they apply to new product introduction.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Leads the development modification and maintenance of quality evaluation and control plans and protocols for processing materials into partially finished or finished products.
Leads the development and implementation of methods and procedures for inspecting testing and evaluating the precision and accuracy of products and production equipment.
Leads the design and analysis of inspection and testing processes mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine responsibility for products or materials that do not meet required standards and specifications.
Assists with managing Part Files that define statistical analysis requirements and any associated control limits as needed for Predisys SPC/SPC.
Audits quality systems for deficiency identification and correction.
Assists in the process for ensuring that corrective actions (CAPA) are completed in accordance with relevant ISO requirements (ISO 9001 and ISO 13485) Nypro Advance Problem Solving methods and that documentation is complete and compliant with requirements.
May specialize in the areas of design incoming material production control product evaluation and reliability inventory control and/or research and development as they apply to product or process quality.
May provide direction and mentoring to less experienced QA Engineers.
Demonstrated competence in Quality Engineering body of knowledge.
Writes reviews approves process validations/qualifications in accordance with Nypro and customer requirements.
Assist in the preparation of Drug Master Files (DMF) submissions (Healthcare GBU only) and Reports. DMFs are to be submitted by Nypros Official Correspondent to the FDA.
Support plant Quality System software validation as needed.
May manage the internal supplier third party and FDA quality audits.
Support all company safety and quality programs and initiatives.
May perform other duties and responsibilities as assigned.
JOB QUALIFICATIONS
KNOWLEDGE REQUIREMENTS

Proficiency in use of personal computers Microsoft Office products (Excel Word and PowerPoint) and e-mail skills required.

Job Summary

The Quality Systems Coordinator at Jabil Inc. plays a vital role in maintaining and improving the companys Quality Management System (QMS). This position ensures compliance with internal procedures industry standards and regulatory requirements contributing to the consistent delivery of high-quality products and services.

Job Responsibilities

* Assist in the development implementation and maintenance of the Quality Management System (QMS) in accordance with relevant standards (e.g. ISO 9001 TL9000 ANSI/ESD S20.20 AS9100 ISO 13485).
* Coordinate and support global internal and external quality audits including scheduling facilitating and documenting findings.
* Manage and track corrective and preventive actions (CAPAs) ensuring timely closure and effectiveness verification.
* Maintain accurate and up-to-date quality documentation including procedures work instructions forms and records.
* Support the control of non-conforming materials and processes including documentation disposition and root cause analysis.
* Facilitate quality training programs for employees ensuring awareness and adherence to QMS requirements.
* Participate in continuous improvement initiatives and projects aimed at enhancing product quality and process efficiency.
* Prepare and present quality performance data and reports to management.
* Collaborate with various departments (e.g. Engineering Operations Supply Chain) to ensure quality requirements are met throughout the product lifecycle.
* Assist in the management of calibration activities for equipment and instruments.

Job Qualifications

* Bachelors degree in a relevant technical field (e.g. Engineering Quality Management Science) or equivalent practical experience.
* 2 years of experience in a quality assurance or quality control role preferably within a manufacturing environment.
* Familiarity with Quality Management Systems (QMS) and relevant industry standards (e.g. ISO 9001 TL9000 ANSI/ESD S20.20 AS9100 ISO 13485).
* Strong understanding of quality tools and methodologies (e.g. CAPA root cause analysis statistical process control).
* Excellent organizational skills with a strong attention to detail and accuracy.
* Proficient in Microsoft Office Suite (Word Excel PowerPoint).
* Ability to communicate effectively both verbally and in writing with all levels of the organization.
* Proven ability to work independently and as part of a team in a fast-paced environment.
* Experience with audit processes and documentation.

* Product regulatory compliance
* Certification in quality (e.g. ASQ Certified Quality Assistant Internal Auditor) is a plus.

* Lead Auditor is a plus

TEN CUIDADO CON LOS FRAUDES: Las oportunidades laborales legítimas en Jabil se pueden encontrar en nuestro sitio web oficial . Ningun solicitante debe pagar para acceder a estas oportunidades de empleo. Al postularte para un empleo en Jabil serás contactado a través del portal oficial de jabil por un correo electrónico con teminacion @; llamada telefónica directa de un integrante del equipo de Jabil; o correo electrónico directo con una dirección de correo electrónico @. Jabil no solicita pagos para realizar entrevistas ni en ningún otro momento durante el proceso de contratación. Jabil tampoco pedirá información personal de identificación como número de seguro social acta de nacimiento información de institución financiera número de licencia de conducir o información de pasaporte por teléfono o correo electrónico. Si crees que estás siendo víctima de robo de identidad o fraude repórtalo a la policía en los siguientes números y repórtala en el sitio web donde la encontraste. Llama a: 911 o 089.

Jabil including its subsidiaries is an equal opportunity employer and considers qualified applicants for employment without regard to race color religion national origin sex sexual orientation gender identity age disability genetic information veteran status or any other characteristic protected by law.

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