At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 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 Nypro’s 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 company's 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
- Bachelor's 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.
TEN CUIDADO CON LOS FRAUDES: Las oportunidades laborales legítimas en Jabil se pueden encontrar en nuestro sitio web oficial Jabil.com. 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 @jabil.com; llamada telefónica directa de un integrante del equipo de Jabil; o correo electrónico directo con una dirección de correo electrónico @jabil.com. 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.
If you are a qualified individual with a disability, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access Jabil.com/Careers site as a result of your disability. You can request a reasonable accommodation by sending an e-mail to
[email protected] with the nature of your request and contact information. Please do not direct any other general employment related questions to this e-mail. Please note that only those inquiries concerning a request for reasonable accommodation will be responded to.
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