Quality Specialist Salary at Rr Donnelley & Sons Co BETA

Chicago Public Schools (CPS) is one of the largest school districts in the United States, serving over 320,000 students in 600+ schools and employing approximately 40,000 people, most of them teachers. CPS has set ambitious goals to ensure that every student, in every school and every neighborhood, has access to a world-class learning experience that prepares each for success in college, career, and civic life. In order to fulfill this mission, we make three commitments to our students, their families, and all Chicagoans: academic progress, financial stability, and integrity. Six core values are embedded within these commitments - student-centered, whole child, equity, academic excellence, community partnership, and continuous learning. The Office of Innovation and Incubation (I&I) provides incubation, management, and oversight of charter, contract, and alternative schools as options for CPS students and families. I&I also leads the district's Academic RFP process, which provides schoo

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Come to work each day with an inclusive and collaborative Business technology team! As an Digital Health Quality Specialist in AbbVie Business Technology Solutions (BTS), youll have opportunities to contribute to the digital transformation of a leading biopharma company, helping to create solutions that impact patients and their communities for the better. ***This is a hybrid role based in Lake County, IL*** Primarily responsible for representing Q

POSITION TITLE: PPAP Coordinator Rev. 01/2025 REPORT TO: Quality Manager POSITION SUMMARY: The PPAP (Production Part Approval Process) Coordinator is responsible for ensuring customer and company quality requirements are met. This will include preparation and review of PPAP documentation, responding to customer requirements for any customer mandated quality initiatives related to PPAP process, and interacting with Inspectors, Engineering, Production, and customers as needed. May perform other duties as assigned by the Quality engineer or Quality Manager. Responsibilities PPAP Management (70% of the time) • Performs, maintains, and submits PPAP’s, to assure builds meet the drawing and the specifications of the customer. • PPAP’s to include PFMEA, Control Plan, Dimensions, Print notes, PSW, Product Specs, Ballooned Print, Pictures, CPK’s, MSA and performance test. • Creates 1st piece inspection folders per Control plan as required. • Verification of supplier PPAP’s and maintains traceabi

Job Summary This role specializes in one or two particular subsection(s) of our Quality Management System (e.g. Device Master Records, customer complaint, product hold, recalls, incoming quality). Responsible for basic building and maintaining quality documentation and processes such as product specifications, manufacturing tolerances, engineering drawings, inspection criteria, testing reports, ERP system analysis, customer complaint analysis and validations. Job Description Responsibilities: Assist in the development and implementation of processes, reports, data analysis and procedures within the defined area of specialization. Collaborate with multiple groups (both internal and external) to solve complex problems and continue to ensure compliance is maintained with FDA, ISO and internal requirements. Facilitate meetings with global business units, sales, marketing, branch personnel to manage project requirements and deadlines. Track and report progress periodically to management. Re

As a Quality Specialist, you will ensure high-quality product production through rigorous inspection, testing, and adherence to ASME and ISO 9001 standards. This role involves conducting inspections, managing regulatory compliance, and implementing quality controls to meet product and process specifications. Key Responsibilities: Perform inspections (incoming, in-process, final) to ensure products meet QMS and regulatory standards before shipment. Coordinate ASME product testing and report results. Document verification and validation reports, securing sign-offs from Authorized Inspectors (A.I.) as needed. Verify product drawings and specifications for ASME compliance. Manage the ASME Welder training and certification program. Stay updated on ASME code changes and update internal documentation. Evaluate manufacturing processes and inspection methods for effectiveness and cost reduction. Lead the Non-Conforming Product (NCP) process, including investigation and trend tracking. Participa

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. **_Quality Specialist_** **Working at Abbott** At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Youll also have access to: + Career development with an international company where you can grow the career you dream of. + Free medical coverage for employees* via the Health Investment Plan (HIP) PPO + An excellent retirement savings plan with high employer contribution + Tuition reimbursement, the Freedom 2 Save (https://www.abbott.com/corpnewsroom/strategy-and-strength/tackling-student-debt-for-our-employees.html) student debt program and FreeU (https://www.abbott.co

**The Opportunity** This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. + Reporting compliance status data to operational quality management + Collaborate with center management in the development and implementation of continuous improvement plans + Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concerns + Responsible for coordinating and managing training activities, policies and processes at the center level. You will report to the Assi

**Requisition ID: 279329** + **Relocation Authorized: None** + **Telework Type: Full-Time Telework** + **Work Location: Chicago, IL** # Extraordinary teams building inspiring projects: Since 1898, we have helped customers complete more than 25,000 projects in 160 countries on all seven continents that have created jobs, grown economies, improved the resiliency of the world's infrastructure, increased access to energy, resources, and vital services, and made the world a safer, cleaner place. Differentiated by the quality of our people and our relentless drive to deliver the most successful outcomes, we align our capabilities to our customers' objectives to create a lasting positive impact. We serve the Infrastructure; Nuclear, Security & Environmental; Energy; Mining & Metals, and the Manufacturing and Technology markets. Our services span from initial planning and investment, through start-up and operations. Core to Bechtel is our Vision, Values and Commitments . They are what we belie