Quality Officer Salary at Fan BETA

Job Description Job Description Working with the State of Illinois is a testament to the values of compassion, equity, and dedication that define our state. Whether you’re helping to improve schools, protect our natural resources, or support families in need, you’re part of something bigger—something that touches the lives of every person who calls Illinois home. No matter what state career you’re looking for, we offer jobs that fit your life and your schedule—flexible jobs that provide the gold standard of benefits. Our employees can take advantage of various avenues to advance their careers and realize their dreams. Our top-tier benefits and great retirement packages can help you build a rewarding career and lasting future with the State of Illinois. The Illinois Department of Public Health is seeking a highly motivated individual to serve as Laboratory Quality Specialist 2. This position will perform duties including performing internal CLIA, ISO 17025, OSHA and Select Agent audits,

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

Quality Specialist Crete Analytical Laboratory Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Quality Specialist in 3600 Eagle Nest Dr, North Building, Crete, IL 60417 USA. Your mission will be to: Organize, prepare and maintain documentation of laboratory quality control efforts required for audits. Complete qu

**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

Quality Specialist Location: Chicago, IL Pay: $25-31/HR, based on experience Shift: M-F, 8:30AM to 5:30PM Qualifications: A minimum of a BA or BS in Biological Sciences or a related technical field is required. Prior experience in the pharmaceutical industry is a must Familiarity with regulatory compliance standards Responsibilities: Support the manufacturing team with various documentation tasks. Review executed batch records across multiple departments (Drug Product, Secondary Packaging, Upstream, and Downstream). Manage filing of change controls, deviations, and CAPAs within the manufacturing department. Track and ensure the timely closure of QMS documents. Utilize investigation tools such as the 5Why or 6M method for critical/major investigations. Collaborate with cross-functional teams to ensure timely closure of investigations and QMS action items. Author batch records, SOPs, and related forms required for manufacturing processes. Submit all GMP documents to QA for review and app

**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

Job Description Job Description Position Overview The Quality Management System (QMS) Specialist supports Formerra’s Quality Program by completing administrative duties to ensure the QMS is up-to-date, internal and external quality assessments are appropriately completed, and documentation and other training resources are available. The QMS Specialist works cross-functionally to align procedures with current state operational processes and identify process improvements. Essential Duties and Responsibilities: Conduct internal quality audits to ensure compliance to the ISO 9001:2015 standard and local procedures. Facilitate customer QMS audits of Formerra and its third-party logistics warehouse providers. Support ISO certification audits from preparation to completion. Ensure corrective and preventative actions (CAPA) are entered into the QMS software, ownership is appropriately assigned, and root cause analysis is completed. Complete customer surveys/questionnaires and other requests fo

Boldly innovating to create trusted solutions that detect, predict, and prevent disease. Discover your power to innovate while making a difference in patients' lives. iRhythm is advancing cardiac care...Join Us Now! At iRhythm, we are dedicated, self-motivated, and driven to do the right thing for our patients, clinicians, and coworkers. Our leadership is focused and committed to iRhythm's employees and the mission of the company. We are better together, embrace change and help one another. We are Thinking Bigger and Moving Faster. About this Role: iRhythm is currently seeking a Quality Operations Manager for its facility located in Deerfield, IL. The Quality Operations Manager will provide quality direction and tactical support to the reverse logistics intake operations, and the clinical operations teams. The role is responsible for all aspects of quality, compliance and execution of the site quality management system supporting intake operations and clinical operations. Our work envi