Quality manager jobs in Dubuque, IA

LHH Recruitment Solutions has partnered with a growing manufacturing organization, and they are seeking a motivated Quality Manager to join their team. You will play a pivotal role in ensuring the highest standards of product quality and process efficiency. You will champion their Quality Management System (QMS) and lead site-wide quality initiatives. This is a unique opportunity for someone who enjoys being influential on hands-on improvements and a desire to make a tangible impact. Key Responsibilities: Serve as the site lead for all quality audits, including IATF 16949, ensuring compliance and continuous improvement. Oversee and enhance the QMS, designing, communicating, and implementing quality processes from the ground up. Manage and resolve customer complaints, returns, and corrective actions (8D), maintaining robust documentation and timely follow-up. Lead, mentor, and develop a team consisting of one Quality Engineer and four hourly Quality Technicians/Inspectors. Collaborate closely with plant supervisors, operators, and cross-functional teams to resolve quality issues and drive best practices. Conduct internal and external audits, manage supplier quality, and ensure all documentation meets industry standards (QS/ISO/IATF/SPC). Prepare and submit PPAP documentation, and maintain customer-specific requirements, FMEA/PFMEA, and process flow charts. Monitor customer portals for compliance updates and proactively address any issues. Foster a culture of quality through training, coaching, and direct engagement at all levels of the organization. Qualifications and Skills: Bachelor's degree in a technical field. ASQ certifications (CQM, CQE, CQA) are a plus. 5+ years of progressive quality experience within the precision metals or metal cutting industry. Demonstrated leadership experience. Proven track record managing a QMS and leading successful IATF audits. Bilingual proficiency in English and Spanish is highly preferred. Strong technical writing, project management, and problem-solving skills. Hands-on and process improvement mindset. Compensation Range: $110,000 - $130,000 Benefits Offered: 2 weeks of vacation, paid sick leave where applicable by state law, Medical Insurance, Dental Insurance Vision Insurance, 401K, and Life Insurance. If you are a passionate Quality Manager looking for a new and rewarding career, please apply today! You don't want to miss out on this opportunity! LHH is a leader in permanent recruitment-and in the placement of top talent. Our areas of specialty include office administration, customer service, human resources, engineering, and supply chain and logistics. Please feel to check us out and apply for other opportunities if this role isn't a perfect match. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit **************************************

Project Manager- Quality Systems North Chicago, IL (Onsite Only - M-F, 40 hrs/week) $84-$89/hr (Rate depends on selected health benefit package) 6-Month Contract | Possible Extension About the Role We're seeking an experienced Manager, Quality Systems to support Quality activities across pharmaceutical, medical device, biologics, cosmetics, and combination product operations. In this role, you will help translate strategic quality objectives into actionable plans while ensuring full compliance with Corporate, FDA, and global regulatory requirements. You will collaborate with cross-functional teams across Quality, Manufacturing, and Regulatory to strengthen processes, drive continuous improvement, and support key Quality System elements including Document Control, Labeling, Validation, Training, Supplier Controls, and Quality Intelligence. This is an excellent opportunity for a seasoned Quality professional who thrives in a fast-paced, regulated environment and is confident in writing procedures, interpreting regulations, and ensuring operational excellence. Key Responsibilities Provide Quality Systems oversight across multiple product categories (pharma, devices, biologics, combination products, cosmetics). Write, revise, and maintain Quality System procedures, work instructions, and process documentation. Support Supplier Controls activities, ensuring vendors and partners align with applicable quality and compliance standards. Ensure all product, process, and system-related quality activities-from raw material inspection through finished goods release-meet internal and regulatory requirements. Translate Quality strategy into clear, tactical objectives for day-to-day operations. Support Quality functions such as Document Control, Device QA, Labeling, Validation, Training, and Quality Intelligence. Collaborate with internal stakeholders to interpret regulatory expectations and implement updates. Drive continuous improvement initiatives to enhance compliance, efficiency, and documentation quality. Required Qualifications Bachelor's degree in Life Sciences (or related field). 8+ years of experience in Quality within pharmaceutical or medical device manufacturing. Strong proficiency writing and reviewing Quality System procedures and process documents. Experience with Supplier Controls in a regulated environment. Excellent written and verbal communication skills, with the ability to explain complex concepts clearly. Nice to Have ASQ Certification (CQE, CQA, or similar). Experience supporting multiple Quality System elements (Validation, Document Control, Training, etc.). Work Schedule Monday-Friday, 40 hours/week 100% Onsite Overtime may occur based on business needs but is not expected. Who Thrives in This Role This position is ideal for someone who: Is highly organized, detail-focused, and fluent in Quality System requirements. Enjoys writing, editing, and improving process documentation. Is comfortable advising cross-functional teams and supporting audits or regulatory updates. Understands the fast-paced nature of pharma/device manufacturing and can adapt to evolving expectations. Our role in supporting diversity and inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

Job Title: Quality Control Manager Job Type: Full-time JOB REQUIREMENTS: Stop production if serious product defects are present. Review and update standard operating procedures or quality assurance manuals. Monitor performance of quality control systems to ensure effectiveness and efficiency. Review quality documentation necessary for regulatory submissions and inspections. Analyze quality control test results and provide feedback and interpretation to production management or staff. Verify that raw materials, purchased parts or components, in-process samples, and finished products meet established testing and inspection standards. Oversee workers including supervisors, inspectors, or laboratory workers engaged in testing activities. Direct product testing activities throughout production cycles. Instruct staff in quality control and analytical procedures. Direct the tracking of defects, test results, or other regularly reported quality control data. Participate in the development of product specifications. Identify quality problems or areas for improvement and recommend solutions. Collect and analyze production samples to evaluate quality. Produce reports regarding nonconformance of products or processes, daily production quality, root cause analyses, or quality trends. Communicate quality control information to all relevant organizational departments, outside vendors, or contractors. Monitor development of new products to help identify possible problems for mass production. Identify critical points in the manufacturing process and specify sampling procedures to be used at these points. Create and implement inspection and testing criteria or procedures. Document testing procedures, methodologies, or criteria. Review statistical studies, technological advances, or regulatory standards and trends to stay abreast of issues in the field of quality control. Coordinate the selection and implementation of quality control equipment, such as inspection gauges. Generate and maintain quality control operating budgets. Instruct vendors or contractors on quality guidelines, testing procedures, or ways to eliminate deficiencies. Confer with marketing and sales departments to define client requirements and expectations. Evaluate new testing and sampling methodologies or technologies to determine usefulness. Review and approve quality plans submitted by contractors. Audit and inspect subcontractor facilities including external laboratories. OTHER EXPERIENCE AND QUALIFICATIONS: Prefer experienced Quality Department Leader with 5 years or greater. Must have great interpersonal skills to work with subordinates, peers, executive staffs. Understand and deals with ISO standards in a precision machining environment

Air Quality Professionals! Staff to Senior Project Manager Level 3 to 15 Years of Environmental Consulting Experience Our client is seeking air quality professionals to join their Environmental Permitting and Compliance Group. Openings are available from Staff through SPM level, depending on experience. Successful candidates will bring a strong foundation in air permitting, regulatory compliance and client service within environmental consulting. Responsibilities • Prepare construction and operating air permit applications across major state and federal programs. • Develop emission calculations and inventories for a variety of industrial and energy sector clients. • Assess applicability of state and federal regulations, including NSR, PSD, Title V, NSPS and NESHAP. • Prepare and submit routine compliance reports and regulatory filings. • Review and interpret stack test and emissions testing results. • Support or lead air dispersion modeling tasks depending on experience level. • Advise clients on permitting strategies, compliance pathways and project planning. • Engage with clients and regulatory agencies as needed. • Contribute to proposal development, scopes of work and level-of-effort estimates. • For PM and SPM levels, manage projects, budgets, schedules and client relationships. Qualifications • Bachelor's or Master's degree in Environmental, Chemical or Civil Engineering or a related technical field. • Three to fifteen years of environmental consulting experience with a focus on air quality permitting and compliance. • Strong understanding of state and federal air regulations and permitting frameworks including NSR, PSD, Title V, NSPS and NESHAP. • Proficiency with emission calculations and standard air quality tools. • Familiarity with air dispersion modeling. Experience with AERMOD or CALPUFF is a plus. • Excellent written and verbal communication skills and the ability to collaborate within multidisciplinary teams. • Strong attention to detail and ability to manage multiple priorities under defined deadlines. • Ability to work independently, including in remote or client-site settings. • For Senior and PM levels, demonstrated project management and client-facing experience.

Why This Role Matters: You're not just filling a seat-you're shaping the future of how we build, test, and deliver software at scale. This is a mission-critical leadership role designed for someone who thrives on transforming complexity into clarity and driving excellence across every layer of the organization. If you've ever wanted to leave a legacy of world-class engineering practices, this is your stage. What You'll Own: You'll be the architect and evangelist of our enterprise-wide Quality Engineering strategy-a blueprint that sets the gold standard for governance, compliance, and modern testing practices across all teams. Your influence will ripple through every pillar of the organization, ensuring that quality isn't just a checkbox, but a culture. Define the QE Playbook: Establish governance frameworks, enforce standards, and set policies that become the backbone of our engineering excellence. Drive Modernization: Champion automation, DevOps, and shift-left testing to slash cycle times and elevate quality. Think big: reducing environment readiness from 4 weeks to 1 week. Lead with Metrics: Build a data-driven quality ecosystem-100% coverage, zero leakage into production, and velocity gains that redefine “doing more with less.” Governance & Influence: Run steering committees, executive reviews, and cross-functional forums that align product, development, and testing under one cohesive vision. Innovation in Practice: Design and implement automation frameworks, test data management strategies, and environment provisioning that scale with speed and precision. Risk & Compliance: Align QE practices with regulatory and security mandates without slowing down innovation. Your Leadership Impact: You'll lead 4-5 direct reports, each managing specialized teams (5-10 people) in: Test Environment Management Test Automation Test Data Management KPI & Governance This is a high-visibility role-you'll be the voice of quality in executive rooms and the hands-on leader who ensures delivery teams have the tools, environments, and data they need to succeed. What We're Looking For: Proven QE Visionary: 15+ years in Quality Assurance for complex systems and large-scale programs. Automation Guru: Deep experience in designing and deploying automation frameworks, CI/CD pipelines, and DevOps quality gates. Strategic Influencer: Ability to define enterprise-wide standards and lead organizational change with confidence. Metrics-Driven Leader: Skilled in risk-based validation and quality reporting that drives decisions. Tech Savvy: Familiarity with microservices, event-driven architecture, and emerging tech like AI/ML in QE. Cloud Expertise: Hands-on experience with large-scale cloud-native projects (AWS preferred). Regulatory Mindset: Comfortable navigating governance, compliance, and audit requirements. Technical Toolkit: Jira, Jenkins, automation frameworks, test management tools, defect tracking systems, and cloud foundational services (AWS VPCs, EC2, Security Groups). Education: BS in Computer Science, Information Systems, or equivalent technical discipline. Why You'll Love It Here: This isn't just about testing-it's about building a culture of quality that accelerates innovation. You'll have the autonomy to make bold decisions, the authority to influence enterprise strategy, and the resources to turn vision into reality. If you're passionate about transforming QE into a competitive advantage, we want you on our team.

As the Electrical Quality Control (QC) Manager, you will oversee and enforce all electrical quality assurance and control procedures on mission-critical data center projects. You'll ensure compliance with project specifications, national electrical codes, and client standards, while coordinating closely with field teams, subcontractors, and commissioning agents. Key Responsibilities Develop and implement the Electrical Quality Control Plan in alignment with project requirements and client expectations Conduct daily inspections of electrical installations (e.g., switchgear, UPS systems, generators, PDUs, grounding systems) Review and approve electrical submittals, shop drawings, and RFIs for compliance Coordinate with commissioning teams to support Integrated Systems Testing (IST) Lead pre-installation meetings with subcontractors to review quality expectations Maintain accurate documentation of inspections, deficiencies, and corrective actions Ensure compliance with NFPA 70 (NEC), IEEE standards, and local codes Participate in client and third-party audits and resolve non-conformance issues Train field staff and subcontractors on quality procedures and best practices Qualifications Bachelor's degree in Electrical Engineering, Construction Management, or related field (or equivalent experience) 5+ years of electrical QC experience in large-scale commercial or mission-critical construction Strong knowledge of data center electrical systems and commissioning processes Familiarity with mission critical QC standards is a plus Proficiency in Procore, Bluebeam, and Microsoft Office OSHA 30 certification preferred Excellent communication and leadership skills Perks & Benefits Competitive salary and performance bonuses Per Diem 401(k) with company match Health, dental, and vision insurance Vehicle allowance or company vehicle Paid time off and holidays Career development and training opportunities Benefits Vacation/PTO Medical Dental Vision 401k Bonus Relocation Telecommute Email Your Resume In Word To Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also: kyle.lesser@cybercoders.com Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : KL2-1858599 -- in the email subject line for your application to be considered.*** Kyle Lesser - Recruiting Manager For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. This job was first posted by CyberCoders on 07/02/2025 and applications will be accepted on an ongoing basis until the position is filled or closed. CyberCoders is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at Benefits@CyberCoders.com to make arrangements.

Our client is actively looking for a Senior Quality Assurance Specialist with a focus on Sterility. This is an on-site position in Fort Dodge, IA. This position offers relocation assistance and visa sponsorship. You should apply if you have: 5+ years of front-line QA experience 3+ years experience in aseptic environments Hands-on experience in sterility projects (media fills, environmental monitoring, sterile boundary mapping, contamination investigations) B.S.in Microbiology, Biology

Aegis is partnered with a growing manufacturing operation in the Elgin, IL area that is looking for a Quality Engineer to build and lead its quality processes. This is a newly created position with major opportunity for ownership, impact, and long-term growth as several senior team members retire over the coming years. The role is perfect for someone who enjoys developing structure, improving systems, and working cross-functionally with engineering, procurement, service, and production. What You'll Do Develop and implement an entirely new Quality Management System (QMS). Lead incoming, in-process, and outgoing inspection methods. Perform root cause analysis, corrective actions, and non-conformance management. Support vendor quality issues and work with procurement on part quality improvements. Conduct finished goods testing, process audits, and documentation updates. Use data, KPIs, and production feedback to solve recurring quality problems. Collaborate closely with engineering and shop-floor teams to maintain quality standards. What We're Looking For 3-5 years of quality engineering or QA/QC experience. Experience improving or developing QMS systems (full build-out not required). Strong background in sheet metal or metal fabrication (or med device as an alternative). Ability to read blueprints and wire diagrams. Experience with non-conformances, RCA, and documentation. Engineering degree in Mechanical, Industrial, Manufacturing, or Electrical preferred. Why This Opportunity Stands Out Brand-new role with significant long-term growth runway. Highly collaborative, small team with a culture of knowledge-sharing. Very strong leadership support and cross-department visibility. Impactful, hands-on work that helps shape the future of the organization.

Exciting Career Opportunity: Quality Engineer- Beautiful Central Wisconsin Are you looking to advance your career while embracing a unique lifestyle in one of the most beautiful regions of the U.S.? Central Wisconsin offers the perfect blend of professional growth and outdoor adventure, all just a short drive from vibrant urban areas and surrounded by breathtaking natural landscapes. We're looking for an experienced Quality Engineer who will regularly lead, Support and be engaged and supporting growth and improvement of the Quality Management System to positively impact Fist Pass Yield and Cost of Quality. This is a hands-on position balancing time between the production floor and support office, maintaining a cross-functional partnership with the Operations, Supply Chain and Sales processes. Key Responsibilities: · Partnering with Operations, Supply Chain and Sales team members to develop and improve documented process, work instructions and process verifications · Leading root cause analysis process including identifying trends, investigating possible causes and working with affected team members to develop and deploy sustainable corrective action as well as creating and maintaining the root cause tool documentation · Supporting new hire, new process, cross training, and process refresher training as it pertains to the understanding of quality processes and process effect on quality · Driving operator engagement in the QMS using change management techniques during times of change · Leading the development and update of control plans, FMEAs and other risk-based process tools · Partnering with Operations to complete data collection, supporting process and product conformance and trending · Maintaining document control process with all new documented and document updates · Leading and participating in Improvement projects as necessary to support FPY/CoQ improvement · Being a Subject Matter Expert on Layered Process Audit, First Article Inspection, and other quality sustainability processes · Developing and delivering on, measurable individual goals that support facility Safety, Quality, and production goals · Communicating clearly and consistently both verbally and written What We're Looking For: · Five to seven years' experience in a Quality Manufacturing Environment · 4-year Degree in Technical Field or equivalent experience preferred · Process and/or Project Management education or experience · Six sigma Lean GB or ability to become certified within eighteen months · Excellent written and oral skills are a must · Experience of dealing directly with customers regarding quality issues · Must be able to work independently with minimum supervision Live in a beautiful, affordable area where you can truly enjoy work-life balance. Central Wisconsin is ideal location for outdoor lovers, with all four seasons offering something special. Family friendly, safe community, affordable living and so much more. Become a part of a 100-year-old company with deep roots in the community and opportunities for career growth and development. Visa sponsorship is not authorized for this position now or in the future Annual Base Salary: $80,000 to $100,000 (DOE) Relocation Package is available.

Step into a high-impact Lab Manager role where you'll lead a growing Quality and Technical Support team within a dynamic chemical manufacturing environment. This position gives you the opportunity to shape lab operations, mentor a young and capable team, and bring structure and process to a department that's ready for strong leadership. It's a hands-on role where your chemistry expertise, problem-solving skills, and ability to work through ambiguity will directly influence product quality, customer satisfaction, and production success. Pay: $95k-$120k Schedule: M-F 7a-4p or 10a-6p (Flexible schedule to accommodate 2nd/3rd shift presence) Type of Job: Direct Hire Location: Bedford Park, IL At this time, Astrix cannot transfer nor sponsor a work Visa for this position. Relocation assistance is not available for this position. Benefits Offered: Medical, Dental, Vision, Life/AD&D, 401K, Vacation, and more! Lab Manager Daily Tasks: What you will do: Lead and mentor the QC and Technical Service lab teams, providing daily guidance, training, and structured processes to support a young, developing staff while maintaining high standards of organization and lab performance. Oversee all QC testing, analytical methods, and troubleshooting to ensure product quality, repeatability, and compliance with customer, regulatory, and internal specifications. Apply chemistry expertise, especially in metalworking fluids, industrial lubricants, water-based systems, or emulsions, to solve complex formulation and performance issues. Collaborate with Operations, Sales, and Technical Management to support production needs, guide application decisions, communicate technical insights, and drive both short- and long-term product performance goals. Drive continuous improvement through root-cause analysis, corrective actions, and data-driven project management, ensuring the lab meets KPI targets, safety standards, and budget requirements. Lab Manager Qualifications/Requirements: Bachelor's Degree in Chemistry with 10+ years of experience in a lab, QC, technical service, or formulation role Experience with metalworking fluids, industrial lubricants, or water-based/chemical manufacturing preferred Proven supervisory or lab leadership experience, with the ability to mentor a developing team, organize workflow, and manage multiple projects in a fast-moving environment. Strong analytical troubleshooting skills with experience in analytical methods, instrumentation, SPC, and root-cause/corrective action problem solving. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

About FAC Services Want to build your career helping those who build the world? At FAC Services, we handle the business side so architecture, engineering, and construction firms can focus on shaping the future. Our trusted, high-quality solutions empower our partners, and our people, to achieve excellence with integrity, precision, and a personal touch. Job Purpose FAC Services is expanding our QA team with a strategic new hire: a Data Quality Engineer who will play a pivotal role in ensuring the quality and reliability of our data infrastructure. This role will focus on testing data pipelines, validating data integrity across systems, and supporting infrastructure automation efforts. You'll collaborate closely with Infrastructure, DevOps, and QA teams to build scalable, test-driven solutions that support our growing data ecosystem. This is a hybrid position, and candidates must reside within 60 miles of Madison, WI. Primary Responsibilities The Data Quality Engineer will be responsible for ensuring the quality and reliability of data pipelines, APIs, and infrastructure automation. This includes designing and executing automated tests for ETL/ELT workflows, validating data integrity across cloud platforms, and performing extensive API endpoint testing. The role also involves supporting Infrastructure as Code (IaC) testing using tools like Ansible, ARM, and Bicep, and contributing to CI/CD pipelines and Azure-based testing initiatives. Data Quality & Pipeline Testing Design and implement automated tests for ETL/ELT pipelines and data marts. Validate data transformations, integrity, and quality across Azure, Snowflake, and Microsoft Fabric environments. Collaborate with developers and data engineers to implement test-driven development (TDD) practices for APIs and data workflows. Ensure confidence in data quality through rigorous testing of data pipelines and integrations. API Endpoint Testing Perform extensive testing of RESTful API endpoints, including functional, regression, and integration testing. Validate API responses, error handling, and performance under various conditions. Work closely with developers to ensure comprehensive test coverage and early detection of issues. Use tools such as Postman, Swagger, or custom scripts to automate and document API testing. Infrastructure as Code (IaC) & Automation Support infrastructure automation testing using tools like Ansible, ARM templates, Bicep, and Power Automate. Contribute to the development of reusable QA frameworks that integrate with existing systems. Participate in the design of automated provisioning and deprovisioning workflows for infrastructure and user hardware. Cloud & System Testing Assist in testing hybrid Azure environments, including network, security, scalability, and fuzz testing. Collaboration & Leadership Work cross-functionally to ensure QA alignment across infrastructure and application teams. Lead by example, demonstrating best practices and continuous improvement. Share knowledge and mentor team members in data quality and automation practices. Qualifications To perform this job successfully, an individual must be able to perform each primary duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Experience 3+ years in QA engineering, specializing in data testing/infrastructure Extensive ETL/ELT testing, data validation, and quality frameworks experience Skilled in SQL and scripting (Python, PowerShell) Knowledge of CI/CD tools and workflows (Git, Azure DevOps) API testing experience; familiar with Swagger documentation Understanding of IaC tools (Ansible, ARM, Bicep) Microsoft Azure expertise Strong communicator and effective team player

MUST HAVE : Good amount of experience with heavy steel metal fabrication and welding Core Responsibilities • Supplier Collaboration • Partner closely with suppliers to ensure the production of high-quality parts. • Conduct multi-stage inspections at supplier sites to verify compliance with specifications. • Support and update project processes as needed. • Address and resolve technical queries from suppliers (e.g., materials, dimensions, coatings). • Supplier Audits • Perform audits for onboarding new suppliers to ensure they meet quality standards. • Scope of Role • This is a purely technical role with no involvement in purchase orders, quotations, or payments or lifting on the floor. Travel Requirements • Approximately 40% travel, primarily within the U.S. • Occasional international travel (e.g., Mexico, Canada). Qualifications • Education: Bachelor's or Master's degree in Mechanical or Industrial Engineering. (Flexible if the candidate has strong relevant experience.) • Experience: 5-10 years (minimum 5 years acceptable). Must-Have Skills Industry Experience Candidates should come from heavy engineering sectors, such as: • Automotive • Aerospace • Locomotive • Truck • Heavy Machinery (e.g., earth-moving equipment, long machinery) *Note: Candidates from medical or small-scale product industries are not suitable for this role. Technical Expertise • Strong knowledge of forging, casting, machining, materials, and welding. • Hands-on experience with heavy sheet metal fabrication and welding of large steel structures/enclosures.

*Employment Type:* Full time *Shift:* Day Shift *Description:* * Manages day-to-day operations for the Laboratory department located in the acute care setting. Responsible for human, fiscal and material resources of the department and ensures staff provides high quality, accessible, cost-effective care and patient-focused services. * Maintains the Laboratory's Quality Management and Safety Programs to ensure the Laboratory meets local, state and Federal regulatory requirements. * Contributes to the formation of the vision, policies, standards and culture * Interviews and hires staff in areas of responsibility * Ensures the staffing level and mix is appropriate for the workload of the sections and shifts * Ensures appropriateness of staff orientation and competency materials and coordinates completion according to facility and regulatory guidelines; completes performance evaluations for direct report personnel * Performs disciplinary action when indicated; writes and maintains work group job descriptions * Ensures compliance with the requirements of laboratory regulatory and accrediting agencies * Evaluates, recommends and coordinates implementation of new tests, instrumentation, and/or methods * Ensures standard operating policies and procedures are current and adhere to the Laboratory's document control system * Assists the Laboratory Director with the development of budgets and monitors expenses appropriate to area of management * Assists with the development of business plans and evaluates capital equipment needs in consultation with the Laboratory Director * Develops and maintains quality management systems and performance improvement initiatives appropriate to the area of responsibility * Coordinates and facilitates the change process * Effectively facilitates communication with direct reports, peers and leaders in the organization * Assists in the formulation and implementation of department goals * Maintains an inventory system that ensures appropriate supply levels. Supervisory Responsibility: Large Group/Multi-Level: The job requires direct responsibility for a large department or unit of greater than 25 employees. In addition to staff, incumbent directly supervises one or more supervisors and/or assistant managers who assist incumbent with managerial responsibilities. Incumbent has multiple shift responsibilities for staff. Education: Bachelor's Degree Special Training: Successful completion of a NAACLS or ABHES accredited clinical laboratory science program or alternate career path that meets certification eligibility requirements. Training Preferred: Three years supervisory or similar experience; Masters degree in Healthcare Administration, Business Administration or related field. Certification in one of the following: * Medical Laboratory Scientist (MLS) or Medical Technologist (MT) by the American Society of Clinical Pathology (ASCP) OR * Medical Technologist (MT) by the American Medical Technologists (AMT). * Valid driver/chauffeur license required, must meet MercyOne's Motor Vehicle Safety Standards, must be at least 18 years of age and be eligible to drive per Iowa state law. Experience: More than 5 years experience required. *Our Commitment * Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.

Lead with Purpose. Lead with Heart. Become Our Next Director of Quality and Compliance. If youre energized by elevating care standards, driving meaningful change, and making a real impact in hospice care, Northern Illinois Hospice wants you on our team. As the regions first hospice since 1979, weve built a legacy of compassion, excellence, and community trustand now, we're looking for a passionate Director of Quality and Compliance to help carry that mission forward. Why Northern Illinois Hospice? We are a warm, mission-driven organization where collaboration isnt a buzzwordits a way of life. Here, your hospice expertise is valued, your ideas matter, and your leadership as the Director of Quality and Compliance directly shapes how we deliver extraordinary hospice care to patients and families. Youll be joining a place where innovation meets heart, and where your growth is supported every step of the way. A Day in the Life As our Director of Quality and Compliance, youll guide quality programs, mentor clinical teams, and lead key committees that ensure we continue setting the standard for hospice excellence. Your day may include partnering with leadership, driving QAPI initiatives, facilitating RCA and FMEA activities, preparing for Joint Commission surveys, and ensuring regulatory and hospice compliance across the organization. Youll help create a thriving, safe, high-performing environmentone that strengthens both team confidence and patient trust. What Youll Do As the Director of Quality and Compliance, you will: Oversee all quality programs and present recommendations to leadership. Lead Quality Committees and QAPI work. Drive performance improvement efforts and facilitate RCA and FMEA analyses. Oversee quality and compliance education, infection control, and emergency preparedness. Ensure compliance with all state, federal, Medicare CoPs, and Joint Commission hospice standards. Serve as liaison to the Joint Commission and lead survey readiness efforts. Oversee the Compliance Program, internal controls, and risk-mitigation practices. Work Schedule Full-time leadership role with regular business hours and administrative on call availability for organizational needs. What You Bring As the Director of Quality and Compliance, youll need: RN licensure in Illinois; BSN required, MSN preferred. 5+ years of progressive hospice leadership, required (Joint Commission experience preferred). Strong knowledge of hospice regulations and quality reporting. Experience leading quality, compliance, and process-improvement initiatives. Valid drivers license and reliable transportation. Pay & Benefits Competitive salary $104,000$156,925, commensurate with experience and education, plus comprehensive benefits including PTO, medical, dental, vision, disability, 401(k) with match, and more. Ready to Lead With Purpose? If you're excited to make a difference as our next Director of Quality and Compliance, apply now. Join Northern Illinois Hospiceand help shape the future of hospice care. Northern Illinois Hospice is an equal-opportunity employer and a drug-free workplace. Requirements: Compensation details: 104000-157000 Yearly Salary PIe56ac424b424-31181-39065141

Job Purpose We are seeking a passionate, tech-savvy and proactive manager to support the design and implementation of a pioneering global digital solution for our Quality Management System (QMS). As a Global Supplier Quality Process Manager, you will work closely with the Global QMS Lead to shape the “to be” processes of the system, being a part of building and deployment of the solution, and spearhead change management initiatives across the organization. The ideal candidate will be a digital enthusiast with a deep understanding of technology and a willingness to push the boundaries of innovation in QMS & Supplier Management. Essential Functions & Responsibilities 1. Design and implementation of supplier management system processes (digitalize the supplier approval, non conformance management, supplier performance, audit tool) Support the creation of “to be” process flows that integrate digital tools and solutions Work with subject matter experts (SMEs) and stakeholders to ensure proposed processes meet global standards and regulatory requirements Ensure new processes sign off within global, regional and local teams GCOE / Regions 2. Support design & build of digital solution Partner with solution Product Owner, collaborators and external vendor to design, build, test and deploy the digital QMS solution Plan and prepare the current document management digital solution for the proper migration to new one Ensure solution's functionalities are aligned with the organization's future-proofing goals Support functional backlog control and gap closure within the solutions team during the streams Coordinate UAT (user acceptance test) within business process team 3. Change management support for the Supplier management processes Develop and implement change management strategies to ensure successful adoption of the new digital supplier management solution across the organization Lead training and communication efforts to ensure a smooth transition to the new digital solution, fostering a culture of continuous improvement and innovation Identify and address any challenges or resistance related to the adoption of new technologies and processes 4. Collaboration and stakeholders' engagement Act as a liaison between business users, IT, external partners to ensure seamless communication and delivery of the solution Prepare updates to senior leadership (project sponsors) on project progress, challenges, milestones Govern change requests Establish and maintain relationship with FSQ global teams to ensure alignment and adherence to project timelines and objectives, leading digital solution adoption Expected Experience & Required Skills 5+ years experience in managing FSQ transformation projects, preferably in the field of Quality Management Systems or enterprise-level software solutions 3+ years experience on Supplier Quality Management System / ISO 9001:2015 implementation and/or maintenance Proven experience in process design, system implementation, and deployment of digital solutions globally Hands-on experience with change management practices in a global or cross-functional environment Familiarity with QMS tools and software platforms (like Siemens, Veeva, ETQ) Familiarity with Food Safety & Quality Global standard system, as BRC, FSSC, or other GFSI recognized scheme Experience with Agile methodologies and project management tools would be high value asset Excellent interpersonal skills, with the ability to articulate complex technical concepts to non-technical stakeholders Proactive, self-starter, with the ability to take ownership of tasks and deliver results with minimal supervision Leadership capabilities, with experience in leading change and supporting through transitions Tech-enthusiast with a passion for digital innovation and staying up-to-date with the latest trends in technology Collaborative, adaptable and able to work in a dynamic and global team environment Meticulous, organized and capable of leading multiple priorities Work Environment & Schedule This position is considered a Normal office environment with moderate travel to customer locations, stores, manufacturing facilities, etc.; offices are open workspaces Additionally, this role requires 40 hours/week schedule, 5 days a week. Our Total Rewards philosophy is to provide a meaningful and flexible spectrum of programs that equitably support our diverse workforce and their families and complement Kraft Heinz' strategy and values. New Hire Base Salary Range: $102,100.00 - $127,600.00 Bonus: This position is eligible for a performance-based bonus as provided by the plan terms and governing documents. The compensation offered will take into account internal equity and may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors Benefits: Coverage for employees (and their eligible dependents) through affordable access to healthcare, protection, and saving for the future, we offer plans tailored to meet you and your family's needs. Coverage for benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. Wellbeing: We offer events, resources, and learning opportunities that inspire a physical, social, emotional, and financial well-being lifestyle for our employees and their families. You'll be able to participate in a variety of benefits and wellbeing programs that may vary by role, country, region, union status, and other employment status factors, for example: Physical - Medical, Prescription Drug, Dental, Vision, Screenings/Assessments Social - Paid Time Off, Company Holidays, Leave of Absence, Flexible Work Arrangements, Recognition, Training Emotional - Employee Assistance Program , Wellbeing Programs, Family Support Programs Financial - 401k, Life, Accidental Death & Dismemberment, Disability Location(s) Chicago/Aon Center Kraft Heinz is an Equal Opportunity Employer - Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes. In order to ensure reasonable accommodation for protected individuals, applicants that require accommodation in the job application process may contact *********************** for assistance.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Lilly is entering an exciting period of growth, and we are committed to delivering innovative medicines to patients around the world. Lilly is working to build a stronger Sterility Assurance function and capability to provide increased technical capacity across the network. The purpose of this position is to provide oversight and drive / maintain harmonization of technical programs that govern implementation and execution of Sterility Assurance control strategies across the Lilly Parenteral Network. This position also influences peers within Lilly globally and at the site level, as well as external to Lilly, to ensure strategies are in-line with technical, quality and regulatory guidance, current expectations and business needs. This role also aids and enables building technical capability at Lilly sites to ensure the vital capabilities are developed and in place to meet business objectives. Finally, this role provides ad-hoc technical support to Lilly PR&D, external contract manufacturing, and non-sterile drug substance (API) manufacturing. Responsibilities: * Assess differences in current sterility assurance programs across the sites and drive harmonization * Work closely with site and multi-functional SMEs to drive cohesion. Ensure control strategies are robust, consistent with regulatory and compliance expectations, and are continuously improved. * Ensure control strategies are robust, consistent with regulatory and compliance expectations, and are continuously improved. * Assume SME leadership role for a specific topic area within Sterility Assurance across the network, including harmonization of aspects of the topic area and facilitation of the knowledge across the network. * Represent TS/MS on network Science Lead Team and other appropriate governance forums. Ensure that Sterility Assurance programs and similar topics are frequently presented to network team in order to align across sites. Ensure that learnings and best practices are shared across sites: set-up appropriate forums in order to achieve this and present case studies to site SMEs. * Provide mentoring leadership to site SMEs to help build continue to build capability, particularly at the newer sites or where deep technical expertise is lacking. * Building, maintaining, and growing capability across the organization in the sterility assurance space * Provide technical support to new sites/ filling lines during design and start-up activities to ensure sterility assurance programs and process/ product requirements are supported at these sites, particularly while the sites are in early stages of building capability. * Provide technical support for significant sterility assurance investigations to help identify root cause and implement appropriate corrective actions. Share best practices / learnings / CAPAs across the other sites. * Benchmark industry trends and emerging regulatory guidance / requirements in the field through building an extensive peer network and attendance at relevant industry and regulatory meetings and advocacy groups. Advance Lilly agenda in the field. Represent Lilly on relevant external bodies related to Sterility Assurance; be influential in terms of representing Lilly's position on technical/ regulatory positions papers and guidance. Assess new technologies to ensure Lilly stays current with new trends and technologies and share with the network with the goal of staying current with industry best practice. * Work with PR&D on new technology / platform development and implementation for pipeline products. Influence the agenda within PR&D to ensure the needs of Manufacturing are met, and the control strategies are fit for-purpose for robust and compliant commercial manufacturing. * Provide ad-hoc technical support to Lilly organizations outside of the PPN including PR&D, external contract manufacturing, and non-sterile drug substance (API) manufacturing. * Engage in providing support during regulatory interactions such as RtQ of submissions, and on-site inspections * Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate Goals Basic Qualifications: * BS Degree required. * MS/PhD in a biological science preferred. * 10+ years' experience working in Parenteral Sterility Assurance / Environmental Monitoring or equivalent roles preferred. * 10+ years' experience in parenteral manufacturing sterility assurance control systems - development of systems, execution and operation of systems and continuous improvement of systems in a highly regulated environment preferred. * Deep technical understanding of sterility assurance, from a science and compliance perspective. Current in technological and compliance developments across the parenteral manufacturing industry (e.g. filling technology, Annex 1 interpretation) * Proficiency in data analysis, ability to prioritize, attention to detail, critical decision-making skills, complex problem-solving abilities * Strong written and oral communication skills * Ability to mentor and develop scientists in the fields of sterility assurance and applied pharmaceutical microbiology * Understanding of cGMP's, policies, procedures, and guidelines relating to sterility assurance * Demonstrated experience influencing site and network leaders to advance technical agenda projects Additional Preferences: * Work closely with senior technical staff in the parenteral network TSMS group to provide full oversight to new and existing facilities. Be available to help with inspection readiness and inspection preparation at each site, particularly the new sites. Provide guidance to investigations and ensure root cause, CAPA are quickly developed. * Support the establishment of a sterility assurance network or hub in global TSMS * Support inspection preparation and execution during health authority on-site or remote inspection as an expert in Sterility Assurance * Experience in leading external committees or conferences to ensure Lilly remains a leader in the sterility assurance space * Work with engineering SME's to support Lilly platforms to maximize the performance and minimize the risk of sterility assurance * Strength in scientific and practical thinking to ensure the best options are selected following a thorough evaluation of applicable options. * Strong capability to influence personnel and management across the organization * Close interaction with quality to enable internal audits that identify risks * Past experience in creating effective working relationships with all levels across internal and external stakeholders impacting the success of sterility assurance. Additional Information: * Approximately 25% travel Lilly currently anticipates that the base salary for this position could range from between $133,500 to $220,000 and will depend, in part, on the successful candidate's qualifications for the role, including education and experience. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Of course, the compensation described above is subject to change and could be higher or lower than the range described above. Further, Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $133,500 - $246,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Give hope. Give health. Make your mark in the fight against cancer. At Accuray, we make a direct and powerful impact on the lives of cancer patients every day - helping them live longer, better lives. But our commitment to innovation offers a truly unique opportunity: the chance to change the fight against cancer - helping to develop, introduce and support new treatment delivery systems and software that will give new hope and new health to cancer patients and cancer survivors around the world. Accuray develops, manufactures and sells radiotherapy systems for alternative cancer treatments. Our radiation therapy for cancer makes treatment shorter, safer, personalized and more effective, ultimately enabling patients to live longer, better lives. Job Description Do you have a passion for quality and a drive to ensure suppliers meet top-tier standards? Accuray is always on the lookout for skilled Supplier Quality Engineers to join our team. If there isn't a current opening that matches your skill set, we encourage you to apply through this General Interest Pipeline. By doing so, you'll be considered for future Supplier Quality opportunities that align with your experience and career goals. WHY WORK FOR ACCURAY? At Accuray, we give hope through innovation. Our goal is to develop cutting-edge radiation therapy solutions that help people diagnosed with cancer get back to living their lives, faster-and every role contributes to this purpose. We're a team of passionate problem-solvers driven by the desire to make an impact. You'll work in a collaborative, inclusive environment where your ideas-and your growth-matters. We offer competitive benefits, flexible work options, and the chance to shape the future of healthcare with AI and advanced technologies. Join us-and help give patients hope for more time to make memories that matter. About The Role and What we Look For Supplier Quality Engineer: The supplier quality engineer is a member of the quality assurance team who plans and performs activities related to the selection, monitoring, and control of purchased materials and suppliers. They work cross-functionally with engineering, procurement, manufacturing, service, and other quality teams to support all phases of the product lifecycle from initial product development through customer support. Successful candidates for this role have a high degree of resourcefulness by delivering timely and effective results in a dynamic and fast-paced environment with a high degree of autonomy. If you have experience in Supplier Quality, we encourage you to apply to this General Interest Pipeline. This allows us to consider you for future openings as they become available. To qualify for this position, candidates must be able to furnish proof that they are authorized to work in the country they are applying on a permanent basis without sponsorship. EEO Statement At Accuray, our commitment to patient-first outcomes drives an inclusive and collaborative work environment where the best ideas rise to the top - and everyone works to push them further. We value diversity in both the professional and personal backgrounds of our employees, as this variety adds rich energy to every team, every project and every work day. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or national origin - including individuals with disabilities and veterans.

Responsibilities will include: Oversee development and implementation of company safety & quality management system Develop and implement a quality plan to meet quality levels established by company guidelines and local regulations Lead and facilitate the quality champion program to analyze and correct nonconformance and complaints Collaborate with engineering to review project readiness and the purchasing of a supplier management strategy Work with company team members and local regulators to establish inspection protocols and ensure compliance Analyze and resolve process quality issues and needs as they relate to process performance and quality requirements Provide data related to KPI's and identify opportunities for improvement Travel to suppliers to ensure quality and process capacities are met Strive to develop a feeling of pride and loyalty to company and team members Champion Affirmitive Action Program in hiring, development and promotion opportunities Become familiar with company policies and train subordinates to follow guidelines Strive to improve leadership and management capabilities for personal development Qualifications BS in Engineering, Quality, Business or rleated degree 6+ years in a manufacturing or construction environment implementing quality programs Strong organizational and problem solving skills Track record of implementing Lean Manufacturing methodologies and Continuous Improvement Strong written and verbal communication skills Leadership ability U.S. Citizen or Green Card holder Additional Information Perks: Established and growing company Competitive pay and benefits packages Plenty of career growth opportunities

At Northwestern Medicine, every patient interaction makes a difference in cultivating a positive workplace. This patient-first approach is what sets us apart as a leader in the healthcare industry. As an integral part of our team, you'll have the opportunity to join our quest for better health care, no matter where you work within the Northwestern Medicine system. We pride ourselves on providing competitive benefits: from tuition reimbursement and loan forgiveness to 401(k) matching and lifecycle benefits, our goal is to take care of our employees. Ready to join our quest for better? Job Description The Program Manager, Quality reflects the mission, vision, and values of Northwestern Medicine, adheres to the organization's Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. The Program Manager, Quality is responsible for planning and coordinating all or a portion of the Quality program for Northwestern Memorial Hospital the direction of the Director of Quality. This role coordinates and leads the quality endeavor, coordinates with peers, and is responsible for implementation and follow up as outlined in the annual quality plan, ongoing priorities of leadership and quality committees, and compliance with relevant standards monitored by The Joint Commission (TJC) and other agencies. This position will advance the use of quality evaluation and improvement strategies to achieve key organizational goals in quality and patient safety. The Program Manager partners with administrative, physician, nursing, ancillary leadership and other system function teams to advance the quality agenda through the development and implementation of plans and strategies that facilitate the achievement of strategic organizational goals. Responsibilities: Provide leadership and operational implementation of assigned Clinical Quality activities Conduct detailed, sophisticated, accurate and creative analyses of data at NMHC and outside NMHC (e.g. benchmarks, comparative data) to identify quality opportunities. Advance performance compared to appropriate external benchmarks and optimize process and outcome metrics. Develop, conduct, implement and improve process improvement activities to improve high quality & high-reliability healthcare. Identify and utilize appropriate quality metrics to evaluate project or performance success based on stated purpose and needed outcomes. Implement effective quality planning Design quality plans, programs and policies, peer review, and best practices in partnership with senior medical and operational leaders. Lead the department to identify quality opportunities and concerns, in collaboration with the Director of Quality. Facilitate the implementation of systems and processes that promote a fair and just culture, and improve patient care. Support effective department operations and growth, and personal development Support, coach, teach, mentor, monitor and evaluate the work of others conducting quality work (as directed) and personally conduct, coordinate, facilitate, and participate in quality assessments, improvement efforts, committees, etc. Oversee effective use of budget and other resources as delegated. Will supervise projects with organizational impact, and intermittent staff assignments. Responsible for self-development and professional engagement, including knowledge of the literature and attendance at professional meetings, preparation of manuscripts, posters and presentations, involvement of with local and national task forces as relevant. Additional/Clarified Essential Functions: Under the leadership of the Quality Director: SME on external rankings methodology and overall impact to hospital ranking, specialties, and procedures and conditions. External Methodology Vizient expert including changes in annual release and advocate for changes when possible Analyze and interpret data, develop reports and dashboards, identify performance challenges and opportunities to improve care; monitor progress Create and lead action plans of multiple workstreams to improve patient outcomes and lead improvement projects in targeted areas. Advocate and collaborate with Vizient for improved and transparent methods. Identify emerging needs for NM strategic priorities, monitoring external measurement and performance and emerging literature. Exhibits confidence, credibility, and professionalism to influence decision-making for NMHC senior leadership Delivers clear, concise, and persuasive messages tailored to executive audiences, ensuring alignment and engagement across teams. Qualifications Required: Bachelor's degree in Nursing or Allied Health Profession or a Master's degree in a healthcare related field 5+ years of work experience, with 4+ years in a healthcare setting, and 3+ years of quality, patient safety, or relevant experience Highly effective and experienced at facilitation of teams including complex multi-disciplinary projects Expert knowledge of quality measures and measurement, mastery of performance improvement methodologies (i.e. DMAIC), analytic tools and methods, including implementation with measurable results Advanced competence with Excel and data analysis Excellent writing and presentation skill Preferred: Master's degree Certified Professional in Healthcare Quality (CPHQ) or Certified Professional in Patient Safety (CPPS) or other evidence of advanced commitment to profession. Familiarity with major sources of measures, literature, and quality- and patient-safety-related federal and state policy. Experience with clinical outcomes, safety, and patient satisfaction data Additional Information Northwestern Medicine is an equal opportunity employer (disability, VETS) and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, disability, sexual orientation or any other protected status. Background Check Northwestern Medicine conducts a background check that includes criminal history on newly hired team members and, at times, internal transfers. If you are offered a position with us, you will be required to complete an authorization and disclosure form that gives Northwestern Medicine permission to run the background check. Results are evaluated on a case-by-case basis, and we follow all local, state, and federal laws, including the Illinois Health Care Worker Background Check Act. Benefits We offer a wide range of benefits that provide employees with tools and resources to improve their physical, emotional, and financial well-being while providing protection for unexpected life events. Please visit our Benefits section to learn more. Sign-on Bonus Eligibility: Internal employees and rehires who left Northwestern Medicine within 1 year are not eligible for the sign on bonus. Exception: New graduate internal employees seeking their first licensed clinical position at NM may be eligible depending upon the job family.