Quality Manager jobs at The Walsh Group - 1273 jobs

Work with Us. Change the World. At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. We are the world's trusted infrastructure consulting firm, partnering with clients to solve the world's most complex challenges and build legacies for future generations. There has never been a better time to be at AECOM. With accelerating infrastructure investment worldwide, our services are in great demand. We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world. We're one global team driven by our common purpose to deliver a better world. Join us. Job Description AECOM is seeking an experienced On-site Quality Assurance Manager to support Federal Projects. Key Responsibilities Provide overall on-site administrative and technical Quality Assurance Management program for a wide range of Site Civil construction activities. Responsible for the organization and direction of the construction Quality Assurance inspections and related activities within assigned areas of responsibility, which may be a single area, multi-area, or a multi-discipline Civil construction project. Interact and be the primary contact for all inspectors and jobsite day to day quality assurance inspection functions and coordinate with client's resident representatives on jobsite activities within assigned area of operations. Attend and/or support meetings and teleconferences as required, including preparing correspondence and maintaining official construction site records. Experience in conducting meetings to resolve problems on construction projects, and briefing DOD clients and management personnel. Responsibilities include implementing and maintaining the Quality Assurance Program and ensuring construction installation and activities are in compliance with design and specifications and industry quality standards. Provide a review of the construction contractor's submittals for completeness and compliance with the specification requirements while monitoring the Submittal and RFI review process. Provide technical consultation and direction as appropriate to lower-level technicians and inspectors. Conduct inspection and investigations and tests that are of considerable complexity, such as of the contractor's on-site plant (storage yards and temporary facilities), materials and equipment Serve in oversight of final inspections, preparation of final punchlist and determination as to the completeness and acceptability of the Work. Prepare, resolve, document, and close out all deficient and noncompliant construction installations Qualifications Minimum Requirements: * BA/BS + 4 years of experience or demonstrated equivalency of experience and/or education. * Due to the nature of the project, US citizenship is required. Preferred Qualifications: * Experience working in a time-sensitive environment with direct client interface and high-level accountability. * Effective written and verbal communication skills. Additional Information * All your information will be kept confidential according to EEO guidelines. About AECOM AECOM is proud to offer comprehensive benefits to meet the diverse needs of our employees. Depending on your employment status, AECOM benefits may include medical, dental, vision, life, AD&D, disability benefits, paid time off, leaves of absences, voluntary benefits, perks, flexible work options, well-being resources, employee assistance program, business travel insurance, service recognition awards, retirement savings plan, and employee stock purchase plan. AECOM is the global infrastructure leader, committed to delivering a better world. As a trusted professional services firm powered by deep technical abilities, we solve our clients' complex challenges in water, environment, energy, transportation and buildings. Our teams partner with public- and private-sector clients to create innovative, sustainable and resilient solutions throughout the project lifecycle - from advisory, planning, design and engineering to program and construction management. AECOM is a Fortune 500 firm that had revenue of $16.1 billion in fiscal year 2024. Learn more at aecom.com. What makes AECOM a great place to work You will be part of a global team that champions your growth and career ambitions. Work on groundbreaking projects - both in your local community and on a global scale - that are transforming our industry and shaping the future. With cutting-edge technology and a network of experts, you'll have the resources to make a real impact. Our award-winning training and development programs are designed to expand your technical expertise and leadership skills, helping you build the career you've always envisioned. Here, you'll find a welcoming workplace built on respect, collaboration and community-where you have the freedom to grow in a world of opportunity. As an Equal Opportunity Employer, we believe in your potential and are here to help you achieve it. All your information will be kept confidential according to EEO guidelines.

A leading life sciences consultancy is seeking a Senior Quality Consultant to deliver quality and compliance-related services. The ideal candidate should have a B.S. in life sciences, 15 years of experience in quality assurance, and be bilingual in Spanish and English. Responsibilities include conducting gap assessments, evaluating inspection readiness programs, and participating in complex investigations. This position allows for remote work and is integral to ensuring the compliance of pharmaceutical products. Apply today for this exciting opportunity in Miami, FL. #J-18808-Ljbffr

A leading life sciences consultancy is seeking a Senior-level Quality Consultant to assist with delivering quality and compliance-related services. Candidates should have a B.S. in life sciences, 15 years of relevant experience, and bilingual skills in Spanish and English. Responsibilities include conducting gap assessments and evaluating inspection readiness programs. Remote work is available, and strong interpersonal and communication skills are essential. #J-18808-Ljbffr

Quality Engineering Manager (Accenture LLP; Charlotte, NC): Accenture LLP has multiple openings for the position of Quality Engineering Manager in Charlotte, NC, and the job duties are as follows: Design and maintain master test plan that encompasses test strategy for functional and end-to-end testing, test environments, and automation approach. Define test models (plans, data, scripts, and expected results) and entry/exit criteria. Drive quality testing solutions by planning and constructing test scripts through use of quality processes and methodologies for Accenture or its clients. Define, track, and publish test metrics, including code coverage, quality, and performance to the team and client. Execute testing efforts by delivering application and component releases. Coordinate and execute regression testing, test automation, performance testing, functionality, and user acceptance testing. Determine and meet time estimates and schedules for testing efforts. Develop, update, and maintain quality testing standards and procedures. Lead others on the testing team and manage process questions and issues. Optimize process and methods to deliver quality work. Allocate test resources and guide on priorities to application tests in a multi-test environment and different testing phases. Act independently to determine methods and procedures for new assignments. Make decisions that impact the team through regular consultation with senior management and adhere to strategic direction provided. Qualification BASIC QUALIFICATIONS: Must have a bachelor's degree in Computer Science, Technology, Computer Information Systems, Computer Applications, Engineering, or related field, plus 5 years of progressive post-baccalaureate experience in the IT consulting industry. Must have 5 years of experience in each of the following: Testing custom and enterprise solutions; Utilizing Agile and Waterfall methodologies to deliver IT projects; Providing solutions in planning, constructing, and executing test scripts; Leading, designing, and implementing test plans and cases for testing phases, including Smoke, Regression, and end-to-end integrations; Performing and leading test execution of all test cycles; Conducting defect triage meetings and presenting status reporting with development and business teams; and Managing teams and work efforts across different shores. Must have 3 years of experience in each of the following: Managing testing, defects, and user stories using Quality Center or JIRA; Designing and implementing test automation frameworks using Tosca; Automating API testing using Soap UI or Postman and performing back-end validations against database technologies including MSSQL Server or Oracle; Executing automation suite in a CI/CD pipeline; and Maintaining automation suite utilizing version control systems in Tosca. Must have willingness and ability to travel domestically approximately 80% of the time to meet client needs. To apply, please click the 'APPLY' button. #LI-DNI #IND-DNI Locations

Quality Engineering Manager (Accenture LLP; Charlotte, NC): Accenture LLP has multiple openings for the position of Quality Engineering Manager in Charlotte, NC, and the job duties are as follows: + Design and maintain master test plan that encompasses test strategy for functional and end-to-end testing, test environments, and automation approach. + Define test models (plans, data, scripts, and expected results) and entry/exit criteria. + Drive quality testing solutions by planning and constructing test scripts through use of quality processes and methodologies for Accenture or its clients. + Define, track, and publish test metrics, including code coverage, quality, and performance to the team and client. + Execute testing efforts by delivering application and component releases. + Coordinate and execute regression testing, test automation, performance testing, functionality, and user acceptance testing. + Determine and meet time estimates and schedules for testing efforts. + Develop, update, and maintain quality testing standards and procedures. + Lead others on the testing team and manage process questions and issues. + Optimize process and methods to deliver quality work. + Allocate test resources and guide on priorities to application tests in a multi-test environment and different testing phases. + Act independently to determine methods and procedures for new assignments. + Make decisions that impact the team through regular consultation with senior management and adhere to strategic direction provided. BASIC QUALIFICATIONS: Must have a bachelor's degree in Computer Science, Technology, Computer Information Systems, Computer Applications, Engineering, or related field, plus 5 years of progressive post-baccalaureate experience in the IT consulting industry. Must have 5 years of experience in each of the following: + Testing custom and enterprise solutions; + Utilizing Agile and Waterfall methodologies to deliver IT projects; + Providing solutions in planning, constructing, and executing test scripts; + Leading, designing, and implementing test plans and cases for testing phases, including Smoke, Regression, and end-to-end integrations; + Performing and leading test execution of all test cycles; + Conducting defect triage meetings and presenting status reporting with development and business teams; and + Managing teams and work efforts across different shores. Must have 3 years of experience in each of the following: + Managing testing, defects, and user stories using Quality Center or JIRA; + Designing and implementing test automation frameworks using Tosca; + Automating API testing using Soap UI or Postman and performing back-end validations against database technologies including MSSQL Server or Oracle; + Executing automation suite in a CI/CD pipeline; and + Maintaining automation suite utilizing version control systems in Tosca. Must have willingness and ability to travel domestically approximately 80% of the time to meet client needs. To apply, please click the 'APPLY' button. #LI-DNI #IND-DNI Requesting an Accommodation Accenture is committed to providing equal employment opportunities for persons with disabilities or religious observances, including reasonable accommodation when needed. If you are hired by Accenture and require accommodation to perform the essential functions of your role, you will be asked to participate in our reasonable accommodation process. Accommodations made to facilitate the recruiting process are not a guarantee of future or continued accommodations once hired. If you would like to be considered for employment opportunities with Accenture and have accommodation needs such as for a disability or religious observance, please call us toll free at **************** or send us an email or speak with your recruiter. Equal Employment Opportunity Statement We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. For details, view a copy of the Accenture Equal Opportunity Statement (******************************************************************************************************************************************** Accenture is an EEO and Affirmative Action Employer of Veterans/Individuals with Disabilities. Accenture is committed to providing veteran employment opportunities to our service men and women. Other Employment Statements Applicants for employment in the US must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States. Candidates who are currently employed by a client of Accenture or an affiliated Accenture business may not be eligible for consideration. Job candidates will not be obligated to disclose sealed or expunged records of conviction or arrest as part of the hiring process. Further, at Accenture a criminal conviction history is not an absolute bar to employment. The Company will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. Additionally, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the Company's legal duty to furnish information. California requires additional notifications for applicants and employees. If you are a California resident, live in or plan to work from Los Angeles County upon being hired for this position, please click here for additional important information. Please read Accenture's Recruiting and Hiring Statement for more information on how we process your data during the Recruiting and Hiring process.

About the Role Our client is seeking an experienced Safety & Quality Manager to lead plant-wide initiatives that ensure safe operations, high-quality output, and strong process discipline. This role plays a critical part in shaping a culture of accountability, continuous improvement, and proactive risk reduction across the facility. You will partner closely with production, maintenance, engineering, and leadership teams to strengthen safety behaviors, reduce operational risks, and reinforce quality standards throughout all stages of manufacturing. Key Responsibilities Safety Leadership Champion a safety-first culture through coaching, training, and daily engagement with floor teams. Conduct regular facility inspections, risk assessments, incident investigations, and follow-up actions to prevent recurrence. Ensure compliance with corporate and regulatory safety expectations. Lead or support emergency preparedness planning, safety observations, and behavior-based safety initiatives. Quality Management Oversee plant-level quality systems, documentation, and standard operating procedures. Monitor product quality trends, customer feedback, and internal data to proactively address quality risks. Lead root-cause investigations and corrective/preventive actions (CAPA). Collaborate with cross-functional teams on process control, testing standards, and continuous improvement initiatives. Continuous Improvement Drive waste reduction, defect reduction, and efficiency improvement efforts across operations. Facilitate structured problem-solving activities (e.g., root cause analysis, process stabilization). Support team members through coaching and development to enhance quality and safety performance. Lean experience is a plus. Team Collaboration & Leadership Partner with supervisors and operators to ensure consistent adherence to plant policies and quality/safety expectations. Provide training on safety practices, quality procedures, and operational standards. Contribute to daily production meetings, audits, and cross-functional projects. Qualifications Bachelor's degree Experience working in a manufacturing or industrial environment is required. Background in safety, quality, or combined operational roles with demonstrated leadership on the plant floor. Familiarity with regulatory or industry compliance requirements. Strong communication, follow-through, and problem-solving skills. Ability to engage and influence employees at all levels. Benefits 401k PTO Medical Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ******************************************* The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements

Job Title: Program Manager Pay Range: $45 - 50/Hr. On W2 (Depending on Experience/Interview) Duration: 2 Year Contract Role (Possible Extension or Temp to Hire for Right Candidate) Shift times: Monday - Friday 08:00 AM to 05:00 PM Job Description: The Management Systems Assessment, ISO Assessor is responsible for providing expertise and knowledge in ISO management systems activities for the company and delivering to objectives supporting ISO certification. This is a position where the candidate must be able to work independently in a team environment. Develop and implement processes and workflows for global compliance as it pertains to Support all business groups in order to realize goals and objectives for ISO certifications. Provide management systems controls training on quality, and environmental, health & safety, compliance and basic quality / environmental / health & safety fundamentals, as required. Work with quality/EHS and technical teams to implement ISO compliant management systems Collaborate with teams to document processes/ flows and to correct discrepant business processes critical to ISO certification Develop systems to ensure quality performance and continuous improvement of the established and reconciled processes. Support and participate in ISO 9001, ISO 14001, & 45001 conformance internal & external audits Ensure audit results are formally recorded and reported and corrective and preventive actions are documented. Follow up and collaborate with team members on corrective actions resulting from internal / external audits Evaluate applicable corrective and preventive action responses to the audit findings for adequacy and timeliness. Elevate issues to management as appropriate. Assist in the establishment of management systems' metrics Drive continuous improvement of the integrated Quality, and EH&S Management Systems. Minimum Qualification Bachelor's degree Excellent written and communication skills in English Demonstrated expertise in promoting and enforcing environmental compliance and other quality conformance. Proficient in information & data collection, verification, and analysis. Excellent time-management and organizational skills; disciplined & detail-oriented. Ability to work independently with minimum guidance. Constructive advocacy, influence & negotiation skills, at all levels as well as across cultures. Preferred Qualification Project Management (PMP or Agile) a plus. Professional certifications ISO Lead Auditor “Russell Tobin offers eligible employees comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors.”

GL Staffing is currently seeking for a Quality Manager - 503B Sterile Manufacturing. The Quality Manager serves as a key Quality presence on the manufacturing floor and supports FDA inspections under the direction of the Director of Quality. Salary: 100k - 115k a year (based on experience) Position Summary The Quality Manager is responsible for managing day-to-day Quality operations for a 503B outsourcing facility engaged in sterile IV bag and vial manufacturing. This role ensures compliance with FDA cGMP requirements (21 CFR Parts 210/211), 503B regulations, and applicable USP standards, while providing hands-on Quality oversight of aseptic processing, batch record review, investigations, validation activities, and product release. This position does not set corporate Quality strategy but is fully accountable for execution, compliance, and inspection readiness within manufacturing operations. Key Responsibilities Quality Operations Manage daily Quality activities supporting sterile manufacturing and aseptic processing operations Review and approve batch production records, deviations, investigations, and CAPAs Execute and support final batch disposition and product release in accordance with approved procedures Ensure documentation accuracy, completeness, and compliance with data integrity (ALCOA+) principles Support deviation trending, root cause analysis, and effectiveness checks Compliance & Quality Systems Ensure ongoing compliance with: FDA 21 CFR Parts 210/211 503B outsourcing facility requirements Applicable USP standards Maintain, revise, and approve SOPs related to Quality systems and sterile manufacturing Manage and support: Deviation and CAPA systems Change control activities impacting sterile operations Vendor qualification, requalification, and supplier oversight Vendor audits and quality agreements Participate in internal audits and inspection readiness activities Serve as a Quality SME during FDA inspections and regulatory audits under direction of the Director of Quality Sterile Manufacturing Oversight Provide hands-on Quality oversight of sterile manufacturing operations, including: Aseptic compounding and filling Sterile filtration processes Automated IV bag filling machines and associated manual processes Manual sterile IV vial production Large-volume automated vial filling machines Mixing and compounding equipment used in sterile manufacturing IV bag filling, sealing, labeling, and packaging operations Review and evaluate: Environmental monitoring data Sterility testing results (USP ) Endotoxin testing (USP ) Particulate testing (USP ) Media fill and aseptic process simulation outcomes Support equipment qualification and process validation activities, including IQ/OQ/PQ, and ongoing validated state maintenance. Cross-Functional Support Work closely with Manufacturing, Validation, Microbiology, Engineering, and Facilities teams Provide GMP and aseptic technique training support to manufacturing personnel Support and review: cGMP validation documentation BMS (Building Management Systems) and CMS (Controlled/Computerized Monitoring Systems) data Participate in risk assessments and continuous improvement initiatives Required Qualifications Bachelor's degree in Chemistry, Biology, Microbiology, Engineering, Pharmacy, or related field preferred but not required Minimum of 3 years of experience in a Quality role within a 503B outsourcing facility Demonstrated hands-on experience with: Aseptic processing and sterile manufacturing oversight Batch record review and product release Deviation investigations and root cause analysis CAPA development, implementation, and effectiveness verification Required experience with Quality Systems and compliance activities, including: cGMP validation processes (equipment, utilities, and processes) BMS and CMS oversight Deviation and CAPA management systems Vendor qualification and supplier management Vendor audits SOP authoring, review, approval, and lifecycle management Working knowledge of: FDA cGMP regulations (21 CFR Parts 210/211) 503B outsourcing facility regulatory requirements USP , , , , and Preferred Qualifications Prior experience with IV bag manufacturing or large-volume parenteral production Background in Microbiology or Sterility Assurance Experience supporting FDA inspections at a 503B outsourcing facility Familiarity with electronic Quality Management Systems (e.g., MasterControl, TrackWise, or similar)

Baker Tilly is a leading advisory, tax and assurance firm, providing clients with a genuine coast-to-coast and global advantage in major regions of the U.S. and in many of the world's leading financial centers - New York, London, San Francisco, Los Angeles, Chicago and Boston. Baker Tilly Advisory Group, LP and Baker Tilly US, LLP (Baker Tilly) provide professional services through an alternative practice structure in accordance with the AICPA Code of Professional Conduct and applicable laws, regulations and professional standards. Baker Tilly US, LLP is a licensed independent CPA firm that provides attest services to its clients. Baker Tilly Advisory Group, LP and its subsidiary entities provide tax and business advisory services to their clients. Baker Tilly Advisory Group, LP and its subsidiary entities are not licensed CPA firms. Baker Tilly Advisory Group, LP and Baker Tilly US, LLP, trading as Baker Tilly, are independent members of Baker Tilly International, a worldwide network of independent accounting and business advisory firms in 141 territories, with 43,000 professionals and a combined worldwide revenue of $5.2 billion. Visit bakertilly.com or join the conversation on LinkedIn, Facebook and Instagram. Please discuss the work location status with your Baker Tilly talent acquisition professional to understand the requirements for an opportunity you are exploring. Baker Tilly is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status, gender identity, sexual orientation, or any other legally protected basis, in accordance with applicable federal, state or local law. Any unsolicited resumes submitted through our website or to Baker Tilly Advisory Group, LP, employee e-mail accounts are considered property of Baker Tilly Advisory Group, LP, and are not subject to payment of agency fees. In order to be an authorized recruitment agency ("search firm") for Baker Tilly Advisory Group, LP, there must be a formal written agreement in place and the agency must be invited, by Baker Tilly's Talent Attraction team, to submit candidates for review via our applicant tracking system. Job Description: Are you interested in joining one of the fastest growing public accounting firms? Would you like the ability to focus on one industry sector and further become an expert for your clients? If yes, consider joining Baker Tilly (BT) as an Audit Senior Manager! This is a great opportunity to be a valued business advisor delivering industry-focused audit and other assurance services to middle market clients. You will work side-by-side with firm leadership to serve clients and build the business, having a direct impact on the firm's success. Additionally, you will be a mentor and coach to a group of talented staff, utilizing your expertise to help develop their technical and professional skills. If you are invigorated by these exciting challenges, then this could be the right opportunity for you! As one of the fastest growing firms in the nation, BT has the ability to offer you upward career trajectory, flexibility in how and where you get your work done and meaningful relationships with clients, teammates and leadership who truly care about you and your development. You will enjoy this role if: You are looking for an opportunity to build your career in a specific industry, becoming an industry expert to the clients you serve. You can see yourself as a trusted business advisor, working face-to-face with clients to find creative solutions to complex accounting and business challenges. You want to work for a leading CPA advisory firm that serves middle market clients and whose owners have both their clients' and employees' best interests in mind and are transparent in their decisions. You value your development and want to work for a firm that provides you the autonomy to own your schedule and career through structured programs (ask us about My Time Off, My Development and Dress for Your Day!). You want to contribute to your engagement team's professional growth and develop your own leadership skills to build a career with endless opportunities now, for tomorrow. What you will do: Be a trusted member of the engagement team providing various assurance and consulting services to industry specific clients, positively impacting their financial statements, profitability, and business operations through: Proactively engaging with your clients throughout the year to understand business goals and challenges. Developing and implementing appropriate testing to assess deficiencies of internal controls and make recommendations for improvement. Managing all fieldwork to ensure quality service and timely delivery of results. Playing an active role in providing valuable financial statement guidance and business recommendations based upon various testing performed and information gathered. Delivering business insight through thoughtful review, analysis, and discussion. Manage client engagement staffing, billings/collections, and ensure client profitability targets are met. Utilize your entrepreneurial skills to network and build strong relationships internally and externally with the goal of acquiring new clients, projects, and revenue. Invest in your professional development individually and through participation in firm wide learning and development programs. Support the growth and development of team members through the Baker Tilly Care and Teach philosophy, helping associates meet their professional goals. Enjoy friendships, social activities and team outings that encourage a work-life balance. Qualifications Bachelor's degree in accounting required, masters or advanced degree desirable CPA required Eight (8)+ years' experience providing financial statement auditing services in a professional services firm desired Five (5)+ years' of supervisory experience, mentoring and counseling associates desired Demonstrated management, analytical, organization, interpersonal, project management, communication skills Ability to lead and supervise others, provide exceptional client service, demonstrate commitment to continuous learning in order to stay current regarding applicable strategies, see the "big picture" as well as the details, display appropriate ethical knowledge and commitment, and exhibit a sense of urgency and commitment to quality and the timely completion of projects. Eligibility to work in the U.S. without sponsorship preferred. The compensation range for this role is $122,300 to $231,870. Actual compensation is influenced by a variety of factors including but not limited to skills, experience, qualifications, and geographic location. #LI-NH1

Aramark Healthcare+ has an immediate need for a System Food Service Quality and Standards Manager for The Children's Hospital of Philadelphia. The System Food Service Quality and Standards Manager will be responsible for engaging with front line managers and front line associates to manage safety, sanitation and compliance in the food service operation, and to develop corrective action plans and assist with implementing these plans. Position may also facilitate training on a 1:1 or group basis. Job Responsibilities Conduct regular on-site Quality Assurance Audits utilizing the Aramark Productivity Portal Develop and implement corrective action plans for locations identified as not meeting Aramark Standards as it relates to food ordering, production and service Focus on implementation and training of Aramark's 5 P's of Food Management Work with client constituents to develop training material for client front line staff Work with VPO, DM's and Director of Culinary to develop various training material to assist in driving operational outcomes to the operating locations Continually seek to improve performance; hold staff accountable for challenging goals Provide leadership in the implementation and maintenance of internal control and business process improvement initiatives. Develop and be accountable for a culture that creates a safe work environment. Develop and execute a process for monitoring, testing and reporting compliance. Identify risks or opportunities to strengthen internal controls and present recommendations for process improvement initiatives. At Aramark, developing new skills and doing what it takes to get the job done make a positive impact for our employees and for our customers. In order to meet our commitments, job duties may change or new ones may be assigned without formal notice. Qualifications Bachelor's degree or equivalent experience Requires at least 1-3 years of experience in a food service management role Healthcare experience required Strong interpersonal skills Ability to maintain effective client and customer rapport for mutually beneficial business relationships Ability to demonstrate excellent customer service using Aramark's standard service model Ability to maintain an effective working relationship with other departments to a unified food service experience for all customers Education About Aramark Our Mission Rooted in service and united by our purpose, we strive to do great things for each other, our partners, our communities, and our planet. At Aramark, we believe that every employee should enjoy equal employment opportunity and be free to participate in all aspects of the company. We do not discriminate on the basis of race, color, religion, national origin, age, sex, gender, pregnancy, disability, sexual orientation, gender identity, genetic information, military status, protected veteran status or other characteristics protected by applicable law. About Aramark The people of Aramark proudly serve millions of guests every day through food and facilities in 15 countries around the world. Rooted in service and united by our purpose, we strive to do great things for each other, our partners, our communities, and our planet. We believe a career should develop your talents, fuel your passions, and empower your professional growth. So, no matter what you're pursuing - a new challenge, a sense of belonging, or just a great place to work - our focus is helping you reach your full potential. Learn more about working here at ***************************** or connect with us on Facebook, Instagram and Twitter. Nearest Major Market: Philadelphia

ANDRITZ Inc. is the world's leading pulp & paper industry supplier with the broadest technology portfolio and more than 2,000 specialists in 40 countries. For more than 150 years, we have been a driving force in the evolution of solutions and services for industries ranging from pulp & paper, food, chemical, and mining & minerals. As the OEM for many of the world's leading brands, we have the solutions and services to transform our customers' business to meet tomorrow's changing demands, wherever they are and whatever the challenge. Product Quality Manager Position Summary ANDRITZ is seeking a seasoned Quality professional with significant experience in Quality Assurance and Quality Control for project-based engineered equipment. The ideal candidate will bring deep welding knowledge, strong familiarity with industry codes (AWS, ASME), and hands-on expertise supporting fabrication for pulp & paper, chemical, power, and related industrial applications. Welding experience is the #1 qualification for this position. Candidates must meet this requirement to proceed. Top Priority Qualifications (Must-Have) Extensive welding experience supporting industrial fabrication and equipment manufacturing. Working knowledge of AWS Codes (especially AWS D1.1, D1.6) - required. Knowledge of metals including carbon steel, stainless, duplex, and alloy materials; welding of structural and pressure-part fabrication - required. Working knowledge of ASME Codes (especially ASME Section V, IX) - desired. CWI Certification and ASNT SNT-TC-1A Level II in any NDE method - preferred. Principal Duties Lead and manage all Quality Assurance activities for assigned engineered equipment projects. Develop Quality Monitoring Plans for large, multi-fabrication projects. Create and implement Inspection and Test Plans (ITPs) for equipment and supplier deliverables. Audit, evaluate, and qualify global suppliers-including Asia and Europe. Provide technical support to engineering and project management regarding quality requirements. Communicate quality expectations across internal departments and with customers. Implement controls to ensure quality compliance across all equipment and components. Coordinate inspections of structural, mechanical, welded, and machined parts. Manage third-party inspectors and cross-division ANDRITZ inspection resources. Review supplier quality programs, documentation, NCRs, and provide stakeholder feedback. Support root cause analysis, corrective action processes, and supplier improvement initiatives. Education & Experience Bachelor's degree in Mechanical, Materials, or Industrial Engineering (Master's is a plus). Minimum 5 years of experience in Quality or Project Management in pulp & paper, power, metals, chemical, or process industries, or within a large fabrication environment. Strong working knowledge of machining, surface preparation, and mechanical testing. Ability to perform dimensional inspections and verify compliance during multiple fabrication stages. Experience with supplier auditing - preferred. Experience with failure analysis and RCA - preferred. Knowledge of pulp & paper equipment - preferred. Ability to travel internationally (Asia and Europe). Work Environment This role requires daily cross-functional interaction with vendors, Sales, Engineering, Production, Quality Control, and Materials. Overnight travel by air or ground is required. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability.

This position for Quality Management Systems (QMS) will ensure compliance with Good Distribution Practices (GDP), 21 CFR regulations, and other applicable standards in a warehouse environment specializing in clinical trial supplies. This role involves implementing, monitoring, and enhancing quality systems to maintain regulatory compliance and ensure operational excellence. Essential Duties and Responsibilities: Manage and oversee the QMS processes, including documentation, control, and implementation of policies and procedures in compliance with GDP, 21 CFR, and industry standards. Conduct routine internal & external audits of warehouse operations to ensure adherence to quality guidelines, regulatory requirements, and standard operating procedures (SOPs). Coordinate and manage deviation investigations, CAPA (Corrective and Preventive Actions), change control processes and Risk Assessments. Ensure Vendor/Customer Verification & Qualification on timely basis also should do audit if required on site of partners site. Accurate documentation check for the each transaction been carried out for the inbound and outbound by the operation team. Ensure accuracy and effective maintenance of the eQMS portal for all quality-related documentation and activities. Reviewing and Authorizing Quality related documents and agreements. Prepare and review quality documentation such as SOPs using eQMS portal, validation protocols, and training records to ensure they meet regulatory and organizational standards. Support regulatory inspections, internal audits, and customer audits by providing necessary documentation and ensuring compliance readiness. Monitor and evaluate the effectiveness of QMS processes through metrics and reporting, identifying areas for improvement. Conduct training sessions for staff on QMS policies, GDP requirements, and regulatory compliance. Collaborate with cross-functional teams, including warehouse operations, logistics, and regulatory affairs, to address quality-related issues and implement improvements. Training the operation team personnel in warehouse. Stay updated on evolving regulatory requirements and incorporate changes into QMS practices. Yearly review on the SOPs if any changes need to be made and upgrade the processes. All documents record should be kept in controlled and secured manner. Work Experience Qualifications: Proven 5+ years of work experience in QMS role within the Pharmaceutical Industry. Result driven orientation having solid customer service attitude with excellent negotiation skills. Previous experience in SAP & MS Office will be an added advantage Must have keen attention to detail and possess proper phone and email etiquette. Ability to stay organized while effectively prioritizing multiple projects at once. High attention to detail when completing projects. Person should be in position to travel for meetings and exhibitions and events. Strong time management skills to complete projects by deadlines. Self-motivated individual who takes ownership of their projects. Administrative skills (MS Office and Google Workspace are required). Maintain excellent verbal, writing, and language skills.

Yoh is hiring a Sr. QA Technician for our Pharmaceutical Manufacturing client in St. Louis, Missouri. This is a great opportunity to expand your skillsets and join a growing team! Job Responsibilities: Ensure completion of require training, work (including document review, batch release, QA on-the-floor, AQLs), and timely release of materials and batches. Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP). Responsible for the thorough and efficient review and disposition of completed batch record documentation ensuring adherence to Good Documentation Practices, cGMPs and applicable local procedures. Responsible for performing and / or overseeing performance of Quality Assurance On The Floor tasks including but not limited to performing AQL inspections, performing clearances for manufacturing areas and providing Quality input and guidance to manufacturing personnel. Responsible for with dispositioning finished product, raw materials/ components and intermediates through an all-inclusive documentation review and cross reference of electronic quality systems. Responsible with release of incoming raw materials and components per applicable local procedures. This may include support for labeling dispositioned raw materials and components with appropriate status indicator labels. Ensure a safe and quality working environment through training, awareness, and compliance to safety/Quality guidelines and SOP's. Ensure the maintenance of department, premises and equipment. Perform all work in compliance with site safety and radiation protection guidelines. Assist with quality investigations in order to determine root cause and applicable CAPAs. Skills/Education Required: Associate Degree in life science or a related field with completion of 4 college-level life science courses required. Bachelor Degree in life science or a related field preferred. Work experience is considered in lieu of degree. Three or more years of quality and production experience in a cGMP environment/facility. Working Conditions: Willing to work in plant producing radioactive materials and complete required safety trainings to work on the floor. The ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment. Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed. Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants. Schedule: 8:00 am - 4:30 pm, Monday - Friday Estimated Min Rate: $20.30 Estimated Max Rate: $29.00 What's In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) Health Savings Account (HSA) (for employees working 20+ hours per week) Life & Disability Insurance (for employees working 20+ hours per week) MetLife Voluntary Benefits Employee Assistance Program (EAP) 401K Retirement Savings Plan Direct Deposit & weekly epayroll Referral Bonus Programs Certification and training opportunities Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is 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, or status as a protected veteran. Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: **********************************

Expand your professional portfolio as a Logistics Quality Specialist II with MAU at our client in Greer, SC. As a Logistics Quality Specialist II, you will provide onsite production support to ensure the supplier's logistical line side delivery performance by using efficient problem-solving processes. This is a long-term contract position with an opportunity for hire by the client. Our client, a premier automotive company, is located in the upstate area of SC. REWARDS: Major Medical Coverage, including dental and vision 401k with Employer Matching Term life Short-term disability Accidental loss Uniform allowance Paid time off Paid holidays Market leading pay Opportunity for advancement REQUIREMENTS: BA/BS degree in Supply Chain Management, Logistics, or Psychology, OR 4+ years of experience in the related area (manufacturing preferred) 4+ years of experience in logistics issue resolution in the following areas: Supply Chain Planning Materials Requirement Planning (MRP) Material Control Production Control Warehouse Operations Receiving Operations VPS LEAN Manufacturing Returnable Container Management JIS WoW and Transport Planning 3 - 5 years of experience with SAP, SCQ Ample, LPKM, GIS, and B2B 3 - 5 years of experience with Wrong Delivery Mislabeling analysis and issue resolution (e.g., L-FMEA approach) Exceptional verbal and written communication skills Onsite experience steering Logistics improvement at Suppliers while developing successful working relationships under stressful conditions RESPONSIBILITIES: Guarantee supplier launch and series capability by completing logistical qualification activities in the PDP (Product Development Process) Represent the company in high-stress, production-critical situations Represent the company and maintain professional relationships with suppliers Establish working networks with peers and management to ensure assignment effectiveness Provide transparency by assigning measures to suppliers, maintaining a list of open points, and creating PowerPoint presentations Organize effective meetings, provide directions, and follow through to ensure measures are met Assume the Supplier Logistics tasks in the event of an emergency Logistics Planning Production Planning Material Control Inventory Analyst Logistics Manager Self-direct to carry out assigned project responsibilities and meet all deliverables within the designated deadlines Perform other duties as assigned MAU Workforce Solutions is an innovative global company with extensive experience providing solutions for success in staffing, recruiting, technology and outsourcing to our clients, employees, and applicants. Headquartered in Augusta, GA since 1973, MAU is a family and minority-owned company offering better processes and better people to create efficiencies and greater profits for our clients. Our relationships with world-class companies, our training programs and our culture of family allow MAU to offer better results, better jobs, and better lives to those who work with us. All Applicants must submit to background check and drug screening Disclaimer: This job description is not designed to be a complete list of all duties and responsibilities required of the position

ANDRITZ Hydropower North America is part of an international technology group with an extensive portfolio of sustainable products and solutions. ANDRITZ aims to make the greatest possible contribution to a sustainable future and help its customers achieve their sustainability goals. The group has around 29,800 employees and over 280 locations in more than 40 countries. As the first equipment manufacturer in North America and a world leader in the design of hydroelectric turbines, ANDRITZ Hydropower North America has more than 185 years of know-how. In a context of energy transition, our hydroelectric innovation projects make sense. From design to construction, our innovative team of experts offers turnkey solutions. By joining ANDRITZ Hydropower, you are contributing to the development of sustainable technology, and a clean future. From water to wire - Be part of the movement! Role Description This is a full-time hybrid role for a Supplier Quality Engineer located in the Charlotte Metro area. The Supplier Quality Engineer will be responsible for evaluating and ensuring the quality of suppliers, managing supplier quality processes, and conducting supplier audits. Day-to-day tasks include monitoring supplier performance, developing and implementing Inspection and Test Plans, and collaborating with cross-functional teams to resolve quality-related issues and improve supplier processes. The role requires a proactive approach to maintaining quality standards and building strong supplier partnerships. Qualifications Expertise in Supplier Evaluation and Supplier Quality Management Proficiency in Quality Management and Quality Control processes Comprehensive knowledge and experience in Supplier Quality practices Strong problem-solving and analytical skills Excellent communication and collaboration abilities Bachelor's degree in Engineering or a related field is preferred Familiarity with industry standards related to quality and supplier management Experience in the renewable energy or hydropower industry is a plus NDE - MT, PT, VT, UT Geometric Dimensioning & Tolerancing Inspection duties may include up to 65% travel All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability. Requisition ID: 19753 Nearest Major Market: Charlotte

ANDRITZ Hydropower North America is part of an international technology group with an extensive portfolio of sustainable products and solutions. ANDRITZ aims to make the greatest possible contribution to a sustainable future and help its customers ac Quality Engineer, Quality, Engineer, Manufacturing, Power

Adecco is assisting a local client recruiting for Sr Quality Engineer opportunities in Fremont, CA. This is an excellent opportunity to join a winning culture and get your foot in provides advanced dental implants, prosthetics, CAD/CAM solutions, and regenerative products, supporting dentists and labs worldwide. If Sr Quality Engineer sounds like something you would be interested in, and you meet the qualifications listed below, apply now! **Job Summary** The Quality Engineer will maintain Bay Material's quality activities related to operations, quality control, supplier quality management, and investigations, ensuring compliance with company procedures, regulatory requirements, and ISO standards. **Duties and Responsibilities:** Manage non-conformances, conduct root cause analysis, and implement corrective and preventive actions (CAPA). Drive continuous improvement initiatives by automating measurement techniques, simplifying SPC requirements, and optimizing processes. Support validation and qualification efforts, including equipment qualification, process validation, PFMEA, and risk assessments. Facilitate technology transfer with suppliers by developing quality plans, sampling plans, and process controls. Perform statistical analyses (SPC, GRR, DOE) to control processes and reduce quality costs. Participate in Design and Process FMEA activities and update risk management files. Provide manufacturing support by troubleshooting production issues and developing inspection methods. Collaborate with QC Inspectors to select and manage metrology equipment. Manage document control processes, including ECOs and work instructions, ensuring compliance with QSR and ISO standards. Maintain compliance through process optimization and accurate record-keeping. Lead cross-functional teams and quality reviews to meet organizational goals. **Required Skill** Bachelor's degree in Engineering, Material Science, Chemistry, or Manufacturing. 5+ years of quality engineering experience in a regulated industry (medical devices, pharma, biotech, or manufacturing). Strong knowledge of ISO standards (ISO 9001, ISO 13485) and FDA regulations (21 CFR Part 820, 21 CFR Part 211). Experience producing technical documents, risk management, and quality plans. Experience in supplier audits, nonconformance investigations, and CAPA. Advanced Microsoft Excel skills; proficiency in MS Office Suite. Familiarity with US and international medical device regulations. Knowledge of quality tools (RCA, Fishbone, SPC, Pareto, process mapping). Six Sigma/Lean Manufacturing skills; APQP/PFMEA/Control Plans experience. **What's in this Sr Quality Engineer position for you?** + Pay rate: $60/hr. + Location- Fremont, CA 94538 (Onsite) + Work Schedule: Mon - Fri 8AM - 5PM + Weekly paycheck. + Dedicated Onboarding Specialist & Recruiter. + Access to Adecco's Aspire Academy with thousands of free upskilling courses. This Sr Quality Engineer is being recruited by one of our Centralized Delivery Team and not our local Branch. For instant consideration for this Sr Quality Engineer position and other opportunities with Adecco in Fremont, CA apply today! **Pay Details:** $60.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to ********************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance **Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Quality Lead - Entry Level 1st Shift Advance Services inc. is hiring Quality Lead for the northwest Houston "climate controlled" plant. This role involves working closely with Quality Management to help oversee the production floor, ensuring quality standards are met consistently, attention to detail is required as well as standing for up to 10 hours a day Shift is Monday to Friday and sometimes sat and sun. Weekends are required if scheduled with some overtime and weekend work as required unless otherwise previously approved to be off of work. Pay $14.00 per hour Key Responsibilities: Support quality assurance processes on the production floor Collaborate with leadership to maintain high standards of production Identify and help resolve quality-related issues Maintain accurate records and reports using basic computer tools Promote a culture of professionalism, respect, and integrity Basic Requirements: Leadership experience (preferred but not mandatory) Strong commitment and reliability Attention to detail Basic computer skills Respectful and professional demeanor Honesty and integrity Problem-solving abilities Ability to work flexible hours, including weekends and extended shifts (10-12 hours as needed) English proficiency Why work for Advance Services, Inc. We are your employment specialists Never a fee Weekly pay Safety and attendance incentives Health Benefits PTO Referral Incentives Apply for this job by clicking the apply button, applying our website and selecting a branch near you or calling our office at************** Please complete online application and Stop in and see our experienced friendly staff at 1530 W Sam Houston Pkwy, Houston, Tx 77043 to be considered for this immediate opportunity. Advance Services is an equal opportunity employer.

Job Title: Quality Lead Employment Type: Full-Time The Quality Lead is responsible for ensuring world-class product quality, delivery performance, and customer satisfaction across assigned production lines. This role serves as the primary quality interface for customers, suppliers, and internal teams, supporting flawless product launches, stable production, and continuous improvement throughout the product lifecycle. The Quality Lead provides tactical leadership over quality systems, staff development, customer concerns, supplier performance, and product safety while ensuring compliance with corporate, customer, and regulatory requirements. Key Responsibilities Customer Interface & Issue Resolution Serve as a primary quality contact for assigned customers, responding to requests and deliverables in a timely and thorough manner Drive continuous improvement in customer scorecards while reducing or eliminating customer rejects Establish root cause and corrective actions for customer returns through effective defect analysis Participate in customer quality reviews, audits, and concern resolution meetings as required Communicate and escalate critical quality concerns appropriately to internal leadership and customers Production Quality & Problem Solving Analyze scrap, defect, and warranty data to identify trends and improvement opportunities Lead structured problem-solving activities using objective measurement, analysis, and quality tools Read and interpret blueprints to verify product compliance and quality improvement Authorize disposition of nonconforming product and stop production when safety or major quality risks are identified Initiate preventive actions to eliminate recurring design, material, or process-related nonconformities Quality Systems & Continuous Improvement Develop, implement, and maintain the Quality Operating System, including policies, procedures, work instructions, and specifications Coordinate quality system audits to ensure compliance with TS, QS, JCI, and customer requirements Identify system gaps and drive timely corrective actions to support world-class quality and delivery Support Kaizen and continuous improvement initiatives across production and quality functions Staff Development & Leadership Maintain appropriate staffing levels to support all quality functions Train and develop quality team members to strengthen technical, analytical, and system knowledge Supervise quality staff to ensure effective resource utilization, cost control, and timely execution of responsibilities Operational Reporting & Plant Support Support daily gate board reviews, KPIs, and month-end operational meetings Provide quality performance reporting and feedback to plant teams Actively participate in plant-wide initiatives and action plan development Supply Chain & Supplier Quality Support new supplier qualification to ensure compliance with customer specifications Monitor supplier performance and ensure adherence to customer and corporate quality standards Collaborate with suppliers to address performance gaps and strengthen quality systems Program & Engineering Support Support program SDT meetings and engineering change activities (SDT, ECO, ECR) Partner with Quality Engineers and Engineering teams to support new launches and design changes Participate in VA/VE initiatives to improve product quality, cost, and efficiency Additional Responsibilities Perform other duties as assigned by the Plant Quality Manager Safety & Compliance Promote product safety and quality at all stages of development and production Ensure compliance with ISO, TS, QS, and customer-specific quality standards Support plant initiatives that promote a safe and compliant manufacturing environment Qualifications Bachelor's degree in Engineering or Quality required ASQ Quality Auditor certification preferred Strong ability to read and interpret blueprints and technical documentation Effective problem-solving, communication, and leadership skills Experience 3-5 years of experience in an industrial or manufacturing environment Experience with ISO 14001, TS 16949, and QS9000 standards Quality audit experience preferred Customer quality system experience preferred Controller and/or laboratory equipment experience preferred