Quality Manager jobs at MCC Label - 215 jobs

Wage: $65,000 - 90,000/year Hours: 1st Shift | Monday - Thursday: 7:00 am - 4:00 pm, Friday: 7:00 am - 11:00 am Are you passionate about quality, compliance, and continuous improvement in a manufacturing setting? Twin City Staffing is hiring a quality engineer for a full-time opportunity with a trusted company in the area. This role plays a critical part in maintaining high standards and ensuring all products and processes meet both internal and external quality requirements. Benefits of the quality engineer: Competitive salary Stable work schedule with early Friday wrap-up Opportunity to work with industry certifications, including NADCAP Career growth and advancement in a collaborative environment Comprehensive Medical Coverage Dental Insurance for a Healthy Smile Vision Care to Keep You Focused Flexible Spending Account (FSA) for Tax-Saving Flexibility Life Insurance to Protect What Matters Most Short- and Long-Term Disability Coverage Accident Insurance for Life's Unexpected Moments Critical Illness Coverage for Peace of Mind Duties of the quality engineer: Lead and coordinate internal and external corrective actions Conduct audits and monitor production processes for compliance with certifications and customer standards Schedule and perform internal/external audits and follow up on findings Collaborate with production teams to resolve quality-related issues Serve as the primary contact for heat treat NADCAP certification and audits Generate reports and quality data to drive continuous improvement initiatives Requirements of the quality engineer: Bachelor's degree in engineering or equivalent industrial/manufacturing quality experience Solid understanding of quality standards and production processes Proficient in Microsoft Excel, Word, and related applications Strong attention to detail, time management, and organizational skills Excellent communication and problem-solving abilities Ability to interpret technical instructions and perform relevant calculations Additional Information: Apply today! To learn more about this quality engineer position, contact Nancy at 763-571-7077. EOE Statement: Twin City Staffing 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 veteran status.

Principal Duties and Responsibilities: Serves as the primary contact for all Quality, Food Safety, and Regulatory issues. Develops, implements, and manages the Quality and Food Safety System Develops, maintains, and ensures compliance of a qualified HACCP program Ensures the effectiveness of the Master Sanitation and Pest Control programs for the facility and any associated food grade storage areas. Manages the Quality Assurance Operations and controlled documentation. Communicates compliance results to operating groups, ensures timely feedback, and provides technical support to operate processes at target. Utilizes customer and consumer complaint data to identify root cause, then communicates and provides support to implement process/product improvements. Determines the disposition of all raw materials, packaging, and finished product HOLD orders. Develops a Quality and Product Safety System that consistently meets regulatory, customer, and third-party audit requirements.

About AkzoNobel Since 1792, we've been supplying the innovative paints and coatings that help to color people's lives and protect what matters most. Our world class portfolio of brands - including Dulux, International, Sikkens and Interpon - is trusted by customers around the globe. We're active in more than 150 countries and use our expertise to sustain and enhance the fabric of everyday life. Because we believe every surface is an opportunity. It's what you'd expect from a pioneering and long-established paints company that's dedicated to providing sustainable solutions and preserving the best of what we have today - while creating an even better tomorrow. Let's paint the future together. For more information please visit ***************** 2024 Akzo Nobel N.V. All rights reserved. Job Purpose The Quality Control Manager holds a strategic and critical role in ensuring the site meets customer expectations while driving cost control and waste reduction. This position exists to lead the Site Quality Control Department, manage customer complaint response, and oversee continuous improvement initiatives related to quality control. The role is responsible for the development, maintenance, and continuous improvement of the site Quality Management System (QMS). Through leadership of key quality activities, this position mentors employees, ensures compliance with quality standards, and supports operational excellence across the site. Key Responsibilities Quality Systems & Compliance * Ensure compliance with all established safety rules, procedures, and the company's Code of Conduct. * Lead and manage the site Quality Management System, including document control, customer complaint handling, corrective and preventive actions. * Monitor changes to management system standards and ensure timely integration into site business processes. * Manage internal and external audits, ensuring readiness, effectiveness, and implementation of corrective actions. Continuous Improvement & Problem Solving * Identify deficiencies in business processes; prioritize improvement initiatives and lead cross-functional teams to implement corrective and preventive actions. * Drive continuous improvement through the use of Lean principles (ALPS) to reduce waste and improve efficiency. * Promote fact-based, data-driven problem solving across the organization. Leadership & Communication * Promote quality system awareness through regular communication and training to ensure organization-wide understanding. * Develop and deliver training programs to strengthen quality knowledge and capability. * Prepare and present reports to site and regional leadership on the effectiveness and health of the Quality Management System. * Lead, direct, coach, and mentor quality team members to support growth and performance. Customer & Supplier Interface * Serve as the Site Management Team (SMT) representative for plant quality issues and customer quality interface. * Partner with Sales and Marketing to ensure customer quality issues are effectively managed and resolved. * Support supplier quality development in collaboration with Purchasing and cross-functional teams. * Collaborate with Regional ISC, Commercial, RDI, CI, and Quality teams to ensure alignment and consistency. Level of Autonomy * Acts independently as the Site Management Team (SMT) authority for plant quality issues. * Serves as the primary customer interface for quality-related matters. * Makes independent decisions related to quality system compliance, audit readiness, corrective actions, and continuous improvement priorities. Job Requirements Education & Experience * Bachelor's degree in Chemistry, Chemical Engineering, Engineering, or a related field (or equivalent combination of education and experience). * Minimum of 7 years of quality systems experience. * Experience with process mapping, quality system development, and statistical analysis tools. * Manufacturing experience required, preferably in a quality leadership role. * Strong working knowledge of Microsoft Word, Excel, PowerPoint, and Visio. * Proven experience leading cross-functional and large teams. * Working knowledge of business management systems and governing standards (e.g., ISO 9000, TS 16949). Essential Qualifications * Demonstrated commitment to safety leadership and compliance. * Strong analytical, problem-solving, and decision-making skills. * Ability to analyze and interpret data using statistical tools (Gage R&R, DOE, t-tests, multi-vari studies). * Ability to work independently while managing multiple priorities. * Strong coaching, leadership, and communication skills. * Excellent written and verbal communication skills in English, with the ability to communicate effectively at all organizational levels. Compensation/Rewards/Benefits The salary range for these skills is: $115,000 to $135,000. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range. This salary range may also be modified in the future. * Medical insurance with HSA * Dental, Vision, Life, AD&D benefits * Annual bonus * 401K retirement savings with 6% company match * Generous vacation, personal and holiday pay * Paid Parental leave * Hybrid work for most exempt roles * Active Diversity & Inclusion Networks * Career growth opportunities on a regional and global scale * Tuition Reimbursement * Employee referral bonus At AkzoNobel we are highly committed to ensuring an inclusive and respectful workplace where all employees can be their best self. We strive to embrace diversity in a context of tolerance. Our talent acquisition process plays an integral part in this journey, as setting the foundations for a diverse environment. For this reason we train and educate on the implications of our Unconscious Bias in order for our TA and hiring managers to be mindful of them and take corrective actions when applicable. In our organization, all qualified applicants receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age or disability. Requisition ID: 50424 #LI-KG1

Looking for a job to get you out of bed? Casper is looking for a QA Manager to join our Technology team. In this role, you'll lead the QA function at Casper and transform how quality is defined, measured, and delivered across the organization. Casper has a history of shipping thoughtful, best-in-class digital experiences - and you'll be the owner of ensuring those high standards are upheld as we scale. If you're motivated, self-driven, energized by iterative development, and passionate about building exceptional software in a fast-moving environment, we'd love to meet you. Casper (Casper.com) believes everyone should sleep better. Casper has a full portfolio of obsessively engineered sleep products-including mattresses, pillows and bedding-designed by the Company's in-house design team. In addition to its e-commerce business, Casper has over 40 retail locations across the United States and its products are available at a number of retailers. When you're not catching zzz's, this is what you'll do... * Partner with Technology teams as well as cross-functional business partners - including e-commerce, marketing, finance, operations, retail, and customer experience - to ensure new launches meet Casper's quality bar * Own and evolve the QA lifecycle as part of our Agile/SCRUM processes * Work with product, design, and engineering to define user stories, acceptance criteria, and test coverage across manual and automated paths * Maintain and improve our site performance through ongoing monitoring and reporting * Lead recurring Accessibility compliance testing cycles * Create, maintain, and execute test plans and test cases * Detect, isolate, reproduce, document, and prioritize defects * Provide clear communication on QA status, product quality metrics, and release readiness across teams * Champion QA best practices and develop a lightweight center of excellence for quality at Casper Our dream candidate is/has... * Has 5+ years of QA Engineering experience, ideally with some leadership or mentorship exposure * Collaborates effectively with both technical teams and non-technical business stakeholders * Has experience with bug/task/test management systems (e.g., JIRA, TestRail) * Has experience with Web/API testing and debugging tools (e.g., Postman, Charles, Fiddler) * Understands CI/CD pipelines and how quality engineering fits into modern DevOps practices * Has experience with automated testing frameworks and is comfortable defining an automation strategy - including selecting modern tools/platforms as needed (e.g., Playwright, WebdriverIO, or other contemporary frameworks) * Has familiarity with AI-assisted testing tools or approaches - such as AI-generated test cases, autonomous regression testing, or leveraging AI agents for repeatable test automation * Is proactive, curious, and passionate about continuously improving quality processes across systems * This is a hybrid role requiring that you work 3 days per week from our NYC office. Targeted Annual Base Salary Range: $120,000-140,000 USD Casper's compensation philosophy ensures that the actual base salary is based on factors including but not limited to skills, education, experience, special training, time in position, and/or years of service. We recognize that annual base salary is just one part of a total rewards package. In addition, we offer a comprehensive benefits package, wellbeing resources, and other perks including: * Medical, vision, and dental insurance to help you with those coughs or cavities (too many waffles)... * Paid Time Off. We believe in the power of rest so take the time you need to recharge. * Dream-worthy gifted products after tenure milestones! * Employee Discount to use on whatever you like (with a few exceptions) and product discounts for friends and family! * … and more! If you dream about this stuff this job is probably right for you. We look forward to learning more about you! #LI-Hybrid

PLATING DONE RIGHT THE FIRST TIME Looking for a job where you can use your experience in quality management? Want to work with a company that has been in existence for over 60 years and values its employees? MPC Plating may have an opportunity for you. ABOUT THE COMPANY Located in Brooklyn, Ohio, MPC Plating was founded as a metal plating operation. Branching out into plastic plating in 1985, MPC now plates exclusively on plastics. MPC has remained a one-stop job shop plater, investing in work-class equipment and developing a team capable of producing products that meet the demanding specifications that our customers require in the Automotive, Appliance, Heavy Truck, and Medical Industries. We offer a competitive wage and benefits, including medical, dental, 401(k), flexible spending account, paid time off, paid holidays, and long-term disability . We have an immediate opening for a full-time Quality Manager. IATF experience is strongly preferred. POSITION SUMMARY: Provides leadership and direction to the MPC Plating quality function, including the overall quality system and associated staff. Develops, implements, and manages effective quality policies and procedures. Essential Duties and Responsibilities • Manages the employees of the Quality Department, including off-site product or process evaluations of contractors • Serves as liaison between Plastics Production and Management, with consistent daily interaction between Production and Plating regarding non-conforming parts • Responsible for the Non-Conformance process • Responsible for overseeing the Return Material Authorization (RMA) process and team • Acts as a customer advocate, developing strong relationships with customer quality departments to ensure they have a positive experience with MPC Plating • Provide data-driven feedback to upper management • Monitors quality system trends using process control methodologies, improvement actions, and ensures proper root cause analysis and corrective actions • Identifies system-wide root causes and works with department managers and teams to predict defects and complaints, then develops and implements solutions to improve • Performs plant-wide audits on quality-related activities and provides improvement plans on findings • Responds formally to customer concerns and issues through off-site visits or formal written responses • Actively participates in the resolution of product quality problems through interface with operations, sales, and customer representatives • Coordinates vendor quality issues • Coordinates IATF Certification effort and ensures we pass IATF Audits • Participates in projects as they relate to quality and associated customer satisfaction issues • Supervises quality testing projects • All other duties as assigned Required Qualifications • Quality management experience, preferably in an automotive and/or plating environment • Quality system experience • Proficient skills in Microsoft Office applications such as Microsoft Project, Excel, PowerPoint, and Word • Proficient in multiple technical disciplines, analytics, and assurance techniques. • Proven ability to lead, motivate, and develop personnel, particularly with project and cross-functional teams. • Proven ability to cultivate and maintain strong customer relationships • Ability to solve practical problems and deal with various concrete variables in situations where only limited standardization exists. • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form • Strong verbal and written communication and team-building skills Preferred Qualifications • Bachelor's degree in Engineering, Business Administration, or related discipline preferred • Working knowledge of IATF16949 quality systems and standard operating procedures • Experience in lean manufacturing and Six Sigma • Experience with Plex ERP system or similar cloud ERP systems MPC Plating is an Equal Employment Opportunity employer. If you need assistance during the application process, please contact Human Resources. Disclaimer The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time as needed.

Busch Vacuum Solutions is a leading manufacturer of vacuum pumps, compressors, and blowers for use in industries such as semiconductor manufacturing, food processing, metallurgy, biomedical, and material handling. Busch Vacuum Solutions has an immediate direct hire opportunity open for a Quality Manager at our manufacturing plant in Virginia Beach, Virginia! The Quality Manager is responsible for leading the quality team and driving all quality-related initiatives in the plant, ensuring continuous improvement in vacuum pump production while upholding the company's high manufacturing standards. This role oversees the quality department, manages customer complaint resolution, strengthens supplier quality through development and assessment, and ensures the validation of internal processes, including automated and semi-automated machining, assembly, and product testing. Serving as the primary point of contact for customers on quality matters, the Quality Manager makes final decisions on quality issues and collaborates closely with the Head of Global Quality and international quality managers to align global standards with site-level strategic initiatives. We are looking for a dynamic, detail-oriented professional with a strong commitment to preventative quality practices, advanced problem-solving skills, and operational excellence, someone who can drive continuous improvement and deliver superior outcomes. If you are a highly motivated quality professional seeking to advance your career and make a meaningful impact, apply NOW to discover why Busch Vacuum Solutions is an exceptional place to grow and thrive! Job Responsibilities * Drives company quality philosophy through a prevention oriented mindset, systems and actions * Achieves quality improvement through a leadership style that inspires both his own team work and the shop floor team work and consistent use of problem solving and other lean tools * Achieves quality improvement through a management style that is rooted in annual planning, goal setting and data / KPI oriented performance measurement * Leads the fulfilment and improvement of the company ISO system 9001:2015 standard. Develops, trains and leads all internal, and customer driven audits and actions * Develops and manages a fiscal department budget. Also able to fully understand and leverage the classic Cost of Quality model to monitor operational quality and help dive costs down * Assist in root cause and corrective action processes * Maintain internal calibration system Experience Required * 3+ years of experience managing ISO Quality Systems * Experience with performance and process capability studies (Cp/CpK), machine capability studies (Cm/CmK), machine qualification processes, statistical analysis, and reporting * Hands-on experience with quality methodologies and problem-solving tools (Six Sigma, 8D, 3D, QRQC, Ishikawa, 5 Why, FMEA, etc.) * Bachelor's degree required; engineering or other technical field preferred * Proficiency in Microsoft Office * Demonstrated expertise in high-precision manufacturing processes, including implementing and analyzing measurement systems and statistical data to achieve world-class machining and assembly standards * Experience working within ERP systems * Ability to read and interpret technical documents and specifications, including GD&T Preferred * 3+ years of proven team leadership or management experience * Certified Quality Auditor (CQA) * Experience with manufacturing software for gauge calibration and data collection * Experience with ERP and CRM systems * Strong background operating in an APQP/prevention-focused environment Personal Qualifications * Strong leadership skills and ability to develop a high-performing team. * Detail-, goal-, and safety-oriented with commitment to operational excellence. * Organized, dependable, and able to work independently or collaboratively. * Excellent problem-solving, decision-making, and communication skills. * Committed to continuous improvement and quality best practices. Job Requirements * Ability and willingness to pass a 10-panel drug screen, 7-year criminal history check * Most felonies are a disqualifier, misdemeanors are considered on a case-by-case basis * Must be willing and able to utilize all required PPE * Ability and willingness to travel (up to 10%) domestically and internationally to include overnights * Employment with Busch Vacuum Solutions requires current work authorization in the United States. Visa sponsorship is not available for this position. Physical Requirements * Frequent sitting, standing, walking; occasional climbing, squatting, kneeling, reaching above shoulder, lifting/carrying/pushing/pulling up to 50 lbs. * All applicants must be able to hear and see audible and visual alarms and must be able to wear all required PPE, such as safety shoes, electrical hazards, safety glasses, and hearing protection. Benefits & Opportunities Busch Vacuum Solutions offers an attractive benefits package, which includes medical, dental, vision, EAP, tuition reimbursement, Legal Plan, 401K, PTO, and more! Opportunity for growth and advancement via on-the-job training, paid training/certifications, tuition reimbursement, and opportunities for advancement within the company. Busch values promoting from within! Work Environment Moderately controlled manufacturing environment, moderate noise levels, fumes, and airborne particles, while working near moving mechanical parts. Reasonable accommodations may be made to help enable qualified individuals with disabilities to perform the essential functions. To accomplish this job successfully, an individual must be able to perform, with or without reasonable accommodation, each essential function satisfactorily. Why work for Busch Vacuum Solutions? As diverse and boundless as the world of vacuum is, so are the jobs and tasks at Busch. We welcome all talents, regardless of education, age, gender, or nationality; worldwide. Nearest Major Market: Virginia Beach

Job Purpose The Director of Quality Assurance will lead and oversee all aspects of the company s quality strategy, ensuring product and process compliance with applicable regulations and standards. This role is responsible for driving continuous improvement initiatives, maintaining certifications, and fostering a culture of quality throughout the organization. Duties and Responsibilities Lead the Quality Assurance department; select, manage, develop, and hold accountable team members to meet department deliverables and responsibilities. Control of suppliers including supplier approval, supplier audits, supplier monitoring and supplier corrective action. Support sustaining engineering of commercialized product from a quality perspective. Support development and design transfer of new products to production from a quality perspective. Manage the document change control process. Review and approve changes to engineering drawings, specifications and procedures. Assess impact on design and processes from a regulatory standpoint. Manage QA Engineering activities (including Design/Development and Sustaining) Lead Risk Management activities ensuring compliance with ISO 14971, including but not limited to the completion of FMEAs, Risk Assessments, and Risk Management Plans/Reports Lead material review board (MRB). Facilitate non-conforming material report (NMR) documentation, material disposition and NMR closure. Monitor and maintain corrective action / preventive action system. Conduct internal quality audits to ensure compliance to Quality System and regulatory requirements. Ensures maintenance of company Quality System is in compliance with US-FDA, MDD/MDR, ISO 13485 and other applicable country specific medical device regulations. Function as a company liaison with regulatory and/or Notified Bodies during certification/recertification audits. Collection and trending of key quality indicators for management review. Assist with regulatory submissions and technical file creation/maintenance for new products and significant changes, as needed. Adheres to all company policies, procedures and business ethics codes. Duties may be modified or assigned at any time based on business needs. Qualifications Bachelor s degree in a technical field such as Engineering or Biological Science and a minimum of ten-years experience in the field of medical device quality/manufacturing, prior experience with medical electronics preferred; Ability to read and interpret engineering drawings, schematics and specifications; Motivated, detail oriented, and well-organized with good communication skills, both written and oral; Proficient computer skills which include the use of Microsoft WORD, EXCEL, and POWERPOINT. Prior use of an electronic document control system, ERP system and FDA eMDR reporting. Certified ISO 13458 Lead Auditor or equivalent. Proficient understanding of FDA / MDD / MDR Regulations. Minimum 5 years of people management experience, including driving results through others, leading team or projects, provide training and guidance. Desirable Accreditations/Knowledge ASQ Certifications such as Manager of Quality/Organizational Excellence, Quality Engineer, Quality Auditor, Supplier Quality Professional, etc. Completion of MDR Certified training course or equivalent. Compensation The anticipated range for this position is $155,000 to $188,000 at an annual base. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, experience and location. Working Conditions A Director of Quality Assurance usually works in an office environment which includes laboratory and manufacturing areas. Occasional domestic/international travel may be required for up to 15%. A Director of Quality Assurance works a standard work week but may be required to work some evenings and weekends to meet the needs of the company. Physical Requirements Must be able to type using the keyboard of a computer. Must be able to talk, listen and speak clearly on the telephone. Must be able to lift and carry up to 50 lbs.

As Manager, Operations - ICQA, you will be responsible for end -to-end operations. You will serve as the department's senior point of escalation for all employees working in CQA. You will own the end-to-end value stream encompassing the ICQA department. You will be responsible for the operations metrics and setting the strategy for your area of the business to deliver on our operational goals. You will oversee hourly employees ensuring coaching, development and mentoring takes place regularly. Additionally, you will collaborate with the Senior Operations Management team to lead your reports through successful project implementations within specific timeframes and exemplify Saks Leadership fundamentals along the way. The Manager, Operations, ICQA, will regularly engage in site safety initiatives, ensuring the required operational procedures align to safety expectations across the department. Role Description ● Provides leadership and direction to the assigned team for each production shift ● Maintains efficient and orderly usage of supplies in their areas of responsibility ● Leads and supports team members and coordinators in the day-to-day operations ● Motivates the employees to achieve and exceed productivity and quality standards ● Works closely with other department Leaders and Management to ensure the goals and needs of the business are met ● Trains and supports processors, material handler and coordinators ● Follows and assists managers in ensuring the department's compliance with all company policies and procedures, as well as safety and industry regulations ● Complete other tasks as assigned Key Qualifications Required Qualifications (Minimum Requirements): ● High School Degree or GED required ● 1-5 years of experience in retail, wholesale, or direct to consumer warehouse operations ● Must possess basic math skills ● Effective verbal communication and problem solving skills. ● Must have understanding of the English language both written and verbal. Must communicate understanding of English during the interview process. ● Analytical skills to identify issues, trends and proper solutions to resolve any supply issues ● Effective verbal communication and problem solving skills. ● Dependable, work with a sense of urgency ● Flexible in tasks and work hours ● Detail oriented with a high degree of accuracy ● Positive attitude and team player mindset ● Proven ability to work independently ● Ability to operate an automated fulfillment system and other supporting systems as required Preferred Qualifications (nice to haves): ● Microsoft Office Suite Intermediate Skills (Excel, Word, PowerPoint, Access, Outlook) ● Google Workspace Proficiency ● May operate non-powered warehouse equipment (i.e., pallet jack) which requires some coordinated movements. ● Ability to operate the automated robotic system and other supporting systems as required ● Demonstrate an understanding with a major WMS package Physical Demands/Environmental Conditions (only required for Fulfillment Center jobs) ● Standing for extended periods of time(scheduled shift (except breaks) ● Lifting up to 50 lbs repeatedly ● Push or pull up to 50 lbs ● Walking extended distances throughout the center ● Bending, stooping, climbing ladders or stairs ● Manual dexterity of hands to count, bag, tag, sort, and package freight ● Must be able to see and hear equipment and warning signals ● Must be able to distinguish between colors 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. Saks.com is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. * The above expected salary range may have some variability based upon factors including, but not limited to, a candidate's overall experience, qualifications, and geographic location. If you are interested in the role, we encourage you to apply and, if selected to move forward in the interview process, you will have a chance to speak with our recruitment team regarding your specific salary expectations.

MGP Ingredients is a leading supplier of premium distilled spirits and food ingredient solutions. Its Distilling Solutions segment provides bourbons, whiskeys, ryes, gins, and vodkas to craft and multinational brands. MGP's own Branded Spirts business is growing following the 2021 acquisition of Luxco, a top spirits producer, bottler, supplier, and importer as well as the 2023 acquisition of Penelope Bourbon, known for its wide range of uniquely blended expressions. Ingredient Solutions delivers nutritional, functional wheat- and pea-based ingredients aligned with consumer trends. The company operates in locations across the Midwestern U.S., and overseas in Northern Ireland and Mexico. THE OPPORTUNITY: Under the guidance of the Branded Spirits Quality Manager, provides quality control leadership for the plant to ensure product safety and quality of all products produced. The Quality Control Manager ensures that the quality management programs and product safety systems such as HAACP, GMPs, SOPs, or any food safety certifications are in support of the manufacturing plant's quality initiatives and in compliance with applicable laws and regulations. The Quality Control Manager also conducts audits of processes, systems, and production to ensure excellent quality production. WHAT YOU WILL BE DOING: Responsible for all quality control programs (Quest), systems and instrumentation. Supervise all Saint Louis quality control associates. Works with R&D to ensure all product specifications are developed for new products and maintained throughout batching process and production for all products. Plans and conducts periodic internal audits to ensure compliance with appropriate procedures. Shall include raw material suppliers and co-packer audits. Works with Luxco Supply Chain and raw material suppliers on issues or defects for proper crediting, root cause analysis and corrective actions. Enters proper documentation into Raw Material Complaints program. Conducts and/or supervises studies to determine cause, effect, and corrective measures required to remedy deviations from desirable standards of quality. Ensures quality procedures, work instructions and associated documentation are properly developed, reviewed, implemented, and updated. Ensure compliance with regulatory requirements. Conduct all quality training or ensure training has been conducted for all plant employees. Demonstrate the ability to conduct independent research and ability to use problem solving/root cause analysis tools. All other duties assigned by the Branded Spirits Quality Manager. WHO WE ARE LOOKING FOR: Bachelor's Degree in Chemistry, Biology, or Chemical Engineering . Five years' experience in the food and/or beverage manufacturing industry of which 3 years is in a quality management role, preferred. Strong knowledge of all governmental regulations concerning beverage manufacturing operations, e.g. HAACP, GMP's. Setting up and controlling all plant procedures and documentation. Controlling all quality systems effectively and accurately to ensure customer satisfaction in the market. Possess excellent technical knowledge and analytical skills. Must possess a strong working knowledge of Microsoft Windows and Office. PHYSICAL REQUIREMENTS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions. While performing the duties of this position, the employee is regularly required to talk or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls. The employee is occasionally required to stand; walk; sit; and reach with hands and arms. Specific vision abilities required by this position include close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate. Includes frequently used office equipment, computer software programs, manuals, books, or other written resources, hand tools, power tools, two-way radios, and other tools/equipment/resources; Includes use of sanitation equipment and lab/field equipment. Various lab equipment, two-way radios will be required to use. If you require a reasonable accommodation in the employee selection process, please direct your inquiries to Caitlin Zbikowski, Talent Manager @ ********************. If the above speaks to you, we're excited to learn more about you! At MGP, we know that our people are our greatest strength. With different perspectives and unique ways of thinking, our employees are as varied as our products. We believe that inclusivity strengthens the organization and champions a company culture that is evolving to reflect all of us. Culture results from our behaviors, our personal commitment, our curiosity, how we collaborate, and the ways we courageously share our perspectives and expect others to do the same. Each of us can make a difference by fostering thinking and actions that empower us to connect, belong and grow together. Compensation is competitive and is commensurate with experience. MGP offers exceptional medical, dental, vision, short and long-term disability, life insurance, 401(k) Match and PTO. All successful candidates for this position will be required to submit to a criminal background check and drug test.

MGP Ingredients is a leading supplier of premium distilled spirits and food ingredient solutions. Its Distilling Solutions segment provides bourbons, whiskeys, ryes, gins, and vodkas to craft and multinational brands. MGP's own Branded Spirts business is growing following the 2021 acquisition of Luxco, a top spirits producer, bottler, supplier, and importer as well as the 2023 acquisition of Penelope Bourbon, known for its wide range of uniquely blended expressions. Ingredient Solutions delivers nutritional, functional wheat- and pea-based ingredients aligned with consumer trends. The company operates in locations across the Midwestern U.S., and overseas in Northern Ireland and Mexico. THE OPPORTUNITY: Under the guidance of the Branded Spirits Quality Manager, provides quality control leadership for the plant to ensure product safety and quality of all products produced. The Quality Control Manager ensures that the quality management programs and product safety systems such as HAACP, GMPs, SOPs, or any food safety certifications are in support of the manufacturing plant's quality initiatives and in compliance with applicable laws and regulations. The Quality Control Manager also conducts audits of processes, systems, and production to ensure excellent quality production. WHAT YOU WILL BE DOING: * Responsible for all quality control programs (Quest), systems and instrumentation. * Supervise all Saint Louis quality control associates. * Works with R&D to ensure all product specifications are developed for new products and maintained throughout batching process and production for all products. * Plans and conducts periodic internal audits to ensure compliance with appropriate procedures. Shall include raw material suppliers and co-packer audits. * Works with Luxco Supply Chain and raw material suppliers on issues or defects for proper crediting, root cause analysis and corrective actions. Enters proper documentation into Raw Material Complaints program. * Conducts and/or supervises studies to determine cause, effect, and corrective measures required to remedy deviations from desirable standards of quality. * Ensures quality procedures, work instructions and associated documentation are properly developed, reviewed, implemented, and updated. * Ensure compliance with regulatory requirements. * Conduct all quality training or ensure training has been conducted for all plant employees. * Demonstrate the ability to conduct independent research and ability to use problem solving/root cause analysis tools. * All other duties assigned by the Branded Spirits Quality Manager. WHO WE ARE LOOKING FOR: * Bachelor's Degree in Chemistry, Biology, or Chemical Engineering required. * Five years' experience in the food and/or beverage manufacturing industry of which 3 years is in a quality management role, preferred. * Strong knowledge of all governmental regulations concerning beverage manufacturing operations, e.g. HAACP, GMP's. * Setting up and controlling all plant procedures and documentation. * Controlling all quality systems effectively and accurately to ensure customer satisfaction in the market. * Possess excellent technical knowledge and analytical skills. Must possess a strong working knowledge of Microsoft Windows and Office. PHYSICAL REQUIREMENTS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions. While performing the duties of this position, the employee is regularly required to talk or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls. The employee is occasionally required to stand; walk; sit; and reach with hands and arms. Specific vision abilities required by this position include close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate. Includes frequently used office equipment, computer software programs, manuals, books, or other written resources, hand tools, power tools, two-way radios, and other tools/equipment/resources; Includes use of sanitation equipment and lab/field equipment. Various lab equipment, two-way radios will be required to use. If you require a reasonable accommodation in the employee selection process, please direct your inquiries to Caitlin Zbikowski, Talent Manager @ ********************. If the above speaks to you, we're excited to learn more about you! At MGP, we know that our people are our greatest strength. With different perspectives and unique ways of thinking, our employees are as varied as our products. We believe that inclusivity strengthens the organization and champions a company culture that is evolving to reflect all of us. Culture results from our behaviors, our personal commitment, our curiosity, how we collaborate, and the ways we courageously share our perspectives and expect others to do the same. Each of us can make a difference by fostering thinking and actions that empower us to connect, belong and grow together. Compensation is competitive and is commensurate with experience. MGP offers exceptional medical, dental, vision, short and long-term disability, life insurance, 401(k) Match and PTO. All successful candidates for this position will be required to submit to a criminal background check and drug test.

Founded over 35 years ago, First Quality is a family-owned company that has grown from a small business in McElhattan, Pennsylvania into a group of companies, employing over 5,000 team members, while maintaining our family values and entrepreneurial spirit. With corporate offices in New York and Pennsylvania and 8 manufacturing campuses across the U.S. and Canada, the companies within the First Quality group produce high-quality personal care and household products for large retailers and healthcare organizations. Our personal care and household product portfolio includes baby diapers, wipes, feminine pads, paper towels, bath tissue, adult incontinence products, laundry detergents, fabric finishers, and dishwash solutions. In addition, we manufacture certain raw materials and components used in the manufacturing of these products, including flexible print and packaging solutions. Guided by our values of humility, unity, and integrity, we leverage advanced technology and innovation to drive growth and create new opportunities. At First Quality, you'll find a collaborative environment focused on continuous learning, professional development, and our mission to Make Things Better . We are seeking a Quality Manager for our First Quality Retail Services located in Lewistown, PA. This position will be responsible for the creation, implementation and monitoring of all corporate & site Quality practices within their site of operation. Leading a team of quality professionals and driving a culture of continual improvement. Play a pivotal role and work collaboratively within the site management team, and drive quality engagement through all levels of the organization. Primary responsibilities include: Provide leadership and planning to develop, implement and maintain quality systems to ensure compliance to regulatory, industry, and customer standards. Serves as the Management Representative for all site compliance and quality systems Supervises the activities of assigned staff and monitor the activities of QA/QC personnel within the QA Department. Assure that all resources utilized for the quality functions are procured, maintained, and perpetuated in a cost effective and timely manner within the goals of the strategic business plan. Take the leadership role in maintaining/changing the quality culture of the company - serve as the visible model of Quality. Educate team members in the quality philosophy and practices, including improvement strategies. Represents the company to vendors, customers, and appropriate regulatory officials in matters related to quality. Administers the quality audit program. Provides training to team members, as required, for implementing quality initiatives. Work with cross-functional teams to prioritize key site projects and determine appropriate resources and timing; integrate lean six sigma activities with quality system activities such as Corrective and Preventive Action (CAPA) and Quality Improvements to assure effectiveness and compliance to customer and regulatory requirements. Develops annual quality plans and recommendations for continual improvement in conjunction with the Quality Leader and Operations Manager Determines methods and implements plans for professional development of personnel within the QA Department. Proposes budgets and monitors budget activity for the QA Department. Provides statistical analysis for evaluation of processes, and issue KPI reports to site leadership and divisional leaders at determined frequencies. Conducts lab tours and explains quality system to visitors. Understands competitive product features in comparison to products. Completes required reports and summaries for regulatory & industry agencies. Assists and substitutes for the Divisional Quality Leader, as needed. Observes all safety rules and always uses the proper safety equipment. Performs other duties as necessary when directed to do so. Follows necessary GMP, FDA, and ISO regulations. Manage master validation plan. Implement, monitor and review online Quality systems, including vision QMS Software, and SPC systems. The ideal candidate should possess the following: Bachelor's degree in an Engineering, Technology, Mathematics, Business, or Science discipline. Three years minimum experience as a Quality Manager, Technical Manager, or QC Supervisor in a manufacturing environment (preferably FDA-regulated environment). Six sigma Green Belt certified, preferred. Supervisory experience. Auditing experience in GMP and/or ISO systems. ASQ Certification or equivalent training (CQE, CQA, CQT, or CQM). Advanced skills in oral and written communications. Standard skills in technical, business, and managerial fields. Standard skills in statistics, procedure implementation, and quality auditing. Competent in interactions with executive management, vendors, and customers. What We Offer You We believe that by continuously improving the quality of our benefits, we can help to raise the quality of life for our team members and their families. At First Quality you will receive: Competitive base salary and bonus opportunities Paid time off (three-week minimum) Medical, dental and vision starting day one 401(k) with employer match Paid parental leave Child and family care assistance (dependent care FSA with employer match up to $2500) Bundle of joy benefit (year's worth of free diapers to all team members with a new baby) Tuition assistance Wellness program with savings of up to $4,000 per year on insurance premiums ...and more! First Quality is committed to protecting information under the care of First Quality Enterprises commensurate with leading industry standards and applicable regulations. As such, First Quality provides at least annual training regarding data privacy and security to employees who, as a result of their role specifications, may come in to contact with sensitive data. First Quality is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, sexual orientation, gender identification, or protected Veteran status.

Testing software that saves lives. Join the Quality Management team at Epic and become the last line of defense for software that impacts the lives of 305 million people worldwide. As a Quality Manager, you'll collaborate closely with developers, crafting intuitive tools for health organizations, testing new features, uncovering bugs in our software, and overall making our software a joy to use. You'll apply your extensive language skills to clearly and accurately prepare a wide range of technical documentation, training materials, and other written materials related to Epic's software. This role offers exceptional flexibility, allowing Quality Managers to specialize in areas such as software usability design, technical automation, or project coordination for customer software installations. Bring your intelligence, curiosity, and creativity, and we'll equip you with the knowledge needed to excel. Together, we'll shape the future of healthcare technology. Learn more about our team at *********************************************** Test the limits of our software for the most innovative health systems on the planet. The top-ranked health systems in U.S. News and World Report are Epic customers. Our community includes major systems like the Mayo Clinic, Johns Hopkins, Cleveland Clinic, and Kaiser Permanente, as well as leading academic medical centers at the University of Wisconsin, University of Michigan, University of California, University of Texas, The Ohio State University, and many more. Live affordably in a city known for its rising tech talent. Epic is located just outside Madison, Wisconsin, the second fastest growing market for tech talent in the United States and home to the state capital and the University of Wisconsin. Madison, a city surrounded by water, has received accolades for being the greenest city in America (NerdWallet), the best city for renters (SmartAsset), the fittest city in America (Fitbit), and the third best metro in the US for young professionals (Forbes Advisor). More than just important work. Our uniquely themed campus was designed to heighten your ability to get stuff done in your office, a conference room, or by the fireplace in a comfy chair. All meals are restaurant-quality but cost only a few dollars, and they're prepared by a team comprised of kitchen talent from restaurants around the country. And, after five years here, you'll earn a four-week sabbatical anywhere in the world. Staff have kayaked in Patagonia, attended a Beyoncé concert in Ireland, built a library in Tanzania, and run a marathon in Antarctica. We offer comprehensive benefits to keep you healthy and happy as you grow in your life and career, and your merit-based compensation will reflect the impact your work has on the company and our customers. You'll also be eligible for annual raises and bonuses, as well as stock grants, which give you an even greater stake in the success of Epic and our customers. Healthcare is global, and building the best ideas from around the world into Epic software is a point of pride. As an Equal Opportunity Employer, we know that inclusive teams design software that supports the delivery of quality care for all patients, so diversity, equity, and inclusion are written into our principles. Please see our full non-discrimination statement at ***************************** Requirements * Bachelor's degree or greater (any major) * Excellent knowledge of one of the following languages: * Arabic * Armenian * Haitian Creole * Hmong * Italian * Russian * Vietnamese * Relocation to Madison, WI area (reimbursed) * Knowledge of Epic software is not required, we will train you! * COVID-19 vaccination * Eligible to work in the United States without visa sponsorship

Job Description The Quality Manager, will lead a dedicated multishift Quality department and play a key role in ensuring our personal care products meet the highest standards of safety, quality, and regulatory compliance. We are looking for a proactive, collaborative leader who excels at developing talent, solving problems and strengthening quality systems in a fast-moving manufacturing environment. Job Responsibilities: Lead the Quality department across two shifts, driving team development, building bench strength, and reinforcing a culture of accountability, continuous improvement and high operational standards. Interacts with customers and internally with UBP production, supply chain, marketing and the R&D groups. Create, revise and manage cGMP procedures and supporting documents and carry out additional duties as needed to uphold quality and regulatory standards. Exercise authority to accept, reject or quarantine raw materials and finished products in accordance with quality standards. Handles customer complaints, nonconformance and corrective actions. Ensure that actions and reports generated conform to regulations/requirements. Plan, schedule, conduct internal audits, analytical methods and validation as well as raw materials suppliers and contractor manufacturers. Coordinates FDA, EPA and third-party certification activities and responds to customer audits and inquiries to ensure compliance and transparency. Works with Customer Service, R&D, and Operation teams to resolve and assist with customer/consumer complaints, internal concerns and new product development and processing. Partners with the Operations team to communicate quality concerns and drive continuous improvement initiatives. Supports the R&D department in multiple aspects: Vendor qualifications, raw material testing, etc. Other duties as required by management. Requirements: At least 5 years of experience in Quality Management Continuous improvement mindset, with strong decision-making ability Effective communicator with ability to collaborate cross functionally Must have previous manufacturing industry experience (preferably in the Beauty Industry) Strong working knowledge of current Good Manufacturing Practices (cGMPs) Adaptable and flexible in a fast-paced environment with changing priorities

The Quality Manager, will lead a dedicated multishift Quality department and play a key role in ensuring our personal care products meet the highest standards of safety, quality, and regulatory compliance. We are looking for a proactive, collaborative leader who excels at developing talent, solving problems and strengthening quality systems in a fast-moving manufacturing environment. Job Responsibilities: Lead the Quality department across two shifts, driving team development, building bench strength, and reinforcing a culture of accountability, continuous improvement and high operational standards. Interacts with customers and internally with UBP production, supply chain, marketing and the R&D groups. Create, revise and manage cGMP procedures and supporting documents and carry out additional duties as needed to uphold quality and regulatory standards. Exercise authority to accept, reject or quarantine raw materials and finished products in accordance with quality standards. Handles customer complaints, nonconformance and corrective actions. Ensure that actions and reports generated conform to regulations/requirements. Plan, schedule, conduct internal audits, analytical methods and validation as well as raw materials suppliers and contractor manufacturers. Coordinates FDA, EPA and third-party certification activities and responds to customer audits and inquiries to ensure compliance and transparency. Works with Customer Service, R&D, and Operation teams to resolve and assist with customer/consumer complaints, internal concerns and new product development and processing. Partners with the Operations team to communicate quality concerns and drive continuous improvement initiatives. Supports the R&D department in multiple aspects: Vendor qualifications, raw material testing, etc. Other duties as required by management. Requirements: At least 5 years of experience in Quality Management Continuous improvement mindset, with strong decision-making ability Effective communicator with ability to collaborate cross functionally Must have previous manufacturing industry experience (preferably in the Beauty Industry) Strong working knowledge of current Good Manufacturing Practices (cGMPs) Adaptable and flexible in a fast-paced environment with changing priorities

Work is Sweet! 'Quality without Compromise' is not just a motto at See's Candies. It is the most important ingredient in our recipe for success. See's Candies has been in business since 1921 and maintains a reputation for producing the highest quality candy and providing superior customer service. See's is a leader in the confectionary industry with over 250 retail shops across the USA. We are seeking friendly, enthusiastic individuals who are passionate about providing great customer service. Summary: POSITION OBJECTIVE: The Supplier Quality Manager is responsible for ensuring that suppliers meet See's quality standards by developing and implementing quality assurance programs, conducting supplier audits, and resolving quality issues. Key duties include collaborating with internal teams, monitoring supplier performance, driving corrective actions, and supporting new product development to ensure a high-quality supply chain. The pay range for this position is expected to be $100,000k-$110,500k annually; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Job Description: POSITION RESPONSIBILITIES: * Quality program development: Create and implement supplier quality assurance programs that align with company goals and industry regulations. * Supplier evaluation and audits: Conduct audits to assess supplier capabilities, processes, and compliance with quality standards. This includes performing initial and surveillance audits and selecting suppliers based on quality standards. * Performance monitoring: Establish metrics to monitor supplier performance, such as defect rates, and use this data to report on performance and drive improvements. * Problem-solving and corrective actions: Lead the analysis of quality issues and coordinate corrective and preventive actions (CAPA) with suppliers to resolve defects and prevent recurrence. * Cross-functional collaboration: Work with internal departments like engineering, procurement, and production to identify and mitigate quality risks, define process parameters, and ensure alignment between supplier capabilities and company requirements. * New product development support: Participate in new product development teams to ensure suppliers are capable of meeting quality standards for new products. * Continuous improvement: Drive a culture of quality excellence and implement continuous improvement initiatives throughout the supply base. * Risk management: Identify and mitigate quality-related risks in the supply chain. MINIMUM QUALIFICATIONS: * A bachelor's degree in life sciences, quality management, or a related field. * Minimum of 2 years of experience in supplier quality management, and SQF experience. Food industry experience is required. * Strong understanding of quality management systems, auditing, and problem-solving methodologies. * Excellent communication, negotiation, and leadership skills are essential for managing supplier relationships and driving cross-functional teams. The total compensation package for this position may also include other elements, in addition to a full range of generous medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. See's is an EOE See's will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable local, state or federal law (including San Francisco Ordinance #131192 and Los Angeles Municipal Code 189.00).

Highly competitive compensation at one of Plastics News Best Places to Work. Hands-on leadership of the Quality Team at a state-of-the-art custom plastic injection molding plant with a global reach. As Quality Manager, you're responsible for leading all aspects of the Quality Management Systems supplying precise plastic parts to both automotive and medical customers. Ensuring products meet all customer, regulatory, and internal quality requirements through robust systems, disciplined process control, and an engaged quality culture. About this Job Lead, coach, and develop a high-performing team of Quality Engineers and QA Technicians. Maintain and continuously improve the Quality Management System (QMS) in accordance with IATF 16949, ISO 13485, and ISO 9001 standards. Lead quality planning activities for new products from design phase through production launch. Partner with Production and Engineering to monitor and improve process capability and reduce internal defects. Serve as primary contact for customer quality issues, audits, and quality performance reporting. Manage and maintain the plant's Environmental Management System (EMS) to comply with ISO 14001 or corporate environmental standards. About this Company Successful plastic injection molding company with global reach and state-of-the-art facilities. Recognized as one of the best places to work (Plastics News) for the past eight years. Multi-national plant locations. Minimum Job Qualifications Bachelor's degree in Engineering, Quality, or a related technical discipline. Minimum 7-10 years of experience in Quality Management within plastics molding or precision manufacturing environments. Demonstrated experience in both automotive (IATF 16949) and medical (ISO 13485 / FDA) regulated sectors. Proven leadership experience managing technical quality teams. Quality Manager/ Quality Assurance Quality Engineering / Engineer Plastic Injection Molding IND123

CAA-GBG is part of the brand management division of Global Brands Group (GBG), one of the world's leading branded apparel, footwear, fashion accessories, and lifestyle product companies. GBG designs, develops, markets, distributes and sells goods for its portfolio of owned brands including, FRYE, Spyder, Juicy Couture, Aquatalia, Buffalo Brands, Jones New York as well as for its extensive portfolio of licensed brands including, Tommy Hilfiger, Calvin Klein, Michael Kors, kate spade, Cole Haan, Under Armour, Nautica and Disney. Job Description Review and establish factory and supplier processes to ensure that they are following established inspection procedures, for example, 4-point fabric inspections, in-line inspections and final aql audits Determine and advise on any outsourced or freelance staff required for inspections when required in peak periods Review customer requirements and making sure they are met Manage factory audits and ensure all required compliance Work with purchasing staff to establish quality requirements from external suppliers Supervise and train staff as required to ensure effective quality control procedures are in place Manage any repairs required on production whether that is in house, out sourced or at the factory Look at ways to reduce waste and increase efficiency Define quality procedures and manage roll-out to all factories Set up and maintain controls and documentation procedures Monitor factory and supplier performance by gathering relevant data and producing statistical reports Analyze returns due to quality issues and communicate with factories/suppliers to ensure issues are resolved and not repeated. Resolve any issues with factories and advise on solutions where necessary to fix any production problems advised Pre-production: Audit inward fabric, hardware and trims and ensuring only quality components are accepted Ensure that no faulty components are sent for production. If minor faults are present in the fabric or hardware, defects should be marked on the fabric/hardware and communicated to cutting/production department Prepare audit report of the fabric, hardware and trims quality Conduct pre-production meeting with relevant parties before production start Production: Perform in - line inspection and end-of-line inspection on production floor of all factories Perform inline inspection, pre-final audit and final inspection in finishing departments Audit of the packed goods prior to offering shipment to buyer QA Responsible for analysis quality reports and prepare improvement plan Ensure the right quality of the final product by conducting quality audits in manufacturing process Qualifications Bachelor's degree in Apparel Design, Textiles, Manufacturing, or similar Previous experience of working in quality control within the fashion industry preferably within denim production Solid background in product testing and implementing testing protocols Good working knowledge of quality assurance and quality control procedures Strong communication and administration skills with excellent attention to detail are essential Knowledge of factory working processes and production processes is essential to this role Good commercial awareness Good prioritization and organization skills Computer skills, proficient in using MS Office Good problem-solving skills and ability to perform under pressure Ability to travel to all factories as required is essential in order to carry out this role effectively Additional Information All your information will be kept confidential according to EEO guidelines.

CAA-GBG is part of the brand management division of Global Brands Group (GBG), one of the world's leading branded apparel, footwear, fashion accessories, and lifestyle product companies. GBG designs, develops, markets, distributes and sells goods for its portfolio of owned brands including, FRYE, Spyder, Juicy Couture, Aquatalia, Buffalo Brands, Jones New York as well as for its extensive portfolio of licensed brands including, Tommy Hilfiger, Calvin Klein, Michael Kors, kate spade, Cole Haan, Under Armour, Nautica and Disney. Job Description Review and establish factory and supplier processes to ensure that they are following established inspection procedures, for example, 4-point fabric inspections, in-line inspections and final aql audits Determine and advise on any outsourced or freelance staff required for inspections when required in peak periods Review customer requirements and making sure they are met Manage factory audits and ensure all required compliance Work with purchasing staff to establish quality requirements from external suppliers Supervise and train staff as required to ensure effective quality control procedures are in place Manage any repairs required on production whether that is in house, out sourced or at the factory Look at ways to reduce waste and increase efficiency Define quality procedures and manage roll-out to all factories Set up and maintain controls and documentation procedures Monitor factory and supplier performance by gathering relevant data and producing statistical reports Analyze returns due to quality issues and communicate with factories/suppliers to ensure issues are resolved and not repeated. Resolve any issues with factories and advise on solutions where necessary to fix any production problems advised Pre-production: Audit inward fabric, hardware and trims and ensuring only quality components are accepted Ensure that no faulty components are sent for production. If minor faults are present in the fabric or hardware, defects should be marked on the fabric/hardware and communicated to cutting/production department Prepare audit report of the fabric, hardware and trims quality Conduct pre-production meeting with relevant parties before production start Production: Perform in - line inspection and end-of-line inspection on production floor of all factories Perform inline inspection, pre-final audit and final inspection in finishing departments Audit of the packed goods prior to offering shipment to buyer QA Responsible for analysis quality reports and prepare improvement plan Ensure the right quality of the final product by conducting quality audits in manufacturing process Qualifications Bachelor's degree in Apparel Design, Textiles, Manufacturing, or similar Previous experience of working in quality control within the fashion industry preferably within denim production Solid background in product testing and implementing testing protocols Good working knowledge of quality assurance and quality control procedures Strong communication and administration skills with excellent attention to detail are essential Knowledge of factory working processes and production processes is essential to this role Good commercial awareness Good prioritization and organization skills Computer skills, proficient in using MS Office Good problem-solving skills and ability to perform under pressure Ability to travel to all factories as required is essential in order to carry out this role effectively Additional Information All your information will be kept confidential according to EEO guidelines.

Haddad is a privately held family business with 100 years' experience in the children's apparel & accessories industry. A leader in the children's wear industry, Haddad Brands is the exclusive global licensee for the most iconic brands in the world, which include Nike, Jordan, Converse, Hurley, Levi's, Polo, Abercrombie and Fitch, Lacoste, Tommy Hilfiger, Calvin Klein and Huggies. Supported by a team of professionals skilled in design, sourcing, production, sales, marketing & distribution of premium quality children's wear, Haddad distributes globally to 100+ countries and maintains sales and sourcing offices in 22 cities globally, including New York, Paris, Hilversum, Shanghai, Egypt, Bangkok, Vietnam, Sri Lanka, London and Montreal. Overview: The International Quality Manager supports global Quality Control operations by providing leadership, oversight, and coordination of product quality execution across all international regions. This role provides assistance with ensuring consistency of standards, alignment with customer requirements, and effective implementation of global QC initiatives. The manager works closely with director of quality control to strengthen overall product quality. Domestic and international travel is required. Key Accountabilities: Support global QC team initiatives by implementing company quality standards across all international regions Provide guidance to regional QC teams to ensure consistent inspector performance, inspection accuracy, and procedural compliance Partner with overseas managing offices and factory management to resolve quality issues, support corrective actions, and improve factory outgoing product quality Review and analyze global and domestic inspection reports, defect trends, and quality metrics to identify areas for improvement Visit factories as required to review production, evaluate quality risks, and verify corrective actions Communicate critical quality findings and risk assessments to the Director of Quality Control and other cross-functional leaders Support retailer chargeback prevention through compliance oversight and documentation accuracy Partner with the Director of Quality control to develop and refine global QC processes, manuals, and training materials Provide pre-production and inline quality support to factories to reduce final inspection failures Maintain consistent quality communication channels between domestic and international teams Recruit top talent, train and develop team members Special projects as assigned Requirements Required Skills/Abilities/Education: Bachelor's degree in Quality Management, Manufacturing, Engineering, or related field preferred 5-7 years of experience in Quality Control or Quality Assurance within apparel, or consumer products Strong knowledge of global manufacturing processes, inspection methods, and quality assurance systems Prior experience working with overseas factories and international QC teams Excellent communication, coaching, and cross-cultural collaboration skills Strong analytical and problem-solving abilities with attention to detail Ability to work independently across multiple regions and time zones Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook) Ability to travel domestically and internationally as required Consistent in-office presence is vital to the role as it is for all Haddad Brands team members, so that we all have a full appreciation, aesthetically and tactilely, of the qualities that define our brand partners' products and set them apart from their competitors. Salary Description $80,000 - $100,000 per year