Quality assurance manager jobs in Berea, SC - 119 jobs

The Area QA Manager role has a national salary range of $85,000- $150,000. DHL Supply Chain offers multiple benefits including Medical, Dental, Vision, Prescription, Discounted Stock Purchase, General Bonus Plan and a generous PTO policy. Are you looking for a challenging and rewarding opportunity in a fast-paced environment? Do you take an analytical approach to design complex and innovative solutions that exceed customer expectations and directly impact a growing business? Do you enjoy being part of a passionate team that works with stakeholders from across the business to create and implement the best solutions for our customers? Job Description Manage and coordinate all aspects of quality assurance activities with various levels of risk and complexity within a variety of scopes across multiple sites. Confirm requests for quality support from the site and communicate policies and procedures. Expert regarding selected governmental regulations for the site(s). Proactive liaison with customer for quality assurance across site(s). Leads a defined group of Quality Assurance resources and key initiatives, disseminating regulatory and corporate policy changes. Develops and implements policy and procedures for sites under their responsibility. Develop, manage, and oversee site quality managers/coordinators. Leads global and cross-sector QA initiatives. Develops and implements processes for regulated hardware, equipment, and software systems (validated as applicable). * Oversee the maintenance and continuous improvement of the overall quality system for multiple sites or multiple customers within a site, including management review, CAPA management, internal quality audits, quality self-assessments, change control, document control, and standard operating procedures/work instructions * Oversee the licenses, permits, and registrations process * Manages the validation process (as applicable) at a sector or network level and associated change control processes * Manage and provide oversight for regulatory compliance with regards to products handled and services performed at site by assessing performance to regulatory guidelines, the contract, and customer requirements; reporting the results to executive management * Work in coordination with continuous improvement team to focus/direct continuous improvement activities/workshops * Review and provide recommendations on regulatory, customer and 3rd party audits * Review and identify trends within the quality assurance metrics for the organization * Primary customer contact for QA related issues/initiatives as needed * Develop, distribute and maintain regular management reports. Compile executive level reports as required * Ensure site suppliers are assessed. Coordinate, prepare, receive, and act on audits Required Education and Experience * Bachelors Degree or equivalent 4 years work experience, required * 7+ years of relevant experience in a regulated environment, required * 5+ years of supervisory or management experience, required * Certification related to quality control (RAC, Six-Sigma, etc.), preferred * People management * Sufficient computer application experience * Strong written and verbal communication * Data analysis experience * Training and facilitation skills * Self management * Problem solving * Project management * Presenting * Report creation * Solution execution * Process development * People development * Quality program start-up experience * Standards development * Customer management Our Organization is an equal opportunity employer. ","title

Are you looking to join a dynamic team that provides its people with the tools to be successfull and opportunities to grow? Universal Logistics is a leading provider of customized transportation and logistics solutions, offering a comprehensive suite of services including transportation, value-added, intermodal, and specialized services utilized throughout entire supply chains. Universal has immediate career opportunities in your area. Apply today to become part of the Universal team! Universal Logistics Holdings, Inc. is a leading asset-light provider of customized transportation and logistics solutions. We provide our customers with supply chain solutions that can be scaled to meet your changing demands and volumes. We offer a comprehensive suite of services including transportation, value-added, intermodal and specialized services that can be utilized throughout your entire supply chain. Currently, we are seeking Warehouse Quality Manager candidates for a position based out of our operation in Greer, SC. where we support an automotive manufacturer in the area. Job Responsibilities: -Process engineering and validation -Developing and maintaining Quality Management System manual, procedures and standard work instructions -Identifying non-conformances with root cause corrective actions to mitigate occurrences and risk -Implementing quality objectives (KPI) across all departments for monitoring and measuring performance -KPI trend analysis -Forecasting operational capacity across all departments -Scheduling Layered Process Audits (LPA) and Process Failure Modes and Effects Analysis (PFMEA) -Inventory management and reconciliation -Standardized training procedure and developing associates -Continuous improvement projects with focus on lean and six sigma principles (PDCA, DMAIC & DMADV) -Developing and generating report card for supplier compliance The ideal candidate will possess knowledge and/or experience in the following areas: -Experience in ISO: 9001, 2015 International Standard Certification -Experience in developing and implementing a Quality Management System -Lean and six sigma principles (PDCA, DMAIC & DMADV) -Understanding of the importance of PEAR in regard to Quality Management System -Experience in managing third-party audits to ensure compliance with regulatory standards Other requirements include: · Bachelor's Degree preferred · Highly organized with a strong attention to detail · Good oral and written communication skills · Eager to learn · Ability to make quick decisions · Good work ethics · Ability to meet deadlines This position offers a competitive wage and benefits package, as well as offering upward mobility within the company. If you are an energetic, self-motivated individual with the drive to become part of a growing organization, do not hesitate, respond today! Look us up on the web at: **************************

PDF Download In the Automotive division, you will shape the mobility of tomorrow. System solutions in the areas of Battery Solutions, Structural Lightweight, Aerodynamics and Propulsion. This means: We protect the environment while also improving the driving experience of millions of vehicles. It is time for a new challenge. And time to arrive where you want to be. We have grown steadily, together as a team. Would you like to grow too? For us and with us? If you answered yes, we have career opportunities for you Do you have what it takes to spur game-changing innovation? Do you crave being a part of the solution, while enjoying training and learning opportunities? Then get ready to join the Röchling Automotive team and become part of the next chapter in our history? Director Quality Americas Where we need you * Developing standards, KPIs and guidelines. • Developing and maintaining relationships with internal and external stakeholders. • Developing competency profiles, training concepts and strategic improvement needs. • Defining and setting functional collaboration inside the network and cross-network. • Identifying and providing CSRs. • Defining functional systems and tools. • Driving escalations to Regional Board and Corporate Board. • Interfacing with other regions and Steering Committees. • Leading the functional management organization and the functional community in the region. Defining functional strategies and priorities. How to convince us * Degree in Engineering or a related discipline. • Strong English communication skills. • Proven leadership experience, managing teams and driving functional results. • Experience as a Quality Manager with solid knowledge of quality systems and compliance. • Strong relationship-management skills with internal and external stakeholders. • Automotive or general manufacturing industry experience. • Intercultural experience working in global or cross regional environments. • Experience managing budgets and resource allocation. • Knowledge of Total Quality Management principles. • Operations Management expertise. • Understanding of Material Science, especially plastics. • Strong problem-solving skills and use of structured methodologies. What we offer The compensation and benefits package will be shared during the advanced stages of the selection process. We offer a competitive framework aligned with market best practices, along with professional development programs and growth opportunities within the organization. Our commitment is to provide our employees with a stable environment that fosters continuous learning and long-term career projection. Interested in joining our team? Please send your resume for consideration. The Röchling Group has been shaping industry. Worldwide. For more than 200 years. We transform the lives of people every day with our customized plastics: they reduce the weight of cars, make medication packaging more secure and improve industrial applications. Our workforce of 11.681 people is located in the places where our customers are - in 83 locations in 25 countries. Share / PDF Download

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES: • Review changes to industry standards and understand how to apply them • Review and coordinate implementation of applicable revisions to internal procedures to maintain and uphold AS9100, ISO9000, and Nadcap standards • Maintain internal auditing program to meet industry and customer requirements • Uphold ITAR compliance • Direct, plan, and lay out the details of inspection standards, methods, and procedures, including those used by the repair station, in complying with all applicable FAR, DFARS, ITAR, and manufacturer's specifications and recommendations • Has final authority in the release of products/services to the customer • Ensure that corrective and preventive actions taken are effective and implemented in a timely manner • Assist, supervise, and direct all personnel assigned to the site's Quality Department • Ascertain that all inspections are properly performed on all completed work and that the proper inspection records, reports, and forms used are properly executed prior to releasing the product/service to customer • Perform the duties of and provide training for Contract Review • Maintain organizational freedom to identify problems related to quality and correct, initiate action for their correction, or stop any work or activity that violates the established quality standards. • Ensure conformance to quality program requirements through external/internal audits, corrective action program and qualify associates through testing and training. • Maintain supplier qualification to establish their ability to perform work meeting quality standards and obtaining process approvals. • Responsible for shop card review prior to certification and shipment. • Responsible for furnace surveys certification and equipment calibration, including recall system, thermocouple wire, and hardness testing standards. • Use personal protective equipment as required by the job, including but not limited to the wearing of safety shoes, gloves, and eye protection • Perform duties safely, responsibly, and proficiently, observing and complying with all safety and health rules (OSHA, MTI, and SDS Standards), including safe operation of all equipment • Perform similar or related work as required, directed or as situation dictates and shall exercise any additional powers that are or may be legally conferred upon the position by the Business Unit Director or President Requirements QUALIFICATIONS AND REQUIRED/PREFERRED SKILLS: • Bachelor's degree supplemented by experience in quality related work and/or extensive knowledge of heat treating, brazing, metallurgy, inspection and customer needs through technical and advanced training, seminars. • Experience and practical knowledge of commercial heat treatment of aerospace alloys including steel, aluminum, titanium, nickel, brass, copper, etc. • Nadcap and/or aerospace industry experience • Thoroughly familiar with commercial (AMS, ASTM), aircraft, and aerospace specifications, ISO, AS, QS and TS quality systems. • AS9100 Lead Auditor • Six Sigma Green Belt or experience • Comprehension of QMS Principles • Read and understand customer specifications and drawings • Excellent written and oral communication skills • Proficient in utilizing Root Cause and Corrective Action principles • Ability to work collaboratively with other staff, vendors, and customers • Capable of mentoring direct and indirect reports • Organized and detail-oriented with strong level of accuracy • Ability to prioritize and adhere to strict deadlines • High level of integrity; ability to handle confidential information • Proficient in Microsoft Office applications to include Word, Excel, PowerPoint, and Outlook

←Back to all jobs at INFINTIUM INC Quality Manager INFINTIUM INC is an EEO Employer - M/F/Disability/Protected Veteran Status Summary:Infintium Fuel Cell Systems, Inc. is developing next generation small and medium fuel cell systems in the Greenville, SC area. We are currently looking for a Quality Manager.This role is responsible for ensuring that our internal and external customers receive quality products & services. Lead activities that drive quality for manufacturing, products, systems, processes and people that will exceed customer expectations. Drive our quality initiatives, quality monitoring methods, and implement best practices. Ensure our quality network and quality team meet all applicable quality standards. Infintium is a small team, the candidate must be capable of setting and meeting goals reliably, with limited oversight. While there are controls and processes currently in place, the candidate will have the opportunity to guide future improvements in the system and ultimately has a significant influence on the company's profitability.The company's facility is located in the Greenville, SC Essential Job Responsibilities Define & proactively manage company production & supplier quality requirements Manage manufacturing & supplier audit programs and facilitate corrective actions Manage investigations, analysis and root cause determination for customer product returns Ensure product development and manufacturing processes meet Infintium quality standards Ensure product design meets or exceeds Infintium product quality standards Manage the calibration program for all measurement devices Administer the Infintium first article and Product Part Approval Process. Support the product platforms in the development of product quality control plans Manage processes to address customer complaints and manufacturing & supplier quality issues. Proactively identify potential product quality issues. Administer and lead company cross-functional Quality Triangle. Influence design features and supplier activities to proactively improve part and product quality partnering with design and development community on new product development projects. Manage Incoming Inspection and Supplier Corrective Action Process Lead the Nonconformity Process through the Material Review Oversee the investigation, identification and implementation of root cause failure analysis and corrective action of all customers returned products Lead the Stop Shipment Processes Document production inspections, final inspection criteria and performs final system inspections Document and analyze production quality results, ensuring requirements are met. Manage the flow of quality inspections to make sure they are timely and complete. Organize and manage Quality Assurance function(s) in close cooperation with customers and Company's Management team (Member of Operational Management Team) and Engineering Department.. Provide weekly standard quality reports Supervise, Coach & Mentor Quality team. Required Job Qualifications (unless Otherwise Noted) Educational Background B.S in Engineering or Technical Field; or at least 10 yrs in a Quality Manager role in Manufacturing Certified Manager of Quality/Organizational Excellence preferred Previous Work Experience 10 + years of experience managing and developing a ISO quality system, implementing lean strategies in organizations, conducting management review of quality system; working with manufacturing, customer service and product development teams in driving quality in products and materials. Special Skills, Experience And Abilities Lean Six Sigma Green Belt required. Six Sigma Black Belt preferred. Direct experience with ISO 9001 compliance auditing and similar standards Direct experience utilizing 8D problem-solving techniques Strong statistics background. Strong project management, mentoring and coaching skills. Proven facilitation, presentation and team skills. Physical requirements/Work environment Standing on a Manufacturing floor up to 8 hours Travel required Local and international travel up to 20% may be required Please visit our careers page to see more job opportunities.

Quality Manager - Manufacturing Greenville, SC Full-Time | Competitive Benefits | Career Growth About Us We're driven by excellence and committed to delivering top-quality results. Our team thrives on collaboration, integrity, and continuous improvement. If compliance and quality leadership are your strengths, we'd love to connect. Your Role · Lead and sustain our Quality Management System (QMS) · Ensure adherence to AS9100, ISO9000, Nadcap, FAR, DFARS, ITAR, and OEM requirements · Manage audits, corrective actions, and product/service release processes · Mentor and guide the Quality team · Oversee supplier qualifications and equipment calibration · Champion safety and regulatory compliance across all operations What You'll Bring · Bachelor's degree plus 10+ years in engineering or quality · Hands-on experience in aerospace heat treatment (steel, aluminum, titanium, etc.) · AS9100 Lead Auditor certification · Six Sigma Green Belt or Lean Manufacturing expertise · Strong grasp of QMS principles and technical specifications · Exceptional communication, leadership, and organizational skills · Proficiency with Microsoft Office Suite Ready to Lead Quality Excellence? Apply today or reach out for more details. Let's build something exceptional together.

Job Description About Us: We are a leading manufacturer committed to excellence in quality and compliance. Our organization operates under strict industry standards and is seeking a highly skilled Quality Manager to join our team. Position Overview: The Quality Manager will oversee all aspects of our Quality Management System (QMS), ensuring compliance with ISO 9001 and AS9100 standards. This role requires a proactive leader with extensive experience in quality assurance, continuous improvement, and regulatory compliance. Key Responsibilities: Manage and maintain the company's QMS in alignment with ISO 9001 and AS9100 requirements. Lead internal audits and coordinate external audits with certification bodies. Develop and implement quality policies, procedures, and training programs. Lead root cause analysis and implements corrective and preventive actions to resolve nonconformities. Monitor and report on quality performance metrics and trends. Collaborate with cross-functional teams to ensure product and process compliance. Interfaces with customers and regulatory bodies on quality matters. Core Duties in Maintaining a QMS. First Article Inspection (FAI) - AS9100 requirement - documenting and validating parts meet all engineering and design specs including surface finish checks and dimensional verifications. Nonconformance Control - Identifying, documenting, and segregating defective items to prevent them from moving forward. Precision Measurement Equipment: Full understanding and experience of CMM (Coordinate Measuring Machines), calipers, micrometers, gauges for inspection purposes. Qualifications: Bachelor's degree in Quality, Engineering, or related field (preferred). ISO Lead Auditor Certification strongly preferred. Minimum 5 years of experience in Quality Management within aerospace or manufacturing. In-depth knowledge of ISO 9001 and AS9100 standards. Strong analytical, problem-solving, and leadership skills. Preferred Skills: Experience with risk-based thinking and continuous improvement initiatives. Familiarity with customer and regulatory requirements in aerospace.

Salary: $105-120K What is your perfect fit? Do you like to work for smaller operations where you can have a larger impact? Are you passionate about quality and want to work for a company that keeps it at the forefront? Are you a leader looking to continue to build those skills? If that describes you, we need to talk! What your future day will look like: Customer liaison for all quality issues Develop quality inspections standards based on customer specifications Create work instructions Prepare control plans Maintain inspection and test records Manage quality personnel, evaluating performance and tracking goals Root cause analysis/corrective actions, APQP, PPAP/FMEA, SPC & GD&T Benefits Offered: Competitive benefits plan Health insurance PTO/Holidays 401K + match Type: Direct Hire To be a champion in this role, you will need: 10+ years in a quality management role Bachelor's degree preferred, associate's required We know you are more than a resume and understand your next career move needs to be the right fit! If this is your first time considering Godshall as your trusted partner, welcome! Once you have applied, we ask that you give us 1-2 business days to review your experience and skills. You will then hear back from one of our recruiting professionals on your next step. If you are checking in to see what types of roles we have, please consider reaching out to your recruiter instead. We will happily update your file and make sure we are considering you for all roles your experience is a perfect fit for! Godshall & Godshall Personnel Consultants, Inc. is an equal opportunity employer and gives consideration for employment to qualified applicants without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, status as a parent or protected veteran status.

The Quality Control Manager provides leadership, coordination, guidance, technical expertise in all areas of quality. The QCM is responsible for the overall daily operations of quality. This position develops and administers quality related policies, procedures, techniques, initiatives, to ensure that all quality policies and practices are followed consistently on the project. The QCM is responsible for the overall daily operations of quality. Requirements: In-depth knowledge of the Construction Standards and Best Practices Working knowledge of the International Building Code Knowledge and experience of diverse project type Ability to delegate tasks to others and supervise performance Excellent analytical skills Very organized and systematic in thinking and processes Computer skills using Procore, Viewpoint, SharePoint, MS Office Associate or bachelor degree in Quality Management, Construction Management, Engineering or related area Minimum of 6 years of construction experience as a Quality Control Manager Essential Job Duties: Works with Project Manager, Superintendents, and subcontractors in developing processes and procedures that effectively accomplish the goal of 100% compliant work that exceeds expectations Collaboration among project team and subcontractors Acts as an advocate for our company by maintaining good corporate ethics and promoting quality, at every opportunity, as a core value of the organization Maintains active relationships with engineers, consultants and industry association Assists teams with developing a project specific quality management plan Supports and follows up to ensure that project teams are following their project specific quality management plan Builds and maintains system templates for various DFOW activities conducted Prepare DFOW for project, as required in Quality Management Plan Participates in project meetings Conducts site visits and inspections of work in place Assists teams with plan and constructability reviews Read and understand specifications, reference codes and standards Review and interpret contract drawings Provides training and coaching for project team members to identify key project risks, related to quality Assist team with risk prevention planning and follow up Works closely with the Quality and Construction Science Department to ensure that we are utilizing advancements in technology to support operational excellence and reduce risk on projects Act independently as CQCM while coordinating all QC functions so as not to delay construction scheduling Determine, communicate, and document deficiencies and ensure they are corrected in a timely manner (NCR Log) Maintain current records providing factual evidence that required quality control activities and / or test have been performed Identifies and resolves problems in a timely manner, gathers and analyzes information skillfully; develops alternative solutions; works well in group problem solving situations: uses reason even when dealing with emotional topics Review shop drawings and submittals for conformance with project specifications and contract requirements Initiate Three Phase Inspection process. Conduct daily observations to ensure that all Three Phases of Inspection are undertaken and implemented as designed and document all results. Examine the work area to assure that all required work has been completed and is in compliance with the contract requirements and resolve any differences Conduct and Chair Preparatory Meetings Chair and document weekly QC meetings with internal and external stakeholders and external team members Verify and document that all matters received for the project are in conformance with the approved submittal, are handled and stored appropriately, and are acceptable for use Oversee daily and weekly QC/QA reports that reinforce activities that are being constructed in conformance with established standards Required Citizenship / Work Permit / Visa Status US Citizen/Green Card Holder Must-Haves *Associate or bachelor's degree in Quality Management, Construction Management, Engineering * Atleast 6 years experience as a Quality control Manager * Must have commercial construction (manufacturing) experience. * We need candidates who have handled projects worth a minimum of $20M. *This person must be focused on vertical construction. * Ideal candidates would have participated in large vertical construction projects such as mid-rise, high-rise, data center, or distribution center projects. * Should have supervised a small team * Should be willing to travel to multiple sites Strict No-Nos NO Oil refinery or RESIDENTIAL construction experience

in Greer, SC. Overall Purpose The Quality Manager is responsible for ensuring a company's policies and procedures comply with regulatory and ethical standards. Quality Manager will be required to travel within the area to perform regular audits, implement company policies, and design control systems. The Quality Manager will perform duties at the professional level in some or all of the following functional areas: quality operating system functions, ISO/IATF/AS Technical Specification, employee relations, training, etc. Maintain proper company documentation. Must be sensitive to company needs, employee goodwill, requirements/goodwill, and industry standards. May Report to General Manager Responsibilities Client relationship & Business development Works with support and site teams to standardize and refine existing processes Interface with customers for specific quality needs Assists support and site teams on specific customer needs and expectations Works directly with teams and customers on non-conformance issues Assists in maintaining Customer-mandated safety and insurance requirements Assists sites and departments in the creation of procedures and work instructions Assists region/site with quality related question or issues Manage schedules and performs internal audits Supports Corrective Action investigation and documentation Supports Continuous Improvement projects Prepares and chairs Health & Safety Committee meetings Analyzes company Health & Safety data Assists Health & Safety Committee in reviewing policies and standards Complies with local and company Health & Safety legislation, laws, and policies Creates and updates core quality system documentation, procedures and work standards Establishes and develops Management Reviews Assists company in compliance management Update and manage the QMS files in the company portal Communicates with site and company Management on audit results Assists Management in establishing and reviewing company and operational KPIs and other metrics Makes specific recommendations based on quality systems needs and metrics Analyzes data collected that support the QMS, Quality Policy and Scope of Business Recommends, supports and assists Management in driving quality and process improvements and financial waste reduction Updates company portal Manage the QSM programs, Lead Auditor Trained Creates robust documentation management systems using e-tools Pursuit of activities required to achieve and maintain ISO9001 registration Create electronic work instructions and navigate company websites and portals Other Any other duties as assigned Knowledge, skills, abilities Hard Skills Proficiency in English High-level Microsoft Office capability, including email, Word, and Excel Familiarity of the Windows PC and browser environments Strong knowledge of LEAN practices, AutoCAD and 8D Six Sigma methodology a bonus Ability to read and understand blueprints Work Instruction Writing Corrective Action Writing Leadership skills to conduct workshops and drive continuous improvement Excellent problem-solving skills Ability to work effectively on a team or individually Process Oriented High-level communication skills Technical writing capabilities Values and attitudes Global team spirit Team player Caring for people Open-minded Excellence Reactive Resilient to pressure Rigorous Customer focus Client oriented Reliable & trustworthy Flexible Initiative Autonomous Innovative Daring Work experience Overall recommendations Heavy Automotive experience in Quality/Operations Experience in warehouse operations- sorting, inspection, packaging and shipping (inbound and outbound) Strong communication skills- written, computer, verbal Expert MS Office software- Outlook, PowerPoint, Excel, Word Familiarity with automotive supplier requirements ISO/TS 16949, 9001 & IATF Audit experience and / or training Efficient time management / multi-tasking / team working skills in a high pressure environment Experience with problem solving, statistical, and analytical skills. Experience leading and managing employees / teams. Experience in Quality Operations SQE certification is a plus Education background Overall recommendations Associate's degree or greater in business management, engineering, or a related field is helpful About TRIGO Global Quality Solutions Founded in 1997, TRIGO is a multinational company providing operational Quality Management solutions for the manufacturing sector, especially in the automotive and aerospace industries. With a team of more than ten thousand professionals present in 20+ countries across 4 continents, TRIGO offers a comprehensive portfolio of Quality Assurance services ranging from inspection to expert auditing, consulting and training. The unrivaled expertise, industrial mindset and extensive global footprint that TRIGO has built up over the last 3 decades has made TRIGO the leading quality solutions provider using the latest innovative and reliable digital systems and standard processes, delivering results in the most demanding industries. TRIGO has recently started to expand its clientele by offering quality services to the medical, chemical and food industries. TRIGO Global Quality Solutions is committed to the core values of equal employment opportunity. We are committed to treating people fairly, and with respect and dignity. We offer employment opportunities based upon an individual's qualifications and performance, free from discrimination or harassment because of race, ancestry, place of origin, ethnic origin, color, citizenship, creed, sex, sexual orientation, age, marital status, family status, and disability.

in Greer, SC. Overall Purpose The Quality Manager is responsible for ensuring a company's policies and procedures comply with regulatory and ethical standards. Quality Manager will be required to travel within the area to perform regular audits, implement company policies, and design control systems. The Quality Manager will perform duties at the professional level in some or all of the following functional areas: quality operating system functions, ISO/IATF/AS Technical Specification, employee relations, training, etc. Maintain proper company documentation. Must be sensitive to company needs, employee goodwill, requirements/goodwill, and industry standards. May Report to General Manager Responsibilities Client relationship & Business development * Works with support and site teams to standardize and refine existing processes * Interface with customers for specific quality needs * Assists support and site teams on specific customer needs and expectations * Works directly with teams and customers on non-conformance issues * Assists in maintaining Customer-mandated safety and insurance requirements * Assists sites and departments in the creation of procedures and work instructions * Assists region/site with quality related question or issues * Manage schedules and performs internal audits * Supports Corrective Action investigation and documentation * Supports Continuous Improvement projects * Prepares and chairs Health & Safety Committee meetings * Analyzes company Health & Safety data * Assists Health & Safety Committee in reviewing policies and standards * Complies with local and company Health & Safety legislation, laws, and policies * Creates and updates core quality system documentation, procedures and work standards * Establishes and develops Management Reviews * Assists company in compliance management * Update and manage the QMS files in the company portal * Communicates with site and company Management on audit results * Assists Management in establishing and reviewing company and operational KPIs and other metrics * Makes specific recommendations based on quality systems needs and metrics * Analyzes data collected that support the QMS, Quality Policy and Scope of Business * Recommends, supports and assists Management in driving quality and process improvements and financial waste reduction * Updates company portal * Manage the QSM programs, Lead Auditor Trained * Creates robust documentation management systems using e-tools * Pursuit of activities required to achieve and maintain ISO9001 registration * Create electronic work instructions and navigate company websites and portals Other * Any other duties as assigned Knowledge, skills, abilities Hard Skills * Proficiency in English * High-level Microsoft Office capability, including email, Word, and Excel Familiarity of the Windows PC and browser environments * Strong knowledge of LEAN practices, AutoCAD and 8D * Six Sigma methodology a bonus * Ability to read and understand blueprints * Work Instruction Writing * Corrective Action Writing * Leadership skills to conduct workshops and drive continuous improvement * Excellent problem-solving skills * Ability to work effectively on a team or individually * Process Oriented * High-level communication skills * Technical writing capabilities Values and attitudes Global team spirit * Team player * Caring for people * Open-minded Excellence * Reactive * Resilient to pressure * Rigorous Customer focus * Client oriented * Reliable & trustworthy * Flexible Initiative * Autonomous * Innovative * Daring Work experience Overall recommendations * Heavy Automotive experience in Quality/Operations * Experience in warehouse operations- sorting, inspection, packaging and shipping (inbound and outbound) * Strong communication skills- written, computer, verbal * Expert MS Office software- Outlook, PowerPoint, Excel, Word * Familiarity with automotive supplier requirements * ISO/TS 16949, 9001 & IATF Audit experience and / or training * Efficient time management / multi-tasking / team working skills in a high pressure environment * Experience with problem solving, statistical, and analytical skills. * Experience leading and managing employees / teams. * Experience in Quality Operations * SQE certification is a plus Education background Overall recommendations * Associate's degree or greater in business management, engineering, or a related field is helpful About TRIGO Global Quality Solutions Founded in 1997, TRIGO is a multinational company providing operational Quality Management solutions for the manufacturing sector, especially in the automotive and aerospace industries. With a team of more than ten thousand professionals present in 20+ countries across 4 continents, TRIGO offers a comprehensive portfolio of Quality Assurance services ranging from inspection to expert auditing, consulting and training. The unrivaled expertise, industrial mindset and extensive global footprint that TRIGO has built up over the last 3 decades has made TRIGO the leading quality solutions provider using the latest innovative and reliable digital systems and standard processes, delivering results in the most demanding industries. TRIGO has recently started to expand its clientele by offering quality services to the medical, chemical and food industries. TRIGO Global Quality Solutions is committed to the core values of equal employment opportunity. We are committed to treating people fairly, and with respect and dignity. We offer employment opportunities based upon an individual's qualifications and performance, free from discrimination or harassment because of race, ancestry, place of origin, ethnic origin, color, citizenship, creed, sex, sexual orientation, age, marital status, family status, and disability.

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The Quality Manager in our Spartanburg, South Carolina facility is responsible for leading quality improvement for an Applied Sterilization Technologies (AST) processing or lab facility. This position leads implementing and maintaining state-of-the-art quality practices and assumes overall responsibility in ensuring that the site maintains operational and quality systems in a state of compliance to domestic and international standards. As a Quality Manager you are responsible for the organization, documentation and maintenance of the quality system to be compliant with, as appropriate, the following standards: ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads the local site efforts focused on quality system improvement, supplier quality, process quality, new service/modality/technology development quality and quality system compliance. The Quality Manager serves as the Management Representative for the site(s) and is responsible for ensuring the quality system meets all applicable regulatory standards. The Quality Manager has the responsibility, duty and decision-making authority to put any product on hold that is identified as potentially non-conforming and escalating as needed for additional reviews by technical teams. This position requires working onsite in our Spartanburg, South Carolina facility. What You'll do as a Quality Manager * Lead the organization's Quality staff to ensure compliance to the overall Quality Management System and drive continuous improvement. * Lead the organization's Quality staff to ensure alignment to operations, support Lean efforts and drive quality improvement for services/processes. * Work closely with site senior management to provide strategic direction and development of the organization's quality strategies and tactics. * Provide quality viewpoints and opinions on future service/technology offerings. * Provide coaching, mentoring and leadership to the Quality staff. * Serve as the site's Management Representative and lead the organization's Management Review process. * Ensure compliance with appropriate domestic regulatory and international standards and requirements. * Lead the organization's continuous improvement process; including data analysis, improvement projects and process capability to improve key metrics as measured by the product/service quality dashboard. * Lead and implement effective production and process controls. * Manage the CAPA, complaint and non-conformance handling processes to insure customer responsiveness and process improvements. * Lean and manage Regulatory Agency and Notified Body inspections and drive the creation and implementation of sustainable and effective remediation plans. * Oversee the completion of Customer audits. * Apply regulatory knowledge and judgment to the evaluation of quality concerns and regulatory compliance issues. * Travel to other AST facilities, domestically and/or globally, to support remediation activities, audits/inspections and/or continuous improvement initiatives. * Overall responsibilities include commitment to ensure external and internal requirements are met according to documented policies, procedures, standards and regulations. * The position requires a level of authority to conduct and direct required activities such as quality planning, personnel management and regulatory compliance. * Perform other duties as assigned. The Experience, Skills and Abilities Needed Required: * Bachelor's Degree in a related scientific/technical field * Minimum of 2 years of experience in a Quality leadership role. * Minimum of 10 years of experience working in an ISO certified environment required. * Minimum of 10 years of combined Manufacturing/Quality Engineering and/or Quality Systems experience. * Minimum of 10 years of experience in manufacturing or processing environment or another technical/scientific field. Preferred: * Minimum of 10 years of experience with medical device or other regulated industries preferred. * Sterilization experience preferred. * Working knowledge of FDA QSR/ EUGMP regulations strongly preferred. * Ability to build relationships and collaborate cross functionally to achieve business goals. Other: * Excellent problem-solving skills * Focus on identification of potential issues and continuous improvement. * Experience working on cross-functional teams and on own initiative. * Effective interpersonal skills, ability to work independently under minimal guidelines and supervision. * Demonstrated excellent organizational, oral and written communications skills. * Must have working familiarity of MS Office applications including Excel, Word, and PowerPoint. * Ability to work in a fast-paced, regulated environment with strict deadlines and ever-changing responsibilities. * Mathematical skills including practical application of fractions, percentages, ratios, proportions, and algebra. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, wellbeing, and financial future. Here is just a brief overview of what we offer: * Market Competitive pay * Extensive Paid Time Off and added Holidays * Excellent Healthcare, Dental and Vision benefits * Long- and Short-Term Disability coverage * 401(k) with a company match * Maternity and Paternity Leave * Additional add- on benefits / discounts for programs such as Pet Insurance * Tuition Reimbursement and continuing education programs * Excellent opportunities for advancement in a stable long-term career #LI-MO1 #LI- Onsite Pay range for this opportunity is $105,400.00 - $136,400.00. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits Open until position is filled. STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit *************** If you need assistance completing the application process, please call ****************. This contact information is for accommodation inquiries only and cannot be used to check application status. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity. The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours.

Quality Manager - Distribution Center (Woodruff, SC) Company: Warehouse Services, Inc. (WSI) Warehouse Services, Inc. is seeking a qualified Quality Manager to join our team at our distribution center in Woodruff, SC. The ideal candidate will be experienced in managing quality systems, driving process improvements, and ensuring compliance with company and customer standards. Duties & Responsibilities Recognize and reward improvement, achievements, and progress Lead and participate in meetings with associates and leadership Implement, monitor, and maintain the Quality Management System (QMS) Support the development and continuous improvement of the QMS Track, analyze, and report key performance indicators on a weekly basis Conduct internal quality audits across the site and provide corrective action guidance Required Qualifications 2-5 years of management experience in quality, operations, or a related field Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook) and Adobe Acrobat Working knowledge of Quality Management Systems (QMS) ISO 9001 auditor certification or willingness to obtain certification Basic understanding of quality tools (5-Why, Fishbone, etc.) Forklift certification or ability to obtain certification Ability to lift up to 55 lbs. Must pass pre-employment background check and post-offer drug screen/physical Pay & Benefits $1,500 Sign-On Bonus $750 Employee Referral Bonus Affordable Medical, Dental, and Vision Insurance Profit Sharing & 401(k) retirement plan Performance reviews at 90 days, 6 months, and annually Company-paid Life Insurance Paid Vacation, Sick Time, and Holidays Steel-Toe Shoe reimbursement Prescription Safety Glasses reimbursement Uniform Allowance

The Quality Manager is responsible for the overall direction and drive towards continual quality improvement focused on improved customer satisfaction. This individual will lead team efforts to: establish and monitor customer/supplier relations, support strategic planning and deployment initiatives, help develop measurement systems to determine organizational improvement, and ensure adherence to customer and regulatory requirements. The Quality Manager will have oversight of Quality for multiple ICS North America buildings comprised of light assembly, machining, distribution, engineering, and labs. Essential Job Duties and Responsibilities Develop and implement quality control processes, evaluate existing processes, and identify areas of improvement. Maintain the Quality Management System that monitors and measures quality standards for the sites in North America. Ensure all accreditations are maintained and extended through QMS execution and communication with customers or approval bodies. Maintain ISO9001:2015 certification, guiding the Quality Engineering team in audit activity and documentation. Drive a culture of quality assurance and quality improvements throughout the campus. Establish and implement appropriate QA/QC programs to reduce COPQ and improve compliance to regulations and standards. Manage a diverse, cross functional Quality team who: Manages the CAPA process for external quality issues. Manages internal quality notification process (QN's) in Manufacturing and Machining. Manages supplier quality deliverables and corrective actions (SCARs) for components. Manages internal and external containment activities. Maintains gage calibration system using GagePack software. Manages and maintains PPAP submissions from Suppliers. Manages regulatory certifications related to product safety and environmental compliance. Supports divisional Trade Compliance requirements for North America Education and Experience Requirements BS in Engineering or Engineering Technology, or equivalent of 15 years of relevant experience in a technical field with quality responsibilities 5 years minimum in a quality role 3 years minimum in a supervisory role Preferred Skills and Abilities Six Sigma Black/Green Belt, CQE, CQA or Lead Auditor certification preferred. Quality certifications like: CQE, CQA, or CQPA preferred. ISO 9001 Lead Auditor certification preferred. Familiar with typical quality assurance processes like, development of quality plans, control plans capability studies, and gage R&R Experience with managing and maintaining a Quality Management System, like an ISO 9001 program. Experience with supervising or managing a quality team responsible for gage calibration. Experience in participating in quality investigations, undertaking root cause analysis, developing corrective action plans, and ensuring the effectiveness of actions undertaken. Excellent communication skills Effective organization and time management skills with the ability to prioritize actives and manage deadlines. Good mechanical skills. Excellent leadership and facilitation skills. Proficient in Microsoft Office Suite. SAP experience a plus. AutoCAD or SolidWorks experience a plus. GD&T experience preferred. Working knowledge of statistical software and/or Minitab. Machining and injection molding experience a plus. Working Conditions and Physical Demands To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Travel Required Estimated 15-20% #LI-TT1 #nordsonindustrialcoatingsystems

Spartanburg Steel Products is a major supplier of metal stampings and welded sub-assemblies for automotive, lawn & garden, agricultural, and construction equipment OEMs throughout the United States: * Motivated, experienced, and stable team, ready to execute. * Stamping press tonnage from 200 to 2000 metric tons. * Transfer, tandem, and progressive production lines. * SSP is IATF 16949:2016 and ISO 14001-2015 certified. * Industry leading quality and delivery PPM performance. Job Description Primary Objectives The Quality Manager is responsible for the evaluation, benchmarking, improvement, design, development and standardization of the plant quality systems by possessing strong leadership, communication and teamwork skills; demonstrating an acute attention to detail, and showing strength in researching and analyzing data in the Quality Department directing the Quality team. Essential Responsibilities (Other duties may be assigned and changed as needed) Represent the quality function on technical support, in conjunction with other internal support groups, regarding issues affecting manufacturing. Initiates and approves supplier/customer production/process control activities and reviews for implementation and effectiveness. Maintain quality control sampling system, procedures, APQP, PPAP and IMDS activities Ensure that the organization's Quality Management System conforms to customer, internal and 3rd party audits (SQF & IMS). Manage, audit and continuously improve IATF16949 systems as well as Customer Specific Requirements. Direct Customer and Supplier liaisons for plant quality activities and concerns including scheduled visits. Establish and maintain all quality documents, samples, customer contact, supplier development, production start - up, product launch, and correction of production variances and warrant analysis. Coach and manage departmental talent, ensuring compliance with HR policies and procedures. Ensure engineering deviation and change management processes are effective, including assurance on the use of authorized approvals, deviation control plans, lot identification and traceability, verification of non-standard process control, root cause analysis, expiry/exit of deviation time period or quantities and closure. Qualifications Requirements Bachelor's degree preferred. Engineering degree preferred. 7+ yrs exp. in Automotive/Mfg. environment required (A Class experience and metal stamping preferred). 5+ yrs in a Management or Supervision position of Quality required. Experience obtaining and maintaining company and customer required quality certifications (i.e. IATF, ISO, Q1) Familiarity with Automotive OEM quality requirements Solid knowledge of quality systems including 8D, MSA, Automotive APQP, PPAP ASQ, CQE, or CQM certification a plus Certified Six Sigma Green Belt or Black Belt a plus. Ability to read and interpret prints, knowledge of GD&T, gage design and function. Additional Information All your information will be kept confidential according to EEO guidelines. * Not accepting candidates through any third-party recruiters at this time. *

Kyocera International, Inc. We're hiring a Quality Manager at our Hendersonville, NC location! Salary Range: $99,087 - $118,000 annually (Final offer based on experience, education, skills, and market factors) Why Kyocera? With nearly 80,000 employees worldwide, Kyocera is a global leader in advanced ceramic technologies used in aerospace, automotive, medical, and semiconductor industries. Our materials power everything from smartphones to space shuttles - and we're just getting started. What Makes Us Stand Out? We don't just offer jobs - we offer careers with purpose, stability, and growth. Here's what you can expect: Generous Time Off 3 weeks of vacation to start (120 hours/year) 10 paid holidays annually Financial Wellness Competitive pay 401(k) with company match Employer-paid pension plan Comprehensive Health Coverage Medical, dental, and vision insurance Life insurance Flexible Spending Account (FSA) Employee Assistance Program (EAP) Investing in You Tuition reimbursement Paid time off to volunteer Flexible schedules Work-Life Balance & Culture Onsite gyms, walking tracks, and employee gardens at larger locations Long-tenured team (many with 30+ years of service!) Inclusive and diverse workforce A company philosophy rooted in doing the right thing as a human being Our Philosophy Kyocera's culture is deeply inspired by our founder, Dr. Kazuo Inamori. His values guide our decisions and shape our workplace. Learn more about our guiding principles here: Kyocera Values Ready to Make a Difference? Apply today and become part of a team that's shaping the future - one innovation at a time. GENERAL DESCRIPTION OF POSITION The Manager of Quality Assurance Possesses a high degree of understanding of manufacturing quality practices, fundamentals and uses them to assess and analyze product quality performance of ceramic products. Able to work independently and with colleagues to research and coordinate determination of root cause of electrical, mechanical, R/D, Proto-type software problems etc. Provides timely professional details and summaries of findings and conducts internal audits and controls. Regularly interfaces with customer representatives and production to manage requirements and deliverables. Requirements: 4-year degree 10+ year experience in quality control 5 years' experience managing quality staff members and technicians Strong analytical skills eligible to work in an ITAR environment Excellent leadership, communication, critical thinking, and organizational skills ESSENTIAL DUTIES AND RESPONSIBILITIES The Quality Assurance Manager is responsible for managing day-to-day quality operations related to KII plant, location, or product line. Will focus on maintaining internal quality management systems, oversee the audit program and work with/manage contract development and manufacturing organizations to ensure compliance with KII and customer programs. The Quality Assurance Manager will report the Senior Quality Manager and ensure he/she is aware of all significant returns, systems issues, and quality related initiatives. Provide quality oversight and manage projects for development and production of KII products and supplier programs. May lead committees, training, and roadmaps for non-quality team members. Participates in meetings and presentations such as MRM, PBC, HE Review, and CAR review Board. Ensure implementation, maintenance, and improvement of quality management systems, including but not limited to procedure writing, document control, deviations, change controls, investigations, CAPAs, CAR and related personnel training. Leads calibration program and hires/trains technicians or outside vendors. Manage KII audit program, including audit preparation, execution of the audit, audit report and follow-up to any findings to Sr leadership. Manage staff of quality engineers and technicians. Train, evaluate, motivate, and develop staff. Routine travel will be required between various locations in the US (10% travel). Will work closely with KII sales, other quality teams, internal audit, and customers weekly. Establishes and monitors process metrics and develops action plans as needed for plant, location, or division. Perform any other related duties as required or assigned. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty mentioned satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. PHYSICAL ACTIVITIES The following physical activities described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and expectations. While performing the functions of this job, the employee is regularly required to sit, reach with hands and arms, talk or hear; frequently required to stand, walk; and occasionally required to use hands to finger, handle, or feel. The employee must occasionally lift and/or move up to 25 pounds, occasionally lift and/or move up to 50 pounds, regularly lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision. ENVIRONMENTAL CONDITIONS There are no harmful environmental conditions that are present for this position. The noise level in the work environment is usually moderate. ADDITIONAL INFORMATION The above statements are intended to describe the work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required. The duties and responsibilities of this position are subject to change and other duties may be assigned or removed at any time. This position may require exposure to information subject to US Export Control regulations, i.e.: the International Traffic and Arms Regulations (ITAR) or Export Administration Regulations (EAR). All applicants must be US persons within the meaning of US regulations. Kyocera International, Inc. values diversity in its workforce, and is proud to be an AAP/EEO employer. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Kyocera International, Inc. Human Resources team directly. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.

**Primary Purpose** With minimal supervision, the Quality Manager directs plant quality assurance efforts with emphasis on identification and solution of process, material or labor problems that could compromise plant and division quality commitments. Trains staff and applies analytical and statistical analyses to achieve required quality results. Provides customer and supplier contacts relating to quality performance of a technical nature. **Responsibilities and Duties** + Plant reporting systems + Accountable for Plant Quality Control Systems to insure that controls are functioning in the areas of process, purchased material and final product quality to maintain internal and external quality costs while ensuring customer expectations are met + Manages Quality Assurance Systems to include the maintenance of warranty data, in-plant scrap data, compliance data, SNR's, customer concerns, etc. + Customer issues, 8D's + Provide customer responses as per customer expectations + Interface with customers both OEM and aftermarket to resolve quality issues/concerns + Daily QA practices + Work with plant cross functional teams + Facilitate and Support problem solving on preventative/corrective action for resolution of issues or concerns related to quality + Coordinate cross functional efforts and provide internal direction to ensure timely completion of assignments + Provide oversite and drive compliance to CSR requirements + Monitor quality reports to identify problems + Perform special studies and analyses at the request of Plant or Division management + Contact customers or suppliers regarding resolution of quality or product liability problems of a technical nature (includes customers and supplier visits) + Accountable for disposition of defective materials and manage the QOS system management + Performs special studies and analyses at the request of plant or division management + Change management + Facilitate and ensure compliance with customer change management notifications and approval requirements. Verify customer submission packages meet customer expectations and are correctly formatted in advance of customer submissions + Administer and sign-off on existing/new process changes/implementation + PPAP + Preparation and submission of PPAP documentation to customer as needed + Managerial + Direct or assist in the selection, hiring and training of Quality Engineers and Quality Technicians + Reports on Quality at all Plant Management reviews + Drives Cost of Quality improvements. Project management in areas involving Quality + Assures QS and ISO requirements are met. Acts as Plant representative during audits + Manages and directs the activities of the Plant Quality Technicians + Submits required monthly reports to Milwaukee (QOS, Environmental, Purchasing) + Administers and signs-off existing/new process specifications (SCO/DCO system, Control Plan) + Responsible for plant Quality Control systems to insure that controls are functioning in the areas of process, purchased material and final product quality to maintain internal and external quality costs while ensuring customer expectations are met + Supervises preparation of all quality reports and analyzes reports to identify problems. Assists plant management to achieve desired results. + Contacts customers or suppliers regarding resolution of quality or product liability problems of a technical nature (includes customers and supplier visits). + Responsible for disposition of defective materials + Project management in areas involving Quality **Qualifications** + Bachelor's degree in Engineering or other technical field + 5+ years of QA management experience in a manufacturing environment; automotive highly preferred, plastic injection molding highly preferred + 5+ years of experience in customer support / communication role demonstrating effective customer skills in all areas of communications + Knowledgeable in program launch processes and CSR + Statistics background + Proficient in Excel, Power point, Program Manager + Experience in ISO9001, IATF, PPAP, SPC and other quality standards. Experience in standards and facilitating continuous improvement using formal quality methodology and tools + Demonstrated ability to effectively lead a QA Team within a manufacturing environment; automotive preferred **What you get:** + Medical, dental and vision care coverage and a 401(k) savings plan with company matching - all starting on date of hire + Tuition reimbursement, perks, and discounts + Parental and caregiver leave programs + All the usual benefits such as paid time off, flexible spending, short-and long-term disability, basic life insurance, business travel insurance, Employee Assistance Program, and domestic partner benefits + Global market strength and worldwide market share leadership + HQ location earns LEED certification for sustainability plus a full-service cafeteria and workout facility + Clarios has been recognized as one of 2025's Most Ethical Companies by Ethisphere. This prestigious recognition marks the third consecutive year Clarios has received this distinction. **Who we are:** Clarios is the force behind the world's most recognizable car battery brands, powering vehicles from leading automakers like Ford, General Motors, Toyota, Honda, and Nissan. With 18,000 employees worldwide, we develop, manufacture, and distribute energy storage solutions while recovering, recycling, and reusing up to 99% of battery materials-setting the standard for sustainability in our industry. At Clarios, we're not just making batteries; we're shaping the future of sustainable transportation. Join our mission to innovate, push boundaries, and make a real impact. Discover your potential at Clarios-where your power meets endless possibilities. **Veterans/Military Spouses:** We value the leadership, adaptability, and technical expertise developed through military service. At Clarios, those capabilities thrive in an environment built on grit, ingenuity, and passion-where you can grow your career while helping to power progress worldwide. All qualified applicants will be considered without regard to protected characteristics. We recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please apply. Diversity of experience and skills combined with passion is key to challenging the status quo. Therefore, we encourage people from all backgrounds to apply to our positions. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, status as a protected veteran or other protected characteristics protected by law. As a federal contractor, we are committed to not discriminating against any applicant or employee based on these protected statuses. We will also take affirmative action to ensure equal employment opportunities. Please let us know if you require accommodations during the interview process by emailing Special.Accommodations@Clarios.com . We are an Equal Opportunity Employer and value diversity in our teams in terms of work experience, area of expertise, and all characteristics protected by laws in the countries where we operate. For more information on our commitment to sustainability, diversity, and equal opportunity, please read our latest report (********************************************** . We want you to know your rights (*********************************************************************************************** because EEO is the law. **A Note to Job Applicants:** please be aware of scams being perpetrated through the Internet and social media platforms. Clarios will never require a job applicant to pay money as part of the application or hiring process. **To all recruitment agencies** : Clarios does not accept unsolicited agency resumes/CVs. Please do not forward resumes/CVs to our careers email addresses, Clarios employees or any other company location. Clarios is not responsible for any fees related to unsolicited resumes/CVs. Clarios is the creator behind the world's most recognizable car battery brands. We are the car battery found in most new vehicles including leading brands such as Ford, General Motors, Toyota, Honda, and Nissan. Our 16,000 employees develop, manufacture, and distribute batteries for virtually every type of vehicle. We recover, recycle, and reuse up to 99% of our battery materials, leading sustainability practices in our industry. **A Note to Job Applicants** : Please be aware of scams being perpetrated through the Internet and social media platforms. Clarios will never require a job applicant to pay money as part of the application or hiring process.

Join independent, family-owned All Juice, a leader in production of juice beverages for regional, national, and international brands. The Quality Manager coordinates the implementation and maintenance of Food Safety and Quality programs. This individual will ensure the highest standards of quality and safety that meet company goals, customer specifications, FDA requirements, SQF requirements in accordance with company policies and procedures. Requirements SQF Practitioner Essential Duties and Responsibilities Organizes and leads the HACCP / HARPC team and the Internal Audit team Performs verification and validation activities Assists with the oversight of Sanitation activities Leads 2nd and 3rd party audit preparation to be always “audit ready” Conduct and manage employee training (HACCP, Food Defense, Allergens, Foreign material, GMP, etc.) Ensures document and record control including change control, storage, retrieval, and destruction (including electronic documents and records) Verifies that packaging, labels, ingredients, and finished products meet standards. Directs beverage handlers and production personnel in sanitary procedures. Assist with new product commissioning Assist with supplier and ingredient approval Assist with Organic, Kosher, etc. programs Report areas of concerns and needed improvements to Plant Manager Other duties as assigned. Benefits: Health, Dental & Vision Insurance-large percentage of premiums employer paid 401(k), with company matching Life Insurance employer paid Flexible Spending Account / Health Savings Account Short-Term Disability and Long-Term Disability Insurance Vacation Sick days/personal days Paid Holidays

About Us: We are a leading manufacturer committed to excellence in quality and compliance. Our organization operates under strict industry standards and is seeking a highly skilled Quality Manager to join our team. Position Overview: The Quality Manager will oversee all aspects of our Quality Management System (QMS), ensuring compliance with ISO 9001 and AS9100 standards. This role requires a proactive leader with extensive experience in quality assurance, continuous improvement, and regulatory compliance. Key Responsibilities: Manage and maintain the company's QMS in alignment with ISO 9001 and AS9100 requirements. Lead internal audits and coordinate external audits with certification bodies. Develop and implement quality policies, procedures, and training programs. Lead root cause analysis and implements corrective and preventive actions to resolve nonconformities. Monitor and report on quality performance metrics and trends. Collaborate with cross-functional teams to ensure product and process compliance. Interfaces with customers and regulatory bodies on quality matters. Core Duties in Maintaining a QMS. First Article Inspection (FAI) - AS9100 requirement - documenting and validating parts meet all engineering and design specs including surface finish checks and dimensional verifications. Nonconformance Control - Identifying, documenting, and segregating defective items to prevent them from moving forward. Precision Measurement Equipment: Full understanding and experience of CMM (Coordinate Measuring Machines), calipers, micrometers, gauges for inspection purposes. Qualifications: Bachelor's degree in Quality, Engineering, or related field (preferred). ISO Lead Auditor Certification strongly preferred. Minimum 5 years of experience in Quality Management within aerospace or manufacturing. In-depth knowledge of ISO 9001 and AS9100 standards. Strong analytical, problem-solving, and leadership skills. Preferred Skills: Experience with risk-based thinking and continuous improvement initiatives. Familiarity with customer and regulatory requirements in aerospace.