Quality Assurance Manager
Quality Manager Location: Richmond, Virginia Working Situation: Onsite We are currently partnered with a leading provider of high-quality folding cartons and boxes, serving various industries including beverages, food, confectionery, and tobacco. We pride ourselves on our commitment to quality, service, and innovation, ensuring our customers receive the best packaging solutions. The Quality Manager will oversee and manage all aspects of quality assurance and quality control within our organization. This role is crucial in ensuring that our folding cartons and boxes meet consistent standards and comply with industry regulations. The Quality Manager will work closely with cross-functional teams to optimize processes, resolve quality issues, and drive continuous improvement initiatives. The Quality Manager will be responsible for: Develop, implement, and maintain quality management systems, policies, and procedures. Conduct inspections, testing, and audits to identify and address defects in folding cartons and boxes. Analyze quality data to identify trends and areas for improvement. Develop and implement corrective and preventative actions. Train and manage production line staff in quality assessment and production practices. Prepare reports by collecting, analyzing, and summarizing data. Ensure products adhere to quality standards and regulatory requirements. Collaborate with leadership to translate quality objectives into actionable plans. Track products through the manufacturing process to guarantee quality at each stage. Perform detailed inspections of final products to ensure they meet industry and company standards. Lead and mentor a team of quality assurance professionals, fostering a culture of quality and continuous improvement. The Quality Manager will have the following qualifications: Bachelor's degree in Quality Management, Engineering, or a related field. Minimum of 5 years of experience in quality assurance or quality control, preferably in the packaging industry. Strong knowledge of quality management systems and standards (e.g., ISO 9001). If you are interested in the Quality Manager position, apply now!
US$90000 - US$135000 per annum
Richmond
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Senior Quality Engineer II - Manufacturing
Senior Quality Engineer II - Manufacturing, Medical Device Location: Atlanta, GA Working Situation: Onsite Join a world leader in medical device innovation, transforming surgical care and improving patients' lives globally. The commitment to cutting-edge research and compassionate healthcare solutions ensures that every day brings new challenges and opportunities for growth. Be part of a team where your expertise and passion will drive impactful advancements in medical technology. We are seeking a Senior Quality Engineer II to join our esteemed global medical device company, celebrated for its groundbreaking advancements in product development. As a pivotal member of our team, you will ensure our products meet the highest quality standards and regulatory requirements. You will have the opportunity to work cross functionally and collaboratively with keys stakeholders at the site. If you have a passion for excellence and a drive to make impactful contributions in the industry, we want to hear from you! The Senior Quality Engineer II will be responsible for: Analyze design drawings for tolerance, inspectability, and quality issues. Collaborate with suppliers to enhance quality and assist in process validations. Train QC Inspectors on inspection techniques and new equipment usage. Participate in internal and external quality audits. Lead or assist in PFMEAs and Risk Assessments. Perform tasks in the Engineering Change Management process. Oversee or support First Article Inspections and review reports. Lead or assist in equipment and process validations (IQ, OQ, PQ). Conduct Measurement System Analysis (Gage R&R) studies. Develop inspection plans for receiving and in-process inspections. Investigate complaints and manage Nonconformances (NCRs). Conduct trend analysis and lead quality review meetings. Perform Root Cause Analysis and define Corrective/Preventive Action Plans (CAPAs). The Senior Quality Engineer II will have the following qualifications: Bachelor's degree in Engineering or Engineering Technology required. Minimum of 2 years' experience in Quality Control or Quality Assurance position in a Medical Device Company required. If you are interested in the Senior Quality Engineer II position, apply now!
US$80000 - US$125000 per annum
Atlanta
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Regional Quality Assurance Manager
Regional Quality Manager Location: Atlanta, GA Working Situation: Onsite, Travel Join a dynamic and innovative packaging manufacturing company committed to excellence in quality management and continuous improvement. This role offers the chance to work cross-functionally with various teams, driving strategic quality initiatives across multiple locations. Be part of a team where your expertise and leadership will significantly impact the organization's quality standards and operational efficiency. We are seeking a Regional Quality Manager to join our team, enhancing and sustaining our Quality Management System. The ideal candidate will have extensive experience in paper packaging, along with a deep understanding of ISO 9001 and FSSC 22000 (Food Safety) standards. If you have a passion for quality and a drive to lead impactful improvements, we want to hear from you! The Regional Quality Manager will have the following responsibilities: Support safety as a top priority in training, job design, and regulatory compliance. Lead quality efforts for regional sites, bringing value and expertise in flexible film and paper packaging. Oversee flexible films manufacturing and paper packaging converting operations, internal audits, and corrective actions. Manage the Document Change System, measurement and test system calibration, and non-conforming material system. Analyze product testing data, plant scrap data, and customer complaints to identify and drive improvements. Lead cross-functional efforts related to product quality and corrective actions. Develop a comprehensive understanding of product manufacturing, usage, and test result implications. Collaborate with Design, Operations, Product Management, Sales, and Supply Chain to drive quality results. Lead quality staff in performance metrics and development of key manufacturing metrics. Track vendor performance, resolve customer complaints, and investigate critical quality defects. Focus on plant-wide issues and inter-plant initiatives, developing synergies and business opportunities. The Regional Quality Manager will have the following qualifications: Bachelors Degree with 5+ years of experience in Paper Packaging Manufacturing 3+ years of experience in Quality Management Systems in Paper Packaging Knowledge of ISO 9001 standards and FSSC 22000 (Food Safety). If you are interested in this Regional Quality Manager opportunity, apply now!
US$100000 - US$125000 per annum
Atlanta
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Quality Engineer - Field Safety Corrective Action (FSCA)
Quality Engineer - Field Safety Corrective Action (FSCA) Location: Atlanta, GA Working Schedule: Onsite Join a world leader in medical device innovation, transforming surgical care and improving patients' lives globally. The commitment to cutting-edge research and compassionate healthcare solutions ensures that every day brings new challenges and opportunities for growth. Be part of a team where your expertise and passion will drive impactful advancements in medical technology. We are seeking a Quality Engineer - Field Safety Corrective Action (FSCA) to join our esteemed global medical device company. This role is pivotal in driving product improvements by performing and supporting product quality complaint evaluations and field safety communications. If you have a Bachelor's degree in Engineering and over 2 years of experience in root cause analysis, project management, and continuous improvement in a regulated environment, we want to hear from you. The Quality Engineer - Field Safety Corrective Action (FSCA) will be responsible for: Developing and managing global policies and procedures for Product Surveillance processes for medical devices. Conducting root cause analysis for returned complaint devices or identified trends as needed. Maintaining test protocols to evaluate returned products according to established specifications and recording detailed results. Collaborating with Design Engineering, Manufacturing Engineering, Product Management, and Quality Engineering teams to drive continuous process and product improvement. Acting as the global representative for complaint investigation, escalation, and trending processes during Agency/3rd Party Audits and assisting in the preparation and submission of audit responses and requests for information to regulatory bodies such as the FDA and Notified Bodies. Providing timely customer feedback through root cause analysis, statistical analysis, and regular forums. Supporting global complaint triage, intake, evaluation, reporting, investigation, closure, and trending activities. Managing supplier relationships from initial notification to receipt of supplier complaint evaluations. The Quality Engineer - Field Safety Corrective Action (FSCA) will have the following qualifications: Bachelor's degree in Engineering or Engineering Technology. Over 2 years of experience in root cause analysis, project management, and continuous improvement in a regulated environment. If you are interested in the Quality Engineer - Field Safety Corrective Action (FSCA) position, apply now!
US$85000 - US$125000 per annum
Atlanta
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Maintenance Manager
OVERVIEW: The Maintenance Manager plays a critical role in ensuring the efficient operation of machinery and equipment within a food manufacturing facility. Reporting directly to the Plant Manager, this position is responsible for leading and managing the maintenance department to ensure preventive maintenance, repairs, and troubleshooting are conducted effectively to minimize downtime and maintain product quality and safety standards. WHAT YOU'LL DO: Lead and oversee all maintenance activities, including preventive maintenance programs, repairs, and troubleshooting of machinery, equipment, and facilities, to ensure continuous operation and minimize production interruptions. Develop and implement maintenance strategies, plans, and schedules to optimize equipment reliability, availability, and performance while maximizing operational efficiency and minimizing maintenance costs. Coordinate with production, engineering, and other departments to prioritize maintenance activities, schedule downtime, and minimize impact on production schedules. Manage maintenance technicians and staff, including hiring, training, performance management, and development, to ensure a skilled and motivated workforce capable of meeting maintenance objectives. Establish and enforce safety protocols and procedures to maintain a safe working environment for maintenance staff, including compliance with OSHA regulations, lockout/tagout procedures, and personal protective equipment (PPE) requirements. Develop and maintain maintenance budgets, track expenses, and manage spare parts inventory to ensure cost-effective maintenance operations. Implement and utilize computerized maintenance management systems (CMMS) to track work orders, maintenance activities, equipment history, and performance metrics. Monitor equipment performance, analyze maintenance data, and identify opportunities for improvement in equipment reliability, efficiency, and maintenance processes. Collaborate with vendors, suppliers, and contractors to procure parts, equipment, and services, negotiate contracts, and manage vendor relationships to support maintenance needs and objectives. Stay current with industry trends, best practices, and technological advancements in maintenance and reliability engineering, and recommend and implement innovative solutions to enhance maintenance effectiveness and efficiency. WHAT YOU'LL NEED: Bachelor's degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, or related field, or equivalent experience Proven experience in maintenance management or related field, with at least 4 years of progressive leadership experience in a food manufacturing environment. Strong knowledge of maintenance principles, practices, and techniques, including preventive maintenance, reliability-centered maintenance (RCM), and predictive maintenance technologies. Demonstrated leadership and team management skills, with the ability to inspire and motivate teams to achieve maintenance excellence. Excellent communication and interpersonal skills, with the ability to interact effectively with employees at all levels of the organization, as well as external stakeholders. Proficiency in computerized maintenance management systems (CMMS), enterprise asset management (EAM) software, and Microsoft Office Suite. Strong analytical and problem-solving abilities, with a focus on data-driven decision-making and continuous improvement. Familiarity with food safety regulations, GMP (Good Manufacturing Practices), and HACCP principles. Ability to work in a fast-paced environment, manage multiple priorities, and adapt to changing business needs. WHAT WE'D LIKE TO SEE: Certification in maintenance management, reliability engineering, or related fields (e.g., Certified Maintenance & Reliability Professional, Certified Plant Maintenance Manager) is a plus
US$100000 - US$120000 per annum
Danville
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Quality Director
Lead Process and Quality Engineering teams to improve processes, productivity, and yield, reduce material non-conformance, and manage customer support activities. Primary Duties: Follow safety rules and ensure a safe work environment. Set and review departmental goals for quality and productivity. Collaborate with Production, Sales, and Marketing to achieve quality objectives. Establish and maintain product acceptance criteria. Investigate and resolve product nonconformance issues. Monitor quality trends and drive continuous improvement. Serve as ISO 9001 Management Representative. Manage customer complaints and RMA disposition. Provide technical support to customers. Guide Quality Engineers in optimizing processes. Develop and manage the departmental budget. Maintain high safety standards. Provide training and development for team members. Ensure compliance with Quality System. Perform other duties as assigned. Roll Milling Experience is a MUST Have Education/Experience Requirements: Bachelor's degree preferred, with 7 years of related experience or equivalent. ISO 9001 Internal Auditor Certification. Skills Requirements: Experience in QMS development. Strong leadership and supervisory skills. Financial report development and budget management. Expertise in quality processes and problem-solving. Knowledge of Quality Management Systems and statistics. Proficient in Microsoft Office. Excellent communication and organizational skills. Proficiency in English. Work Environment: Office environment with frequent production facility visits. Occasional travel required. Salary: Commensurate with experience. Benefits: 401(k) plan Retirement plan Vacation and paid holidays Health, vision, and dental insurance Short-term and long-term disability insurance Life insurance for employees and dependents
US$140000 - US$200000 per annum
Iowa City
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Quality Manager
Qualtiy Manager Job Summary: The Quality Manager will be responsible for overseeing and enhancing the quality management system, ensuring compliance with industry standards, and leading continuous improvement initiatives. The ideal candidate will have extensive experience in IATF 16949, ISO 9001, Lean Manufacturing, Kaizen events, and Continuous Improvement (CI) projects. Key Responsibilities: Develop, implement, and maintain the Quality Management System (QMS) in compliance with IATF 16949 and ISO 9001 standards. Lead and manage quality assurance and control processes to ensure product quality and customer satisfaction. Conduct regular audits and assessments to identify areas for improvement and ensure compliance with industry standards. Facilitate and lead Kaizen events and CI projects to drive process improvements and operational efficiency. Collaborate with cross-functional teams to address quality issues and implement corrective and preventive actions. Monitor and analyze quality performance metrics, and report findings to senior management. Provide training and support to employees on quality standards, procedures, and best practices. Stay updated with industry trends and advancements to continuously enhance the quality management system. Qualifications: Bachelor's degree in Engineering, Quality Management, or a related field. Minimum of 8 years of experience in quality management within the automotive industry. In-depth knowledge of IATF 16949, ISO 9001, Lean Manufacturing, and Continuous Improvement methodologies. Proven experience in leading Kaizen events and CI projects. Strong analytical, problem-solving, and decision-making skills. Excellent communication and interpersonal skills. Ability to work effectively in a fast-paced, dynamic environment. Preferred Qualifications: Certified Quality Engineer (CQE) or similar certification. Experience with Six Sigma methodologies. Proficiency in quality management software and tools. Benefits: Competitive salary and benefits package. Opportunities for professional growth and development. Collaborative and innovative work environment.
US$140000 - US$150000 per annum
Charlotte
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Quality Engineer
Quality Engineer Position Overview: We are seeking a highly skilled and detail-oriented Quality Engineer to join our team. The Quality Engineer will be responsible for ensuring that our products meet the highest standards of quality and performance. This position will involve working closely with various departments to identify and resolve quality issues, develop and implement quality control processes, and continuously improve our manufacturing and production practices. The Quality Engineer will have the following responsibilities... Develop, implement, and maintain quality control systems and processes. Conduct inspections and tests on products and materials to ensure compliance with quality standards. Identify, document, and resolve quality issues and non-conformances. Analyze quality data and trends to identify areas for improvement. Collaborate with cross-functional teams to develop and implement corrective and preventive actions. Provide training and support to staff on quality control procedures and best practices. Prepare and present quality reports and documentation to management and stakeholders. Participate in internal and external audits to ensure compliance with industry standards and regulations. The Quality Engineer should have the following qualifications... Bachelor's degree in Quality Engineering, Industrial Engineering, Mechanical Engineering, or a related field. At least 1-5 years of experience in a quality engineering role within a manufacturing or production environment. Strong knowledge of quality control methodologies, tools, and standards. Proficient in statistical analysis and quality assurance software. Excellent problem-solving and analytical skills. Strong communication and interpersonal skills. Ability to work independently and as part of a team. Attention to detail and a commitment to continuous improvement. Benefits 401k Insurance Bonus
US$50000 - US$70000 per annum
Atlanta
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Americas Quality Assurance Director
Join a leading global medical device manufacturing company committed to advancing health care through innovative products and solutions. We are seeking a highly experienced and strategic Senior Director of Quality to oversee our global quality assurance and regulatory compliance initiatives. The ideal candidate will have extensive experience in quality management within the medical device industry, with a strong focus on multisite oversight responsibilities. The position is in Massachusetts and the company is offering relocation assistance. Key Responsibilities: Lead and manage the global quality assurance strategy, ensuring compliance with all regulatory standards, including FDA, ISO 13485, and other relevant international regulations. Oversee quality management systems across multiple manufacturing sites, ensuring consistency and alignment with corporate quality objectives. Develop and implement policies and procedures to ensure quality standards are met and continuously improved. Collaborate with cross-functional teams, including R&D, operations, and supply chain, to integrate quality into all aspects of product development and manufacturing. Drive the development and execution of quality improvement initiatives, including root cause analysis and corrective action processes. Establish and maintain effective communication with regulatory agencies and ensure timely reporting and resolution of any compliance issues. Provide leadership and mentorship to quality assurance teams across multiple sites, fostering a culture of quality and accountability. Monitor industry trends and emerging regulations to proactively address potential impacts on quality practices. Qualifications: Bachelor's degree in Engineering, Life Sciences, or a related field; advanced degree preferred. Minimum of 10 years of experience in quality management within the medical device industry, with at least 5 years in a leadership role. Proven experience in multisite oversight, managing quality operations across multiple manufacturing facilities. Strong knowledge of FDA, ISO, and other global regulatory requirements for medical devices. Exceptional analytical and problem-solving skills, with a track record of driving quality improvements. Excellent communication and interpersonal skills, with the ability to influence at all levels of the organisation. Demonstrated ability to lead and motivate teams in a fast-paced, global environment. Salary: $200k-225k + Bonus + Benefits If you are interested, don't hesitate to apply!
US$190000 - US$225000 per annum
Milford
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