Quality assurance technician jobs in Springfield, OH

We are seeking a Process Technician to support operations at a single manufacturing site and across customer locations. This role is critical in ensuring smooth onboarding of new jobs, validating processes handed off by R\&D, and maintaining sustainable production practices. Additionally, the Process Technician will provide technical support to ensure products remain in spec, lead quality and efficiency improvements, and assist with new product development initiatives. The ideal candidate will be highly organized, detail-oriented, and skilled at translating technical requirements into practical, repeatable processes while responding quickly to production challenges. Why work at MCC: Competitive Compensation Generous benefits package including medical, dental, vision, disability, life insurance, and 401(k) Paid Holidays: New Year's, Memorial Day, Fourth of July, Labor Day, Thanksgiving, Day after Thanksgiving, Christmas Eve, Christmas Day, plus two floating Holidays Key Responsibilities: Job Onboarding: Lead the introduction of new products or jobs into production, ensuring readiness and alignment with plant capabilities. Training & Support: Develop and deliver training for floor personnel on new processes, equipment, and best practices. Process Validation: Confirm that R\&D handoffs are feasible and sustainable for long-term production. Technical Support: Provide proactive and reactive support to operators, ensuring products remain in spec and resolving issues quickly. Documentation & Standards: Create and maintain detailed process documentation, SOPs, and quality standards. Trials & Testing: Plan and execute trials to validate processes, troubleshoot issues, and optimize performance; conduct lab evaluations and comparative analysis with competitive products. Continuous Improvement: Identify opportunities to streamline workflows and enhance efficiency in label manufacturing and related operations. Customer Interaction: Support customer and MCC-sponsored new product development projects; participate in coater trials and customer visits, occasionally requiring on-site work across shifts. Quality Oversight: Maintain lab/testing equipment and calibrations; initiate raw material complaints (SNAR), track corrective actions, and manage quality holds. Qualifications: Bachelor's degree in engineering or related field (or equivalent experience); 2- or 4-year degree or 2-4 years of related experience/training acceptable. Experience in manufacturing environments, preferably in labels or similar industries. Strong problem-solving skills and ability to manage multiple priorities. Math skills (including Algebra) and knowledge of printing/converting materials and technologies. Excellent communication and training skills; ability to write reports, business correspondence, and procedure manuals. Ability to travel for internal and customer visits and trials. Other Considerations: Occasional lifting of rolls/samples up to 40-45 lbs. Work around coating and slitting equipment; safety shoes may be required. Professional attire for customer visits; flexible hours for multi-shift coverage. #AppcastOPT For over a century, Multi-Color Corporation (MCC) has crafted premium labels for the world's most iconic and recognizable brands. Our labels elevate emotional connections with consumers and help brands stand out in competitive markets. Honoring our rich history as a market leader, we focus on the future by developing sustainable packaging solutions and consumer-driven innovations. MCC combines global reach with the personalized touch of local service through our network of facilities across 25+ countries. More than 12,000 teammates come together to make our industry-leading work possible and bring our True Colors to life. Join us at MCC, where every product is Labeled with Care. Learn more at ***************** If you need assistance or an accommodation in applying, please contact our Human Resources Department at ***********************. Multi-Color is committed to providing equal employment opportunities and prohibits discrimination based on race, color, religion, sex, national origin, age, disability, veteran status, or any other protected characteristic under applicable law.

What Makes a Honda, is Who makes a Honda Honda has a clear vision for the future, and it's a joyful one. We are looking for individuals with the skills, courage, persistence, and dreams that will help us reach our future-focused goals. At our core is innovation. Honda is constantly innovating and developing solutions to drive our business with record success. We strive to be a company that serves as a source of “power” that supports people around the world who are trying to do things based on their own initiative and that helps people expand their own potential. To this end, Honda strives to realize “the joy and freedom of mobility” by developing new technologies and an innovative approach to achieve a “zero environmental footprint.” We are looking for qualified individuals with diverse backgrounds, experiences, continuous improvement values, and a strong work ethic to join our team. If your goals and values align with Honda's, we want you to join our team to Bring the Future! Job Purpose Quality Analyst with the core role and responsibility to assure quality products to our final customer / customer plants through suspect product containment and repair activity. Key Accountabilities Lead and Investigate quality defects to determine suspect range and confirm containment actions Collect and analyse data related to Transmission Plant manufacturing/supplier quality concerns Negotiate containment activity within Transmission Plant manufacturing areas and customer facilities Perform measurement analysis on transmission components Perform functional analysis on Transmission assemblies; properly repair any concern items Perform gauge calibrations Qualifications/Experience/Skills Minimum Educational Qualifications: Bachelors/Associates degree in a technical field or equivalent experience in Quality or Technical role Minimum Experience: 0-4 years experience based on education. Preferred at least 1 Year of experience in a quality related role Other Job-Specific Skills: Positive Attitude, open minded and team player Ability to review technical data and make timely decisions based to contain suspect product Strong communication skills (written or oral) and decision making Strong self-motivation and desire to work in a manufacturing environment Working Conditions 30% office area; 30% laboratory area; 40% production areas Overtime of ~ 4-8 hours per week Ohio facilities) What differentiates Honda and make us an employer of choice? Total Rewards: Competitive Base Salary (pay will be based on several variables that include, but not limited to geographic location, work experience, etc.) Paid Overtime Regional Bonus (when applicable) Industry-leading Benefit Plans (Medical, Dental, Vision, Rx) Paid time off, including vacation, holidays, shutdown Company Paid Short-Term and Long-Term Disability 401K Plan with company match + additional contribution Relocation assistance (if eligible) Career Growth: Advancement Opportunities Career Mobility Education Reimbursement for Continued Learning Training and Development programs Additional Offerings: Tuition Assistance & Student Loan Repayment Lifestyle Account Childcare Reimbursement Account Elder Care Support Wellbeing Program Community Service and Engagement Programs Product Programs Free Drinks Onsite Honda is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, veteran status, or any other protected factor.

**Locaion:** 950 Stelzer Road,Columbus,Ohio,43219 **Shift & Schedule:We have two shift available:** + 2nd Shift | Monday-Friday, 2:00 PM - 10:00 PMor + 3rd Shift | Monday-Friday, 10:00 PM - 6:00 AM Overtime, weekends, and holidays as needed The Production Technician II operates assigned workstations and supports operations through autonomous maintenance, preventative maintenance, changeovers, and minor adjustments to ensure optimal line efficiency. **Key Responsibilities** + Operate and monitor production equipment; replenish materials as needed + Set up machinery and ensure production materials are available + Perform quality checks and adjust processes based on data findings + Troubleshoot line issues and handle empty cases + Train other operators on equipment use + Perform basic Autonomous Maintenance (CIL) activities + Demonstrate knowledge and application of 5S principles + Clean and sanitize equipment and work areas as required + Accurately record operational data **Physical Requirements** + Regularly required to stand, walk, see, and smell + Frequent use of hands and wrists + Occasionally required to sit, stoop, kneel, push/pull totes, and stack by hand + Ability to lift, push, and pull 50 lbs repeatedly **Total Rewards:** + Starting pay: **$24.60** per hour. The employee will move to a higher rate of **$25.87** per hour in the quarter after their 6-month anniversary. **Benefits** (Effective Day One, Where Applicable): + Medical, Dental, and Vision Insurance + Disability Coverage + Paid Time Off (including vacation and sick leave) + 401(k) with company match + Tuition Reimbursement + Mileage Reimbursement _Benefits are subject to eligibility requirements and applicable collective bargaining agreements._ **Requirements:** + High school diploma or GED preferred + 2+ years of experience operating high-speed production machinery + Experience monitoring product quality in a manufacturing environment **Company Overview:** Keurig Dr Pepper (NASDAQ: KDP) is a leading beverage company in North America, with a portfolio of more than 125 owned, licensed and partner brands and powerful distribution capabilities to provide a beverage for every need, anytime, anywhere. We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values. We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale. Whatever your area of expertise, at KDP you can be a part of a team that's proud of its brands, partnerships, innovation, and growth. Will you join us? We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~29,000 employees to grow and develop. We offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work. Keurig Dr Pepper is an equal opportunity employer and recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law. A.I. Disclosure: KDP uses artificial intelligence to assist with initial resume screening and candidate matching. This technology helps us efficiently identify candidates whose qualifications align with our open roles. If you prefer not to have your application processed using artificial intelligence, you may opt out by emailing your resume and qualifications directly to **************** in lieu of clicking Apply. Please include the job title and location or Job ID # in the email subject line. Keurig Dr Pepper is an equal opportunity employer and affirmatively seeks diversity in its workforce. Keurig Dr Pepper recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law.

Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. We are seeking a dedicated and detail-oriented QC Lab Technician to join our Quality Control team. This role is responsible for performing routine and non-routine testing of in-process samples, final products, and raw materials to ensure compliance with internal and external specifications. Shift: Rotating 12-hour night shifts (7:00 PM - 7:30 AM) Key Responsibilities * This position is responsible for equipment, as well as, set up, operation, calibration (as required by method and instrument parameters), routine maintenance and troubleshooting of laboratory instrumentation. * Conduct routine testing of raw materials, in-process samples, and finished products. * Perform additional analyses as requested by supervisors or other departments. * Operate and maintain laboratory instruments including (but not limited to): ICP-MS, GFAA, LC, GC, GPC, NMR, FTIR, titration equipment, density meters, and turbidity meters. * Accurately document results and maintain records in the Laboratory Information Management System (LIMS). * Manage multiple samples and tasks simultaneously in a fast-paced environment. * Work independently during night shifts, ensuring timely and accurate testing. * Maintain a clean, organized, and safe laboratory environment. * Communicate effectively with team members and other departments regarding results and issues. Qualifications * Bachelor's degree in Chemistry or a related field is highly preferred * Previous experience in a laboratory setting, preferably in a QC or analytical lab. * Familiarity with LIMS systems and standard lab documentation practices. * Strong problem-solving skills and attention to detail. * Excellent organizational and multitasking abilities. * Effective written and verbal communication skills. * Ability to work independently and take initiative. Preferred Skills * Hands-on experience with analytical instruments: LC, GC, GPC, NMR, FTIR. * Proficiency in wet chemistry techniques including titration, density, and turbidity measurements. * Prior experience in a regulated lab environment. * Preferred experience working in the semiconductor or chemical field. Join our Talent Community to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.

Production Tech (Inspector) Working at our Beavercreek Site: GE Aerospace operations have been part of the Beavercreek community for over 70 years! Our Beavercreek facility manufactures gas turbine tubes, ducts, and manifolds, and also has complex machining, fabrication and investment casting capabilities. Product engineering, new product development and testing is performed on site. This facility also does repair and overhaul of tubes, ducts, and manifolds. We have been awarded OSHAS's highest safety rating. * Wages are $22.75 + per hour based on experience. * Additional $1.50 Premium Pay for 2nd or 3rd Shift! Role Overview: * Practically apply fractions, percentages, ratios and proportions. * Apply variety of principles to solve practical problems and deal with a variety of variables in situations where limited standardization exists. * Define problems, collect data, establish facts and draw valid conclusions. * Interpret service manuals, blueprints and related documents * Use standards shop measuring devices (calipers and micrometers) * Able to lift and exert 10 to 25 pounds of force frequently and 20 to 50 pounds of force occasionally * Certain areas may require mandatory/random drug testing The Ideal Candidate: * Team Player and willing to operate in a professional environment * Takes Pride in the work they are doing * Excellent attendance and punctuality history and availability to work overtime as needed * Makes decisions based on experience and available data * Strives to meet or exceed job requirements * Able to work effectively when receiving general supervision (This involves performing routine assignments alone.) * Able to carry out operations according to set procedures or sequences. * Ability to receive and act on constructive feedback Required Qualifications: * High School graduate or equivalent * 6 months experience in manufacturing and/or quality or Aerospace environment Preferred Qualifications: * Understanding or ability to learn the use of measuring gauges such as manual calipers. Additional Information: Safety. Your safety is important to us, so we provide most protective gear including hearing protection if needed. Strong safety focus with daily/monthly reviews and we have been awarded OSHAS's highest safety rating. GE Aerospace provides a $125 voucher towards the purchase of safety shoes as well as a voucher for safety prescription glasses if needed. Surroundings. You'll be operating and working around moving machines - stand-up forklifts, mobile carts, cranes, etc. Due to normal machining operations there may be dust, fumes, or smoke (not over OSHA Permissible Exposure Levels (PEL)). Inclusive Culture. Team oriented, ability to share ideas and make recommendations with peers and leadership Activity. In addition to sitting and standing while operating equipment, some activities may require standing in one place for long periods, walking around, or climbing stairs. Temperature. Most areas are climate controlled Closing: We strive to keep a fun and enjoyable shop atmosphere while maintaining the highest level of quality work output. We work together to make the impossible happen and we are looking for people like YOU to join us! We're looking for team-oriented individuals with the ability to share ideas and make recommendations with peers and leadership. This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3)). Additional Information GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). Relocation Assistance Provided: No

Under the supervision of the Quality Manager, the Quality Assurance Technician conducts audits on the process, products and systems in the Configuration environment and other areas as required. Using defined tools and scripts, the Tech identifies issues, analyzes those found during testing, and documents the findings. The Technician also provides support in assessment, implementation and maintenance of quality systems and processes that meet or exceed ISO standards and customer specific requirements. Reports out KPIs as needed to achieve the goals and objectives of the organization. Responsibilities Performs quality audits on the production product and processes in the configuration lab. Analyzes, troubleshoots, and documents problems, isolates and finds root causes, drives corrective and preventative actions using quality tools and audits improvements for effectiveness Conducts data analysis and test validations using statistical process control as well as RPN, (risk priority number) Audits adherence to standard work and work flow processes. Documenting risks and potential errors. Administers the non-conforming database for analysis and reporting Assists operations with COPQ (cost of poor quality) tracking Collaborates with technicians and leads to drive quality, continuous improvement and process controls, including standard work. Participates in requirement/design reviews and Quality Assurance strategy meetings Tracking CI Projects - stats, Control Analysis / PDCA. Submits proposals for improvements and participate in continuous improvement activities Assists Process Improvement Engineering Monitors, measures and reports out KPI (key performance indicators). Maintains customer scorecards / Incident charts Documents test results and reports project status Reports quality information at Tier Meetings Reports on COPQ Tracking Performs all other duties or special projects as assigned. Min USD $21.63/Hr. Max USD $27.04/Hr. Qualifications Degree requirements: Associate's Degree or the equivalent combination of education and work experience Working knowledge in Hardware and Software configurations Familiar with Microsoft Office software: Word, Excel, PowerPoint and Access is beneficial Strong attention to detail for quality adherence Problem solver with ability to research, investigate and problem-solve issues working with multiple people. Basic knowledge of ISO 9001 standards with ability to understand the application of the requirements Familiar with document control practices Working knowledge of Standard work or Work Instruction Documents Working knowledge of quality tools and / or problem solving tools, such as Fishbone diagrams, 8-D problem solving, Pareto charting Detail oriented with item by item focus, meticulous attention to detail with ability to proofread for accuracy

Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in risk management. As a Tech Risk & Controls Lead in Enterprise Technology - Employee Platforms, you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities Ensure effective identification, quantification, communication, and management of technology Risk, & operational Risk, focusing on root cause analysis and resolution recommendations. Develop and maintain robust relationships, becoming a trusted partner with LOB technologists, assessments teams, and data officers to facilitate cross-functional collaboration and progress toward shared goals. Collaborate and partner with all Employee Platform (EP) TRC Leads to drive EP wide initiatives. Execute reporting and governance of controls, policies, issue management, and measurements, offering senior management insights into control effectiveness and inform governance work. Proactively monitor and evaluate control effectiveness, identify gaps, and recommend enhancements to strengthen risk posture and regulatory compliance. Be responsible for delivery, governance and oversight of employee platforms risk portfolio including CORE, Archer, FARM, Harmony, KRI and KPI Management (GTMetrics, etc). Required qualifications, capabilities, and skills 5+ years of experience or equivalent expertise in technology risk management, information security, or related field, emphasizing risk identification, assessment, and mitigation. Familiarity with risk management and operational risk frameworks, industry standards, and financial industry regulatory requirements. Proficient knowledge and expertise in data security, risk assessment & reporting, control evaluation, design, and governance, with a proven record of implementing effective risk mitigation strategies. Demonstrated ability to influence executive-level strategic decision-making and translating technology insights into business strategies for senior executives Strong understanding of risk management principles and practices. Ability to evaluate and enhance control effectiveness. Experience in preparing for and supporting internal audits and 2LOD assessments. Proficiency in identifying, assessing, and mitigating vulnerabilities within the technology environment. A natural curiosity to explore, question, and understand complex systems and processes and take appropriate action. Preferred qualifications, capabilities, and skills CISM, CRISC, CISSP, or similar industry-recognized risk and risk certifications are preferred. Data governance and data controls experience. Familiarity and intellectual curiosity on AI/ML risk & control considerations. Cloud native experience (i.e., AWS).

Job Description STAQ Pharma is currently hiring for a Quality Assurance Specialist to join our team here in Columbus Effectively encourage and motivate associates to be successful and remain focused on Quality, Transparency, Safety and Availability objectives compatible with the company's mission and vision. Responsible for providing oversight of the Quality System; including managing control of documents (SOPs, WI, Specifications, Batch Records, etc.) that impact the identity, strength, quality, and purity of finished product, and providing support on Quality management projects. Duties/Responsibilities: Lead the document control program to ensure procedures meet CGMP requirements Manage training documentation and track employee compliance with training plans Issue GMP documents including Master Batch Production Records, Room and Equipment Logs, Document Change Orders, etc. Support in-process and finished product lot acceptance sampling and inspection Participate in investigations and problem solving of raw material, in-process, and finished product non-conformances with production personnel and/or supplier Develop and implement corrective and preventive actions geared toward continuous process improvements Support the finished product label printing and issuance process Write and implement standard operating procedures to meet and maintain FDA cGMP, USP, and state licensure requirements Provide supplier related support to production and receiving inspection team Other duties and tasks, as assigned Required Skills/Abilities: Excellent independent judgement and interpersonal skills Excellent mathematical, written communication, and verbal communication skills Strong technical writing skills and attention to detail Knowledge of and proficiency in the use of basic statistics Familiarity with Good Manufacturing Practices and FDA Regulations Supplier Auditing experience Knowledge of ERP System Proficient in using Microsoft Word, Excel, PowerPoint, Outlook: experience with OneNote and Publisher a plus Education and Experience: 2-5 years of Quality Assurance experience Pharmaceutical, Medical Device, or biotechnology industry experience, preferably in support of manufacturing B.S. or B.A. on Sciences or a relevant field or equivalent experience Professional certification in Quality Engineering or Quality Auditing, preferred Physical Requirements: Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 15 pounds at times.

We are immediately hiring for a Quality Analyst here in the Dayton, Ohio area! This position is going to help support a laboratory team that focuses on manufacturing and processing for nerve regeneration for patients. This is a long-term career opportunity for someone looking to grow in the sciences! Candidates must have a Bachelors Degree in a scientific field and at least 6 months of industry experience. INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT ************** TO SET UP AN IMMEDIATE PHONE INTERVIEW! Job Description The Quality Analyst is primarily responsible for document review to ensure compliance with FDA and other necessary regulations. Responsibilities * Review batch production and manufacturing records as part of lot release activities. * Coordinate and track CAPA, NCR, and Deviation records, ensuring timely completion. * Manage the site environmental monitoring (EM) testing program. * Assist teams in problem-solving and root cause analysis for quality events. * Provide input based on experience with batch release requirements. * Conduct Quality Control activities including incoming material, in-process, and finished product inspections for medical devices and human tissue-based products. * Maintain accurate records of Quality Control activities, adhering to Good Documentation Practices. * Support gowning qualification and training. * Ensure timely issuance, review, and approval of Microbiology and EM testing results. * Implement corrective and preventive actions for recurring product/process discrepancies. * Assist in hosting onsite regulatory audits and inspections. Qualifications * Must have a Bachelors Degree in a Scientific field and at least 6 months of industry experience. * May consider candidates with an Associates Degree in a scientific field and additional, relevant industry experience. Job Type & Location This is a Contract position based out of Vandalia, OH. Pay and Benefits The pay range for this position is $26.50 - $26.50/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Vandalia,OH. Application Deadline This position is anticipated to close on Dec 16, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

JobID: 210661484 JobSchedule: Full time JobShift: Base Pay/Salary: Jersey City,NJ $142,500.00-$200,000.00 Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in risk management. As a Tech Risk & Controls Lead - Resiliency within JPMorgan Chase, you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities * Ensure effective identification, quantification, communication, and management of technology risk, focusing on root cause analysis and resolution recommendations * Develop and maintain robust relationships, becoming a trusted partner with LOB technologists, assessments teams, and data officers to facilitate cross-functional collaboration and progress toward shared goals * Execute reporting and governance of controls, policies, issue management, and measurements, offering senior management insights into control effectiveness and inform governance work * Proactively monitor and evaluate control effectiveness, identify gaps, and recommend enhancements to strengthen risk posture and regulatory compliance * Provide SME knowledge and oversight of resiliency testing activity Required qualifications, capabilities, and skills * 5+ years of experience or equivalent expertise in technology risk management, information security, resiliency or related field, emphasizing risk identification, assessment, and mitigation * Familiarity with risk management frameworks, industry standards, and financial industry regulatory requirements * Proficient knowledge and expertise in resiliency protocols, testing, data security, risk assessment & reporting, control evaluation, design, and governance, with a proven record of implementing effective risk mitigation strategies * Demonstrated ability to influence executive-level strategic decision-making and translating technology insights into business strategies for senior executives Preferred qualifications, capabilities, and skills * CISM, CRISC, CISSP, or similar industry-recognized risk and risk certifications are preferred

Who We Are Born from a mission to make prescription eyewear affordable and accessible to everyone, Zenni Optical has been changing the way people see the world since 2003. With complete prescription pairs for adults and kids starting at under $10, we've grown into a global brand with over 51 million pairs of glasses sold - and counting! Based in the San Francisco Bay Area, we're proud to be the Official Eyewear of the San Francisco 49ers, Boston Celtics, Monster Jam, Ghost Gaming, TSM, Major League Pickleball and more. We've also partnered with tastemakers and designers like Chase Stokes, Jrue Holiday, and George and Claire Kittle to bring our brand to life in bold, meaningful ways. Innovation is at the heart of everything we do at Zenni - from our revolutionary EyeQLenz™ with Zenni ID Guard™ glasses to our cutting-edge VR Vision Screener, we're constantly exploring new ways to improve vision and enhance lives. For more information, please visit zenni.com/press. Candidate safety is important to us. Please note that all official communication will only be sent ********************** addresses. About the Role We are looking for a highly motivated QA Analysis Technician who is eager to learn and develop in the optical field onsite in Obetz, Ohio. The ideal candidate has strong organizational skills, open to feedback, and looking to grow their career. If you are open to light physical labor (frames and lenses for eye glasses) and working with a fantastic team to help people everywhere buy more affordable glasses, we'd love to hear from you! The Obetz location offers a brand new and climate controlled facility with free daily meals and snacks! You'll have the opportunity to move up in the organization based on performance reviews. Want to learn more about our team? Watch our story and see how we're making an impact-check out the video below! 🎬👇 Shift: Monday - Thursday 7:00 am - 5:30 pm (must be available for overtime as needed, including weekends) Compensation: $17 - $19/hour (based on applicable experience) Responsibilities: Utilize automation for quality analysis Point out cosmetic defects Maintain good housekeeping, 6S Ensure daily / weekly / monthly goals are met Adherence to all company policies, processes, and procedures (i.e. Health & Safety Awareness) Report to management on activities and issues Basic Qualifications: Ability to stand or sit for the duration of the shift Fine attention to detail Strong organizational skills Good literacy and numeracy skills You are proactive and have a strong ability to identify & problem solve Follow instructions and production schedules Preferred Qualifications: Previous quality analysis experience is a plus Previous experience with utilizing pass / no pass standards Previous warehousing experience is a bonus! Perks & Benefits: Annual Bonus Program Employee Paid - Health Care Plan (Medical, Dental & Vision) Retirement Plan (401K & matching) Life Insurance (Basic, Voluntary & AD&D) Paid Time Off (Vacation, Public Holidays) Training & Development Dental insurance Employee assistance program Flexible spending account Health savings account Vision insurance Free Lunch Daily Referral program As a condition of employment for this role, you will be required to undergo pre-employment drug testing in accordance with our company policies and applicable law. We look forward to hearing from you! We strive to build a diverse team of individuals with a broad range of experience and perspectives. We encourage you to apply even if you don't feel you meet all the qualifications. Zenni Optical is an equal opportunity workplace and considers applications without regard to race, color, national origin, gender identity, sexual orientation, age, citizenship, marital status, disability, or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our donors, and provide the science behind the medicine through our diagnostic laboratories. Versiti brings together outstanding minds with unparalleled experience in transfusion medicine, transplantation, stem cells and cellular therapies, oncology and genomics, diagnostic lab services, and medical and scientific expertise. This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced cost of care for hospitals, blood centers, hospital systems, research and educational institutions, and other health care providers. At Versiti, we are passionate about improving the lives of patients and helping our healthcare partners thrive. Position Summary Under the direction of the department leadership, prepares quality biological blood components within the prescribed time following regulatory and operational standards as specified in the Standard Operating Procedures and departmental procedures. WHEN YOU WILL WORK: 3rd Shift: Sunday-Thursday, 11:00pm-7:30am On-call availbility as needed Full Time, Non-Exempt role Training schedule may differ from traditional schedule. COMPENSATION: $18.04/hr.+ based on experience - paid training provided Benefits eligible including medical/dental/vision insurance options, 7% 401(k) match, EAP, employee wellness program, generous PTO, and more. Shift differentials for evenings/weekends Evenings (after 6:00pm) - $1.50/hr. Weekends - $2.00/hr. Total Rewards Package Benefits Versiti provides a comprehensive benefits package based on your job classification. Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and Long-term disability, life insurance, 7% match dollar for dollar 401(k), voluntary programs, discount programs, others. Responsibilities Manufactures Red Blood Cells (RBCs), Fresh Frozen Plasma and Recovered Plasma Manufactures Neonatal RBCs. Sterile docks Pedipaks to Platelet Apheresis, Neonatal RBCs Performs leukoreduction of Whole Bloods and RBCs Manufactures Cryoprecipitate, Pooled Cryoprecipitate and Cryo Reduced Plasma Labels products to meet regulatory and inventory requirements Manufactures additional specialty products as needed by customer base Follows procedures pertaining to the proper storage of RBCs, platelet products and frozen products Performs and documents equipment function checks and QC as required Maintains a level of productivity that allows department to achieve production goals Works weekend, holiday rotations and on-call, as needed Other duties, as assigned Performs other duties as assigned Complies with all policies and standards Qualifications Education High School Diploma required equivalent required Experience Less than 1 year 1-6 months related experience and/or training or equivalent combination of education and experience required Knowledge, Skills and Abilities Ability to read, interpret, and write documents such as operating forms, operating and maintenance instructions, and other department manuals required Above average attention to detail and problem-solving skills required Ability to apply judgment to written or oral instructions required Aptitude for computers and data entry skills required Ability to manage interruptions in a fast-paced environment required Customer service and communication skills required Able to organize work to provide productive work flow needed in component manufacturing required Flexibility to work independently and with a team required Organized, able to prioritize and handle multiple tasks at one time required Be able and available to work a flexible working schedule as required based on volume and timing of blood collections required Ability to work independently with limited written or oral instruction required Understands military time required Tools and Technology General office equipment (computer, printer, fax, copy machine) required Microsoft Suite (Word, Excel, PowerPoint, Outlook) required Software systems (Blood Establishment Computer Systems, Title21) required Lab specific equipment, including, but not limited to: • Sealers • Centrifuge • Water bath • Scales required Not ready to apply? Connect with us for general consideration.

Job Title: Quality Assurance Associate Job Title: Quality Assurance Associate Job Type: Full-time About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them. Description: We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated [Job Title] to join our team. In this role, you will be responsible for [briefly describe key responsibilities and tasks]. You will work closely with [mention teams or departments the role collaborates with] to [describe the role's contribution to the company's success. Job Purpose: Under the supervision of the Quality Assurance Supervisor, this person is responsible for performing field QA activities: in process checks in the aseptic processing area, approval for area clearance, AQL inspection for finished products, retention sampling for finished products, batch record review, final product release, review and approve operation documents and forms, and approval / rejection of in-coming raw materials, components, and final product labels. Ensure compliance of operations personnel with the company's procedures and Good Manufacturing Practices (GMPs). This position will also be responsible for identifying any deviations or non-conformances, writing deviation reports, performing root cause analysis, writing/revising standard operating procedures and forms, and tracking metrics, when required. Key Responsibilities: • Regular and predictable onsite attendance and punctuality. • Perform monitoring of Compounding in the aseptic processing area. • Perform AQL inspection for Finished products • Perform in-coming raw material, component, and labeling inspection and release • Review executed batch records to ensure compliance with approved procedures, and communicate and resolve discrepancies with manufacturing operators and supervisors. • Provide Quality support to Manufacturing personnel on the floor - providing guidance during GMP events and initiation of deviations and investigations. • Lead small scope projects, as assigned. • Prepare and/or revise SOPs to ensure compliance with regulations and current practices. Keep current with regulations and industry best practices and update SOPs to improve compliance. • Prepare all necessary reports in a timely manner to meet compliance requirements and business needs. • Participate in Process Validation activities, including protocol execution and reporting, as necessary. • Working knowledge of FDA regulations and application of GMPs. Qualifications: We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them: • Minimum: Associates Degree in Science or equivalent with 2 to 5 years applicable Quality Assurance experience. • Preferred: Bachelor's Degree in Science or equivalent with 1-2 years applicable laboratory, pharmaceutical manufacturing, or related experience (QA preferred) Compensation: Base Salary: $ 65,000 to $ 75,000 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process. What We Offer*: • Annual performance bonus, commission, and share potential • Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute • A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries • 3 personal days (prorated based on hire date) • 11 company paid holidays • Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits • Employee discount program • Wellbeing rewards program • Safety and Quality is a top organizational priority • Career advancement and growth opportunities • Tuition reimbursement • Paid maternity and parental leave *Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms. Recruiters: Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma. Equal Opportunity Employer: Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.

What Quality Assurance contributes to Cardinal Health Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Assurance develops and implements a compliant and cost effective quality system that assures products and services are reliable, safe and effective. This job family provides oversight of production/manufacturing activities, training to operational and quality control personnel, and educates business leaders on Quality policies and procedures and ensures that all products and services are properly reviewed for quality and documented. Job Summary The Principal Specialist, Quality Assurance is responsible for reviewing all customer threshold activity requests for controlled substances in compliance with set standards. This job reviews inbound requests, assesses them for risk and escalates according the standard operating procedures. The Principal Specialist, Quality Assurance assists the Manager, Regulatory Management in data entry activity and documentation drafting/filing. This job ensures the consistent application of set threshold methodologies across the organization. Responsibilities Responsible for ensuring quality standards and procedures are followed at the Cardinal Health NPHS Warehouse. Authority for approval and disposition of raw materials, components, closures, APIs, and products at the Cardinal Health NPHS Warehouse. This includes review of analytical results which may support material release. Supporting and documenting investigations where required. Organizes documentation to ensure procedure timelines are met Additional responsibility may include overarching systems which support the warehouse, for example, equipment and facility (i.e., temperature management and mapping), packaging and labelling. QA site lead for SAP material management activities. Document and report quality and compliance issues to QA management as necessary. Prioritizes and ensures work is delivered in an efficient way. May assist in the material qualification of new materials May serve as a delegate or representative Performs other job duties as assigned. Qualifications 4-8 years of experience, preferred Quality and/or Operations Warehouse experience preferred Bachelor's degree in related field, or equivalent work experience, preferred What is expected of you and others at this level Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects Understands technical/release material issues and evaluates their potential impact on quality and compliance. Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including but not limited to maintaining required trainings as appropriate to position requirements. Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback. Will contribute to the development of policies and procedures Works on complex projects of large scope Develops technical solutions to a wide range of difficult problems Solutions are innovative and consistent with organization objectives Completes work independently; receives general guidance on new projects Work reviewed for purpose of meeting objectives May act as a mentor to less experienced colleagues Anticipated salary range: $79,700 - $113,800 Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vision coverage Paid time off plan Health savings account (HSA) 401k savings plan Access to wages before pay day with my FlexPay Flexible spending accounts (FSAs) Short- and long-term disability coverage Work-Life resources Paid parental leave Healthy lifestyle programs Application window anticipated to close: 10/07/2025 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here

The QA Compliance Specialist position exists to support the execution of quality & regulatory functions in the organization to ensure compliance with the AV-SH quality/business systems to applicable regulations, standards and corporate policies. Responsible for compliance with applicable Corporate and Divisional Policies and procedures. Support external audit activities (FDA, FDB, ISO registrar audits etc.). Audit areas of client s Vascular Quality System. Support administration of Quality System processes (CAPAs, Internal Audits etc.). Generate and distribute periodic open CAPA and Internal Audit Corrective Action (IACA) reports. Track and trend compliance activities on a periodic basis. This may include CAPA & IACA metrics etc. Generate compliance metrics for Management Reviews. Assist the organization to receive timely feedback on open corrective actions. Participate in cross divisional activities to integrate quality system information. Conduct review and update Quality System procedures as necessary. Assist in developing & conducting Quality System training as necessary. File Quality Records (audit reports, IACAs, CAPAs etc.). Ensure that all responsibilities are carried out in compliance with governing regulations and standards. Other duties as assigned. Education: Bachelor Degree or equivalent plus 4 + years of related work experience or equivalent combination.

The Panther Group has an immediate need for a Manufacturing Technician in the Kettering, OH area. This position employs an individual for the operation of a computer-based laser machining work center. This individual's primary responsibility will be to laser process components through instructions that may be in the form of drawings and written or verbal direction. Employees must become familiar with procedures and are aided with direct supervision. This position is part of a team, and a heavy emphasis will be placed on the individual's ability to participate in a team environment. Responsibilities: Perform simple to medium complexity tasks related to customer specific process requirements. Must be able to comprehend documentation requirements. Verify system conditions or equipment status before operation. Inspect components to ensure specifications have been met. Enter data as required. Train other employees in production processes or equipment usage as requested by Supervisor. Maintain a clean and safe work area. Follows instructions of the Supervisor and/or Production Manager and conducts all work according to company policy and good safe labor practices. The use of laser radiation (non-ionizing) sources will be used only in a manner that is safe for all employees and visitors. The various wavelengths of laser light utilized will be taken into consideration in this and other personal protection policies by the laser operator. Employee must conduct themselves in a professional and appropriate manner and is responsible for maintaining a high standard of conduct and job performance. Required Qualifications: Minimum one year experience in a manufacturing environment High School Diploma or GED Good dexterity, as many jobs require the handling of many small components. Preferred Qualifications: Experience with automated or manual inspection equipment Familiarity with ISO Quality Systems particularly in medical device manufacturing. Use of optical inspection equipment. This may be defined as a magnifier, microscope, and/or equipment used for measuring capacity.?? Pay range $17.00 - $21.60 / hour depending on shift #INDENG

JBK Manufacturing is recruiting for a Quality Control Technician. We are a growing company and we are looking for qualified candidates that are looking for growth opportunities and a long time career. As a Quality Control Technician, you will uphold the safety of our company and supervise the production process to guarantee that all our products meet quality expectations. Perform regular product evaluations, record inspection results, and recommend improvements to the production process. Quality control inspectors examine products and materials for defects or deviations from specifications. RESPONSIBILITIES: Read blueprints and specifications. Monitor operations to ensure that they meet production standards. Recommend adjustments to the assembly or production process. Inspect, test, or measure materials or products being produced. Measure products with calipers, gauges, CMM or micrometers Accept or reject finished items. Remove all products and materials that fail to meet specifications. Discuss inspection results with those responsible for products. Report inspection and test data Resolve quality related issues in a timely manner. REQUIREMENTS: Minimum of 3 years' experience working in Quality Control in a manufacturing environment. Proven experience as quality inspector or relevant role A keen eye for detail and a results-driven approach Responsible and trustworthy Familiarity with quality testing machines and systems Experience with calipers, gauges, CMM and micrometers Thorough knowledge of quality control standards and testing methodologies. Certification of quality control is a strong advantage (ISO 9000 etc.) Working knowledge of MS Office High School Degree; Further qualifications will be a plus Location: Dayton, OH Benefits offered: Paid time off Health insurance Dental insurance Vision insurance Retirement benefits Healthcare spending/reimbursement JBK Manufacturing is an Equal Opportunity Employer, committed to fostering diversity in its staff, and strongly encourages applications from the entire spectrum of a diverse community. Job Type: Full-time Pay: $21.00 - $25.00 per hour Benefits: 401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance Schedule: 10 hour shift Day shift Monday to Friday Overtime Weekends as needed Work Location: In person

The Quality technician inspects and test product and materials per customer specifications and meets regulatory requirements maintaining quality and safety standards. She/He prepares and keeps records of final inspections, follows traceability, and maintains supporting documentation as required by QQE and their customers. Primary Responsibilities Clean parts as required Inspect and test product for both cosmetic flaws, dimensional, and/or other product characteristics per prescribed methods and requirements Identify and follow critical control points and preventive measures Verify and record required data such as critical features and certifications as needed Handle product in such a way to reduce the introduction of additional contamination and damage Verifies CMM print outs and identify any discrepancies. Communicate with Office and shop personnel any problems or concerns about product quality or customer requirements Write non-conformance reports as required Review routers for completeness and accuracy as routers come into inspection. Laser engraves parts as needed per procedure Print and scan barcode labels, shipping labels and shipping papers as required Print shipping labels and shipping papers as required Package product per both QQE and customer requirements Perform tasks to meet the requirements of the QQE Quality Management System such as record and document control Print and scan barcode labels as needed Monitor operations for quality achievement and compliance with established processes and procedures by executing internal audits as assigned Participate and support the implementation of new programs and changes by performing and supporting continuous improvement initiatives Support and be part of corrective and preventive action plans May interact with internal and external customers and meet customer requirements Other duties as assigned Qualifications: Knowledge: Must be a high school graduate and have experience in process improvement techniques. Preferably with an associate's degree in an industrial or manufacturing technology field or an equivalent combination of education and experience. A degree with a quality background is preferred. 2-3 years of experience in manufacturing and/or quality environment. Abilities: Good conceptual capabilities and must be meticulous in their work. Must have attention to detail and ability to exercise sound judgment; also, must be able to read drawings and identify critical features. Must have the ability to communicate verbally and in writing, work as part of a team to ensure achievement of company goals, consistently follow set procedures on inspection techniques and practices as QQE and customers require, and legible penmanship is a must since many inspections require documentation that they will be required to fill in. Skills: Working knowledge of controls and instrumentation, as well as computers to be able to work and maintain records, etc. Must be skilled in quality processes and knowledgeable about measurement and test equipment. Proficient in the use and operation of measuring tools such as micrometers, calipers and profilometer. Physical Demands: Must be able to lift 50 Lbs. and eyesight of 20/20 with or without corrective lenses

Job DescriptionDescription: About Us: Westrafo America is the first US based facility specializing in the design and manufacturing of high-quality transformers. We are committed to excellence and are looking to expand our team with dedicated professionals who share our passion for electrical engineering and manufacturing. Position Overview: We are seeking a detail-oriented Quality Control Inspector to join our team. The ideal candidate will be responsible for ensuring that our transformers meet the highest quality standards and comply with industry regulations. This role is critical to maintaining our reputation for quality and reliability as we scale our operations. Key Responsibilities: Conduct inspections of raw materials, in-process components, and finished products to ensure compliance with specifications and standards. Develop and implement quality control procedures and guidelines. Perform testing and analysis on transformers to identify defects or areas for improvement. Document inspection results and maintain accurate records of quality metrics. Collaborate with production teams to address quality issues and implement corrective actions. Conduct root cause analysis for quality defects and develop strategies for prevention. Ensure compliance with safety and regulatory standards in all quality control processes. Participate in continuous improvement initiatives to enhance product quality and operational efficiency. Qualifications: High school diploma or equivalent; associate or bachelor's degree in engineering or a related field preferred. Previous experience in quality control or manufacturing, preferably in the electrical or transformer industry. Knowledge of quality control standards and methodologies (e.g., ISO 9001). Strong attention to detail and analytical skills. Proficient in using measurement tools and equipment (calipers, micrometers, etc.). Excellent communication and teamwork skills. Ability to work independently and manage multiple tasks effectively. Benefits: Competitive salary and performance-based bonuses. Health, dental, and vision insurance. Retirement savings plan. Opportunities for professional development and career advancement. A dynamic and innovative work environment. Requirements: