Quality assurance technician jobs in Indianapolis, IN

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. Job Summary: This role provides essential Quality Assurance oversight for API External Manufacturing operations, ensuring compliance with cGMP and regulatory requirements for all products manufactured by third-party partners. Job Responsibilities: * Lead and manage quality aspects of external API manufacturing sites, including but not limited to batch record review, disposition, deviation management, and change control. * Conduct and/or participate in quality audits of external manufacturing sites to assess compliance with cGMP, regulatory expectations, and Eli Lilly's quality standards. * Review and approve quality-related documents, such as manufacturing master batch records, validation protocols and reports, stability data, and analytical methods. * Collaborate cross-functionally with internal teams (e.g., Supply Chain, Regulatory Affairs, Technical Services) and external manufacturing partners to resolve quality issues and drive continuous improvement. * Provide expert QA guidance and support during new product introductions and technology transfers to external manufacturers. * Develop, implement, and maintain quality agreements with external manufacturing organizations. * Investigate and troubleshoot complex quality incidents, deviations, and out-of-specification results, determining root causes and implementing effective corrective and preventive actions (CAPAs). * Represent Eli Lilly's quality interests during regulatory inspections at external manufacturing sites. * Mentor and provide technical guidance to junior QA associates. Job Qualifications: * Bachelor's degree in a scientific discipline (e.g., Chemistry, Biochemistry, Pharmacy, Chemical Engineering) or related field. * Minimum of 5-8 years (Senior Associate) or 8+ years (Principal Associate) of experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry, with a strong focus on API manufacturing and external supply. * In-depth knowledge of cGMP regulations (FDA, EMA, HPRA, etc.) and global pharmacopeial requirements. * Proven experience in auditing external manufacturing sites. * Strong understanding of API manufacturing processes, analytical techniques, and quality control principles. * Demonstrated ability to make sound quality decisions and effectively communicate complex technical and quality information to diverse audiences. * Excellent problem-solving, analytical, and critical thinking skills. * Ability to work independently and as part of a team in a fast-paced, dynamic environment. * Proficiency in quality management systems (e.g., TrackWise, Veeva). * Willingness to travel domestically and internationally to external manufacturing sites as required. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

: Crown Equipment Corporation, one of the world's largest lift truck manufacturers, offers local support on a global scale with more than 15 manufacturing facilities worldwide and more than 500 retail locations in over 80 countries. Our global sales and service network provides our customers with a local resource for a wide variety of quality material handling equipment, fleet management solutions, warehouse products and support services to meet their needs anytime, anywhere. Job Posting External Primary Responsibilities * Responsible for the daily tactical quality support of manufacturing components/processes and assembly processes/outputs. * Implement containment actions for non-conformances ensuring impact to production is minimal. * Participate in quality assurance audits. * Maintain/update quality control documents. * Utilize basic inspection equipment and blueprint reading. * Assist in the evaluation and disposition of non-conforming product. * Provide metrics and input for the Quality function to other departments. * Review and verify corrective actions for effectiveness to prevent reoccurrences Qualifications * A two-year college degree and/or ASQ Certification as a Quality Technician preferred. * Three to five years' experience in quality and/or manufacturing related fields desirable. * Must have good problem solving skills. * Working knowledge of advanced mathematics, including statistical techniques, SPC, Capability Analysis and Gage R+R is required. * Must be able to apply quality tools for continuous improvement (FMEA). * Must know basic inspection and testing concepts, how to read blueprints and GD+T information. Must possess good communication skills - both verbal and written. * Must possess the ability to work effectively and maintain a professional composure with other employees. * Requires understanding of basic PC computer application skills, including database, spreadsheets and word-processing. Work Authorization: Crown will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas or who need sponsorship for work authorization now or in the future, are not eligible for hire. No agency calls please. Compensation and Benefits: Crown offers an excellent wage and benefits package for full-time employees including Health/Dental/Vision/Prescription Drug Plan, Flexible Benefits Plan, 401K Retirement Savings Plan, Life and Disability Benefits, Paid Parental Leave, Paid Holidays, Paid Vacation, Tuition Reimbursement, and much more. EOE Veterans/Disabilities Nearest Major Market: Indianapolis Job Segment: Quality Assurance, Maintenance, Database, Warehouse, Technician, Technology, Manufacturing

Job Description Who we are Skjodt-Barrett is a world-class manufacturer of food solutions and custom ingredients for North America's most beloved and trusted brands. We take pride in working closely with our customers to understand their unique needs and create innovative, individualized solutions that deliver joy to their customers. A family-founded company started over 35 years ago, we are backed by the investment company Axel Johnson Inc (AJI). With their investment and support, we are well-positioned to foster growth and explore new opportunities. Our customers, blue-chip international brands and mid-sized producers alike, are why we exist. Our teams of innovators, communicators, and managers are the people who meet their needs, build trust, and exceed their expectations. Who we need Reporting to the Quality Assurance Supervisor, we are looking for a Senior Quality Assurance Technician to join our state-of-the-art food production plant in Lebanon, Indiana. You will play a critical role in performing and supporting daily QA activities across both the production floor and the laboratory. You will execute sampling programs, conduct verification checks, support investigations, maintain quality documentation, and provide guidance to QA Technicians to ensure compliance with internal standards and regulatory requirements. This is an on-site role. Who you are You bring hands-on experience as a QA Technician in a regulated manufacturing environment - food, beverage, pharmaceutical, or similar. You understand how quality programs operate in real production settings, and you are motivated by the opportunity to elevate standards and contribute to a culture of continuous improvement. You want to work for a company where your contributions are valued, where you can collaborate across teams, and where you can grow your career in QA and beyond. What's in it for you Autonomy and influence. You will play an essential role in maintaining our position as a leading manufacturer of innovative food products. You will independently perform technical sampling, verification checks, and quality monitoring programs, while providing support to QA Technicians and contributing to daily operational excellence. Impact. You will help strengthen our quality culture by ensuring every product meets the highest standards of safety, compliance, and consistency. Your work in inspections, investigations, sampling, and documentation will directly influence production performance, customer satisfaction, and audit readiness. Career development. You will join a collaborative QA team that values transparency, respect, and learning. This role is ideal for a seasoned QA Technician ready to step into a senior-level position with the opportunity to gain deeper investigative experience, support Quality Management System programs, and grow toward leadership or specialized QA roles. How you will make an impact: Perform sampling and testing. You will complete internal and external sampling activities, fulfill customer sample requests, collect retained samples, and maintain retention programs. You will conduct routine sampling for environmental monitoring programs in light, water, air, and nitrogen. Work on the production floor and in the lab. You will divide your time between the floor and the laboratory, performing hands-on verification checks, reviewing product quality, conducting testing, and supporting QA Technicians completing line checks. Lead verification and inspection activities. You will perform GMP self-inspections, conduct verification checks (including equipment verifications), complete routine audits, and ensure all documentation is accurate and audit-ready. Support investigations. You will assist in deviation investigations, including participating in equipment inspections, completing swabbing, coordinating sample pulls, gathering documentation, and collaborating with Production, Maintenance, and Warehouse teams to support root cause analysis and corrective actions. Collaborate across teams. You will work closely with Production, Maintenance, Warehouse, and Purchasing to ensure product quality and program compliance. You will support equipment or process deviations, help locate warehouse samples, and verify that standards are maintained. Support QMS program execution. You will complete administrative tasks, including program trackers, verification logs, routine reports, and other documentation required to support QA programs. You will help ensure that all programs are current, accurate, and audit-compliant. Provide support for QA Technicians. You will assist floor Technicians with questions, troubleshooting, sample pulls, and verifications. You will provide off-shift or PTO coverage to ensure continuity of testing, inspections, and documentation. What you bring to the role: The experience. You have experience in quality assurance, quality control, or a related function within a regulated manufacturing environment. You understand how manufacturing quality programs operate and have hands-on experience conducting sampling, inspections, audits, and verifications. The technical skills. You have strong knowledge of GMP, HACCP, and quality management systems. You are proficient in Microsoft Office and quality data systems. You bring analytical thinking, accuracy, and a strong attention to detail. The adaptability and communication. You are able to work across departments, building relationships with Production, Maintenance, Warehouse, and other teams. You communicate clearly, adapt to shifting priorities, and maintain composure in a fast-paced environment. The approach. You bring a continuous improvement mindset, strong organization, and a proactive sense of ownership. You are not new to quality-you have the confidence and experience to step into a senior technical role and support both daily operations and long-term quality initiatives. Why join? We've got great taste. We care deeply about fostering a culture of transparency, responsibility, and integrity. It's what drives us to make great-tasting, convenient, and healthy ingredients and finished products that our customers depend on. With a focus on nurturing and growing our employees' careers and professional satisfaction, we believe in open communication, idea sharing, and knowledge building. Skjodt-Barrett is committed to building an inclusive culture that helps to create longevity, growth, and innovation in the food industry. We are working towards a sustainable future. We believe that what's good for people and the planet is good for profit. It is everyone's responsibility to do their part. We recognize the growing need to prioritize sustainability in manufacturing, and we continue to take steps to evolve. We strive to accelerate the adoption of sustainable packaging and food products to be a responsible partner for our customers and for the greater good. We take our role as a supply chain partner to heart and adhere to a strict Supplier Code of Conduct to ensure that our vendors uphold the integrity and values we live by. We believe actions speak louder than words. Every day, we come together to exceed the expectations of our customers, each other and ourselves, inspired by our values: We care. About family, honesty, and respect. We communicate. Across every level, often, effectively, and clearly. We Empower. With trust, integrity, and accountability. We Deliver. Every time, through teamwork, innovation, and results. Apply now. At Skjodt-Barrett, we aim for diversity, equality, accessibility and inclusion in all of our operations and interactions. We welcome and appreciate candidates with a range of backgrounds and experiences. If you have 70% of the qualifications we are looking for and want to play an integral role in delivering innovative food product solutions, apply to express your interest. What you can expect from our interview process: A virtual interview with a Talent Advisor discussing your interest in the role and the company. The conversation will be recorded using BrightHire, an AI-powered video interview tool. More details will be shared when you are invited to interview. An on-site interview with the Plant QA Manager and QA Supervisor, including a tour of the facility to give you a closer look at the environment and team. A virtual interview with the QA Director and Plant Manager, where you will discuss your experience in quality, your approach to collaboration, and your alignment with the team's needs. Skjodt-Barrett welcomes and encourages applications from people with disabilities. Please let us know what accommodations you require across the selection process. #LI-DNI Powered by JazzHR VmGGuldjBu

Job DescriptionMust be able to read tape measure up to 1/8 of an inch. Understand/read blueprints. Working in concrete industry. Minutemen Staffing provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Job Scope: The Quality Control Technician is to be proficient in every aspect of performing the functions of this position. The Quality Control Technician's overall responsibility, and objective, is to ensure that all aspects of the SQF, Quality, and Food Safety Programs are followed by all employees, vendors, visitors, etc. Duties and Responsibilities: Routinely check operator paperwork for accuracy and completeness. Routinely check labels, bags, and seals for accuracy. Assure checks are documented clearly, cross referenced and traceable. Communicate results of routine QA tests to production personnel. Notify supervisory personnel and Quality Control and Food Safety Manager of product quality or plant conditions which may have a negative impact on product quality and work together to correct the situation. In the case of finished product, perform follow-up testing until situation is corrected and product disposition is resolved in a quality conscious manner. As directed and trained, conduct various tests for incoming ingredients, including sieve, NIR, moisture, and mycotoxin testing. Maintain and report hold/reject product and assure its proper disposition. Collect routine ingredients and finished product samples, as required (detailed in QA Manual). Train and educate all personnel on quality and food safety practices. Promptly respond to calls for assistance clearly communicating and ETA of arrival. Promptly respond to quality/food safety concerns, following up as needed. Follow First In First Out (FIFO) and enforcing other departments to follow the same process. Continuously work with and/or assist production, maintenance, and sanitation personnel as needed throughout the shift. Maintain a clean work environment and stock supplies as needed for next shift. Ensure, and hold accountable, all personnel, visitors, vendors, etc. comply with all Standard Operating Procedures (SOPs) in addition to all SQF, Quality, and Food Safety Programs. Maintain accurate, complete, and legible paperwork. Assist Quality Control and Food Safety Manager with all other duties/tasks as needed. Be an employee champion who will maintain a strong and positive working relationship with all employees with the utmost integrity, confidentiality, and ethical values. Additional Job Functions: Assist in maintaining a positive team environment and good working relationship by maintaining a positive attitude toward all Diamond team members, vendors, and customers. Participate effectively in a team atmosphere by modeling and promoting conflict resolution, diversity, ethical practices, and organizational citizenship. Responsible for other duties as deemed necessary by Management. QUALIFICATIONS: Must be willing to/have availability to work any shift (day or night shift). Ability to work independently without immediate direction or oversight. Self-motivated with a high degree of initiative and integrity Excellent communication skills, both oral and written, to effectively communicate in a professional manner. Excellent interpersonal skills (communication, listening, team player, cooperative, approachable). Ability to be organized, flexible, and perform acceptably under pressure. Must be able to take directions, work efficiently and safely. Must be able to stand, sit, and walk for long periods including on a catwalk. Must be capable of lifting, carrying, pushing, and pulling up to 50 pounds routinely. Must be capable of overhead work and manual dexterity for manipulating or moving objects. Must be able to climb both stairs and ladders up to a high elevation. Must be able to balance, stoop, kneel, crouch, and crawl. Must be able to operate a forklift. Must be able to perform moderate to heavy labor under constant machine operation and other noise. Education & Experience Recommendations: Quality experience at a food processing facility preferred. High School Diploma or GED required.

The Quality Control Technician will be a member of the Quality Control Department. As a member of the team, he/she/they will be involved in routine QC sampling and testing of utilities, raw materials, in-process/finished product/stability drug product and incoming components in accordance with GMP (Good Manufacturing Practices) and safety guidelines. Technician will also support lab organization/operation by performing activities such as supply ordering, glassware washing and preparation, laboratory cleaning, and any other additional tasks deemed necessary for laboratory operation. Additionally, tasks including but not limited to second person verification of analytical data, laboratory investigations support, and equipment calibrations and maintenance support may be required of this role. The Quality Control Technician is an entry/developmental position with opportunities to grow within the laboratory. This is a 2nd Shift Position. Hours: 3pm-11:30pm Essential Job Functions: * Be team oriented and willing to act as both a facilitator of special projects and a contributor to special projects when needed. * Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures. * Collaborate with internal departments and teams to resolve quality issues regarding facility, products manufactured and released, and goods ordered for the laboratory. * Handle and dispose of Laboratory waste while adhering to Environmental, Health, & Safety standards required in a GMP lab. * Performs sample management activities for Quality Control Chemistry Laboratory including management of samples from clean utilities, components, raw materials, in-process samples, finished product samples, and stability samples * Perform common chemistry testing on utilities samples, incoming components and raw materials, in-process samples, finished product samples, and stability samples according to validated methods as well as special testing deemed necessary by special testing or protocols. * Perform common laboratory procedures such as pH, weighing with analytical balances, glassware washing/preparation, daily equipment calibration verifications, and peer review of test parameters and reagent preparations. * Assist, as needed, with sample preparation and testing related to but not limited to validation protocols, laboratory studies, and cleaning validations. * Execute work orders and routine preventative maintenance on QC laboratory instrumentation, as needed, using written SOPs, work order directive or be available assist/escort vendors with access to systems/materials when vendors perform maintenance. * Provide support during laboratory investigations when needed. * Maintain laboratory documentation to ensure organization and regulatory compliance. Special Job Requirements: * Demonstrates excellent written and oral communication skills with the ability to clearly and concisely articulate complex issues to a range of target audiences. * Thrives in a team environment but can work autonomously with strong self-management and organizational skills. * Commits to a culture of quality with skills including attention to detail, on time delivery, and efficiency. * Upholds customer-centric mindset. * Bachelor's degree in science (Chemistry or Biochemistry preferred) or equivalent industry experience. * Strong math and documentation skills * Strong oral and written communication and interpersonal interaction skills. * Ability to work in a highly regulated and fast paced environment. * Ability to lift up to 50 lbs. * Exceptional computer skills evidenced by hands-on work with automated data management and/or data analysis systems (LIMS, JMP, Minitab, etc.) Additional Preferences: * Working knowledge of laboratory instrumentation such as pH meters, UV/VIS, FTIR, UHPLC/HPLC/GC, TOC analyzer, density meter and freezing point depression osmometer. * Experience with Good Documentation Practices (GDP) and other GxP principles. * Experience with Continuous improvement, Six Sigma, and/or Lean principles. * Experience in an isolator-based aseptic drug product manufacturing facility. * Experience performing container closure integrity testing (CCIT). Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

QUALITY TECH PURPOSE * This role is to provide quality inspection, continuous improvement, and general quality support within the organization. This position requires attention to detail, ability to understand and follow established processes, and product evaluation skills. A successful candidate will be competent in reading and understanding basic blueprints and completing routine inspections. ESSENTIAL DUTIES The Quality Technician may be responsible for performing any of the following types of inspections: * Incoming Inspections: evaluate incoming materials and components for conformance to specific criteria. Incoming inspections will be performed using dimensional, visual, and process related criteria to determine suitability for use. A base understanding of metrology, traceability, and product preservation is required for this function. * In-process Inspections: evaluate product in various stages of the process either internally or after being processed by a third party. Accurate recordkeeping and an understanding of proper document control practices is essential to success in this role * Final Inspections: evaluation of product prior to release for shipment to the customer. This will include assisting with completing and compiling documentation for First Article Inspection packets as well as production inspection records. * Ability to interact with all areas of production to maintain efficient product throughput. * Review production records for accuracy and compliance. * Ability to work in clean room environment including adherence to gowning, cleanliness, and procedural standards. * Work with a high level of precision and detail. * Participation in auditor development program and ability to learn and master auditing practices and principles. * Work in a team environment for an increased productivity and quality by ensuring quality and timely outputs while working with a continuous improvement mindset. * Understand and follow all company policies and safety procedures. * All other duties as assigned by the supervisor. PHYSICAL DEMANDS/WORK ENVIRONMENT * Capacity to work indoors in an office, laboratory, and/or manufacturing environment. * Ability to work in a stationary position for prolonged periods of time. * Capability to lift objects or equipment weighing up to 40 pounds with or without reasonable accommodation. * Physical aptitude to use basic hand tools in a laboratory and/or manufacturing environment. * Ability to attend meetings locally for trainings. MINIMUM REQUIREMENTS * 2 Year technical degree or equivalent prior quality experience in a production environment working with multiple products/product lines. * Available to work first shift with occasional overtime on evenings/weekends if needed. * Intermediate computer and math skills including ability to use Excel and Microsoft Teams. * Ability to evaluate requirements, understand technical documents, and keep thorough, organized records. * Familiarity with reading part prints and detailed specification review. * Ability to use hand tools and measuring devices such as calipers, micrometers, height gauges, surface roughness meters, Go/no-go gauges, pin gauges, comparators, borescopes, sight pipes, etc... * Communicate effectively. * Ability to perform multiple tasks while adhering to procedural guidelines with minimal supervision. * Provia, Syteline, and Excel spreadsheets experience in a work environment a plus. * Prior ISO Class 5 clean room experience a plus. * Experience with Vision Systems, CMMs, Comparators, borescopes or Sight Pipes a plus. For internal use only: Quality001

Join MIASA Automotive as a Quality Technician in Yorktown, IN Are you passionate about ensuring the highest quality standards in the automotive industry? MIASA Automotive is seeking a talented Quality Technician to join our team in Yorktown, IN. As a Quality Technician, you will play a crucial role in maintaining and improving the quality of our products through continuous monitoring, testing, and improvement initiatives. Your expertise and attention to detail will be instrumental in upholding our reputation for excellence and customer satisfaction. Responsibilities: Develop and implement product FMEAs and Quality Control Plans for new and existing products. Develop and implement supporting inspection instructions and criteria to maintain compliance with customer requirements. Reviews and organizes statistical data on quality of production by line, shift, department to produce recommendations. Continuously reviews the economics of the quality program and makes recommendations for improvement. Establishes and maintains effective work relationships with internal and external customers which broadly includes suppliers and stakeholders. Maintains the professional competence, knowledge and skills necessary for the satisfactory performance of all assigned responsibilities. Other duties as assigned Qualifications: Ability to manage projects with limited supervision. Excellent written and verbal communication skills. Systematic problem solving skills. Working knowledge of Quality Systems and related tools. Planning and organization. Experience in conducing or preparing for IAFT system audits Minimum three years of manufacturing environment. Eight Discipline Problem Solving training or experience Core Competencies: Basic knowledge of GD&T Adhere to rules, regulations and/or policies and procedures If you are a detail-oriented professional with a passion for quality assurance, we want to hear from you. Join MIASA Automotive as a Quality Technician and take your career to the next level! About MIASA Automotive: MIASA Automotive is a leading manufacturer of automotive components and systems, specializing in interior and exterior lighting solutions. With a strong commitment to quality, innovation, and customer satisfaction, we have established ourselves as a trusted partner to top automotive brands worldwide. Our state-of-the-art facilities and dedicated team of professionals ensure that we deliver cutting-edge products that exceed industry standards. At MIASA Automotive, we are driven by a passion for excellence and continuous improvement, making us a preferred choice for automotive lighting solutions. To ensure a safe and compliant work environment, all candidates receiving a conditional offer of employment will be required to successfully complete a criminal background check and pre-employment drug screening. Employment is contingent upon passing both screenings.

Responsibilities • Support receiving inspection process including visual and dimensional verification of mechanical assemblies per engineering requirements and operations schedules. Complete and electronically store receiving inspection checklists. • Utilize calipers, tape measures, blueprints, and Microsoft excel. • Perform data collection/analysis and electrical hardware functionality/verification per work instructions, checklists, and engineering requirements. Utilize Microsoft Excel, Word, and PowerPoint, multimeters, test fixtures, tape measures, CAN-testing tools, and proprietary software. • Ensure that each final assembly has a complete quality document package including completed checklists, data files and product pictures. • Ensure that non-conforming products are identified appropriately with a complete description and inform the appropriate department. Ensure that deviations from requirements, if applicable, are approved prior to acceptance of product. Qualifications • Must be able to organize and prioritize job related duties based upon operations schedules. • Ability to handle dynamic priorities and remain flexible. • Must have the ability to work independently and self-motivated • Must have excellent oral/written communication skills. Ability to communicate clearly with multiple departments. Must have proficient use of computers and Microsoft Office suite • Must be able to use basic hand tools including wrenches, drivers, and riveters • Must be able to lift 50 pounds, sometimes in a twisting or bending form. • High school diploma minimum. Electrical background is a plus • Mon-Fri 7AM to 3:30PM core hours • Occasional overtime including weekends required

DHL Supply Chain is Hiring! At DHL, you will play a part in one of the world's most essential industries. There has never been a better time to join DHL Supply Chain. In a global business like ours, the opportunities are endless. So, join us. Work with us. Grow with us. The core responsibilities of this role include: * Completing quality checks on finished goods. * Assisting supervisory staff in correcting quality issues. Position: Qulaity Tech II Shift: 3rd Shift Sunday to Thursday 11:00 PM to 7:00 AM Pay: $20.00 per hour Additional Incentives: $1.00 Shift Differential In addition to the general job description below, the ideal candidate will also possess the following skills and/or experience: Experience in WMS systems (Manhattan) Be part of the world's largest logistics company! DHL Supply Chain has been certified as a Great Place to Work in the US and Canada! Our excellent benefits packages includes: * Affordable medical, dental, and vision coverage available beginning on your 30th day * PTO program for all associates, including paid holidays and vacation * 401(k) with generous company match * Tuition reimbursement program * Excellent training and career advancement opportunities Grow your skills. Shape your world. Role Purpose: Execute assigned tasks to support establishment, maintenance, alignment and continual improvement of the QA System. Responsible for day-to-day Quality Assurance activities to ensure compliance with governmental regulations, customer requirements, quality assurance policies and procedures and accommodating requests for support. Key Accountabilities: * Perform Quality audits, inspections and documentation. * Perform daily quality assurance activities as required or directed by management. * Monitor and report level of QMS implementation, compliance and effectiveness through audit activities, observation, review of quality metrics and customer feedback. * Support QA training for new and existing associates. * Support coordination of QA license, permit and registration activities. * Work with Quality Assurance, Ops Performance and Process Improvement teams to progress Quality initiatives. Required Education and Experience: * High School Diploma or Equivalent * Forklift operator certificate or satisfactory completion of forklift training program with the first 30 days of employment * Associate degree or equivalent in related field of study, preferred Our Organization is an equal opportunity employer. #LI-Onsite #LI-DNI ","title

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. Job Summary: This role provides essential Quality Assurance oversight for API External Manufacturing operations, ensuring compliance with cGMP and regulatory requirements for all products manufactured by third-party partners. Job Responsibilities: Lead and manage quality aspects of external API manufacturing sites, including but not limited to batch record review, disposition, deviation management, and change control. Conduct and/or participate in quality audits of external manufacturing sites to assess compliance with cGMP, regulatory expectations, and Eli Lilly's quality standards. Review and approve quality-related documents, such as manufacturing master batch records, validation protocols and reports, stability data, and analytical methods. Collaborate cross-functionally with internal teams (e.g., Supply Chain, Regulatory Affairs, Technical Services) and external manufacturing partners to resolve quality issues and drive continuous improvement. Provide expert QA guidance and support during new product introductions and technology transfers to external manufacturers. Develop, implement, and maintain quality agreements with external manufacturing organizations. Investigate and troubleshoot complex quality incidents, deviations, and out-of-specification results, determining root causes and implementing effective corrective and preventive actions (CAPAs). Represent Eli Lilly's quality interests during regulatory inspections at external manufacturing sites. Mentor and provide technical guidance to junior QA associates. Job Qualifications: Bachelor's degree in a scientific discipline (e.g., Chemistry, Biochemistry, Pharmacy, Chemical Engineering) or related field. Minimum of 5-8 years (Senior Associate) or 8+ years (Principal Associate) of experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry, with a strong focus on API manufacturing and external supply. In-depth knowledge of cGMP regulations (FDA, EMA, HPRA, etc.) and global pharmacopeial requirements. Proven experience in auditing external manufacturing sites. Strong understanding of API manufacturing processes, analytical techniques, and quality control principles. Demonstrated ability to make sound quality decisions and effectively communicate complex technical and quality information to diverse audiences. Excellent problem-solving, analytical, and critical thinking skills. Ability to work independently and as part of a team in a fast-paced, dynamic environment. Proficiency in quality management systems (e.g., TrackWise, Veeva). Willingness to travel domestically and internationally to external manufacturing sites as required. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

:** Crown Equipment Corporation, one of the world's largest lift truck manufacturers, offers local support on a global scale with more than 15 manufacturing facilities worldwide and more than 500 retail locations in over 80 countries. Our global sales and service network provides our customers with a local resource for a wide variety of quality material handling equipment, fleet management solutions, warehouse products and support services to meet their needs anytime, anywhere. **Job Posting External** **Primary Responsibilities** + Responsible for the daily tactical quality support of manufacturing components/processes and assembly processes/outputs. + Implement containment actions for non-conformances ensuring impact to production is minimal. + Participate in quality assurance audits. + Maintain/update quality control documents. + Utilize basic inspection equipment and blueprint reading. + Assist in the evaluation and disposition of non-conforming product. + Provide metrics and input for the Quality function to other departments. + Review and verify corrective actions for effectiveness to prevent reoccurrences **Qualifications** + A two-year college degree and/or ASQ Certification as a Quality Technician preferred. + Three to five years' experience in quality and/or manufacturing related fields desirable. + Must have good problem solving skills. + Working knowledge of advanced mathematics, including statistical techniques, SPC, Capability Analysis and Gage R+R is required. + Must be able to apply quality tools for continuous improvement (FMEA). + Must know basic inspection and testing concepts, how to read blueprints and GD+T information. Must possess good communication skills - both verbal and written. + Must possess the ability to work effectively and maintain a professional composure with other employees. + Requires understanding of basic PC computer application skills, including database, spreadsheets and word-processing. **Work Authorization:** Crown will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas or who need sponsorship for work authorization now or in the future, are not eligible for hire. No agency calls please. **Compensation and Benefits:** Crown offers an excellent wage and benefits package for full-time employees including Health/Dental/Vision/Prescription Drug Plan, Flexible Benefits Plan, 401K Retirement Savings Plan, Life and Disability Benefits, Paid Parental Leave, Paid Holidays, Paid Vacation, Tuition Reimbursement, and much more. EOE Veterans/Disabilities

Job Description Job Scope: The Quality Control Technician is to be proficient in every aspect of performing the functions of this position. The Quality Control Technician's overall responsibility, and objective, is to ensure that all aspects of the SQF, Quality, and Food Safety Programs are followed by all employees, vendors, visitors, etc. Duties and Responsibilities: Routinely check operator paperwork for accuracy and completeness. Routinely check labels, bags, and seals for accuracy. Assure checks are documented clearly, cross referenced and traceable. Communicate results of routine QA tests to production personnel. Notify supervisory personnel and Quality Control and Food Safety Manager of product quality or plant conditions which may have a negative impact on product quality and work together to correct the situation. In the case of finished product, perform follow-up testing until situation is corrected and product disposition is resolved in a quality conscious manner. As directed and trained, conduct various tests for incoming ingredients, including sieve, NIR, moisture, and mycotoxin testing. Maintain and report hold/reject product and assure its proper disposition. Collect routine ingredients and finished product samples, as required (detailed in QA Manual). Train and educate all personnel on quality and food safety practices. Promptly respond to calls for assistance clearly communicating and ETA of arrival. Promptly respond to quality/food safety concerns, following up as needed. Follow First In First Out (FIFO) and enforcing other departments to follow the same process. Continuously work with and/or assist production, maintenance, and sanitation personnel as needed throughout the shift. Maintain a clean work environment and stock supplies as needed for next shift. Ensure, and hold accountable, all personnel, visitors, vendors, etc. comply with all Standard Operating Procedures (SOPs) in addition to all SQF, Quality, and Food Safety Programs. Maintain accurate, complete, and legible paperwork. Assist Quality Control and Food Safety Manager with all other duties/tasks as needed. Be an employee champion who will maintain a strong and positive working relationship with all employees with the utmost integrity, confidentiality, and ethical values. Additional Job Functions: Assist in maintaining a positive team environment and good working relationship by maintaining a positive attitude toward all Diamond team members, vendors, and customers. Participate effectively in a team atmosphere by modeling and promoting conflict resolution, diversity, ethical practices, and organizational citizenship. Responsible for other duties as deemed necessary by Management. QUALIFICATIONS: Must be willing to/have availability to work any shift (day or night shift). Ability to work independently without immediate direction or oversight. Self-motivated with a high degree of initiative and integrity Excellent communication skills, both oral and written, to effectively communicate in a professional manner. Excellent interpersonal skills (communication, listening, team player, cooperative, approachable). Ability to be organized, flexible, and perform acceptably under pressure. Must be able to take directions, work efficiently and safely. Must be able to stand, sit, and walk for long periods including on a catwalk. Must be capable of lifting, carrying, pushing, and pulling up to 50 pounds routinely. Must be capable of overhead work and manual dexterity for manipulating or moving objects. Must be able to climb both stairs and ladders up to a high elevation. Must be able to balance, stoop, kneel, crouch, and crawl. Must be able to operate a forklift. Must be able to perform moderate to heavy labor under constant machine operation and other noise. Education & Experience Recommendations: Quality experience at a food processing facility preferred. High School Diploma or GED required.

QUALITY_CONTROL - QUALITY_TECHNICIAN_I PURPOSE * This role is to provide quality inspection, continuous improvement, and general quality support within the organization. This position requires attention to detail, ability to understand and follow established processes, and product evaluation skills. A successful candidate will be competent in reading and understanding basic blueprints and completing routine inspections. ESSENTIAL DUTIES * The Quality Technician may be responsible for performing any of the following types of inspections: * Incoming Inspections: evaluate incoming materials and components for conformance to specific criteria. Incoming inspections will be performed using dimensional, visual, and process related criteria to determine suitability for use. A base understanding of metrology, traceability, and product preservation is required for this function. * In-process Inspections: evaluate product in various stages of the process either internally or after being processed by a third party. Accurate recordkeeping and an understanding of proper document control practices is essential to success in this role * Final Inspections: evaluation of product prior to release for shipment to the customer. This will include assisting with completing and compiling documentation for First Article Inspection packets as well as production inspection records. * Ability to interact with all areas of production to maintain efficient product throughput. * Review production records for accuracy and compliance. * Ability to work in clean room environment including adherence to gowning, cleanliness, and procedural standards. * Work with a high level of precision and detail. * Participation in auditor development program and ability to learn and master auditing practices and principles. * Work in a team environment for an increased productivity and quality by ensuring quality and timely outputs while working with a continuous improvement mindset. * Understand and follow all company policies and safety procedures. * All other duties as assigned by the supervisor. PHYSICAL DEMANDS/WORK ENVIRONMENT * Capacity to work indoors in an office, laboratory, and/or manufacturing environment. * Ability to work in a stationary position for prolonged periods of time. * Capability to lift objects or equipment weighing up to 40 pounds with or without reasonable accommodation. * Physical aptitude to use basic hand tools in a laboratory and/or manufacturing environment. * Ability to attend meetings locally for trainings. MINIMUM REQUIREMENTS * 2 Year technical degree or equivalent prior quality experience in a production environment working with multiple products/product lines. * Available to work first shift with occasional overtime on evenings/weekends if needed. * Intermediate computer and math skills including ability to use Excel and Microsoft Teams. * Ability to evaluate requirements, understand technical documents, and keep thorough, organized records. * Familiarity with reading part prints and detailed specification review. * Ability to use hand tools and measuring devices such as calipers, micrometers, height gauges, surface roughness meters, Go/no-go gauges, pin gauges, comparators, borescopes, sight pipes, etc... * Communicate effectively. * Ability to perform multiple tasks while adhering to procedural guidelines with minimal supervision. * Provia, Syteline, and Excel spreadsheets experience in a work environment a plus. * Prior ISO Class 5 clean room experience a plus. * Experience with Vision Systems, CMMs, Comparators, borescopes or Sight Pipes a plus. For internal use only: Quality001

Job DescriptionJoin MIASA Automotive as a Quality Technician in Yorktown, IN Are you passionate about ensuring the highest quality standards in the automotive industry? MIASA Automotive is seeking a talented Quality Technician to join our team in Yorktown, IN. As a Quality Technician, you will play a crucial role in maintaining and improving the quality of our products through continuous monitoring, testing, and improvement initiatives. Your expertise and attention to detail will be instrumental in upholding our reputation for excellence and customer satisfaction. Responsibilities: Develop and implement product FMEAs and Quality Control Plans for new and existing products. Develop and implement supporting inspection instructions and criteria to maintain compliance with customer requirements. Reviews and organizes statistical data on quality of production by line, shift, department to produce recommendations. Continuously reviews the economics of the quality program and makes recommendations for improvement. Establishes and maintains effective work relationships with internal and external customers which broadly includes suppliers and stakeholders. Maintains the professional competence, knowledge and skills necessary for the satisfactory performance of all assigned responsibilities. Other duties as assigned Qualifications: Ability to manage projects with limited supervision. Excellent written and verbal communication skills. Systematic problem solving skills. Working knowledge of Quality Systems and related tools. Planning and organization. Experience in conducing or preparing for IAFT system audits Minimum three years of manufacturing environment. Eight Discipline Problem Solving training or experience Core Competencies: Basic knowledge of GD&T Adhere to rules, regulations and/or policies and procedures If you are a detail-oriented professional with a passion for quality assurance, we want to hear from you. Join MIASA Automotive as a Quality Technician and take your career to the next level! About MIASA Automotive: MIASA Automotive is a leading manufacturer of automotive components and systems, specializing in interior and exterior lighting solutions. With a strong commitment to quality, innovation, and customer satisfaction, we have established ourselves as a trusted partner to top automotive brands worldwide. Our state-of-the-art facilities and dedicated team of professionals ensure that we deliver cutting-edge products that exceed industry standards. At MIASA Automotive, we are driven by a passion for excellence and continuous improvement, making us a preferred choice for automotive lighting solutions. To ensure a safe and compliant work environment, all candidates receiving a conditional offer of employment will be required to successfully complete a criminal background check and pre-employment drug screening. Employment is contingent upon passing both screenings. #hc178642

Job Description Responsibilities • Support receiving inspection process including visual and dimensional verification of mechanical assemblies per engineering requirements and operations schedules. Complete and electronically store receiving inspection checklists. • Utilize calipers, tape measures, blueprints, and Microsoft excel. • Perform data collection/analysis and electrical hardware functionality/verification per work instructions, checklists, and engineering requirements. Utilize Microsoft Excel, Word, and PowerPoint, multimeters, test fixtures, tape measures, CAN-testing tools, and proprietary software. • Ensure that each final assembly has a complete quality document package including completed checklists, data files and product pictures. • Ensure that non-conforming products are identified appropriately with a complete description and inform the appropriate department. Ensure that deviations from requirements, if applicable, are approved prior to acceptance of product. Qualifications • Must be able to organize and prioritize job related duties based upon operations schedules. • Ability to handle dynamic priorities and remain flexible. • Must have the ability to work independently and self-motivated • Must have excellent oral/written communication skills. Ability to communicate clearly with multiple departments. Must have proficient use of computers and Microsoft Office suite • Must be able to use basic hand tools including wrenches, drivers, and riveters • Must be able to lift 50 pounds, sometimes in a twisting or bending form. • High school diploma minimum. Electrical background is a plus • Mon-Fri 7AM to 3:30PM core hours • Occasional overtime including weekends required

DHL Supply Chain is Hiring! At DHL, you will play a part in one of the world's most essential industries. There has never been a better time to join DHL Supply Chain. In a global business like ours, the opportunities are endless. So, join us. Work with us. Grow with us. The core responsibilities of this role include: Ensure accurate checking, inspecting and/or counting of all products for both inbound and outbound departments and ensuring all product is free of damage or defect. Position: Quality Tech II Shift: Monday - Friday 7am - 3pm Pay: $20.00 per hour In addition to the general job description below, the ideal candidate will also possess the following skills and/or experience: Supply Chain, Quality Control, Auditing, Product Compliance, Material or Product Inspection A minimum of one (1) years' experience in the following: * Ensure accurate checking, inspecting and/or counting of all products for both inbound and outbound departments and ensuring all product is free of damage or defect. * Auditing product and packaging/labeling to maintain highest level of product compliance and accuracy * Ensure the quantity, quality, labeling, and shipping address of orders correspond to customer specifications or other requirements. * Experience using a commercial WMS (warehouse management system) such as Blue Yonder, Red Prairie, JDA, SAP, etc. * Microsoft Office software, including Excel. Be part of the world's largest logistics company!DHL Supply Chain hasbeen certified as a Great Place to Work in the US and Canada! Our excellent benefits packages includes: * Affordable medical, dental, and vision coverage available beginning on your 30thday * PTO program for all associates, including paid holidays and vacation * 401(k) with generous company match * Tuition reimbursement program * Excellent training and career advancement opportunities Grow your skills. Shape your world. Role Purpose: Execute assigned tasks to support establishment, maintenance, alignment and continual improvement of the QA System. Responsible for day-to-day Quality Assurance activities to ensure compliance with governmental regulations, customer requirements, quality assurance policies and procedures and accommodating requests for support. Key Accountabilities: * Perform Quality audits, inspections and documentation. * Perform daily quality assurance activities as required or directed by management. * Monitor and report level of QMS implementation, compliance and effectiveness through audit activities, observation, review of quality metrics and customer feedback. * Support QA training for new and existing associates. * Support coordination of QA license, permit and registration activities. * Work with Quality Assurance, Ops Performance and Process Improvement teams to progress Quality initiatives. Required Education and Experience: * High School Diploma or Equivalent * Forklift operator certificate or satisfactory completion of forklift training program with the first 30 days of employment * Associate degree or equivalent in related field of study, preferred Our Organization is an equal opportunity employer. #LI-Onsite #LI-DNI ","title

Quality Control - Quality Technician The Quality technician I may be responsible for performing any of the following types of inspections: Incoming Inspections: evaluate incoming materials and components for conformance to specific criteria. Incoming inspections will be performed using dimensional, visual, and process related criteria to determine suitability for use. A base understanding of metrology, traceability, and product preservation is required for this function. In-process Inspections: evaluate product in various stages of the process either internally or after being processed by a third party. Accurate recordkeeping and an understanding of proper document control practices is essential to success in this role Final Inspections: evaluation of product prior to release for shipment to the customer. This will include assisting with completing and compiling documentation for First Article Inspection packets as well as production inspection records. Ability to interact with all areas of production to maintain efficient product throughput. Review production records for accuracy and compliance. Ability to work in clean room environment including adherence to gowning, cleanliness, and procedural standards. Work with a high level of precision and detail. Participation in auditor development program and ability to learn and master auditing practices and principles. Work in a team environment for an increased productivity and quality by ensuring quality and timely outputs while working with a continuous improvement mindset. Understand and follow all company policies and safety procedures. All other duties as assigned by the supervisor. PHYSICAL DEMANDS/WORK ENVIRONMENT Capacity to work indoors in an office, laboratory, and/or manufacturing environment. Ability to work in a stationary position for prolonged periods of time. Capability to lift objects or equipment weighing up to 40 pounds with or without reasonable accommodation. Physical aptitude to use basic hand tools in a laboratory and/or manufacturing environment. Ability to travel and/or attend meetings locally for trainings. MINIMUM REQUIREMENTS 2 Year technical degree or equivalent prior quality experience in a production environment working with multiple products/product lines. Available to work first shift with occasional overtime on evenings/weekends if needed. Intermediate computer and math skills including ability to use Excel and Microsoft Teams. Ability to evaluate requirements, understand technical documents, and keep thorough, organized records. Familiarity with reading part prints and detailed specification review. Ability to use hand tools and measuring devices such as calipers, micrometers, height gauges, surface roughness meters, Go/no-go gauges, pin gauges, comparators, borescopes, sight pipes, etc... Communicate effectively. Ability to perform multiple tasks while adhering to procedural guidelines with minimal supervision. Provia, Syteline, and Excel spreadsheets experience in a work environment a plus. Prior ISO Class 5 clean room experience a plus. Experience with Vision Systems, CMMs, Comparators, borescopes or Sight Pipes a plus. For internal use only: Quality001

DHL Supply Chain is Hiring! At DHL, you will play a part in one of the world's most essential industries. There has never been a better time to join DHL Supply Chain. In a global business like ours, the opportunities are endless. So, join us. Work with us. Grow with us. The core responsibilities of this role include: Ensure accurate checking, inspecting and/or counting of all products for both inbound and outbound departments and ensuring all product is free of damage or defect. Position: Quality Tech II Shift: Weekend Days (7a to 7p), Fri - Sun Pay: $20/hr plus $1/hr shift differential In addition to the general job description below, the ideal candidate will also possess the following skills and/or experience: Supply Chain, Quality Control, Auditing, Product Compliance, Material or Product Inspection A minimum of one (1) years' experience in the following: * Ensure accurate checking, inspecting and/or counting of all products for both inbound and outbound departments and ensuring all product is free of damage or defect. * Auditing product and packaging/labeling to maintain highest level of product compliance and accuracy * Ensure the quantity, quality, labeling, and shipping address of orders correspond to customer specifications or other requirements. * Experience using a commercial WMS (warehouse management system) such as Blue Yonder, Red Prairie, JDA, SAP, etc. * Microsoft Office software, including Excel. Be part of the world's largest logistics company!DHL Supply Chain hasbeen certified as a Great Place to Work in the US and Canada! Our excellent benefits packages includes: * Affordable medical, dental, and vision coverage available beginning on your 30thday * PTO program for all associates, including paid holidays and vacation * 401(k) with generous company match * Tuition reimbursement program * Excellent training and career advancement opportunities Grow your skills. Shape your world. Role Purpose: Execute assigned tasks to support establishment, maintenance, alignment and continual improvement of the QA System. Responsible for day-to-day Quality Assurance activities to ensure compliance with governmental regulations, customer requirements, quality assurance policies and procedures and accommodating requests for support. Key Accountabilities: * Perform Quality audits, inspections and documentation. * Perform daily quality assurance activities as required or directed by management. * Monitor and report level of QMS implementation, compliance and effectiveness through audit activities, observation, review of quality metrics and customer feedback. * Support QA training for new and existing associates. * Support coordination of QA license, permit and registration activities. * Work with Quality Assurance, Ops Performance and Process Improvement teams to progress Quality initiatives. Required Education and Experience: * High School Diploma or Equivalent * Forklift operator certificate or satisfactory completion of forklift training program with the first 30 days of employment * Associate degree or equivalent in related field of study, preferred Our Organization is an equal opportunity employer. #LI-Onsite #LI-DNI ","title