Quality control technician jobs in Kokomo, IN - 290 jobs

Trident Consulting is seeking a " Production Technician for one of our clients in " Indianapolis IN”. A global leader in business and technology services Job Title: Production Technician Type: Contract 1st shift (0700 - 1530), Mon to Fri Rate: $27 - $30 per hour Interviews: virtual or onsite ***Must have previous isolator experience. ***HM seeks a candidate with Pharmaceutical manufacturing experience. Position Overview: This is a mid-level position in the aseptic filling group within the Manufacturing department. It utilizes those with experience and the training needed to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through a number of job functions and be required to demonstrate increasing skill levels while demonstrating leadership capabilities. NOTE: This position has exposure to SIP100 PPE will need to be worn, which is provided by EMD Major Position Activities & Responsibilities: • Become certified for entry into the GMP cleanroom space to be able to perform sanitization, stock/replenish supplies, equipment setup, and all related aseptic filling operations. • Execute aseptic fill processes using batch records and SOPs. • Responsible for verifying the calibration of all related equipment and sanitization of supplies to support production • Increasing level of competency in the manufacturing area procedures. Assigned job duties will include Aseptic and clean room areas, Component Preparation, Filling and Capping • Learn the functions necessary to work in the Fill suite. This will include the operation of the associated equipment. • Ability to perform tasks with minimal supervisor direction. • Provide training for new team members. • Able to understand the manufacturing schedule and coordinate tasks to achieve the schedule. • Provide floor leadership in the absence of a supervisor or PT3 technicians. • Transport and/or dispose of hazardous chemicals. • Perform all other duties as assigned. • Must immediately notify supervisor if affected by an infectious disease or open lesions on the body, as individuals are not permitted to enter manufacturing areas or handle products if these conditions exist. Scope: • This position has no direct reports. Background Qualifications: • High school diploma or the equivalent. College coursework preferred • Minimum 3-5 years, including relevant aseptic filling experience in a cGMP pharmaceutical manufacturing facility. • Must possess working knowledge and understanding of GMP compliance regulations. • Must possess knowledge and experience in the aseptic filling process, along with equipment cleaning, preparation, and assembly. Experience in stopper prep, capping, and packaging preferred. • As persons in this role are engaged in the open manufacture of medicinal products, individuals must not be affected by an infectious disease nor have open lesions on any exposed surface of the body. • Must be able to comprehend and follow detailed procedural instructions in written and verbal form. • Must possess adequate working knowledge of arithmetic functions to accurately perform or check calculations required in the product documentation. • While performing the duties of this job, the employee is regularly required to use their hands and arms. The employee is frequently required to stand. The employee is occasionally required to sit, walk, stoop, kneel, bend, crouch, or crawl, talk or hear. The employee must regularly lift and /or move up to 10 pounds, and frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, and peripheral vision. • Must possess fluent English (written and verbal) skills in order to read, comprehend, and communicate GMP compliance documentation as well as Standard Operating Procedures. • Computer skills in Microsoft Office, such as Word and Excel are a plus. Trident Consulting is a premier IT staffing firm providing high-impact workforce solutions to Fortune 500 and mid-market clients. Since 2005, we've specialized in sourcing elite technology and engineering talent for contract, direct hire, and managed services roles. Our expertise spans cloud, AI/ML, cybersecurity, and data analytics, supported by a 3M+ candidate database and a 78% fill ratio. With a highly engaged leadership team and a reputation for delivering hard-to-fill, niche talent, we help organizations build agile, high-performing teams that drive innovation and business success. Learn more: tridentconsultinginc.com. Some of our recent awards include: Trailblazer Women Award 2025 by Consulate General of India in San Francisco. Ranked as the #1 Women Owned Business Enterprise in the large category by ITServe. Received the TechServe Excellence award

Driven by Vision | Industrial-Strength Construction| Powered by Passion Are you looking to work for a successful, stable, and growing company that rewards employees with annual bonuses and exceptional benefits? BMWC is an industrial construction company seeking a Site Quality Inspector to join the Quality Team. This crucial position allows you to contribute to the delivery of large-scale industrial construction projects. You will be part of a top-performing project team and report to an expert in the industry. This position regularly interacts with project managers, project engineers, site supervisors, and company operations leaders. RESPONSIBILITIES As a Site Quality Inspector, you will: Be responsible for inspecting all site welds and ensuring compliance with governing guidelines. Stop and report all unsafe conditions and acts. Understand the governing construction codes. Understand the inspection and test plan requirements applicable to the work scope. Ensure welders are qualified for the welding being performed. Inspect the welds, assigns numbers for the weld map, create weld logs. Perform all aspects of Hydro-test and Turnover Package maintenance. Utilize punch lists to identify incomplete items and present to supervision. Compile all appropriate documents in the turnover package. REQUIREMENTS AND QUALIFICATIONS Minimum of 2 years professional experience with piping inspection Turnover package creation Experience with at least one of the following: Heat Maps, Weld Maps, Hydro Packages Certified Welding Inspector with AWS or similar Knowledge of ASME codes and applications Has administered weld tests, as required Ability to manage multiple tasks simultaneously in a constantly changing environment Proficiency with Microsoft Office; Excel, WORD, Outlook, and technical aptitude to learn new systems BENEFITS Competitive Pay with Bonus PTO and paid holidays 401K/Profit Sharing with company match Medical, Dental and Vision Insurance Life, AD&D and Disability benefits Pet Insurance Tuition Reimbursement Paid Volunteer Time Off ABOUT US BMWC tackles the world's toughest and most daunting industrial construction challenges. Our work encompasses an array of industrial sectors, including aerospace, chemical, electric power, food and beverage, oil and gas, pharmaceutical and biotechnology, and semiconductor. As one of the premier specialty construction companies in the country, our employees enjoy a focus on growth and development, work/life balance, and one of the best safety records in the industry. We are 100% management-owned, making our employees' development and advancement paramount to our success.

Join a Global Leader in Workforce Solutions - Net2Source Inc. Who We Are Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 32 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision-Right Talent. Right Time. Right Place. Right Price. Position: Laboratory Technician Payrate: $19-$20/hr. on W2 Location: Indianapolis IN Duration: 12+ Months (Possible Extension) Key Responsibilities: Prepare media, sterilize equipment using autoclave, and clean/rinse glassware Handle plant material: tagging, moving, inoculating, and harvesting Safely handle and apply research chemicals (fungicides, etc.) while wearing proper PPE, including PAPR (Powered Air-Purifying Respirator) Maintain lab and greenhouse cleanliness, manage waste, and stock supplies Assist with routine test setups and fungal culture preparation/inoculation Requirements: Background in Biology, Plant Pathology, or related field (preferred) 1-2 years of relevant lab/greenhouse experience can substitute for a degree Knowledge of plant science and handling fungal cultures Strong work ethic, attention to detail, and ability to work independently and in a small team Comfortable wearing PAPR and handling chemicals (OSHA Respirator Medical Evaluation required) Why Work With Us? We believe in more than just jobs-we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter. Our Commitment to Inclusion & Equity Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics. Awards & Recognition America's Most Honored Businesses (Top 10%) Fastest-Growing Staffing Firm by Staffing Industry Analysts INC 5000 List for Eight Consecutive Years

*Lab EHR Technologist Contract Opportunity* Our client is seeking 1-2 experienced Med Tech-level professional to provide on-site operational support for the Roche Sysmex project. This role is non-technical and focuses on lab operations, not Epic or technical build activities. Candidates must have direct experience with Roche lab operations and/or Sysmex Caresphere, with familiarity in Navify middleware. *Responsibilities/Experience Needed*: -Support high-volume lab testing and ensure accurate sample processing through Roche Sysmex systems. -Validate results in Cerner and maintain proper documentation. -Provide on-site assistance during go-lives, including potential off-hours and extended (>40 hours) support. -Collaborate with lab teams to manage workflow and troubleshoot operational issues. -Travel extensively across Indiana, primarily central and southern regions, with overnight stays as needed. *Job Type & Location* This is a Contract position based out of Indianapolis, IN. *Pay and Benefits*The pay range for this position is $40.00 - $45.00/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 Indianapolis,IN. *Application Deadline*This position is anticipated to close on Jan 26, 2026. h4>About TEKsystems: We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. About TEKsystems and TEKsystems Global Services We're a leading provider of business and technology services. We accelerate business transformation for our customers. Our expertise in strategy, design, execution and operations unlocks business value through a range of solutions. We're a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. We're strategic thinkers, hands-on collaborators, helping customers capitalize on change and master the momentum of technology. We're building tomorrow by delivering business outcomes and making positive impacts in our global communities. TEKsystems and TEKsystems Global Services are Allegis Group companies. Learn more at TEKsystems.com. 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.

Starting Pay $23.000 increasing to $24.00 after completion of training. Shift and Schedule * 12 hour shift (7pm - 7am) * Continental schedule (2/2/3) The Quality Control Technician is responsible for inspecting and assessing the quality of injected plastic products to ensure they meet established company and customer standards during incoming quality control, in process quality control and outgoing quality control. They use a variety of precision tools and equipment to measure and test materials, as well as identify defects or deviations in the manufacturing process. Their insights drive continuous improvement initiatives within the production team, ensuring consistent product quality. Additionally, they collaborate with the manufacturing team and other departments to implement corrective actions and improve overall production standards. Responsibilities for this position include: * Perform incoming quality control inspections on components by interpreting, measuring, and verifying dimensions meet tolerances according to drawings using standard measuring tools and equipment. * Test raw materials using melt flow index tester and moisture analyzer. * Perform in process quality control on product during the manufacturing process for adherence to company and customer requirements using equipment and visually inspection. * Audit product and process for conformance to standards. * Interpret and report testing results and compare them to established specifications and control limits. Generate inspection reports and accept or reject finished goods. * Conduct routine and non-routine analyses of in-process materials, raw materials, and finished goods. * Record inspection and testing data into appropriate systems. Maintain accurate and up-to-date logs. * Review documentation for compliance and maintain traceability records. * Collaborate with production teams to address quality-related issues (product & process). * Familiar with computers, able to navigate excel, email, data entry, multiple operating systems, take photos of product and upload them to designated location. Requirements Requirements * Intelligence: Requires the ability to learn and understand relatively complex principles and techniques related to administrative and clerical duties; to make independent judgments without supervision; to acquire knowledge of topics related to primary occupation. * Verbal Aptitude: The ability to record and deliver information, explain procedures, and follow oral and written instructions. * Numerical Aptitude: Requires the ability to utilize mathematical formulas; add, subtract, multiply, and divide figures. * Physical lifting and movement: Ability to walk or stand 12 hours a day. Ability to lift, push, pull or move 35 pounds and stoop, bend, or reach above the shoulders. Qualifications: * High School Diploma or equivalent. * Good written and verbal communication skills required. * Able to make a decision based on data and standards. * Previous quality experience in a manufacturing environment is preferred. * High attention to detail and commitment to maintaining accurate documentation. * Ability to work collaboratively in a team environment and contribute to a positive, supportive at

ABOUT COMPAL We are in the business of collaborative innovation and making those ideas happen. As one of the world's leading manufacturers of notebook PCs, smart devices, data center equipment and LCD products, and automotive electronics, we take pride in bringing breakthrough design concepts to life with world class R&D, manufacturing, and supply chain management. Innovation is in our DNA and no challenge is too big for our award-winning design teams. Unparalleled experience across a broad range of technologies translates into projects being delivered with the highest design integrity and quality. Compal has 80,000 employees across 8 countries in USA, Mexico, Brazil, Poland, India, China, Vietnam, and Taiwan to provide engineering, manufacturing, service support to our customers. OUR CULTURE We believe innovation happens when people do what they love and have the opportunity to grow. Compal is powered by some of the brightest talent from around the world, working together to push creative and technical boundaries on behalf of our clients and their products. Every day we strive to create an environment where people can grow and learn from each other, while receiving the support to do the best while working on what they love. ABOUT THE ROLE The Quality Technician plays a key role in ensuring compliance with customer, industry, and internal quality standards in printed circuit board assembly (PCBA) manufacturing. This position has a strong focus on process audits, ESD compliance auditing, and initial investigation of material and process issues. The Quality Technician documents findings and reports directly to the Quality Engineer, supporting corrective actions and continuous improvement efforts. Major responsibilities: Perform process audits across PCBA manufacturing operations to verify compliance with work instructions, quality standards, and regulatory requirements. Conduct ESD (Electrostatic Discharge) audits to ensure personnel, workstations, and equipment meet established ESD controls. Perform initial investigations of material issues or process issues identified during production, including defect containment, data collection, and communication of findings. Document and communicate inspection, audit, and investigation results, and report findings to the Quality Engineer for review and action. Carry out in-process, first article, and final inspections of PCBs to verify compliance with IPC-A-600, IPC-A-610, and customer requirements. Issue non-conformance reports (NCRs) and assist with root cause and corrective action activities under guidance of the Quality Engineer. Monitor adherence to ISO 9001, IATF 16949, and customer-specific quality requirements. Support calibration and maintenance of inspection/test equipment, ensuring accurate and reliable measurements. Collaborate with production staff and supervisors to provide feedback on quality issues, recommend corrective actions, and reinforce best practices. Participate in continuous improvement initiatives to strengthen process controls, reduce defects, and improve yields. DESIRED QUALIFICATIONS: High school diploma or equivalent; associate degree or technical training in electronics, quality, or manufacturing preferred. Experience in PCBA manufacturing or electronics assembly environment strongly preferred. Familiarity with IPC-A-600 and IPC-A-610 acceptance standards. Prior experience in process auditing, ESD auditing, or material/process investigations is highly desirable. Understanding of ISO 9001 and IATF 16949 quality management systems. Strong analytical, problem-solving, and organizational skills. Effective verbal and written communication skills for reporting and cross-functional collaboration. WORK ENVIRONMENT: Combination of production floor and inspection/office environment. Requires use of microscopes, precision measuring instruments, and test equipment. May involve standing, sitting, or bending for extended periods; occasional overtime as needed to meet customer deadlines. TRAVEL: Less than 10% BENEFITS AT COMPAL USA (INDIANA) Inc. Medical, dental vision and prescription drug insurance Life insurance Short- and long-term disability Excellent 401k plan with matching contributions Generous PTO policy Company paid holidays Compal USA (Indiana) Inc. is an equal-opportunity employer and is committed to providing a workplace free from harassment and discrimination. All employment is decided on the basis of qualifications, merit, and business need without regard to any protected status.

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

Title: Environmental Monitoring Technician Temp to perm potential 6am/8am start time - 8 hours a day Monday-Friday 3 positions on first shift Aseptic Technique/comfortable in clean rooms entry level microbiologist water collection GDP willingness to learn Background Qualifications: High School diploma required as minimum. Associates degree and/or related certification in Microbiological Sciences highly preferred. Experience with aseptic technique and/or working in aseptic environments. Ability to gown aseptically for Manufacturing and Aseptic Filling areas. As persons in this role are engaged in sampling and environmental monitoring during open manufacture of medicinal products, individuals must not be affected by an infectious disease nor have open lesions on any exposed surface of the body. Working hours will require flexibility with available work hours. Sufficient mobility to work in manufacturing processing areas is required. Major Position Activities & Responsibilities: Environmental monitoring of the aseptic area during production fills or weekly monitoring Must immediately notify supervisor if affected by infectious disease or open lesions on body, as individuals are not permitted to enter manufacturing areas or handle product if these conditions exist. Water collection and testing of WFI, Clean Steam, and the Deionized Water Performs media fill qualification and release in support of environmental monitoring program. Perform sampling activities in support of environmental investigations Maintenance of the cleanliness of the microbiology laboratory area, refrigerators, and incubators Handling of wastes including hazardous wastes. Attendance at mandatory annual hazardous waste training meeting(s). Demonstration of competency in training by passing test(s) administered by the company or consultant providing such training. Responsible for adhering to the Environmental, Health and Safety program. Performs special projects and other duties as assigned. As a part of the employees job requirements, the employee may be required to handle wastes including hazardous wastes. The employee must attend mandatory annual hazardous waste training meeting(s) and show a competency in that training by passing test(s) administered by the company or consultant providing such training.

Starting Pay $23.000 increasing to $24.00 after completion of training. Shift and Schedule 12 hour shift (7pm - 7am) Continental schedule (2/2/3) The Quality Control Technician is responsible for inspecting and assessing the quality of injected plastic products to ensure they meet established company and customer standards during incoming quality control, in process quality control and outgoing quality control. They use a variety of precision tools and equipment to measure and test materials, as well as identify defects or deviations in the manufacturing process. Their insights drive continuous improvement initiatives within the production team, ensuring consistent product quality. Additionally, they collaborate with the manufacturing team and other departments to implement corrective actions and improve overall production standards. Responsibilities for this position include: Perform incoming quality control inspections on components by interpreting, measuring, and verifying dimensions meet tolerances according to drawings using standard measuring tools and equipment. Test raw materials using melt flow index tester and moisture analyzer. Perform in process quality control on product during the manufacturing process for adherence to company and customer requirements using equipment and visually inspection. Audit product and process for conformance to standards. Interpret and report testing results and compare them to established specifications and control limits. Generate inspection reports and accept or reject finished goods. Conduct routine and non-routine analyses of in-process materials, raw materials, and finished goods. Record inspection and testing data into appropriate systems. Maintain accurate and up-to-date logs. Review documentation for compliance and maintain traceability records. Collaborate with production teams to address quality-related issues (product & process). Familiar with computers, able to navigate excel, email, data entry, multiple operating systems, take photos of product and upload them to designated location. Requirements Intelligence: Requires the ability to learn and understand relatively complex principles and techniques related to administrative and clerical duties; to make independent judgments without supervision; to acquire knowledge of topics related to primary occupation. Verbal Aptitude: The ability to record and deliver information, explain procedures, and follow oral and written instructions. Numerical Aptitude: Requires the ability to utilize mathematical formulas; add, subtract, multiply, and divide figures. Physical lifting and movement: Ability to walk or stand 12 hours a day. Ability to lift, push, pull or move 35 pounds and stoop, bend, or reach above the shoulders. Qualifications: High School Diploma or equivalent. Good written and verbal communication skills required. Able to make a decision based on data and standards. Previous quality experience in a manufacturing environment is preferred. High attention to detail and commitment to maintaining accurate documentation. Ability to work collaboratively in a team environment and contribute to a positive, supportive at

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. Organization Overview: The Technician - QC in Indianapolis Active Pharmaceutical Ingredient (IAPI) group performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The technician completes second person verification of other's results. The technician also participates in laboratory analytical investigations, equipment evaluations and qualification, and some quality system improvement initiatives by executing well-defined protocols and procedures. The technician shares technical information and best practice within plant sites or group. Responsibilities: Sample Analysis and Reporting * Verify (SPV) analytical data of other analysts within the lab as requested. * Accurately and safely perform analytical test methods or related support activities as per procedures or protocols. Uses technical knowledge in the review and interpretation of data for conformances to procedures, standards, protocols, and/or real-time recognition of aberrant data and results. * Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards and GMP requirements. * May perform holistic review of data for release of data from the laboratory. Problem Solving * Recognizes when a deviation from test methods, procedures, et cetera has occurred and initiates analytical investigations and participates in a Root Cause Investigations. * Participates in investigations for deviations. * Assists in troubleshooting equipment and methods as required. Continuous Improvement Initiatives * Assist in improvement of quality systems by creating or revising worksheets and other lab documentation systems. * Identifies and communicates opportunities for improvement initiatives in daily work activities. * Reviews SOPs for executable as written. * Shares technical information and best practice within plant sites or group. Lab Operations * Assist with drafting protocols for non-routine testing or validation with appropriate guidance. * Assist in developing equipment qualification protocols with appropriate guidance. * Perform routine equipment calibrations or maintenance. * Comply with and assist with implementing safety standards. * Execute notification to management when required by procedures or standards. * Initiate lab deviations * Train and mentor others. Assist with developing training materials. Basic Requirements: * Associate's degree in a science field related to the lab (e.g., chemistry for Chem. Labs) or 1+ years of demonstrated relevant experience in a GMP analytical lab Additional Skills/Preferences: * Proficiency with computer systems LIMS, Empower, Excel, etc. * Ability to work in a lab environment, including wearing appropriate PPE and other safety required equipment and considerations. * Demonstrate strong math and documentation skills. * Demonstrate strong oral and written communication and interpersonal interaction skills. Additional Information: * Sunday-Thursday 8 Hour Evening to Night Shift. * Tasks may require repetitive motion and standing for long periods of time. * Must be able to lift at least 5 liters of liquid. * Overtime or weekend work required, as necessary. 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 $18.02 - $34.90 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

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.

Description & Requirements Smurfit Westrock (NYSE:SW) is a global leader in sustainable paper and packaging solutions. We are materials scientists, packaging designers, mechanical engineers and manufacturing experts with a shared purpose: Innovate Boldly. Package Sustainably. Guided by our values of integrity, respect, accountability and excellence, we use leading science and technology to move fiber-based packaging forward. GENERAL PURPOSE: Responsible for ensuring all sorting activities are aligned with Smurfit Westrock's AQL Standards, aligned with acceptable defect tolerances, and customer specifications prior to releasing for shipment. The QC Sorting Inspector will report directly to the Quality Control Lead, and ultimately the site's Quality Manager. The QC Sorting Inspector will ensure that data is collected for product being sorted including hours spent in sorting activities, along with scrap quantities to ensure inventory accuracy. The QC Sorting Inspector will prioritize sorting activities at the direction of the Quality Lead and site Quality Manager to ensure timely release of sorted material for shipment to meet the customer's demands. Essential Job Functions * General knowledge and understanding of all manufacturing processes * A very clear understanding of what is good, acceptable product and what is non-conforming. * A very clear understanding of their role in ensuring the quality of the product in the operation. * A very clear understanding of all quality documentation procedures. * The ability to read and understand customer specifications. * Follows all standard operating procedures relevant to the job, position and department. * Performs all assigned work effectively and on schedule. * Follows instructions accurately. * Maintains records of daily activities and results, using specified forms * Keeps work area neat and clean. * Performs other job duties as assigned. Qualifications * Knowledge of the folding carton manufacturing process. * Must have the ability to read and interpret documents such as safety rules, customer specifications, and quality procedures. * Must have basic computer skills - data entry. * Must have the ability to perform basic arithmetic including additions, subtraction, multiplication and division. * Must be able to maintain good attendance. * Must pass color vision test. * Must pass color hue test. * Must be able to ability to use rulers, calipers, micrometers and all other testing equipment. * Must have ability to recognize common packaging defects (cracking, sharpness, heavy scores, line-up, tearing, flat scores, one-sided scores, light cutting, loose fibers, pressure marks, etc.). * Must be willing to work overtime as needed; significant overtime may be required during busy periods. * Must be able to perform all essential functions of the job with or without reasonable accommodation. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions. Employee is required to: sit, stand, be mobile, talk, see, and hear. Candidates are required to undergo a drug screening after receiving a conditional job offer, but before starting employment. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law.

ABOUT THE COMPANY Our founders, food industry veterans Mike and Tisha, knew that food wasn't what it used to be, so they wanted to make it better - by creating a new kind of farm. A farm that grows up to 300 times more food than an ordinary farm on a smaller footprint, without a drop of pesticides. Farms powered with 100% renewable energy, growing with 95% less water and delivering food within 48 hours for longer freshness for our customers and less food waste. 80 Acres Farms is a vertical farming leader, operating commercial farms in Ohio, Kentucky, and soon-to-be Georgia in addition to research and development farms in Arkansas and The Hauge, Netherlands. All farms utilize state-of-the-art technology and analytics developed by the Company's subsidiary, Infinite Acres. 80 Acres Farms branded salads, microgreens, herbs, and tomatoes are available at retailers and food service distributors, including Kroger, Whole Foods, The Fresh Market, Dorothy Lane Markets, Sysco, and US Foods from Michigan to Florida. 80 Acres Farms is supported by world-class investors and partners, including General Atlantic, Siemens, Barclays, Ocado, Priva, and Signify/Philips. If you're interested in making a difference, join our team in changing how the world eats. POSITION OVERVIEW The Quality Technician is responsible for driving the 80 Acres Farms quality and food safety program across all processes at the farm. With strong knowledge of 80 Acres Farms Food Safety and Quality procedures the Quality Technician will perform process audits, product monitoring and verification checks, shelf-life evaluations and collection of food safety and quality data as applicable. The Quality Technician will be responsible for on-time identification and escalation of food safety and quality issues at the farm level, assist in food safety and quality training, support implementation of corrective actions, conduct and participate in root cause analysis and continuous improvement projects. This is a great entry level position that provides a foundation that supports growth in a Quality career path. Key responsibilities and duties: * Monitor and verify compliance with food safety and quality programs and procedures on a day-to-day basis. * Evaluate and document effectiveness of cleaning and sanitation of equipment prior to start-up. Verify general areas are maintained in sanitary conditions throughout operations shifts. * Evaluate product adherence to specification at different stages in the process, including harvest, mixing, and packing. * Collect environmental and product samples in compliance with schedule. * Collect and evaluate shelf-life samples in compliance with schedule. * Verify and calibrate food safety and quality metric monitoring devices such as metal detector, scales, and temperature recorders. * Monitor and verify implementation of corrective actions at the farm level. * Ensure farm compliance with food safety regulations. * Support continuous improvement projects as needed. Qualifications: * 1+ year experience with food handling or processing * Familiarity of GMPs and HACCP * Inquisitive and detail-oriented mind set * Comfortability in computer systems and programs * Degree or applicable experience in Agriculture, Food Science, Chemistry (Preferred) ENVIRONMENT * Repetitive motion throughout the shift * Standing or walking for a long duration of time * Crouching and kneeling * Lifting up to 50lbs * Will be exposed to 39-degree temperatures when working in the leafy packaging area BENEFITS WE OFFER YOU * Health, dental, and vision insurance starting day one of employment * Two weeks paid vacation * One week paid health & wellness time * 10 paid holidays * Parental leave * 401k with up to 4% Company match * Annual tuition reimbursement * Company-paid life insurance * Short and long-term disability insurance ABOUT OUR HIRING PRACTICES Statistics show that underrepresented communities don't apply for a job unless they meet 100% of the qualifications. Don't worry if you think you can't check every box on the list; we'll provide all the on-the-job training you need. 80 Acres Farms is an equal opportunity employer. You're defined by more than just your job title, and we want you to feel comfortable bringing your true self to work. We value your talents, your traditions, your take on the world, and everything else that makes you unique. We strive to be to be a place where a diverse mix of talented people want to come, to stay, and to do their best work. 80 Acres Farms participates in E-Verify. As required by law, your employment with the Company is contingent upon you providing legal proof of your identity and authorization to work in the United States. Employment decisions are made without regard to protected characteristics. All candidates will be given the same consideration.

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

Requirements Qualifications: 1+ year experience with food handling or processing Familiarity of GMPs and HACCP Inquisitive and detail-oriented mind set Comfortability in computer systems and programs Degree or applicable experience in Agriculture, Food Science, Chemistry (Preferred)

Company: Bryan Steam At Bryan Steam LLC we pride ourselves on providing world leading craftsmanship to satisfy the needs of our customers around the world. Our team is passionate about growth, quality and teamwork. We believe in continuous improvement. If you are a self-starter and like resolving tough challenges, you might be a great fit for our team. We are seeking a Quality Technician to join our team! This position assists in a variety of laboratory tests on assigned projects. You would assist in fabrication and testing of prototype boilers. Conduct tests and record data in accordance with procedures outlined by advisory or regulatory agencies. This position assists with request for technical assistance from customers and salespersons concerning Bryan Steam produced products and or services. Essential duties and responsibilities include the following: other duties may be assigned: * Must be able to travel out of state with short notice * Set up boilers and burners according to standard test procedures of ANSI/CSA (American National Standard) IBR (Institute of Boiler and Radiation Manufacturers), SBI (Steel Boiler Institute), or similar advisory or regulatory agency. * Conduct tests and record data in accordance with procedures outlined by these agency requirements. * Fabricate simple parts and models from drawings for prototype testing- perform basic pipe fitting, welding, assembly and adjustment of units to obtain proper operation. * Wire electric controls for burners and boilers to ensure proper operator and safety. * Assist in other laboratory functions as required, including maintenance and calibration of equipment and general clean-up. * Other duties as needed Qualifications/Requirements: * One year certificate from college or technical school; or three to six months related experience/training or combination. * Be able to read and understand prints * Problem solving skills * Team player * Self-motivated and goal oriented * Need to be able to multitask * Strong communication skills Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is required to stand, walk, use hands to finger, handle, or feel and talk or hear. The employee is occasionally required to sit; reach with hands and arms; bend, stoop, kneel crouch, talk and hear, stand for long periods of time; walk and climb up stairs/steps. The employee must regularly lift and/or move up to 25 pounds. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of a production worker. While performing the duties of the job, the employee may be exposed to moving mechanical parts, forklift traffic, hot sand, loud noise, chemicals, high temperatures, hot surfaces, molten metal, sharp objects or edges, grinding with wheels and carbides, silica dust and water. We offer a comprehensive benefits package including, but not limited to: * Medical, dental, and vision coverage * 401(k) plan * Weekly pay * Paid holiday * Vacation * Prescription safety glasses * Short term disability * Life insurance * Employee Assistance Program

Our customer is seeking 1-2 experienced Med Tech-level professional to provide on-site operational support for the Roche Sysmex project. This role is non-technical and focuses on lab operations, not Epic or technical build activities. Candidates must have direct experience with Roche lab operations and/or Sysmex Caresphere, with familiarity in Navify middleware. -Support high-volume lab testing and ensure accurate sample processing through Roche Sysmex systems. -Validate results in Cerner and maintain proper documentation. -Provide on-site assistance during go-lives, including potential off-hours and extended (>40 hours) support. -Collaborate with lab teams to manage workflow and troubleshoot operational issues. -Travel extensively across Indiana, primarily central and southern regions, with overnight stays as needed. *Skills* roche sysmex, navify, caresphere, middleware, lab operations *Top Skills Details* roche sysmex,navify,caresphere,middleware *Additional Skills & Qualifications* Required: Direct operational experience in Roche lab operations and/or Sysmex Caresphere. Familiarity with Navify middleware in lab operations. Ability to work on-site and travel extensively across Indiana. Preferred: Previous experience supporting go-live activations in a lab environment. Strong understanding of high-volume testing processes. *Experience Level* Intermediate Level *Job Type & Location*This is a Contract position based out of Indianapolis, IN. *Pay and Benefits*The pay range for this position is $40.00 - $45.00/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 Indianapolis,IN. *Application Deadline*This position is anticipated to close on Jan 19, 2026. h4>About TEKsystems: We're partners in transformation. We help clients activate ideas and solutions to take advantage of a new world of opportunity. We are a team of 80,000 strong, working with over 6,000 clients, including 80% of the Fortune 500, across North America, Europe and Asia. As an industry leader in Full-Stack Technology Services, Talent Services, and real-world application, we work with progressive leaders to drive change. That's the power of true partnership. TEKsystems is an Allegis Group company. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. About TEKsystems and TEKsystems Global Services We're a leading provider of business and technology services. We accelerate business transformation for our customers. Our expertise in strategy, design, execution and operations unlocks business value through a range of solutions. We're a team of 80,000 strong, working with over 6,000 customers, including 80% of the Fortune 500 across North America, Europe and Asia, who partner with us for our scale, full-stack capabilities and speed. We're strategic thinkers, hands-on collaborators, helping customers capitalize on change and master the momentum of technology. We're building tomorrow by delivering business outcomes and making positive impacts in our global communities. TEKsystems and TEKsystems Global Services are Allegis Group companies. Learn more at TEKsystems.com. 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.

Description & Requirements Smurfit Westrock (NYSE:SW) is a global leader in sustainable paper and packaging solutions. We are materials scientists, packaging designers, mechanical engineers and manufacturing experts with a shared purpose: Innovate Boldly. Package Sustainably. Guided by our values of integrity, respect, accountability and excellence, we use leading science and technology to move fiber-based packaging forward. GENERAL PURPOSE: Responsible for ensuring all sorting activities are aligned with Smurfit Westrock's AQL Standards, aligned with acceptable defect tolerances, and customer specifications prior to releasing for shipment. The QC Sorting Inspector will report directly to the Quality Control Lead, and ultimately the site's Quality Manager. The QC Sorting Inspector will ensure that data is collected for product being sorted including hours spent in sorting activities, along with scrap quantities to ensure inventory accuracy. The QC Sorting Inspector will prioritize sorting activities at the direction of the Quality Lead and site Quality Manager to ensure timely release of sorted material for shipment to meet the customer's demands. Essential Job Functions * General knowledge and understanding of all manufacturing processes * A very clear understanding of what is good, acceptable product and what is non-conforming. * A very clear understanding of their role in ensuring the quality of the product in the operation. * A very clear understanding of all quality documentation procedures. * The ability to read and understand customer specifications. * Follows all standard operating procedures relevant to the job, position and department. * Performs all assigned work effectively and on schedule. * Follows instructions accurately. * Maintains records of daily activities and results, using specified forms * Keeps work area neat and clean. * Performs other job duties as assigned. Qualifications * Knowledge of the folding carton manufacturing process. * Must have the ability to read and interpret documents such as safety rules, customer specifications, and quality procedures. * Must have basic computer skills - data entry. * Must have the ability to perform basic arithmetic including additions, subtraction, multiplication and division. * Must be able to maintain good attendance. * Must pass color vision test. * Must pass color hue test. * Must be able to ability to use rulers, calipers, micrometers and all other testing equipment. * Must have ability to recognize common packaging defects (cracking, sharpness, heavy scores, line-up, tearing, flat scores, one-sided scores, light cutting, loose fibers, pressure marks, etc.). * Must be willing to work overtime as needed; significant overtime may be required during busy periods. * Must be able to perform all essential functions of the job with or without reasonable accommodation. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions. Candidates are required to undergo a drug screening after receiving a conditional job offer, but before starting employment. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law.

Company: Bryan Steam At Bryan Steam LLC we pride ourselves on providing world leading craftsmanship to satisfy the needs of our customers around the world. Our team is passionate about growth, quality and teamwork. We believe in continuous improvement. If you are a self-starter and like resolving tough challenges, you might be a great fit for our team. We are seeking a Quality Technician to join our team! This position assists in a variety of laboratory tests on assigned projects. You would assist in fabrication and testing of prototype boilers. Conduct tests and record data in accordance with procedures outlined by advisory or regulatory agencies. This position assists with request for technical assistance from customers and salespersons concerning Bryan Steam produced products and or services. Essential duties and responsibilities include the following: other duties may be assigned: Must be able to travel out of state with short notice Set up boilers and burners according to standard test procedures of ANSI/CSA (American National Standard) IBR (Institute of Boiler and Radiation Manufacturers), SBI (Steel Boiler Institute), or similar advisory or regulatory agency. Conduct tests and record data in accordance with procedures outlined by these agency requirements. Fabricate simple parts and models from drawings for prototype testing- perform basic pipe fitting, welding, assembly and adjustment of units to obtain proper operation. Wire electric controls for burners and boilers to ensure proper operator and safety. Assist in other laboratory functions as required, including maintenance and calibration of equipment and general clean-up. Other duties as needed Qualifications/Requirements: One year certificate from college or technical school; or three to six months related experience/training or combination. Be able to read and understand prints Problem solving skills Team player Self-motivated and goal oriented Need to be able to multitask Strong communication skills Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is required to stand, walk, use hands to finger, handle, or feel and talk or hear. The employee is occasionally required to sit; reach with hands and arms; bend, stoop, kneel crouch, talk and hear, stand for long periods of time; walk and climb up stairs/steps. The employee must regularly lift and/or move up to 25 pounds. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of a production worker. While performing the duties of the job, the employee may be exposed to moving mechanical parts, forklift traffic, hot sand, loud noise, chemicals, high temperatures, hot surfaces, molten metal, sharp objects or edges, grinding with wheels and carbides, silica dust and water. We offer a comprehensive benefits package including, but not limited to: Medical, dental, and vision coverage 401(k) plan Weekly pay Paid holiday Vacation Prescription safety glasses Short term disability Life insurance Employee Assistance Program