Quality control analyst jobs in Parma, OH

Synthetic Chemist - Material Science | Ohio (On-site) We're working with a global leader in advanced materials, seeking a hands-on chemist to drive innovation and performance breakthroughs in the rubbers space. This is a unique opportunity to join a high-impact team focused on pioneering new additives and sustainable solutions for next-generation products. About the Role: You'll lead investigations into complex chemical systems, collaborating with multidisciplinary experts to engineer transformative products. Reporting directly to technical leadership, you'll have the autonomy to shape research direction, influence product development, and see your innovations swiftly implemented in real-world applications. What You'll Do: Conduct detailed studies of reaction mechanisms, kinetics, and material properties in rubber and polymer systems. Utilize advanced analytical techniques and computational methods to characterize and predict performance outcomes. Develop mechanistic models and propose new pathways for superior material properties. Collaborate with scientists, process experts, and industry partners to integrate insights into product design and manufacturing. Scout and evaluate emerging technologies to drive sustainability and performance, including renewable materials and alternatives to conventional additives. What You Bring: Ph.D. in Organic Chemistry, Physical Chemistry, Polymer Science, or related field. Proficiency with analytical instrumentation and data interpretation. Strong problem-solving skills and ability to apply chemical principles to practical innovations. Excellent communication skills for technical documentation and team collaboration. Prior experience in the rubber industry is a plus.

As a Quality Control Lab Technician, 3rd Shift, you will validate finished good properties of wet samples that come into QC and prepare those samples for coating. You are responsible for property testing that is reported to the customer and is critical for accurate performance of the coating. You will work onsite in Cleveland, OH and you will report to the QA Lab Supervisor. The shift for this role is 10pm to 6:30am and you will train on first shift. PPG offers excellent Medical, Dental, & Vision Benefits; matching 401k + retirement savings; and Paid Vacation, Holiday pay. Main Responsibilities: Wet property testing of samples; i.e. viscosity, pH and resistivity Make up of electrocoat bath for coatings testing Coating of panels via electrodeposition Low level analytical testing of intermediates and finished goods Dry film testing; i.e. hardness, defect evaluation, gloss, color, etc. Batch approval and submission preparation Will lead and work on independent quality projects as needed Initiate and support out-of-specification investigations. Qualifications: High School diploma or GED required. College chemistry and math are preferred, but basic knowledge of mathematics and scientific principles required. Ability to understand record and verbalize detailed information accurately. Able to lift over 25 pounds in order to handle materials. 1+ year of Quality Lab or similar experience preferred About us: Here at PPG we make it happen, and we seek candidates of the highest integrity and professionalism who share our values, with the commitment and drive to strive today to do better than yesterday - everyday. PPG: WE PROTECT AND BEAUTIFY THE WORLD™ Through leadership in innovation, sustainability and color, PPG helps customers in industrial, transportation, consumer products, and construction markets and aftermarkets to enhance more surfaces in more ways than does any other company. To learn more, visit *********** and follow @ PPG on Twitter. The PPG Way Every single day at PPG: We partner with customers to create mutual value. We are "One PPG" to the world. We trust our people every day, in every way. We make it happen. We run it like we own it. We do better today than yesterday - everyday. PPG provides equal opportunity to all candidates and employees. We offer an opportunity to grow and develop your career in an environment that provides a fulfilling workplace for employees, creates an environment for continuous learning, and embraces the ideas and diversity of others. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, color, creed, religion, national origin, age, disability status, marital status, veteran status, sexual orientation, gender identity or expression. If you need assistance to complete your application due to a disability, please email ******************. PPG values your feedback on our recruiting process. We encourage you to visit Glassdoor.com and provide feedback on the process, so that we can do better today than yesterday. Benefits will be discussed with you by your recruiter during the hiring process. #LI-Onsite The base salary range for this position is $43,000 to $50,000. PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The QC Laboratory Specialist is in our Mentor, OH location responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This QC Laboratory Specialist is responsible for performing quality inspection in accordance with the requirements for ISO, FDA QSR, and STERIS policies. This would include but is not limited to testing raw material, in-process, and finished goods using the various analytical instrumentation (i.e. HPLC, FTIR and/or UV Spectrophotometers) and with supervision to perform failure investigation. This position requires working onsite in our Mentor, OH location. The hours for this role are Monday through Thursday 6:00 am to 3:30pm and Fridays 6:00 am to 10:00 am. What You'll do as a QC Laboratory Specialist * Decontaminates, cleans, and sterilizes glassware and other containers. * Monitors and maintains laboratory equipment including calibration. * Prepares media and reagents. * Performs routine product and raw material testing of samples. * Performs product and raw material testing of samples. * Prepares reagents, standard solutions, equipment for use, etc. * Recognizes and communicates unexpected results in a timely manner and completes Out of Specification forms (OOS), Non-conformance Reports (NCR) and Incoming Rejection Forms (IRs) for nonconforming or rejected materials. * Writes and revises standard operating procedures (SOPs) under supervisor's direction, using Quality software to change, submit and review documents. * Participates in Investigations (complaints, failure, calibrations, equipment, etc.). The Experience, Skills and Abilities Needed Required: * Bachelor's degree in biology, chemistry or related technical field. * In lieu of a Bachelor's degree, an Associates' degree in biology, chemistry or related technical field, and a minimum of four years' experience in a laboratory environment is required, preferably in a regulated industry (i.e. FDA / ISO13485). Other: * Ability to work in a fast-paced environment with strict deadlines. * Make recommendations on improvements to test methods and procedures. * Make decisions on experimental steps and data analysis within defined parameters and guidelines. * Recognize and communicates unexpected experimental results. * Interpret data with direction. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, wellbeing, and financial future. Here is just a brief overview of what we offer: * Market Competitive pay * Extensive Paid Time Off and added Holidays * Excellent Healthcare, Dental and Vision benefits * Long- and Short-Term Disability coverage * 401(k) with a company match * Maternity and Paternity Leave * Additional add- on benefits / discounts for programs such as Pet Insurance * Tuition Reimbursement and continuing education programs * Excellent opportunities for advancement in a stable long-term career #LI-MO1 #LI- Onsite Pay range for this opportunity is $43,000 to $55,000. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits Open until position is filled. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

Performs a variety of duties relating to Research & Development in a facility specializing in sauces, dressings, marinades, and other fluid goods. These duties include but are not limited to the development of new products from initial bench-top concept to a commercially producible product, provide technical support to other departments such as sales and production, and reverse engineering recipes. ESSENTIAL DUTIES AND RESPONSIBILITIES include the follow: Knowledge of food ingredient functionality Ability to read and analyze formulas Ability to write product spec's and procedures Ability to collect and analyze data Reverse engineering recipes Must be able to use lab analytical equipment Knowledge and understanding of GMP's, SSOP's, Allergens, food safety rules and regulations Knowledge of USDA and FDA regulations Complies with all company policies and procedures Must have excellent communication skills Understand and adhere to government regulations and documentation requirements Must be able to provide written or face to face reports on progress on projects Ability to work well with others Coordinates sauce tasting panels. EDUCATION and/or EXPERIENCE Two to four years related experience and/or training; or equivalent combination of education and experience. Competency in Microsoft Office Suite as well as Microsoft Windows. This position requires a well organized individual that is self motivated and takes charge, is dependable and responsible, enjoys new opportunities and challenges, enjoys working with and developing people, deals with criticism calmly and effectively, is careful about detail and is thorough in completing tasks as assigned and on time, is flexible and open to change LANGUAGE SKILLS Able to read, analyze, and interpret ingredient specifications and recipes, general business periodicals, and or governmental regulations. Able to write and develop specific, accurate, and scalable recipes and procedure manuals. Able to effectively present information and respond to questions from customers, staff and owners. MATHEMATICAL SKILLS Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of weights and measures. Ability to apply concepts such as ratios, and proportions for ingredient and nutritional information. PHYSICAL DEMANDS While performing the duties of this job, the employee is frequently required to reach with hands and arms; and talk or hear. The employee is required to regularly stand, stoop, kneel and walk. The employee must occasionally lift and/or move up to 30 pounds. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus. WORK ENVIRONMENT The noise level in the office environment is usually quiet. Exposure to outdoor elements is possible on a daily basis. Must be responsible for dressing accordingly and being prepared for any type of weather.

Quality Control / Level II NDE (VT) Place of Work: Orrvilon Manufacturing Division in Orrville, OH Holtec International seeks qualified applicants for its Quality Control / Level II NDE (VT) and dimensional position in the Quality department based at Orrvilon Manufacturing Division in Orrville, OH. Specific Areas of Responsibility: Perform NDE on ASME Section III, Section VIII Vessels and nuclear power plant components. Perform specific inspections and specific evaluations for acceptance or rejection determinations according to written instructions and to record results. Perform NDE Examinations in conjunction with receipt and in-process inspections on material purchased for use in fabrication. Familiar with the tools and equipment and shall have demonstrated proficiency in their use. Capable of determining the calibration status of inspection and measuring equipment is in proper condition for use, and that inspection, examination and test procedures are approved. Capable of assisting production in the set-up of material and/or components for receipt inspection, as required. Minimum Technical Requirements: Must demonstrate the ability to read the equivalent of the size and letters of the Jaeger I chart at a minimum distance of 12 inches and distinguish and differentiate the contrasts between colors illustrated on an Ishihara Test Chart. Inspection personnel performing work on elevated surfaces shall be capable of wearing the required fall protection equipment. Inspection personnel shall be physically capable of crawling in and out of small manways, climb inside vessels, towers, heaters, or other confined spaces for inspection activities, often wearing Self Contained Breathing Apparatus (SCBA) as required to comply with safety regulations. Any fear of closeness (claustrophobia) should be identified. Inspection personnel shall be able to lift, carry, push, pull or otherwise move objects weighing up to 50 pounds Will work in various areas of the plant location. Dependent upon the area, environmental conditions can be hot, cold, dirty, greasy, wet and noisy. May work alone with minimal supervision or with other personnel. Inspection personnel shall possess fundamental written and verbal communication skills. Inspection personnel shall be fluent (written and verbal) in the English language. Computer skills to include MS Office applications. Desirable Qualifications: High School diploma or equivalent with at least three years of inspection related experience. Two years of inspection related experience with a completion of 2 years of college in technical or engineering related discipline from a university, college, or technical school. One year of inspection related experience with a degree in engineering or science from a university or accredited college. Qualified and certified to ASNT-TC-1A in two or more of the following NDT Methods that will be utilized: Visual Examination (VT). Certified Level II Visual Examination (VT). Experience in working with the following codes/standards: ASME, AWS, ISO and other standards are desired. Previous Level II Certification to ASNT-TC-1A including documented objective evidence of classroom and on the job training experience As a technology trailblazer and a prominent innovator in clean energy (nuclear and solar) industry, Holtec strives to foster a meritocratic work environment conducive to continuous learning and professional growth of its associates. Holtec is an equal opportunity employer with a long-standing commitment to social equity and environmental justice. The company gives special preference to disabled veterans as a part of its recruitment policy. Detailed information on the Company can be obtained by consulting the website: holtecinternational.com. Candidates interested in considering a career at the Company should submit their resume' along with at least three references.

Job Description Chemical Analyst / Lab Technician - 3rd Shift ???? Entry Level | ???? Thursday-Sunday, 8:00pm-6:00am (4×10-hour nights) We're looking for a detail-oriented Chemical Analyst/Lab Technician to join our team. You'll perform a mix of classical wet chemistry (titrations, gravimetric analysis, pH measurements) and modern instrumental techniques (GC, FTIR, ICP) to support quality control, product development, and process optimization. What You'll Do: Test raw materials, in-process samples, and finished products Perform classical analyses: • Acid/base & redox titrations (Acid Value, Iodine Value) • Gravimetric analyses (density, filterable impurities) • pH & moisture determination Operate, calibrate, and maintain lab instruments: GC, FTIR, ICP-OES, Karl Fischer titrators Interpret results and keep accurate, detailed records (SOP & GLP compliance) Assist in method development, validation, and troubleshooting Follow all lab safety protocols and PPE requirements Contribute to continuous improvement initiatives What We're Looking For: ✅ Bachelor's degree in Chemistry (preferred), Biology, Chemical Engineering, or related field ✅ Solid foundation in classical chemistry techniques & analytical instrumentation ✅ Knowledge of Good Laboratory Practices (GLP) ✅ Strong organizational & problem-solving skills ✅ Ability to work independently and in a team environment Work Environment: Laboratory-based with routine chemical and instrumentation use PPE required

The Quality Control Inspector is to inspect the quality of the grating for all specified jobs. This requires knowledge of the job travelers that show quantity, grating type, material type, finish, and any special quality notes. SUMMARY: The Quality Control Inspector is to inspect the quality of the grating for all specified jobs. This requires knowledge of the job travelers that show quantity, grating type, material type, finish, and any special quality notes. The QC inspector will have knowledge of galvanizing quality, on-grip process, and quality, as well as acceptable manufacturing standards. The QC inspector will be required to know and implement the NAAMM standards. Quality Control Inspector in assigned Business Units. Work with all levels of the organization including, the Business Unit Manager, Supervisors, and Associates to create a smooth, defect-free process. Sample production from every station to significantly reduce/eliminate escapes from your assigned Business Unit. Approve and/or perform first-article inspections on a job requiring this level of oversight. Assure all associates are trained/certified (if required) to operate to perform the tasks they are being asked to perform. Assist in the training, development, and/or creation of proper training materials as required. Perform any required QCHECKs in the Business Unit. The measurement of effectiveness will be a reduction of IRRs in the Inspector's assigned Business Unit and no escapes from the Inspector's assigned Business Unit to other areas. Inspect output samples using industry-appropriate methods, such as comparing to standards, measuring dimensions, and examining functionality. Using gauges such as tape measure, calipers, and micrometers to measure products and assure Quality is built into the product. Reviewing blueprints and specifications to compare to produced goods. Check that the production line adheres to standards and procedures and complies with the Customer standards. Ask the Question: "Is there an SOP for this Process". Record inspection results by recording job numbers of inspected parts, summarizing issues and actions taken to keep production running with no significant pauses in the process. Use iAuditor to record the jobs inspected. Significant reworks, re-makes, and wastes will be input to the IRR System as needed. Helping train the production team on quality control measures to improve product excellence. Assist Associates in Transaction Control (Epicor). Help Associates attain defect-free entries. Monitor transactions to verify that the Associates are performing the task as required. Propose improvements to the production process. Assisting in the development of test methods and inspection plans. Help determine the causes of product defects and reworks. During product inspections, verify all equipment is calibrated correctly. Monitor the scrap hoppers three times during your shift and advise of any abnormalities. When needed, assist in the Sales Order Deviation Process. Always review issues immediately with the Business Unit Manager, Supervisors, and Quality Manager. This job description does not describe all activities, duties, responsibilities, or physical demands that are required of the employee for this job. Likewise, the work environment described is merely representative. Duties, responsibilities, activities, physical demands, and work environment may change at any time with or without notice. ESSENTIAL DUTIES/RESPONSIBILITIES: Read travelers to ensure quantity, grating type, material type, finish, and any special quality notes are accurate. Inspect the quality of grating for all specified jobs. Reject any product that is not within specifications. Work with Production to repair the product if possible. Document non-conformance and report/return to the business unit or origin. Implement NAAMM standards. Support correction as needed. Knowledge of IRR process. Evaluate internal processes and suggest ideas for improvement. Update IRR process documents as changes occur. Review sales order packets using the five-point checklist application. Back up Quality Assurance as needed. Performs other related duties as assigned. EDUCATION, WORK EXPERIENCE, AND PROFICIENCIES: Requires a high school diploma or equivalent is required. The candidate must have strong computer skills in Microsoft Office Suite (Word, Excel, and Outlook). In addition, one or more years of experience with a manufacturing facility. The candidate must have excellent reasoning skills, be detail-oriented, accurate and complete assignments on time with little supervision. Must take initiative and be a self-starter. Must have knowledge of galvanizing quality, on-grip process, and quality as well as acceptable manufacturing standards. Experience with ERP systems and knowledge of internal processes and procedures is preferred. EEO STATEMENT: Ohio Gratings, Inc. is an equal opportunity employer and affords equal opportunity to all applicants without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other characteristic or status protected under local, state, or federal laws.

Job Description We are looking for a person to inspect parts and assist with supervision of quality control activities on the first shift. This is a hands-on position. Responsibilities: The quality control inspector is responsible for reviewing current production parts to ensure that they meet customer requirements. The inspector works with the operators to inform them what acceptance standards are and notifies supervisors when a problem is found. The quality control inspector may at times rework parts before final shipments. Requirements: Manufacturing experience Some quality control inspection experience in a manufacturing environment. Some supervisory experience. Willingness to work in a foundry environment to do the required tasks. Preferred: Experience with handheld measurement tools such as calipers and dial indicators Experience with castings

Full-time Description Company Background: Headquartered in Akron, OH, Flexsys is a chemical manufacturing company with operations in the US, Europe, Latin America, and Asia. It produces tire additives that enhance the strength and durability of tires for leading manufacturers around the world. We are a global supplier of rubber chemicals and solutions including insoluble sulfur, anti-degradants, and stabilizers. The company's singular focus is on delivering better solutions for manufacturers of tires and other rubber products that enhance product performance, optimize production efficiency, and ensure supply chain success. As the largest manufacturer of tire-industry additives in the world, and a newly independent entity, Flexsys brings a track record of innovation, quality, specialized expertise, a highly collaborative approach, and a commitment to growth - working together with our customers as a valuable partner, helping to meet their critical objectives. General Description: Flexsys has an immediate opening for a Laboratory Analyst in the Akron Rubber Laboratory. The rubber laboratory functions as both a research lab and quality control lab for Flexsys products developed and used in the rubber industry. The Laboratory Analyst is located in Akron but is a part of the global tire additives team providing support to production facilities in the America's, Europe, and Asia/Pacific regions. The laboratory collaborates closely with the tire additives research and development teams to provide research support in new product development and quality assurance of our products. The Laboratory Analyst position promotes continuous on-the-job learning and provides an environment focused on working in a highly integrated team setting. If you are excited to work in a highly innovative environment and want to work for a company with a collaborative spirit, we would love to hear from you. Performing routine sample analysis including, but not limited to: o Accurate and precise weighing of chemicals. o Ability to follow sample preparation in accordance with customer requests. o Operating internal mixers and two-roll mills. o Perform physical, mechanical, and rheological laboratory testing using automated and manual laboratory instrumentation. o Work safely around chemicals and machinery. o Follow Standard Operating Procedures. o Maintain a clean work area. o Assist in preventative maintenance of equipment. o Using a Laboratory Information System to report results. o Supporting all initiatives to improve the laboratory. Requirements o Minimal Education level - High School Graduate or equivalent. o Ability to function in a high-paced, quality-focused laboratory environment. o Ability to work in high-performing teams both safely and responsibly. o High sense of urgency and self-starter mentality. o Strong written and verbal communication skills. o Ability to quickly adapt to a dynamic environment. o Ability to focus on multiple projects at a time. o Ability to lift to 50 pounds. An ideal candidate would possess the following: o Previous laboratory experience and/or industrial experience. o Hands on rubber mixing and milling would be ideal but not required. o Familiar with ASTM testing. o Experience with internal mixers. o Mechanical Aptitude. o Strong knowledge of Microsoft Excel and Word. An Equal Opportunity Employer (EOE): race/color/religion/sex/sexual orientation/gender identity/ national origin/disability

Lingo Staffing is Now Hiring for a Quality Control Inspector in Hartville, OH Hours: 1st Shift: 7:30am- 4pm ($15) 2nd Shift: 3:30pm-12:00am ($16/hr) Days: Monday-Friday Pay: $15/hr (1st shift) • $16/hr (2nd shift) Short Description: We are seeking reliable and detail-oriented Quality Control Inspectors for a fast-paced plastics manufacturing environment in Hartville, OH. QC Inspectors are responsible for performing first-piece inspections, monitoring in-process quality, completing documentation, auditing packaging, identifying defects, and ensuring all production meets LMT's established quality standards. Candidates must be comfortable working independently, communicating across shifts, and maintaining accuracy throughout the shift. Requirements: Minimum 1 year experience in manufacturing or similar environment (plastics preferred) High school diploma or GED Ability to inspect parts visually and identify defects (splay, burns, shorts, contamination, flash, etc.) Ability to complete inspection paperwork, production sheets, and documentation accurately Able to use scales, gauges, check fixtures, and basic testing tools Ability to read, compare, and verify first-piece samples Strong attention to detail and accuracy Ability to follow written and verbal instructions Good communication skills; able to communicate across shifts Must be dependable and able to work with minimal supervision Must be willing to comply with a national background check ? Physical Requirements: This position requires the ability to walk extended distances (approximately 2.5+ miles per day) and remain on your feet for the entire shift. Employees must be able to bend, twist, stand, stoop, and lift as part of daily duties, with or without reasonable accommodation. We Are Seeking Candidates Who Have Held the Job Titles of: Quality Inspector, Quality Assurance Technician, Manufacturing Inspector, Production Inspector, or Assembly Quality Checker #INDAKR

1st Shift - $18.50/hr starting, 19.00/hr fully trained! Schedule: Monday - Friday 7:00am - 3:30pm Since 1985, our core business has been enteral device product development, design, manufacturing, and engineering in a state-of-the-art facility near Cleveland, Ohio. AMT's steady growth consistently creates job opportunities in Northeast Ohio. We are always searching for new talent and would love for you to join our team! We strive to keep the small company feeling while still reaching users all over the globe. Quality Control Associate Position Summary: Process work orders by filling orders with raw materials for production floor. Package finished goods for shipment. Quality Control Associate Duties and Responsibilities: This list is not comprehensive but meant to represent the most common or important duties of the position. Other duties are required and/or assigned * Package finished product for shipping (boxing and labeling). * Stage finished product for loading. * Responsible for quality control. No damaged product is sent out. No damaged raw material is accepted in. * Fulfilling daily orders. * Clean and maintain work area. * Other duties as assigned. Requirements Quality Control Associate Minimum Qualifications: * Must be 18 years or older to apply. Language Skills: * Ability to read, analyze, and interpret general business periodicals, technical procedures, or governmental regulations. Mathematical Skills: * Ability to apply concepts of basic math. Reasoning Ability: * Ability to solve practical problems and interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Essential Job Functions: Critical features of the Quality Control Associate are described below. They may be subject to change at any time due to reasonable accommodation or other reasons. * Mental: Must be able to effectively communicate with others; complete and understand analysis of numbers; read, analyze and interpret written materials; compliance with company policies; respond appropriately to feedback to make improvements; maintain positive working relationships; troubleshoot and solve problems. * Physical: Must be able to hear and verbally communicate. Must be able to lift up to 50 lbs, sit, stand, and walk for hours at a time. Moderate noise level and limited exposure to physical risk. Knowledge, Skills, and Abilities Required: Ability to establish priorities, work independently with minimal supervision, and facilitate teamwork. Basic computer skills needed to use various software packages. Equipment Used: Pallet Jack, computer, basic office equipment Special/ Additional Requirements: Persons in this position may be required to pass a drug, alcohol, and/or criminal background check. AMT is an Equal Opportunity/Affirmative Action Employer. Benefits: * Insurance: AMT offers major medical, dental, and vision insurance at the first of the month following 30 days of service. * Other Benefits: AMT offers several other voluntary benefits including hospital indemnity, critical illness, term life insurance & long term disability (company paid), among others. * 401k: AMT matches 100% of your contribution, up to 3% of your salary. * Paid Time Off (PTO): In addition to nine paid holidays, AMT provides employees with paid time off (determined by length of service), starting on day one Other Exciting Perks! * Tuition Reimbursement * Employee Assistance Program * Annual Employee Appreciation Picnic! * Employee Referral Bonus Program * Work Conditions: Clean work environment that is located in an air conditioned and temperature controlled environment. You are also allowed to have in headphones and listen to music as you work!

We are adding to our Pharmaceutical Quality Control Chemistry Staff. We are currently seeking entry level individuals to: Perform analytical testing of raw material, in-process product, final product release and stability testing. Clear documentation of test activities in approved worksheets and laboratory notebooks. Execute mathematical calculations as outlined in test methods. Assess data to determine if the material tested meets specifications. Peer review of quality control data. Participate in investigational testing and assist with root cause analysis. Create and review SOP s and author Change Controls. Other general lab related duties as necessary. We are seeking individuals with: Bachelor's degree in Chemistry, Biochemistry, Biology, or related field One to two years' experience with hands on testing such as pH, titrations, determination of physical appearance, UV, IR and other wet chemistry tests. Instrumentation work with KF, HPLC, and GC, including instrumentation software a plus. Hands-on analytical chemistry experience Prior success working with regulatory, USP, GLP, GDP, and cGMP requirements. Ability to use Microsoft Suite of tools. Pharmaceutical experience a plus.

Dyson Corporation headquartered in Painesville, OH is seeking a quality control professional for reviewing and testing materials, components, and finished products to ensure they meet specifications and quality standards using various tools like calipers, gauges, and micrometers. The quality department performs inspections on materials and products, monitoring production processes, documenting issues and corrective actions, ensuring compliance with standards, and collaborating with various teams to resolve problems. PRINCIPAL DUTIES AND RESPONSIBILITIES: Inspect in-process and finished products using micrometers, calipers, gauges, and other precision tools. Review and maintain quality records for accuracy and completeness. Interpret blueprints and work orders to verify product specifications. Document nonconforming materials and support corrective actions. Collaborate with production and engineering teams to resolve quality issues. Maintain a clean and organized work area. Meet production goals and perform additional duties as assigned. REQUIREMENTS: High School Diploma or GED required. 1-3 years of quality control experience in a manufacturing setting. Proficient in using inspection tools: micrometers, calipers, thread & pin gauges, surface plates, and height gauges. Ability to read and interpret technical documents and blueprints. Strong communication skills and a team-oriented mindset. PHYSICAL REQUIREMENTS: Ability to work on the shop floor for extended periods. Must be able to lift up to 50 lbs. Strong visual acuity is essential. Dyson Corporation is a leading manufacturer of large diameter fasteners and forgings, proudly headquartered in Painesville, Ohio. With over 130 years of industry expertise, we are committed to precision, quality, and innovation. Join a team where craftsmanship meets opportunity. What We Offer Career Growth: Opportunities to advance within the Quality, Production, or Engineering departments. Training & Development: On-the-job training and mentorship to support your professional growth. Team Culture: Work with experienced professionals in a collaborative and supportive environment. Stability: Be part of a company with a long-standing reputation for excellence. Dyson Corporation offers a competitive pay range and industry leading benefits while also being committed to working with and providing reasonable accommodation to individuals with disabilities. Dyson Corporation is an equal opportunity employer - M/F/Veteran/Disability. We are a drug-free workplace and conduct pre-employment screening as a condition of employment.

Nearly 40 years and still growing, this progressive, high-quality custom welding, fabrication, and maintenance solutions industry leader is looking for an autonomous self-thinking Quality Control Inspector with a desire to get better every day through technical and team driven solutions [Duties ] Dimensionally/visually inspect fabrications/welds for fitment and completion to drawing requirements. Interpret and apply blueprint drawing requirements with strong attention for details Visually inspect (VT) welds and fitments & Penetrant inspect (PT) welds. (As needed) [Requirements ] Prior role in Quality Department for structural welding and fabrication services. Ability to read and interpret blueprints Quality Inspection experience with weld quality, measurements, specifications, surface quality, paint, and coatings quality [Details ] $22 - $25 an hour + benefits (health insurance, retirement plan, and paid vacations/holidays) Full time permanent career opportunity Monday - Friday, 7am-3:30pm (Overtime required when necessary) To apply for this fabulous opportunity, send your resume to ****************** OR call ************ and ask for DaWayne for more info.

Production Team Member - Quality Control Lab Technician Paulo Cleveland - 4428 Hamann Pkwy Willoughby, OH 44094 Wage: $19.57 + shift premium Additional Shift Premium: +$1.00 for 3rd shift Opening is on 2nd, schedule is M-TH and Sunday. Training will be on 1st shift. Paulo Products company is the largest privately held Heat Treat company in the United States and has been in business for over 75 years. We have 5 locations in the Midwest and have recently expanded into South America. We are looking to fill a Quality Control Lab Technician role in our plant in Willoughby, OH (44094). This is a permanent position that offers stability and the opportunity to grow within the company. Paulo is looking for people who are seeking a career, not just a job. Experience in heat treating isn't necessary, but a willingness to learn, grow, and improve your skills is. KEY RESPONSIBILITIES: * Support production by verifying cycle, process, calibration and part conformance to customer specifications. Prepare data, graphs, orders, logs and certifications for customers and management. Maintain files for part/process conformance & customer specifications. * Notify Production & QA Management of non-conforming product on timely basis to avoid it being shipped or run in next operation. * Make checks on loads in process as needed/required * Review furnace/equipment charts for accuracy and compliance to requirements. * Prepare certs/ cert packages per customer requirements and review for compliance * Perform hardness testing as required by customer requirements and review for compliance * Verify hardness and pyrometry calibrations/surveys are maintained to requirements. * Perform order writing as required, mainly on the off shift. * Send random samples of braze materials for cert verification. Collect results and compare. Report all non-conformances to Braze/Production Management. * Answer phones as needed, either handling the call or sending it to the proper authority. * Prepare all records with accuracy, neatness, & completeness that allows for future reviews. * Assure all records generated are filed properly and maintained * Handle log-in & closure of Reject Reports - consistent with the CAIR flow chart. Handle needed Customer contacts for reject reports and production issues. * Maintain needed reference/QMS record materials such as furnace charts, specs, requirements, logs. * Updating specification matrixes, completing customer documentation notice packets, and submit new specs for CHQ or internal review. * Identify, document, & maintain new or changed certification/cert packet special requirements per customer * Customer contact as required by leader or management. * Assure important/key information is shared with other quality people to maintain QC objectives & goals.

The Quality Control Inspector is to inspect the quality of the grating for all specified jobs. This requires knowledge of the job travelers that show quantity, grating type, material type, finish, and any special quality notes. SUMMARY: The Quality Control Inspector is to inspect the quality of the grating for all specified jobs. This requires knowledge of the job travelers that show quantity, grating type, material type, finish, and any special quality notes. The QC inspector will have knowledge of galvanizing quality, on-grip process, and quality, as well as acceptable manufacturing standards. The QC inspector will be required to know and implement the NAAMM standards. Quality Control Inspector in assigned Business Units. Work with all levels of the organization including, the Business Unit Manager, Supervisors, and Associates to create a smooth, defect-free process. Sample production from every station to significantly reduce/eliminate escapes from your assigned Business Unit. Approve and/or perform first-article inspections on a job requiring this level of oversight. Assure all associates are trained/certified (if required) to operate to perform the tasks they are being asked to perform. Assist in the training, development, and/or creation of proper training materials as required. Perform any required QCHECKs in the Business Unit. The measurement of effectiveness will be a reduction of IRRs in the Inspector's assigned Business Unit and no escapes from the Inspector's assigned Business Unit to other areas. Inspect output samples using industry-appropriate methods, such as comparing to standards, measuring dimensions, and examining functionality. Using gauges such as tape measure, calipers, and micrometers to measure products and assure Quality is built into the product. Reviewing blueprints and specifications to compare to produced goods. Check that the production line adheres to standards and procedures and complies with the Customer standards. Ask the Question: "Is there an SOP for this Process". Record inspection results by recording job numbers of inspected parts, summarizing issues and actions taken to keep production running with no significant pauses in the process. Use iAuditor to record the jobs inspected. Significant reworks, re-makes, and wastes will be input to the IRR System as needed. Helping train the production team on quality control measures to improve product excellence. Assist Associates in Transaction Control (Epicor). Help Associates attain defect-free entries. Monitor transactions to verify that the Associates are performing the task as required. Propose improvements to the production process. Assisting in the development of test methods and inspection plans. Help determine the causes of product defects and reworks. During product inspections, verify all equipment is calibrated correctly. Monitor the scrap hoppers three times during your shift and advise of any abnormalities. When needed, assist in the Sales Order Deviation Process. Always review issues immediately with the Business Unit Manager, Supervisors, and Quality Manager. This job description does not describe all activities, duties, responsibilities, or physical demands that are required of the employee for this job. Likewise, the work environment described is merely representative. Duties, responsibilities, activities, physical demands, and work environment may change at any time with or without notice. ESSENTIAL DUTIES/RESPONSIBILITIES: Read travelers to ensure quantity, grating type, material type, finish, and any special quality notes are accurate. Inspect the quality of grating for all specified jobs. Reject any product that is not within specifications. Work with Production to repair the product if possible. Document non-conformance and report/return to the business unit or origin. Implement NAAMM standards. Support correction as needed. Knowledge of IRR process. Evaluate internal processes and suggest ideas for improvement. Update IRR process documents as changes occur. Review sales order packets using the five-point checklist application. Back up Quality Assurance as needed. Performs other related duties as assigned. EDUCATION, WORK EXPERIENCE, AND PROFICIENCIES: Requires a high school diploma or equivalent is required. The candidate must have strong computer skills in Microsoft Office Suite (Word, Excel, and Outlook). In addition, one or more years of experience with a manufacturing facility. The candidate must have excellent reasoning skills, be detail-oriented, accurate and complete assignments on time with little supervision. Must take initiative and be a self-starter. Must have knowledge of galvanizing quality, on-grip process, and quality as well as acceptable manufacturing standards. Experience with ERP systems and knowledge of internal processes and procedures is preferred. EEO STATEMENT: Ohio Gratings, Inc. is an equal opportunity employer and affords equal opportunity to all applicants without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other characteristic or status protected under local, state, or federal laws.

Major Job Responsibilities: Responsible for End-of-Line Quality inspections for ALL units leaving Twinsburg facility. Tracking defects by type and communicating findings daily to management team. Preparing Quality Alerts to aid supervisors in communication to line. Assist in training of new employees from quality perspective May assist in process audits, random quality spot checks throughout process. Essential Duties and Responsibilities: Complete Quality inspection documents for all units Asist Completion Coordinator with transferring units to appropriate carts Review customer returns to assist Engineering on determining root cause of failure Recommend adjustments to production process Any other activities as seen fit to aid in success of Intigral Requirements Education and/or Experience: Minimum of 3 years experience with Intigral Must have keen eye for attention to detail Must have good communication skills Must be organized

As the QC Shader Technician, you will perform the testing on various color panels and prep them for the evaluation for the color shaders for automotive paints. You will work onsite full time in Cleveland, OH reporting to a Shift Supervisor. PPG offers excellent Medical, Dental, & Vision Benefits; 401k retirement savings; and Paid Vacation, Holiday pay. Main Responsibilities: Data entry into color portal and quality database Customer communication Prepare pre-ship samples for customers Use color measurement instruments and software to ensure accurate color shading Facilitate batch approval process Other duties as assigned and needed Qualifications: High School Diploma or GED is required Must be able to use color measurement instruments and software for color analysis and shading About us: Here at PPG we make it happen, and we seek candidates of the highest integrity and professionalism who share our values, with the commitment and drive to strive today to do better than yesterday - everyday. PPG: WE PROTECT AND BEAUTIFY THE WORLD™ Through leadership in innovation, sustainability and color, PPG helps customers in industrial, transportation, consumer products, and construction markets and aftermarkets to enhance more surfaces in more ways than does any other company. To learn more, visit *********** and follow @ PPG on Twitter. The PPG Way Every single day at PPG: We partner with customers to create mutual value. We are "One PPG" to the world. We trust our people every day, in every way. We make it happen. We run it like we own it. We do better today than yesterday - everyday. PPG provides equal opportunity to all candidates and employees. We offer an opportunity to grow and develop your career in an environment that provides a fulfilling workplace for employees, creates an environment for continuous learning, and embraces the ideas and diversity of others. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, color, creed, religion, national origin, age, disability status, marital status, veteran status, sexual orientation, gender identity or expression. If you need assistance to complete your application due to a disability, please email ******************. PPG values your feedback on our recruiting process. We encourage you to visit Glassdoor.com and provide feedback on the process, so that we can do better today than yesterday. Benefits will be discussed with you by your recruiter during the hiring process. #LI-Onsite The base salary range for this position is $40,000 to $43,000. PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. The QC Laboratory Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This position is responsible for performing quality inspection in accordance with the requirements for ISO, FDA QSR, and STERIS policies. This would include but is not limited to testing raw material, in-process, and finished goods using the various analytical instrumentation (i.e. HPLC, GC) and with supervision perform failure investigation. This is a second shift position. Will train Monday - Friday 2:00pm-10:30pm. Will move to Monday - Friday 4:00pm-12:30am when training is complete. What You'll Do as a Quality Control Lab Specialist Decontaminates, cleans, and sterilizes glassware and other containers. Monitors and maintains laboratory equipment including calibration. Prepares media and reagents. Performs routine product and raw material testing of samples. Performs product and raw material testing of samples. Prepares reagents, standard solutions, equipment for use, etc. Recognizes and communicates unexpected results in a timely manner and completes Out of Specification forms (OOS), Non-conformance Reports (NCR) and Incoming Rejection Forms (IRs) for nonconforming or rejected materials. The Experience, Skills and Abilities Needed Required: * Associate degree * Minimum four (4) years experience relevant lab testing in a regulated environment (i.e. FDA/ISO 13485). Will accept less years of experience and lab testing in an academic setting with Bachelor degree. What STERIS Offers We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future. Here is a brief overview of what we offer: * Market Competitive Pay * Extensive Paid Time Off and (9) added Holidays * Excellent Healthcare, Dental and Vision Benefits * Long/Short Term Disability Coverage * 401(k) with a company match * Maternity and Paternity Leave * Additional add-on benefits/discounts for programs such as Pet Insurance * Tuition Reimbursement and continued education programs * Excellent opportunities for advancement in a stable long-term career #LI-KL1 Pay range for this opportunity is $44,412.50 - $54,862.50. This position is eligible for bonus participation. Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc. STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits Open until position is filled. STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.