Quality control analyst jobs in Cincinnati, OH - 104 jobs

General Electric Credit Union is a not-for-profit, member-owned full service financial institution headquartered in Cincinnati with branches in Ohio and Kentucky. At GECU, we pride ourselves on maintaining quality service, being an employee-friendly workplace, and developing our team members while teaching you the skills to lead you to career advancement opportunities. Overview: The Quality Control Specialist is responsible for supporting compliance of credit union operations by ensuring accuracy and completeness of various documents related to deposit accounts, loans, mortgages, or other specialized accounts and reviewing reports to verify adherence to federal and state regulations, thereby playing a critical role in identifying and mitigating risk. Essential Responsibilities: Review business deposit and commercial loan accounts within the required timeframe, ensuring accuracy and compliance with federal/state regulations and GECU guidelines Review specialized accounts, including estate and trust accounts, to ensure compliance with federal/state regulations Review tracking spreadsheets and procedures related to deposit accounts, loans, mortgage, and account maintenance with internal staff, recommending strategies to prevent errors Train team members Perform other duties to support the department as necessary Education and Experience: High school diploma or GED required; bachelor's degree in business, finance or related field preferred Minimum of three years of auditing or financial quality control experience within the financial industry Knowledge, Skills, and Abilities: Strong understanding of federal and state regulations related to financial institutions including various types of deposit accounts and loans High level detail-orientation with a focus on accuracy Good analytical and problem-solving skills Excellent written and verbal communication skills Effective time management with the ability to prioritize tasks Proficiency in Microsoft Office Suite At GECU, we want to support your wellbeing by offering a wide range of benefits: Health, Dental and Vision insurance Life and Disability insurance options Paid Time Off starts accruing once hired and take your birthday off - paid 401k Retirement plan with up to a 10% match of your base gross compensation Tuition reimbursement opportunities & professional development Volunteer opportunities -and earn additional PTO hours! On-site clinics for Vaccines and Mammograms And many more! Come join GECU as we are a curated culture of respect, understanding, and mutual recognition. We believe forming bonds and connecting with each other only stands to strengthen the service we provide to our members in our mission of improving the Quality of Financial lives! General Electric Credit Union is an Equal Opportunity Employer

A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Position Summary The Analyst II, QC Microbiology role supports the Microbiology Department by performing quality-related tasks for pharmaceutical products to include documenting and conducting testing on a variety of samples, such as raw materials, in-process and finished products, stability samples, water, gas, and environmental samples. Job Responsibilities * Read SOPs (Standard Operating Procedures) and excerpts from technical documentation. * Write, review, and revise SOPs (Standard Operating Procedures) and/or work instructions for cGMP (Good Manufacturing Practices) manufacturing of commercial product. * Complete required training and may train others. * Conduct troubleshooting activities. * Gather, organize, and communicate operational information to others. * Facilitate team meetings to discuss progress, initiatives, and/or other matters. * Actively participates in investigations involving manufacturing process areas, related to QC processes or data, such as sampling, deviations potentially affecting QC results, investigational sampling, and testing. * Assist with coordinating activities of support groups. * Identifies trends in data in order to provide accurate descriptions, identify root causes, and/or identify solutions or improvements. * Demonstrates proficiency on authoring Quality records (Deviations, CAPAs, and Change Controls). * Identify temporary and permanent fixes to address issues. * Alert supervisor or manager when problems occur outside of SOPs (Standard Operating Procedures). * Collect, record, and report metrics. * Monitor equipment and/or systems for performance and problem indicators. * Wear gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities. * Consult cross-functionally as an SME (Subject Matter Expert) on systems and/or processes within a functional area. * Perform logbook reviews. * Lead or participate in process improvement activities and teams to meet strategic goals. * Use MAXIMO and/or CMMS (Computerized Maintenance Management System) to manage logistics. * Interact with regulatory agency individuals during audits and inspections, when necessary. * Author, review, and revise documentation needed for cGMP (Good Manufacturing Practices) manufacturing of commercial product. * Attend inter-departmental meetings to discuss matters involving the coordination of multiple departments. * Coordinate qualification activities. * Perform routine sampling activities on the facility utilities. * Recommend compliance resolutions to management. Minimum Qualifications * Working knowledge of cGXP requirements and a strong familiarity with production operations. * Good problem solving skills. Preferred Qualifications * Bachelor's degree in biology, microbiology, or related discipline. * At least 2 year of laboratory experience in pharmaceutical industry. * Prior experience supporting microbiological testing in a sterile pharmaceutical operation environment. This position may also include the following conditions: This role is primarily non-sedentary. May include but not limited to standing, walking, repetitive motion, and chemical usage. All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role. The items described here are representative of those that must be met successfully to perform the essential functions of this job. Sponsorship or support for work authorization, including visas, is not available for this position. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $60,000.00 - $82,500.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Job Summary The Analyst, QC Aseptic Control is responsible for reviewing sampling and laboratory data and autonomously performing tasks related to environmental monitoring to support regulatory requirements of a sterile manufacturing site. The position requires operating equipment in various classified/non-classified areas up to a Grade A aseptic environment and in a laboratory setting, and includes the maintaining of gowning qualification. This is a Monday - Friday Day shift position. Position Responsibilities: Supports coordination of workflow for Environmental Monitoring team. Verifies QC data, while monitoring for trends and abnormalities. Trained and able to perform all Environmental Monitoring technician responsibilities (including maintaining aseptic qualification) when needed. Review completed production documentation (for example: logbooks) for quality, completeness, and cGMP (Good Manufacturing Practices) compliance. Troubleshoots methods and processes. Train others on systems, software, equipment, machines, procedures, and/or processes. Answer compliance and process questions from others. Communicate policies and procedures to employees. Fill in for Analyst II/Team Lead when absent. Gather, organize, and communicate operational information to others. Lead and coordinate investigations and studies with little supervision. Lead process improvement activities and teams to meet strategic goals. Other duties that support Environmental Monitoring, Operations, or Laboratory processes may be assigned. Minimum Qualifications: General experience in a pharmaceutical production or quality control environment (GMP/GDP) Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language. Good attention to detail is required. Must be capable of keeping accurate records and performing mathematical calculations Preferred Qualifications: Bachelor's degree, scientific discipline Significant experience in a sterile or cGXP environment Lab experience Sponsorship or support for work authorization, including visas, is not available for this position. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $24.00 - $34.50 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

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

Work Schedule 12 hr shift/days Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials Job Description Compensation: $21.75/HR Shift: Thursday - Saturday Days - 6:00am - 6:30pm Shift Differential: +10% Location: Cincinnati, OH - 2110 East Galbraith Road As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Join our Pharma Services team and be a part of a leading contract development and manufacturing organization (CDMO) offering end-to-end services for drug development, clinical trial logistics, and commercial manufacturing! Biotech and biopharma companies trust us for our speed, flexibility, and quality across every phase of drug development. Our Drug Product team supports customers in the formulation, production, and packaging of high-quality drug products! Our dedicated colleagues offer a wide range of services, including formulation development, process optimization, scale-up, fill-finish services, packaging, and labeling. Their efforts ensure the efficient production of various drug products, such as sterile injectables and oral dosage forms. Location/Division Specific Information: The Cincinnati, OH site is a Center of Excellence for specialized oral solid dose manufacturing and drug development within the Pharma Services Group. How Will You Make an Impact?: As a Formulation Technician you will be responsible for performing operations related to the manufacturing of pharmaceutical products through equipment set-up, operation, clean up and maintenance in compliance with all regulatory cGMP requirements and company policies and procedures. A Day in the Life: Accurately follows production documents, standard operating procedures (SOP's) and current good manufacturing practices (cGMPs) Maintains consistent and accurate documentation of activities to include batch production, cleaning, assembly, material transportation, and waste disposal. Follow approved batch records (BPR's), clean up sheets, and equipment assembly sheets. Safely operates computer-controlled equipment used in dispensing, granulation, compression or coating. Disassembles, cleans, and re-assembles equipment using basic hand tools to include mixers, extruders, dryers, tablet press, encapsulation, coating pans, printers, or tablet inspection machines. Education: High school diploma or equivalent required. Experience: Preferred: Previous work experience in manufacturing, operations, production or lab setting or related field Preferred: Experience in a cGMP environment Knowledge, Skills, Abilities: Mechanical aptitude/proficiency and ability to disassemble and reassemble various types of equipment (GMP facility preferred) Basic reading comprehension and math skills to follow sophisticated technical instructions and complete BPR calculations. Ability to maintain compliance in all SOP, cGMP, EHS and other training curriculum as assigned. Physical Requirements / Work Environment: Manipulate/handle materials, equipment, tools, up to 100 lbs and lift containers weighing up to 40 lbs. Position requires wearing personal protective equipment to include white zone gowning requirements and various styles of respirators (1/2 face, 3-M hood, full face, and dust mask). Hand-scoop 5 lbs. intermittently throughout the workday. Operate a stand up fork lift and walkie stacker What We Offer: Compensation: Competitive Hourly Pay Rate! Additional shift differential for 2nd shift and 3rd shift positions Annual performance-based bonus Annual merit performance-based increase Excellent Benefits: Benefits & Total Rewards | Thermo Fisher Scientific Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Designated Paid Holidays 401K Tuition Reimbursement Employee Referral Bonus Career Advancement Opportunities

Legacy Talent Search is currently seeking candidates for a Quality Control role in Cincinnati, OH. Our client is a well-established industry leader known for innovation and their commitment to delivering the highest-quality products. With a focus on continuous improvement, they pride themselves on maintaining excellence at every stage of their manufacturing and inspection processes. Key Responsibilities: · Perform inspections using proper CMM (Coordinate Measuring Machine) methods while maintaining clear and concise instructions/programs. · Utilize working knowledge of CMM programming to support accurate and efficient inspections. · Inspect, measure, and document results on all required paperwork to ensure compliance with internal standards and customer specifications. · Report any deviations or nonconformities promptly to the appropriate parties. · Conduct routine quality checks on components and finished goods to ensure consistency and product integrity. · Maintain a clean, organized, and safe inspection environment in alignment with company quality and safety requirements. · Collaborate with production, engineering, and quality teams to resolve issues and support continuous improvement efforts. · Assist in maintaining calibration records, inspection documentation, and quality control logs. Qualifications: · 1+ years of experience in Quality Control within a manufacturing or industrial environment. · Ability to maintain clear and concise instructions/programs for proper CMM inspection methods. · Working knowledge of CMM Programming. · Strong attention to detail with the ability to identify and report deviations. · Ability to accurately inspect, record, and document results. · Excellent work ethic, teamwork skills, and communication abilities. · High school diploma or equivalent required. What We Offer: · Competitive hourly wage. $24-$28 DOE. · Comprehensive benefits package, including health insurance and paid time off. · Opportunities for professional growth and advancement within the company. · A supportive and inclusive workplace culture. · The chance to contribute to a company that values precision, quality, and continuous improvement. At Legacy Talent Search, we are more than just a staffing agency. We are dedicated to supporting the growth of the American economy and way of life, one job at a time. With a focus on rebranding the staffing industry, we work tirelessly to show how a specialized recruiting team can drive productivity. Our legacy is built on people and community-how we help others is how we leave our mark. Join us today and discover how we #recruitdifferently. Legacy Talent Search is an equal opportunity employer.

Job Description Quality Control Technician - Floater; works all shifts as needed. The Quality Control Technician is responsible for ensuring NWF's quality and safety standards on all finished products. Shift Differential offered. Essential Functions: Evaluates finished products for quality and acceptability. Performs all necessary analysis as required, and according to the product specification. Communicates product quality issues to Production Supervisors, Production Managers, and QC Manager & Supervisor and shipping and customer service staff. Logs all analysis test results and batch information in the I-Series (AS400) & maintain analysis records and documents necessary for documentation compliance. Monitors line equipment for functionality, safety, and cleanliness. Checks metal detectors (CCP), magnets, and scales and performs critical control point & GMP audits. Assist in all foreign material & product non-conformance investigations. Performs batch set-up checks, assists in correcting the setups, and logs discrepancies. Places product on hold as necessary and release when appropriate. Rejects product as necessary and completes rejection forms including root cause and corrective action analysis. Checks allergen cleanout effectiveness as needed. Perform Pre - Op audits when necessary (for example: equipment down for maintenance). Perform production scale checks and lab equipment calibration based on the calibration schedule. Collect micro samples as needed and places micro hold products on hold. Performs special tasks as assigned by the QC manager. Maintains retain sample area and control sample file. Follows all GMPs and Safety Procedures. Requirements High School Diploma or G.E.D.; Associate's Degree or Bachelor's Degree preferred. Minimum of 1-2 years of quality control/assurance work experience; preferably in food manufacturing. Ability to use quality control analysis equipment Must be able to read, write and communicate in English. Mathematical Skills Computer Skills & Data Processing skills Required Ability to stand and walk for a prolonged period during the shift Ability to climb ladders to work platforms Able to lift 50 pounds Must have the flexibility to work overtime and/or weekends. Must be legally authorized to work in the United States without assistance or support from NWFs. Newly Weds Foods is an Equal Opportunity Employer Minorities/Veterans/Females/Disabled Newly Weds Foods will only employ those who are legally authorized to work in the United States without assistance or support from Newly Weds Foods. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen.

Responsibilities * Prepare samples according to project protocol and/or related SOPs; * Maintain compliant laboratory documentation; * Perform data analysis and data checking; * Interpret results obtained for accuracy and acceptability; * Clean and sterilize laboratory equipment; and * Other duties deemed necessary. Qualifications * A minimum of a Bachelor's degree, with previous experience in a research laboratory; * Knowledge of GLP, cGMP, and ICH guidelines; * Strong organizational and communication (written and oral) skills; and * Knowledge of Microsoft Word, Excel, and Powerpoint. Travel: None Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Cincinnati Perks * Cincinnati Campus Overview * Flexible work environment * Competitive PTO packages, starting at 20+ days * Competitive compensation and benefits package * Company-sponsored employee appreciation events * Employee health and wellness initiatives * Community involvement with local nonprofit organizations * Discounts on local sports games, fitness gyms and attractions * Modern, ecofriendly campus with an on-site fitness center * Structured career paths with opportunities for professional growth * Discounted tuition for UC online programs Awards * Named a Top Workplace in 2024 by The Cincinnati Enquirer * Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 * Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Aviation Repair QC Inspector Job Description CTL Aerospace is a full service NADCAP certified composite-manufacturing company providing services to the major aerospace and governmental organizations since 1946. CTL specializes in the manufacturing of Fiber Reinforced Polymer Structures. We are seeking talented professionals to work in a fast-paced, team-oriented environment as an Aviation Repair QC Inspector at our northern Cincinnati, Ohio location (less than 30 minutes from Dayton and/or northern Kentucky). Experience in aircraft turbine engine component repair. Experience in composite component manufacture or repair. Experience within aerospace or aviation repair or manufacture field. Proficient in the use of precision measuring hand tools to measure component defects. The ideal candidate will be flexible to perform other visual inspections as needed such as preliminary, hidden damage, in-process, and final inspections on metal/composite civil aviation articles with the current technical data provided in the manufacture's instructions for continued airworthiness, Service Bulletins, service letters, Airworthiness Directives, government and industry standard practices, and other data acceptable and approved by the FAA. Evaluation of hardware at designated steps throughout the repair process. Inspection of hardware from outside processes. Job Requirements The individual will be thoroughly familiar with the scope and limitations of the method in which is being performed. The individual will be able to organize, and inspection findings results and be familiar with the codes, standards and other contractual documents that control the method being utilized. CMM Drug Free Workplace. FAA Regulations. Measurement Tools. Visual Inspection. Inspection in any field with the use of calibrated measuring equipment. Inspection in any field with composite/honeycomb, materials. Airframe and Powerplant license preferred (but not required). Aviation, aerospace, or industrial turbine engine manufacture/repair/inspection experience preferred. This position requires you to undergo a DOT/FAA pre-employment drug test for the following prohibited drugs (as defined in 49 CFR § 40.3) prior to being hired or transferred into a Department of Transportation (DOT) safety-sensitive position as defined in 14 CFR part 120[1]: • Marijuana, • Cocaine, • Opioids, • Phencyclidine (PCP), and • Amphetamines. ________________________________________ [1] A safety-sensitive function, as described in 14 CFR part 120, §§ 120.105 and 120.215, includes a flight crew member, flight attendant, flight instructor, aircraft dispatcher, aircraft maintenance or preventive maintenance, ground security coordinator, aviation screener, air traffic controller, and operations control specialist. CTL Aerospace will provide a pay rate commensurate with experience and an excellent benefits package. To learn more about our company, please visit **************************** CTL Aerospace is an EEO/M/F/Disability/VET and Drug Free Employer Veteran Founded Small Business

We are hiring and looking for a talented individual with hands-on experience in a QC role for a job shop/manufacturing environment position. Must have experience with quality inspections, blue prints, in process inspections, first article inspections, final inspections, and much more! Requirements Must have 3 yrs + QC experience working in a manufacturing environment Must have 3+ years of experience with measuring instruments such as micrometers, V-blocks, sine bars, calipers, dial indicators, angle plates, snap gauge, gauge blocks, height gage, level protractors, optical comparators, bore gages, etc. Faro Arm/Laser experience is highly preferred Must have very solid GD&T and math aptitude Must have a great work ethic, collaborative, team player Must have strong blue print reading skills Born in US, or INS certificate of naturalization REQUIRED Thanks for your interest in Magna Machine! EEO Disabilities/Veterans

Environmental Enterprises, Inc. is a specialty environmental management and disposal company. We are dedicated to protecting the environment by providing quality environmental services, recycling options, and waste disposal at competitive rates through innovative technologies and superior technical support. We are currently looking to fill the challenging and rewarding position of Chemical Treatment Technician. We are seeking dependable individuals with strong work ethic, willingness to learn and take initiative. Full time benefits include: Excellent health coverage, dental, vision, life and disability insurance Paid vacation & sick time Six paid holidays 4o1(k) match Paid company provided training. First shift Monday-Friday, competitive pay at a stable company! PRIMARY TASKS : Load, unload, process hazardous and nonhazardous chemical waste materials at a permitted waste treatment facility independently or with supervision. PHYSICAL DEMANDS (non-inclusive): This position is physical in nature and requires: walking, standing, climbing, bending, reaching, lifting (up to 70 pounds), carrying, pushing/pulling, and twisting. This position involves working with and around chemicals & environmental contaminants. Work is performed in outdoor and indoor environments and workers are subject to heat and cold while donning required PPE. At times, the technician may be required to wear a respirator, supplied air and full protective suit. DETAILS OF ASSIGNMENT : Processing of hazardous chemical waste safely in accordance with company procedures and EPA, DOT and OSHA regulations Moving drums, including safe operation of a fork truck Utilize barcode system to Review laboratory data to determine proper handling and disposal of materials Responsible for keeping operating areas, walls, pipes and floor in a clean and safe condition Perform chemical compatibility checks to prevent reactions and other issues Performs work in a safe manner, following all safety procedures QUALIFICATIONS: High school diploma or equivalent One year applicable experience 24 or 40 Hour Hazwoper certificate preferred Be able to communicate clearly, both verbally and in writing Environmental Enterprises Incorporated is an Equal Opportunity Employer M/F/Disabled/Vets

It's fun to work in a company where people truly BELIEVE in what they are doing! We're committed to bringing passion and customer focus to the business. Reporting to the QC Manager, the position is responsible for providing technical support regarding the chemistry of products, adherence to quality specifications and compliance to safety, regulatory and environmental rules and regulations. This is a Monday - Friday, second shift, 2:00pm to 10:00pm role. KEY RESPONSIBILITIES: Employs safe work habits and complies with all applicable safety requirements. Provide daily production support including testing, adjusting and disposition of raw materials, products and packaging. Works closely with Quality Assurance, Plant Management, Production Teams and EHS to ensure overall quality and safety of products produced and distributed from the Sharonville Plant. Provide technical support with regards to waste minimization, environmental compliance, and timely disposition of returns, discrepant product and materials. Utilize SPC methods in data collection, root cause analysis, corrective/preventive action effectiveness and cost saving/avoidance analysis. Any other responsibilities delegated by the Quality Assurance Manager. MINIMUM QUALIFICATIONS: One to three years of wet chemistry testing experience. Statistical Process Control, Data Analysis, PC skills Must have strong problem-solving abilities specifically in technical matters. Must be able to effectively communicate with all levels of personnel at multiple locations Must have the ability to take a leadership role in all Quality Assurance matters. Must be able to excel in a team environment. EDUCATION QUALIFICATIONS Bachelor of Science degree in Chemistry, Chemical Engineering, or related science DuBois provides equal employment opportunities to all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, sexual orientation, marital status, religion, age, disability, gender identity, gender expression, genetic information, service in the military, veteran status, or any other protected status in accordance with applicable federal, state, and/or local law and/or regulation.

Aerospace QC NDT Inspector Overall Summary of Job Quality Control Inspector's role is to ensure all repairs and operations are in compliance with FAA /EASA / ISO / AS and company's guidance. Essential Functions Ensure company procedures and FAA/EASA /ISO/AS Standards are followed, records maintained, forms and required paperwork. Ensure all repairs are in compliance with FAA regulations. Control and maintain technical documents and publications. Perform calibrations, read and interpret blueprints and specifications. Initiate and participate in corrective actions, rework problem solving and audit processes. Perform dimensional / visual inspections using standard inspection gages and CMM Perform FPI and UT inspections Promote an attitude to serve the customer, instilling a sense of urgency throughout the Inspection Department Minimum Qualifications: Graduation from high school and Technical School and three years of experience minimum in a variety of trades or any equivalent combination of education and experience which would provide the required knowledge, skills, and abilities. Ability to work from sketches, drawings, and blueprints. Ability to follow oral and written instructions and to communicate effectively. Complete understanding of current NDI procedures. Ability to work cooperatively with others. Excellent work history and attendance record. Pre-employment drug screen required.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. • Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. • Set up instruments and conduct sample tests; utilize a variety of methods to assure compliance to established standards and testing controls; interpret test results and prepare and submit reports related to test results. • Perform, interpret, evaluate and record standard process control laboratory tests on ; perform calculations as needed and record results; notify appropriate personnel of abnormal or critical results and significant changes in lab results. • Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; assure an adequate supply of test materials to perform daily testing; perform preventive maintenance on equipment. • Prepare periodic and special reports concerning quality control and results of laboratory tests; prepare analytical results reports to relay qualitative and quantitative data; submit to manager of quality. Qualifications: • 2 years of experience in a related laboratory. HPLC, UV- IR spectrometry, NMR, GCMS (Mass Spec, Gas Chromatography, Total Organic Carbon and etc. Technical record-keeping techniques. • Perform a variety of laboratory testing. • Perform mathematical calculations applicable to chemistry testing. Work cooperatively with others. • Must be able to read, write, speak and understand fluent English. Strong understanding of GMP concepts and requirements. • Able to demonstrate accuracy and thoroughness while completing work in a timely manner. • Follows instructions, policies, and procedures. Non-Essential Skills - Operate, maintain and repair equipment required to perform related duties. Qualifications Education Requirements: Bachelor's of Science degree in chemistry or closely related field. Physical Demands: While performing the duties of this job, the employee is frequently required to stand and use hands to finger, handle, or feel. The employee is occasionally required to walk; sit, talk and hear. The employee must occasionally lift and/or move up to 50 pounds. The employee is occasionally exposed to moving mechanical parts or airborne particles. The noise level in the work environment is usually moderate. These physical demands are representative of the physical requirements necessary for an employee to successfully perform the essential functions of this job. Reasonable accommodation can be made to enable people with disabilities to perform the described essential functions of this job. Additional Information Best Regards, Anuj Mehta ************

IRI believes in commitment, integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Job Description • Perform a variety of analytical laboratory testing of raw material, processed material and finished products and assure compliance with applicable laws, rules and regulations • Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. • Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. Set up instruments and conduct sample tests • Utilize a variety of methods to assure compliance to established standards and testing controls; • Interpret test results and prepare and submit reports related to test results • Perform, interpret, evaluate and record standard process control laboratory tests on ; • Perform calculations as needed and record results; • Notify appropriate personnel of abnormal or critical results and significant changes in lab results • Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; • Assure an adequate supply of test materials to perform daily testing; • Perform preventive maintenance on equipment. • Prepare periodic and special reports concerning quality control and results of laboratory tests; prepare analytical results reports to relay qualitative and quantitative data; submit to manager of quality Qualifications • 2 years of experience in a related laboratory. HPLC, UV- IR spectrometry, NMR, GCMS (Mass Spec, Gas Chromatography, Total Organic Carbon and etc. Technical record-keeping techniques • Perform a variety of laboratory testing. Perform mathematical calculations applicable to chemistry testing. • Work cooperatively with others. Must be able to read, write, speak and understand fluent English • Strong understanding of GMP concepts and requirements. • Able to demonstrate accuracy and thoroughness while completing work in a timely manner • Follows instructions, policies, and procedures. • Bachelors of Science degree in chemistry or closely related field. Additional Information Regards Ricky 732-49-1925

Job Description Legacy Talent Search is currently seeking candidates for a Quality Control role in Cincinnati, OH. Our client is a well-established industry leader known for innovation and their commitment to delivering the highest-quality products. With a focus on continuous improvement, they pride themselves on maintaining excellence at every stage of their manufacturing and inspection processes. Key Responsibilities: · Perform inspections using proper CMM (Coordinate Measuring Machine) methods while maintaining clear and concise instructions/programs. · Utilize working knowledge of CMM programming to support accurate and efficient inspections. · Inspect, measure, and document results on all required paperwork to ensure compliance with internal standards and customer specifications. · Report any deviations or nonconformities promptly to the appropriate parties. · Conduct routine quality checks on components and finished goods to ensure consistency and product integrity. · Maintain a clean, organized, and safe inspection environment in alignment with company quality and safety requirements. · Collaborate with production, engineering, and quality teams to resolve issues and support continuous improvement efforts. · Assist in maintaining calibration records, inspection documentation, and quality control logs. Qualifications: · 1+ years of experience in Quality Control within a manufacturing or industrial environment. · Ability to maintain clear and concise instructions/programs for proper CMM inspection methods. · Working knowledge of CMM Programming. · Strong attention to detail with the ability to identify and report deviations. · Ability to accurately inspect, record, and document results. · Excellent work ethic, teamwork skills, and communication abilities. · High school diploma or equivalent required. What We Offer: · Competitive hourly wage. $24-$28 DOE. · Comprehensive benefits package, including health insurance and paid time off. · Opportunities for professional growth and advancement within the company. · A supportive and inclusive workplace culture. · The chance to contribute to a company that values precision, quality, and continuous improvement. At Legacy Talent Search, we are more than just a staffing agency. We are dedicated to supporting the growth of the American economy and way of life, one job at a time. With a focus on rebranding the staffing industry, we work tirelessly to show how a specialized recruiting team can drive productivity. Our legacy is built on people and community-how we help others is how we leave our mark. Join us today and discover how we #recruitdifferently. Legacy Talent Search is an equal opportunity employer.

Environmental Enterprises, Inc. is a specialty environmental management and disposal company. We are dedicated to protecting the environment by providing quality environmental services, recycling options, and waste disposal at competitive rates through innovative technologies and superior technical support. We are currently looking to fill the challenging and rewarding position of Chemical Treatment Technician . We are seeking dependable individuals with strong work ethic, willingness to learn and take initiative . Full time benefits include: Excellent health coverage, dental, vision, life and disability insurance Paid vacation & sick time Six paid holidays 4o1(k) match Paid company provided training. First shift Monday-Friday, competitive pay at a stable company! PRIMARY TASKS: Load, unload, process hazardous and nonhazardous chemical waste materials at a permitted waste treatment facility independently or with supervision. PHYSICAL DEMANDS (non-inclusive): This position is physical in nature and requires: walking, standing, climbing, bending, reaching, lifting (up to 70 pounds), carrying, pushing/pulling, and twisting. This position involves working with and around chemicals & environmental contaminants. Work is performed in outdoor and indoor environments and workers are subject to heat and cold while donning required PPE. At times, the technician may be required to wear a respirator, supplied air and full protective suit. DETAILS OF ASSIGNMENT: Processing of hazardous chemical waste safely in accordance with company procedures and EPA, DOT and OSHA regulations Moving drums, including safe operation of a fork truck Utilize barcode system to Review laboratory data to determine proper handling and disposal of materials Responsible for keeping operating areas, walls, pipes and floor in a clean and safe condition Perform chemical compatibility checks to prevent reactions and other issues Performs work in a safe manner, following all safety procedures QUALIFICATIONS: High school diploma or equivalent One year applicable experience 24 or 40 Hour Hazwoper certificate preferred Be able to communicate clearly, both verbally and in writing Environmental Enterprises Incorporated is an Equal Opportunity Employer M/F/Disabled/Vets

Aerospace QC NDT Inspector Overall Summary of Job Quality Control Inspector's role is to ensure all repairs and operations are in compliance with FAA /EASA / ISO / AS and company's guidance. This individual has the responsibility and authority to carry out assigned tasks. Essential Functions Ensure company procedures and FAA/EASA /ISO/AS Standards are followed, records maintained, forms and required paperwork. Ensure all repairs are in compliance with FAA regulations. Control and maintain technical documents and publications. Perform calibrations, read and interpret blueprints and specifications. Initiate and participate in corrective actions, rework problem solving and audit processes. Perform dimensional / visual inspections using standard inspection gages and CMM Perform FPI and UT inspections Promote an attitude to serve the customer, instilling a sense of urgency throughout the Inspection Department Minimum Qualifications: Graduation from high school and Technical School and three years of experience minimum in a variety of trades or any equivalent combination of education and experience which would provide the required knowledge, skills, and abilities. Ability to work from sketches, drawings, and blueprints. Ability to follow oral and written instructions and to communicate effectively. Complete understanding of current NDI procedures. Ability to work cooperatively with others. Excellent work history and attendance record. Pre-employment drug screen required.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. • Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. • Set up instruments and conduct sample tests; utilize a variety of methods to assure compliance to established standards and testing controls; interpret test results and prepare and submit reports related to test results. • Perform, interpret, evaluate and record standard process control laboratory tests on ; perform calculations as needed and record results; notify appropriate personnel of abnormal or critical results and significant changes in lab results. • Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; assure an adequate supply of test materials to perform daily testing; perform preventive maintenance on equipment. • Prepare periodic and special reports concerning quality control and results of laboratory tests; prepare analytical results reports to relay qualitative and quantitative data; submit to manager of quality. Qualifications: • 2 years of experience in a related laboratory. HPLC, UV- IR spectrometry, NMR, GCMS (Mass Spec, Gas Chromatography, Total Organic Carbon and etc. Technical record-keeping techniques. • Perform a variety of laboratory testing. • Perform mathematical calculations applicable to chemistry testing. Work cooperatively with others. • Must be able to read, write, speak and understand fluent English. Strong understanding of GMP concepts and requirements. • Able to demonstrate accuracy and thoroughness while completing work in a timely manner. • Follows instructions, policies, and procedures. Non-Essential Skills - Operate, maintain and repair equipment required to perform related duties. Qualifications Education Requirements: Bachelor's of Science degree in chemistry or closely related field. Physical Demands: While performing the duties of this job, the employee is frequently required to stand and use hands to finger, handle, or feel. The employee is occasionally required to walk; sit, talk and hear. The employee must occasionally lift and/or move up to 50 pounds. The employee is occasionally exposed to moving mechanical parts or airborne particles. The noise level in the work environment is usually moderate. These physical demands are representative of the physical requirements necessary for an employee to successfully perform the essential functions of this job. Reasonable accommodation can be made to enable people with disabilities to perform the described essential functions of this job. Additional Information Best Regards, Anuj Mehta ************