Quality control analyst jobs in Kettering, OH

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.

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.

About this opportunity : The QC Analyst II is responsible for executing quality control analytical tasks, including in process manufacturing testing, for one or more projects to support testing and release of oligonucleotides. Key Responsibilities: * Sample, test and release raw materials and finished products per established procedures with minimal errors * Provide analytical support to Manufacturing and Process Development * Perform routine analyses using techniques such as: Wet Chemistry, Karl Fischer, UV-Vis, FT-IR, Raman, LC, GC, LCMS, and NMR * Train and/or assist other QC Analysts on applicable analytical techniques * Assist in the development and/or qualification of test instructions and protocols * Author technical documentation (e.g. methods, procedures) * Represent Quality Control on internal project teams * Perform GDP peer review * Maintain laboratory compliance * Execute tasks to deliver project results on time * Contribute to a positive work atmosphere * Responsibilities may also include water system and environmental monitoring testing Job Experience and Technical Skills: * Degree in Chemistry or related field. BA/BS with 2+ years of related work experience. * Understand and edit laboratory SOPs * Operate laboratory instruments * Knowledge of undergraduate general chemistry and organic chemistry * Basic Word, Excel, and PowerPoint abilities * Perform algebraic and basic statistical calculations correctly * Proficient in written and spoken English. Experience with technical writing. The annualized salary for this position is between $63,200.00 - $77,400.00.

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, QC Aseptic Control (Night Shift) 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 Night Shift position - 12-hour rotating schedule from 6pm - 6:30am (2 days on /2 days off /3 days on)** Position Responsibilities: Supports coordination of workflow for Environmental Monitoring team. Verifies QC data, while monitoring for trends and abnormalities. Performs project work and leads laboratory investigations. 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 is a plus 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.

About this opportunity : The QC Analyst II is responsible for executing quality control analytical tasks, including in process manufacturing testing, for one or more projects to support testing and release of oligonucleotides. Key Responsibilities: Sample, test and release raw materials and finished products per established procedures with minimal errors Provide analytical support to Manufacturing and Process Development Perform routine analyses using techniques such as: Wet Chemistry, Karl Fischer, UV-Vis, FT-IR, Raman, LC, GC, LCMS, and NMR Train and/or assist other QC Analysts on applicable analytical techniques Assist in the development and/or qualification of test instructions and protocols Author technical documentation (e.g. methods, procedures) Represent Quality Control on internal project teams Perform GDP peer review Maintain laboratory compliance Execute tasks to deliver project results on time Contribute to a positive work atmosphere Responsibilities may also include water system and environmental monitoring testing Job Experience and Technical Skills: Degree in Chemistry or related field. BA/BS with 2+ years of related work experience. Understand and edit laboratory SOPs Operate laboratory instruments Knowledge of undergraduate general chemistry and organic chemistry Basic Word, Excel, and PowerPoint abilities Perform algebraic and basic statistical calculations correctly Proficient in written and spoken English. Experience with technical writing. The annualized salary for this position is between $63,200.00 - $77,400.00.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: MilliporeSigma in Miamisburg, OH is hiring an Associate Production Scientist. In this role, you will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. Responsibilities: * Safely perform operations to meet quality expectations * Ensure quality throughout the process * Complete the volume of work required to achieve group/departmental goals and meet deadlines * Participate as needed in quality audits * In compliance with change control procedures, improve processes through application of scientific knowledge, experience, and principles * Identify opportunities for process improvement Physical Attributes: * Wearing appropriate protective gear, (hard hats, glasses/goggles, chemical resistant suits, gloves, safety shoes) and other personal protection equipment "PPE" to protect from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles * Working in outdoor weather conditions while moving material, filling material and waste handling * Lifting and/or moving to 50 pounds unassisted and ability to push and pull heavy materials to complete assignment. Lifting more poundage with assistance. * Utilize close vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus Who You Are: Minimum Qualifications: * Bachelor's degree in Chemistry, Biochemistry, Biology or other Science discipline Preferred Qualifications: * Bachelor's degree in Chemistry * Experience with safe chemical handling methods * Excellent communication skills both oral and written * Computer skills * Mechanical skills * Troubleshooting skills * Interpersonal skills * Organizational skills * Knowledge of ISO Quality standards Pay Range for this position: $27.00 - $46.00/hour The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. RSREMD What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Perform on-line inspections on component and finished product audits. Tests and inspects products at various stages of production process and compiles statistical data (location specific) to determine and maintain quality and reliability of products. Releases conforming lots, documents non-conforming lots and assures record accuracy for traceability according to established inspection procedures and work instructions. Supports and documents the results of the calibration system, test method validation and pest management systems (location specific). Basic Qualifications - High school diploma or GED required - 0-3 years of work experience or equivalent. - Math and problem-solving skills equivalent to a high school education. Preferred Qualifications - 5 or more years of work experience or equivalent and/or certification (CQT, CQI, CQA etc.) through a recognized body such the ASQ American Society of Quality and works under limited supervision. - Knowledge of process capability. - Test Method Validation

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

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 ************

Work Schedule Weekend 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.) 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. 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: Required: No previous work experience required 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

Job Description About the Role: The Quality Controller plays a crucial role in ensuring that parts meet the established quality standards before they reach the market. This position involves conducting thorough inspections and tests on materials and finished goods to identify any defects or areas for improvement. The Quality Controller will collaborate closely with production teams to implement quality assurance processes and corrective actions. By maintaining high-quality standards, this role directly contributes to customer satisfaction and the overall reputation of the company. Ultimately, the Quality Controller is responsible for fostering a culture of quality and continuous improvement within the organization. Minimum Qualifications: High school diploma or equivalent. Proven experience in quality control or a related field. Attention to detail, ability to follow direction, and be consistent in processing parts. Preferred Qualifications: Previous experience in a quality control or manufacturing environment. Familiarity with quality management systems and tools. Responsibilities: Prepare recycled, dismantled vehicle parts for resale, to include washing, tagging, inspection. Report any defects or non-conformities for further investigation or resolution. Support the implementation of quality improvement initiatives and corrective actions. Collaborate with production staff to ensure adherence to quality protocols and procedures. Direct QC Helper in preparation process to ensure all processes are followed and quality parts are sold to customer. Skills: The required skills for this position include attention to detail, which is essential for accurately prepping parts and identifying defects. Strong communication skills are necessary to effectively report findings and collaborate with team members. Basic analytical skills will be utilized to assess quality data and contribute to problem-solving efforts. Preferred skills, such as familiarity with quality management systems, will enhance the QC Helper's ability to support quality initiatives. Overall, these skills are vital for maintaining high standards of quality and ensuring customer satisfaction.

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.

Job Details PJ Ohio Mfg Facility - Mt Orab, OH Full Time $17.00 - $20.00 Hourly DayQuality Control Inspector $17-$20 pr hour paid weekly/ Retention bonus $1000/ Attendance bonus of $3 per hour on the first 40 hours worked each week paid out as $240 bi-weekly. Benefits available after 60 days following the 1st of the month, including 80 hours of Paid Time off (PTO). Quality control inspectors' tasks include running tests, keeping a record of defects, analyzing products, and overseeing procedures. Quality control inspectors may work from a variety of locations, from assembly lines to the Shipping department. This may involve long hours of standing at a time, depending on the location. This job is well suited for people with an eye for detail, who have an aptitude for math, and who have technical skills. Duties and Responsibilities Checks the quality of trailers for Big Tex and PJ Trailers by conducting tests, monitoring production processes, and identifying malfunctions. Appropriate usage of all required PPE. Collaborates with the plant manufacturing team and operations staff to deliver the highest quality product possible. Tracks quality assessments to ensure the plant output meets expectations daily. Utilizes checklists, standard work, quality standards, engineering standards, and iAuditor templates to monitor the manufacturing process and report on plant quality KPI's. Follows product through the entirety of the manufacturing process to ensure each step is completed as intended. Performs detailed inspections of raw materials and final products and confirm they are manufactured to standard. Tracks, records, and maintains quality assurance data. Performs other duties as required. Required Abilities Ability to demonstrate organizational skills and pay close attention to detail. Ability to communicate effectively in written or verbal form. Ability to work in a fast-paced production environment. Ability to frequently lift, push, pull, and maneuver up to 40+ pounds. Frequently exposed to outside temperatures and weather. Continuously exposed to a manufacturing/industrial environment. Qualifications High school diploma or equivalent is required. Two years of experience in a manufacturing environment preferred. Good verbal and written communication skills. Mathematical skills. Attention to detail. Organizational skills

Quality Control Inspector Make sure the military gets the best product available by joining our team of expert inspectors! First and second shift positions are available! FUNCTION: Inspect castings, forgings, fabrications, assemblies and machined workpieces for conformance to specifications and blueprints, using standard and precision measuring devices/instruments, formulas and shop mathematics. PRIMARY DUTIES AND RESPONSIBILITIES: Reads and analyzes blueprints and engineering specifications to obtain product information, such as specified material, surface finish, and dimensions. Computes angles, radii, and other unspecified dimensions of workpiece. Measures dimensions, such as length, height, distance and angles using standard and precision measuring instruments such as CMMs, micrometers, V-blocks, sine bars, calipers, dial indicators, angle plates, snap gauge, gauge blocks, height gage, level protractors, optical comparators, bore gages, ultrasonic equipment and profilometer. Inspects first run parts, including fabrications and assemblies. Write reports regarding inspection and testing results. Position castings, forgings or finished parts on surface plate and layout reference points and centerlines. Examine defective parts to determine cause of defect and recommend changes or modifications. REQUIRED EDUCATION/KNOWLEDGE: High school diploma or GED is required. Two years of related quality inspection based experience is preferred. Training in Statistical Process Control (SPC) data collection techniques and evaluating is preferrable. REQUIRED EXPERIENCE/SKILLS: Experience in a manufacturing environment using various standard measurement gages, preferably in aerospace or defense contracts. Proven problem-solving skills, with proven ability to establish an effective course of action. Eye Examination minimum requirement - Jaeger 1 at 12” with corrective lenses and the Ishihara Color Blindness Test. Exams are required on an annual basis. Equal Opportunity Employer M/F/D/V All applicants will be considered for this position based upon experience and knowledge, without regard to race, color, religion, national origin, sexual orientation, ancestry, marital, disabled or veteran status. GTC is committed to creating and maintaining a workforce environment that is free from any form of discrimination or harassment.

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.

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

We are seeking Quality Control Chemist, to Conduct QC testing on raw materials, in-process samples, and finished products to deliver accurate, timely results aligned with ISO and cGXP requirements. Support method development, data review, and QA/regulatory needs. Location: Montgomery County, OH Hours: Day Shift 4AM-4PM or Overnight Shift 4PM-4AM (rotating 3 days per week, 1 day every other weekend) Pay: $28-30 hour Contract to Hire Responsibilities Perform routine calibrations and maintain equipment readiness. Run analytical tests per SOPs using a variety of instruments and wet chemistry techniques. Support production with in-process testing and ensure smooth shift handoffs. Lead OOS investigations and track CAPA effectiveness. Assist with method improvements, troubleshooting, and equipment maintenance. Maintain and update product specifications across internal systems. Qualifications Bachelor's degree in Chemistry or related field with 5+ years of lab experience. Knowledge of GLP, ISO 9001, and preferred experience with cGMP/GDP and FSSC 22000/ISO 22002. Hands-on experience with GC, GC-MS, HPLC, LC, titrations, spectroscopy, physical testing, and related techniques. Strong documentation, communication, and problem-solving skills. Ability to work rotating shifts and overtime as needed; organoleptic testing ability required. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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 ************

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