Team lead for quality control full time jobs

JobID: 210661484 JobSchedule: Full time JobShift: Base Pay/Salary: Jersey City,NJ $142,500.00-$200,000.00 Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in risk management. As a Tech Risk & Controls Lead - Resiliency within JPMorgan Chase, you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities * Ensure effective identification, quantification, communication, and management of technology risk, focusing on root cause analysis and resolution recommendations * Develop and maintain robust relationships, becoming a trusted partner with LOB technologists, assessments teams, and data officers to facilitate cross-functional collaboration and progress toward shared goals * Execute reporting and governance of controls, policies, issue management, and measurements, offering senior management insights into control effectiveness and inform governance work * Proactively monitor and evaluate control effectiveness, identify gaps, and recommend enhancements to strengthen risk posture and regulatory compliance * Provide SME knowledge and oversight of resiliency testing activity Required qualifications, capabilities, and skills * 5+ years of experience or equivalent expertise in technology risk management, information security, resiliency or related field, emphasizing risk identification, assessment, and mitigation * Familiarity with risk management frameworks, industry standards, and financial industry regulatory requirements * Proficient knowledge and expertise in resiliency protocols, testing, data security, risk assessment & reporting, control evaluation, design, and governance, with a proven record of implementing effective risk mitigation strategies * Demonstrated ability to influence executive-level strategic decision-making and translating technology insights into business strategies for senior executives Preferred qualifications, capabilities, and skills * CISM, CRISC, CISSP, or similar industry-recognized risk and risk certifications are preferred

**SIGNING BONUS AVAILABLE FOR A LIMITED TIME! APPLY TODAY!** State Bank, a growing Community Bank, has an opportunity for a self-motivated and leadership-minded individual to join and lead our team of Quality Control Analysts. We are seeking a Full Time Quality Control Manager. This position is responsible for leading our Quality Control Analysts Group in order to establish advanced quality controls and to implement continuous improvement standards and procedures for State Bank. A B.S. or B.A. or equivalent preferred, or experience in lieu of degree; Mortgage Lending, HMDA and Quality Control training or practical experience. Experience in mortgage and commercial lending or related positions required. Consumer, SBA, and Retail banking deposit experience preferred. State Bank offers an extensive benefits package including paid vacation and PTO, medical/dental/vision insurance, company-paid life and AD&D insurance, a company-matched 401(k) retirement plan, company-provided short and long-term disability, quarterly incentive payouts, a community volunteer program, and growth opportunities. Apply today and see why State Bank is a great place to work! Equal Opportunity Employer

**Now hiring! Senior Quality Specialist** **Greenville, OH - Onsite - Domestic Relocation Availalable -** We are looking for a Senior Quality Specialist to join our team in Greenville, OH. **Come create chemistry with us!** At BASF, we create chemistry through the power of connected minds. By balancing economic success with environmental protection and social responsibility, we are building a more sustainable future through chemistry. As the world's leading chemical company, we help our customers in nearly every industry meet the current and future needs of society through science and innovation. The Senior Quality Specialist plays a critical role in ensuring that products, processes, and services consistently meet both internal and external quality standards. This position is instrumental in maintaining compliance with global frameworks such as IATF 16949, ISO 9001, VDA 6.3, and internal O&M requirements. You will champion Six Sigma continuous improvement initiatives to eliminate process inefficiencies and waste as well as share expertise through coaching and training team members to build quality awareness and capability. Provides expertise in disciplined methodologies for defining, measuring, analyzing, improving and controlling the quality in every one of the company's products, processes and transactions--with the goal of eliminating defects, improving efficiency and reducing costs. These improvements are strategically critical in that they allow the company to continue to provide the goods and services required by our customers while operating in the lowest possible cost structure. **As a Senior Quality Specialist, you create chemistry by...** Key Duties: + Provide expertise in disciplined methodologies for defining, measuring, analyzing, improving and controlling the quality in the company's products, processes and transactions--with the goal of eliminating defects, improving efficiency and reducing costs. (These improvements are strategically critical in that they allow the company to continue to provide the goods and services required by our customers while operating in the lowest possible cost structure).Key + DutiesLeading root cause investigations for non-conformances and implementing effective corrective and preventive actions (CAPA). + Optimizing quality systems and ensuring alignment with global standards. + Driving continuous improvement initiatives using Six Sigma methodology to eliminate process waste. + Coaching and training associates to build organizational quality capability. Core Competencies & Tools + Bulk Material & Manufacturing Process Expertise + Automotive Core Tools (APQP, PPAP, FMEA, MSA, SPC) + Data Analysis & Statistics for quality performance monitoring + SAP QM Module (with focus on Non-Conformance Management) + MinTab proficiency + Ability to present to leadership and problem solve + Office Suite & Dashboarding (Power BI and similar tools) **If you have the following experience...** + Solid data analytics and statistical background required - preferably in automotive industry + IATF and MiniTab required + Degree in Engineering, Analytics, Chemistry or related field + Strong Project Management Skills + Lean/Six Sigma/Kaizen training & implementation experience + Good communication, presentation, coaching, teaching, and interpersonal skills + Comfortable working with all levels of management & staff + History of successfully implemented Six Sigma Projects, Lean Manufacturing, IATF internal and external audits, Core Tolls, CSR, etc. + Minimum 3 years' experience working as a Black Belt **Create your own chemistry with you@BASF** At BASF, you will have the chance to do meaningful work towards building a more sustainable future. In addition to competitive compensation and benefits, BASF provides you with access to a wide range of elements to help you be your best. It's what we call **you@BASF** . We are committed to providing benefits, programs, and opportunities that support our employees' overall well-being, personal growth, and a safe, collaborative, and inclusive work environment. Just some of the many benefits we offer include: + Flexible work arrangements whenever possible + Highly competitive retirement savings plan with company match and investment options + Well-being programs that include comprehensive mental health support for you and your household family members + Family forming benefits (fertility, adoption and surrogacy reimbursement, maternity/parental leave, and more) + Back-up child and elder care with discount programs for families of all ages and stages + Mentoring and career development opportunities that allow you to share, learn, and thrive + Matching gifts program that allows you to deepen the impact of your contributions to qualified charities. + Employee crisis support for when the unexpected happens + Access to our BASF wine cellar, employee discounts, and much more! **About us** As one of the largest chemical companies in North America we have been finding solutions for your everyday needs and addressing the most complex economic, environmental, and sustainability challenges for more than 150 years! At BASF we empower our employees with the tools, guidance and opportunities they need to advance and succeed in work and life. Giving you the support you need to be your best and fulfill your personal ambitions is what helps us create chemistry. After all, our success is linked to yours. Whatever path you envision, BASF is a great place to build a rewarding, successful career. Belong to Something Bigger. #belongat BASF **Privacy statement** BASF takes security & data privacy very seriously. We will never request financial information of any kind via email, private text message or direct message on any social medial platform or job board. Furthermore, we will never send a candidate a check for equipment or request any type of payment during the job application process. If you have experienced any of the above, please contact ************* to report fraud. **Equal employment opportunities** We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, age, citizenship, color, religion, sex, marital status, national origin, disability status, gender identity or expression, protected veteran status, or any other characteristic protected by law. Applicants must be currently authorized to work in the United States on a full-time basis.

Job Description Senior Quality Technical Publication Specialist * US Citizenship is required for this role * On- Site -Cincinnati, Ohio, If you're ready for the challenge of working for a dynamic organization, Dayton T. Brown, Inc. has a career opportunity for a Senior Quality Technical Publication Specialist to join our growing Technical Publications Division. Our three divisions, Engineering and Test, Technical Services, and Mission Systems, make DTB a diverse and welcoming place to work and thrive. Dayton T. Brown, Inc.'s technical writers, illustrators, engineers, programmers, analysts, Logisticians, and data specialists provide world-class technical documentation, information systems, training programs, and logistics data support services. We are experts in mechanical, electrical, and hydraulic equipment that will perform systems analysis, information development, technical writing, data conversions, and graphics preparation, while providing solutions for today's sophisticated delivery requirements. Our Technical Services team utilizes the most up-to-date and appropriate software and systems to undertake and complete your project. We know current documentation standards and specifications, including the ever-evolving S1000D standard. Responsibilities include, but are not limited to: We are seeking a qualified and motivated Senior Quality Technical Specialist to join our team in a full-time, on-site capacity. This position is based in Cincinnati, Ohio, and requires daily in-person attendance. Remote work or telecommuting is not authorized for this role . The ideal candidate will bring a strong commitment to collaboration, communication, and hands-on engagement with our team and operations. If you thrive in a dynamic, in-person work environment and are ready to contribute to impactful projects, we encourage you to apply. You will also be responsible for the following: Review and verify technical documents for grammatical accuracy, formatting, consistency, and compliance with style guides and industry standards (S1000D, ISO). Perform content audits and validations across document versions to ensure alignment with source data, engineering changes, and product updates. Collaborate with writers, illustrators, engineers, and subject matter experts (SMEs) to resolve discrepancies and improve document quality. Develop, maintain, and execute QA checklists, review protocols, and content approval workflows. Identify documentation quality issues, track errors, provide training, and recommend corrective actions. Collect, analyze, and report documentation quality metrics, including error rates, review cycle times, first pass yield (FPY), compliance scores, and rework levels to support continuous improvement. Establish baseline KPIs and trends related to documentation accuracy, review efficiency, and publishing cycle times. Contribute to process improvement efforts related to documentation standards, templates, and QA methodologies. Ensure compliance with company documentation policies and applicable regulatory standards (e.g., FAA, FDA, ISO 9001, AS9100, etc.). Perform internal audits on processes and procedures to ensure adequacy of work instructions/operating procedures and compliance with customer requirements. Lead Corrective Action Request (CAR) and Root Cause Analysis (RCA) events. Monitor and analyze product conformity to meet customer requirements. Monitor and analyze performance of on-time delivery and customer satisfaction. Develop and maintain strong relationships with customers. Required Qualifications: 2 or 4-year degree/or equivalent experience. 7+ years' experience in quality assurance for technical documentation or publication development. Strong knowledge of technical writing standards and style guides. Strong familiarity with S1000D standards. Experience with content management systems (CMS), version control tools, and XML environments. Excellent attention to detail and ability to simplify complex technical concepts. Strong analytical skills with experience in collecting and reporting QA metrics. Strong organizational and communication skills. Strong relationship building, decision-making and problem-solving skills. Ability to work in pressure situations. Strong computer skills and be proficient in all Microsoft Office applications and markup/review tools. US Citizenship - Required. Security Clearance -Active Secret - Required, or the ability to obtain and maintain a U.S. Government Secret security clearance. U.S. Preferred Qualification: ASQ Quality Certifications DoD Aviation Maintenance Quality Assurance experience Turbine Engine experience A&P Certification International Organization for Standards (ISO) experience Experience with Lean, Six Sigma, and Total Quality Management (TQM) As a Dayton T. Brown employee, you can expect a fun working environment that provides security and career advancement and so much more such as: Tuition reimbursement A stable, successful organization Innovative work environment Advancement potential Private medical, vision, and dental insurance Profit sharing, 401K with company match! Work/Life balance and family values. Dayton T. Brown, Inc. is an equal opportunity employer - Veterans and Disabled Job Posted by ApplicantPro

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we're making better health outcomes easier to achieve. Hims & Hers is a public company, traded on the NYSE under the ticker symbol "HIMS." To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company's outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit *********************************** About the Role: Hims & Hers is seeking an experienced Quality Control Specialist to join our Quality Unit located in New Albany, Ohio. The position of Quality Specialist will focus on driving continuous improvement efforts that benefit and delight the Hims customer. We are looking for a highly motivated individual to help support and report to the Quality Control Manager. The Quality Specialist role is responsible for the inspecting and/or testing of product(s) before, during and after manufacturing process(es) to ensure products align with company and regulatory standards, as well as other processes necessary to quality operations. The position performs and leads activities "on the floor" in support of dispositioning product and/or raw materials while ensuring compliance with Quality Assurance (QA) policies and procedures, USP, SOPs, and where applicable cGMP. Assist with relevant environmental monitoring programs. We are hiring for our PM Shift: 9pm to 7:30am You Will: * Perform in process and post production quality checks, including testing, assessing products in the compounding suites ("shop floor") to ensure product acceptability. * Perform line clearance, where applicable. * Perform AQLs during the visual inspection process * Provide reports and trending data to QA management * Support departments in reporting, handling and escalation of investigations * Support external manufacturer non-conformance investigations to improve Quality processes. * Manage product retain samples. * Support change control system to provide improvement solutions * Support quality processes in the pharmacy - including inspections, pH meters and scale checks, non-conformance/deviation/complaint investigations, implement corrective action activities, training activities, etc. * Document & review of records: SOP generation, batch record review, COA acceptance, USP monographs, etc. * Recommend training needs, provide reports to QC Manager and Lead Pharmacist to ensure compliance with quality standards * Assist with incoming raw material inspections, as needed per the guidelines for collection, testing, and reporting quality data. * Assist with drafting SOPs and protocols to follow internal global policies, USP and other applicable regulatory guidelines * Ensures compliance with USP , USP , USP and cGMP cleaning standards * Assist in audit activities with all appropriate third party audits & internal audits as required to ensure compliance. * Assist with the management of samples to be tested with contract laboratories. You Have: * B.S. in chemistry, microbiology, biology, quality management, engineering, or related discipline * 2+ years experience in the area of quality assurance/control, process/quality engineering, and/or product formulation * A Pharmacy Technician license or willingness to obtain one within the first six months of employment (we cover costs and will help you obtain your trainee hours). * Experience within a 503b outsourcing facility or experience in cGMP or regulated environment with knowledge of FDA 21CFR 210 and 211, a plus * Aseptic processing experience and knowledge of ISO 14644 * Working knowledge of USP-NF standards , , including monographs * Ability to manage multiple tasks simultaneously, with strong time management and organizational skills. * Excellent interpersonal skills, communication skills and technical writing * Solid understanding of product testing including understanding best practices for testing product against defined specifications * Ability to multi-task and work independently. Highly motivated self-starter. * Solid computer skills with Word, Excel, PowerPoint, and Google platform applications. * Excellent skills in decision making, data collection and analysis, organizing and planning. * Working knowledge and application of statistical analysis including probability and trend analysis * Knowledge and experience in documentation and facility auditing * Some travel may be required Our Benefits (there are more, but here are some highlights): * Competitive salary & equity compensation for full-time roles * Unlimited PTO, company holidays, and quarterly mental health days * Comprehensive health benefits including medical, dental & vision, and parental leave * Employee Stock Purchase Program (ESPP) * 401 (k) benefits with employer matching contribution Conditions of Employment: * This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown, and other items as required. * This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR). * Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve hour shift. Must be able to lift up to 50lbs. * Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs. We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply-even if you're not sure if your background or experience is a perfect match. Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address. To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.

Schedule: 2nd Shift (4:00PM - 3:30AM) The Quality Control Technician will be responsible for all aspects of the quality programs and functions. These include maintaining all HACCP, food safety records, plant audits, mock recall programs and training the plant on these issues and procedures. Performs testing to validate the microbiological quality of current and new ingredients, suppliers, and packages. Provides test data to assure the production of high quality products. Tests current and new concentrate ingredients in process and finished concentrates, and beverages products in development and finished products. The QC Technician will also work with the R&D Team on new product launches. ESSENTIAL DUTIES AND RESPONSIBILITIES: Knowledge of all cleaning agents and applications, external, internal, cleaners, and sanitizers. Properly document and follow all procedures set forth in the frequency guide and standards. Ability to properly fill out batch reports, calculate variations in batch sizes, proper attributes, standards, and other data required on batch report documented per formula. Ability to properly measure and follow proper mixing procedures. Ability to evaluate and troubleshoot batch and make corrections. Ability to perform all testing, evaluations, and documentation of results while following procedures. Ability to troubleshoot and take corrective action on the line. Ability to properly prepare batch tanks for batching, tank rinsing, tank sanitation, odor, and tasting. Full knowledge and capabilities to perform internal pest control program, location of stations, checking and cleaning of stations, and proper documentation on hand of pest control program. Assist supervisors in resolving Quality Control issues, tracking quality trends, recommending and implementing plans to improve quality and production efficiency. Responsible for compliance with Federal and State legislation by establishing and enforcing quality standards; testing materials and product. Ability to collect, analyze and summarize process quality information and trends. Computer literacy required with proficiency in Microsoft Office products including Excel and Word. Typically faces situations that have a variety of interpretations and require careful evaluation. LANGUAGE SKILLS: Ability to read, analyze, and interpret common information, reports and other documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or company representatives. Ability to effectively present information to management. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk, stand for long periods of time, sit and talk or hear. The employee frequently is required to use hands and fingers, to handle, or feel, sit for long periods of time, stand frequently, bend, squat, reach and turn to access files and office equipment. Must be able to lift up to 50 pounds. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Field positions will be exposed to various unfamiliar conditions where Personal Protective Equipment (PPE) must be worn and which may include, but are not limited to manufacturing and warehouse plants, and other locations as directed by supervisor. The noise level in the work environment is usually moderate, but increases significantly in warehouse and manufacturing plants. MINIMUM QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. High School Diploma or GED preferred or equivalent experience. 2-3 years hands-on work experience in the carbonated soft drink industry preferred. Experience in quality control testing procedures and internal and external sanitation of beverage equipment with a clear understanding of all aspects of blending, product attributes recordkeeping, yields, etc. Strong computer skills, including Microsoft business applications and various reporting software. Exceptional interpersonal and verbal communication skills Understands and can follow all OSHA required training. Must be 18 years or older Favorable background and drug exam. Ability and willingness to work a flexible Full Time schedule that may include weekends and holidays. Must be able to provide own transportation to various locations in organizational service areas, as required by duties. Shasta Beverages, Inc. provides equal employment opportunities to all applicants for employment without regard to race, color, religion, sex, national origin, age, disability, gender, genetics, gender identity, disabled veterans or sexual orientation.

Job Location: Paninesville, Ohio Job type: Full-time Type of role: On-site Work Schedule: DuPont Schedule (12-hour rotating shift) About Lubrizol The Lubrizol Corporation, a Berkshire Hathaway company, is a specialty chemical company whose science delivers sustainable solutions to advance mobility, improve wellbeing and enhance modern life. Founded in 1928, Lubrizol owns and operates more than 100 manufacturing facilities, sales, and technical offices around the world and has about 8,000 employees. For more information, visit ***************** We value diversity in professional backgrounds and life experiences. By enabling a consistent, unbiased, and transparent recruitment process, Lubrizol seeks to create a positive experience for candidates so we can get to know them at their best. We recognize unique work and life situations and offer flexibility, ensuring our employees feel engaged and fulfilled in every aspect of life. Join Our Thriving Team at Lubrizol as a Quality Control Lab Analyst Unleash Your Potential. At Lubrizol we're transforming the specialty chemicals market and looking for exceptional talent to join us on this journey. If you are ready to join an international company with talent around the world, and want to make a real impact, we want you on our team. What You'll Do: Performs all QC Lab activities, including but not limited to: all Standard Work Process (SWP), Management Systems, and analytical responsibilities. What We're Looking For: * Provide internal and external customers with the highest level of customer service in responsiveness while performing QC activities. * Interface with all corporate, commercial, supply chain, customer experience, and lab / operations personnel. * Communicate between departments when reporting results and execute SWP / SOP in an exemplary manner. * Perform all test methods without supervision within precision and accuracy standards. * Prepare all solutions needed for testing. * Perform testing on raw material, in-process, finished good, and miscellaneous samples. * Document all data in corresponding laboratory notebook, SAP, LIMS as business needs dictate. * Dispose of all chemicals safely * Perform required testing pertaining to customer complaints, discrepancies, & laboratory investigations. * Report results to operations, in a timely manner. * Review and approve laboratory results as needed. * Assist in the performance of qualifications and validations of instruments, test methods, and basic PMs. * Troubleshoot/self-evaluate OOS results. * Assist in writing SWP, SOPs, methods, protocols, and reports. * Perform daily laboratory maintenance. * Oversee the training of new employee's basic laboratory skills and functions. * Perform simple problem solving and participate in improving daily work Skills That Make a Difference: * Associate degree in chemistry or a related technical field or 5 years' experience in an industrial manufacturing laboratory. * Experience with one of the following analytical techniques: * physical property testing * wet chemistry * advance instrumental analytical techniques. * Highly self-motivated individual, focused on providing high quality laboratory data in an efficient manner, while exhibiting excellent workplace skills. * Solid background in Microsoft Office and computer-based instrument control systems for analytical equipment. * Excellent verbal and written communication skills. * Advanced problem-solving skills and the ability to make competent, independent, decisions in a timely manner to ensure excellent progress on assigned tasks. * Ability to effectively manage multiple and or changing priorities with minimal to no supervision. * Must possess the ability to interact effectively and professionally with internal customers, external customers, vendors, and various stakeholders. Considered a Plus: * Bachelor's degree in chemistry with 1-5 years relevant experience. * Industrial chemical manufacturing laboratory experience is preferred with 1-5 years' experience. * Analytical experience with advanced instrumental techniques like GC, LC, ICP, and NMR. * Analytical experience with wet chemistry and physical property testing. * Experience with LIMS and SAP QM modules. * Experience with proper usage and administration of Lab notebooks / elog notebooks. * Experience with root cause problem solving techniques and tools. * Experience with Statistical Quality Control methodologies. * Experience working in ISO9001/14001 environments. * Experience with internal auditing a plus. Perks and Rewards That Inspire: * Competitive salary with performance-based bonus plans * 401K Match plus Age Weighted Defined Contribution * Competitive medical, dental & vision offerings * Health Savings Account * Paid Holidays, Vacation, Parental Leave * Flexible work environment Learn more at benefits.lubrizol.com! Ready for your next career step? Apply today and let's shape the future together! It's an exciting time to be part of Lubrizol. Lubrizol is not staying put. We are continually learning and evolving. Our passion delivers our success - not only for Lubrizol but for those who count on us every day: our employees, customers, and communities. As a diverse, global team, we work together to solve some of the world's most pressing challenges. We impact everyday lives through science only Lubrizol can deliver, and we never stop pushing to do it better. One of the founding principles of The Lubrizol Corporation more than 90 years ago was treating every employee with dignity and respect. That same commitment is only stronger today. More than that, we are committed to providing an environment where every employee can be the best they can be, no matter their race, color, religion, sex, national origin, sexual orientation, gender identity, disability, or protected veteran status, or any other characteristic. #LI-CS1

Job Title: Quality Assurance Associate Job Title: Quality Assurance Associate Job Type: Full-time About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them. Description: We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated [Job Title] to join our team. In this role, you will be responsible for [briefly describe key responsibilities and tasks]. You will work closely with [mention teams or departments the role collaborates with] to [describe the role's contribution to the company's success. Job Purpose: Under the supervision of the Quality Assurance Supervisor, this person is responsible for performing field QA activities: in process checks in the aseptic processing area, approval for area clearance, AQL inspection for finished products, retention sampling for finished products, batch record review, final product release, review and approve operation documents and forms, and approval / rejection of in-coming raw materials, components, and final product labels. Ensure compliance of operations personnel with the company's procedures and Good Manufacturing Practices (GMPs). This position will also be responsible for identifying any deviations or non-conformances, writing deviation reports, performing root cause analysis, writing/revising standard operating procedures and forms, and tracking metrics, when required. Key Responsibilities: • Regular and predictable onsite attendance and punctuality. • Perform monitoring of Compounding in the aseptic processing area. • Perform AQL inspection for Finished products • Perform in-coming raw material, component, and labeling inspection and release • Review executed batch records to ensure compliance with approved procedures, and communicate and resolve discrepancies with manufacturing operators and supervisors. • Provide Quality support to Manufacturing personnel on the floor - providing guidance during GMP events and initiation of deviations and investigations. • Lead small scope projects, as assigned. • Prepare and/or revise SOPs to ensure compliance with regulations and current practices. Keep current with regulations and industry best practices and update SOPs to improve compliance. • Prepare all necessary reports in a timely manner to meet compliance requirements and business needs. • Participate in Process Validation activities, including protocol execution and reporting, as necessary. • Working knowledge of FDA regulations and application of GMPs. Qualifications: We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them: • Minimum: Associates Degree in Science or equivalent with 2 to 5 years applicable Quality Assurance experience. • Preferred: Bachelor's Degree in Science or equivalent with 1-2 years applicable laboratory, pharmaceutical manufacturing, or related experience (QA preferred) Compensation: Base Salary: $ 65,000 to $ 75,000 annually. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process. What We Offer*: • Annual performance bonus, commission, and share potential • Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute • A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries • 3 personal days (prorated based on hire date) • 11 company paid holidays • Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits • Employee discount program • Wellbeing rewards program • Safety and Quality is a top organizational priority • Career advancement and growth opportunities • Tuition reimbursement • Paid maternity and parental leave *Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms. Recruiters: Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma. Equal Opportunity Employer: Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.

Full-time Description As the Quality Assurance & Control Supervisor, you will be at the forefront of ensuring that our products meet rigorous safety and reliability standards. You will be responsible for overseeing the quality control team, training employees, triaging tasks, and effectively communicating product standards and customer expectations. This role is essential in recommending process improvements and expediting resolutions to any quality concerns.#ZR Essential Functions: Lead, train, and develop QC inspectors, and oversee daily operations to ensure adherence to the production schedule. Manage the QC department workflow in accordance with the company's prioritization system. Actively participate in root cause analysis of internal and customer-rejected assemblies. Perform inspections: visual, dimensional, PT, and UT. Responsible for inspections, first article, customer-required, as needed. Ensure completion of inspection documentation for fabricated components. Lead or participate in continuous improvement activities, organizing and conducting investigations with departments involved, and driving the resolution of quality issues. Conduct internal audits and audit training programs as required. Responsible for complying with and enforcing the company's Quality Management System Work cross-functionally within the Quality Department to prepare and maintain quality documentation, procedures, forms, and training as it relates to various regulatory and quality standards. Responsible for Quality Inspection and regulatory documents such as inspection reports, calibration records, NCRs, MRBs, and Corrective / Preventive action (CAPAs in QMS software IMSXpress. Work cross-functionally with sales, engineering, and production departments to meet all QC standards for Alloy Engineering. Participate with QA in completing and maintaining KPIs such as Quality Goals, or company initiatives (ITPS, quality plan, and quality agreements). Perform other duties as assigned by the supervisor. Requirements Proven experience in Quality inspection or Manufacturing settings with NDT disciplines (visual, dimensional, PT, UT is preferred). Familiarity with ASME, AWS, or welding code standards preferred. Supervisory experience preferred. Strong attention to detail and problem-solving skills. Excellent communication skills and decision-making abilities. Results-driven with a focus on continuous improvement. Physical Requirements: Sit, stand, and climb stairs daily. Lift at least 50 pounds The standard shift is ten hours per day, with steel-toe boots and safety glasses required. Periods of stress may occur. An Equal Opportunity Employer, Including Disability / Vets Salary Description $75,000-$100,000 based on experience

Job DescriptionJob Title: Logistics Quality Control (QC) Specialist Department: Logistics Reports To: Logistics Manager / Quality Manager Type: Full-Time The Logistics Quality Control (QC) Specialist is responsible for ensuring all packaged cannabis products meet internal quality standards and Ohio regulatory requirements before being released to the vault as finished goods and prior to outbound distribution. This role serves as a critical control point between Packaging, Inventory, and Logistics, verifying product accuracy, compliance, and documentation integrity. The ideal candidate is highly detail-oriented, self-motivated, and capable of working independently in a fast-paced, regulated environment. Key ResponsibilitiesFinished Goods & Lot Quality Control ● Perform detailed QC inspections on all packaged lots received from the Packaging Department prior to vault intake. ● Verify lot integrity, SKU accuracy, unit counts, weights, packaging configuration, heat/tamper seal and labeling compliance. ● Ensure all required regulatory information is present and accurate, including: License numbers Batch/lot numbers Harvest and packaging dates Net weight Required warning statements ● Confirm packaging meets internal quality standards and is free of defects, damage, or contamination. ● Accurately document QC approvals, rejections, and findings per SOP requirements. Order Quality Control & Fulfillment Verification ● Conduct final QC checks on all outbound orders prior to shipment or delivery. ● Verify each order is 100% accurate, including: Correct SKUs and product types Correct lot numbers Correct quantities and unit configurations Matching manifest and sales order documentation ● Ensure orders comply with Ohio cannabis transportation and distribution regulations. ● Identify, escalate, and document discrepancies before orders leave the facility. Compliance & Documentation ● Maintain accurate and complete QC records in accordance with Ohio Division of Cannabis Control (DCC) regulations. ● Ensure inventory movements and lot releases are accurately reflected in the state seed-to-sale tracking system. ● Adhere strictly to GMP, SOPs, and internal quality policies. ● Support audits and inspections by providing documentation and traceability records when requested. Cross-Functional Communication ● Communicate QC findings clearly and professionally with Packaging, Inventory, Logistics, and Management teams. ● Escalate quality or compliance risks immediately and participate in root cause analysis as needed. Support continuous improvement initiatives by identifying trends or recurring issues. Required Qualifications ● Previous experience in quality control, logistics, inventory, or regulated manufacturing preferred. ● Strong attention to detail with the ability to spot discrepancies quickly and accurately. ● Ability to work independently with minimal supervision. ● Strong organizational and documentation skills. ● Comfortable working in a highly regulated environment with strict compliance standards. ● Ability to stand, walk, and handle packaged products throughout the shift. Preferred Qualifications ● Experience in the cannabis industry, particularly in packaging, inventory, logistics, or QC. ● Familiarity with Ohio cannabis regulations and seed-to-sale tracking systems. ● GMP or quality systems experience. ● Experience performing lot and order audits in a warehouse or distribution environment. Core Competencies ● Exceptional attention to detail ● Independent decision-making ● Regulatory compliance mindset ● Clear written and verbal communication ● Integrity and accountability Powered by JazzHR n1JebPyvvy

Job Description Quality Supervisor, QMS Dayton, OH • Tier 1 Automotive • Full time Our client is a leading Tier-1 automotive supplier that has an immediate opening for a Quality Supervisor. In this position, you'll own the system that keeps production honest. You'll coordinate all QMS activities, so they meet IATF 16949, customer, and internal requirements. If you live for clean audits, airtight document control, and gauges that are always in spec, this is your seat. What you'll do Serve as the QMS Representative for third-party IATF 16949, external, and internal audits Run internal audits, including LPA, QMS, and CAR follow-ups Lead document control and gage calibration systems, maintain records, and close internal audit findings Plan, coordinate, and train all QMS Audit Program activities Publish daily and monthly scrap reports for Cost of Quality tracking Audit customer-specific requirements each year and drive required QMS changes Build and maintain procedures, forms, and process maps to defined guidelines What you bring High school diploma required, additional technical education a plus Auditor certification for IATF 16949 preferred, Lead Auditor is a plus 2 or more years of IATF 16949 auditing experience in automotive manufacturing 2 or more years in a supervisory role Hands-on gage calibration experience Advanced Excel skills, including databases, formulas, pivot tables, and charts Strong written and verbal communication, high attention to detail, organized and self-directed Multi-site manufacturing experience is a plus Key metrics you will own QMS audit completion to schedule On-time Cost of Quality analysis IATF 16949 compliance Gage calibration compliance Work environment Split between office and plant Occasional exposure to typical manufacturing conditions, such as dust, odors, or noise Why join Visible ownership of the QMS with leadership support Tier 1 stability and career growth Competitive pay, bonus, benefits, and 401(k)

Job Description Job Title: Quality Control Specialist Friday, Saturday & Sunday 7:00am - 7:30pm We are seeking a detail-oriented and reliable Quality Control Specialist to join our team on a full- time basis. This role is essential in ensuring that products meet our quality standards and comply with regulatory requirements. Key Responsibilities: Perform routine quality inspections on incoming materials, in-process production, and finished goods Document inspection results and report any deviations or non-conformances Assist with sample collection and testing according to established protocols Maintain accurate and organized quality records Communicate effectively with production and QA teams to resolve quality issues Support continuous improvement initiatives and compliance with GMP standards Qualifications: Food Science, Microbiology, or working towards this type of degree preferred Previous experience in quality control or manufacturing environment is a plus Strong attention to detail and ability to follow procedures Basic computer skills (Excel, data entry), Google Drive Ability to work independently and manage time effectively Familiarity with GMP and quality standards preferred

System One is seeking a NDE Quality Oversight professional for a long-term contract to hire, full time opportunity, onsite in Orville, Ohio. The ideal candidate will have a strong background in nuclear quality assurance, NDE, and fabrication operations, with a deep understanding of NQA-1 and ASME standards. This role will focus on ensuring quality through oversight, auditing, and compliance within a nuclear fabrication environment. Responsibilities: + Provide quality assurance oversight of NDE (Non-Destructive Testing) and fabrication operations. + Ensure compliance with NQA-1, ASME, and other nuclear quality standards. + Conduct audits to maintain quality program integrity. + Review and approve procedures, ensuring alignment with applicable standards. + Generate and review final quality packages for completeness and accuracy. + Collaborate with teams to identify and resolve quality issues. Qualifications: + Required Experience: + Hands-on expertise in nuclear quality programs, including NQA-1 and ASME standards. + Proficiency in NDE techniques and fabrication processes. + Experience in auditing, procedure review, and final package generation. + Must be local to Orrville, OH or willing to commute (no per diem provided). + Strong communication and organizational skills. System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. Ref: #161-Managed Staffing Charlotte System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

This is a remote part-time position only available to US residents of Ohio and Texas We are primarily looking to staff part time, Mon-Fri 8am-6pm EST/8am-5pm CDT This role is not eligible for anyone currently employed full time elsewhere Job Overview: This is a remote, part-time, entry-level position. We are looking for a Part Time Production QC Associate to help ensure the deliverability of our product. Production QC Associates primarily test our content by sending SMS messages across various providers and carriers and log the results, while making changes as necessary. You will be provided with a company laptop and set of three cell phones to use for testing. If you are a computer savvy person with a keen eye for detail, who's self-motivated and a quick learner, we are interested in hearing from you! Compensation: $10-12/hour Hours: Part time, 12-28 hours/week Mon-Fri (8am-6pm EST/8am-5pm CDT). Flexible hours to fit your schedule! Specific Duties, Activities, and Responsibilities: Test for the reliable delivery of SMS Text messages through extensive review of QC test results across multiple cellular carriers. Adjust, retest, and document changes made to SMS campaigns. Map specific pre-determined responses to frequent messages Assist with miscellaneous data audits as needed Skills/Qualifications: Computer capability - Microsoft Office (Word/Outlook/Excel) College level English language grammatical skills. Strong organizational skills - attention to detail, and exceptional verbal/ written skills Problem-Solving - ability to interpret data, draw conclusions, and spot trends. Work Ethic - Self-motivated and able to work independently or with a team Cell Phone Reception - It is a requirement that you have adequate cell phone reception with the following cellular carriers: AT&T, T-Mobile, and Verizon Wireless What is Drips? Drips is an AI driven conversational SMS marketing platform; the first Conversational Texting company of its kind, founding a new category and leading the way for some of the biggest brands in the world to improve engagement rates and outcomes for their prospects and customers. Operating completely remote, Drips helps clients increase lead conversions by communicating with their customers in the same way that people communicate with each other. Using conversational SMS, calls, email, and direct mail campaigns, Drips automates conversation in a way that works, and works well. Drips enables brands to connect with consumers through an AI-powered conversational outreach strategy that includes human-like two-way texting, scheduled calling, and voicemail messages. Backed by a proprietary natural language processing model, our platform has handled over half a billion humanized conversations to date, enabling us to deliver automation at a scale that no other competitor in the messaging industry has been able to match. That's why we're the platform of choice for some of the world's most recognizable brands. Drips' focus on empowering brands to capture intent and drive meaningful conversations has sparked rapid growth since the company was founded in 2016. And we are looking to accelerate the next era of growth and expansion of our team. Check us out! ************************** ****************************************** *************************************** **************************************

Location: Indianapolis, IN or Mason, OH. This role requires associates to be in-office 1 - 2 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance. This approach combines structured office engagement with the autonomy of virtual work, promoting a dynamic and adaptable workplace. Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law. An RCA Intern will be responsible for supporting our Risk, Controls, and Assurance team in ensuring the stability and compliance of internal controls over financial reporting and audit/regulatory compliance obligations. Key regulations and standards supported by these efforts include Generally Accepted Accounting Principles (GAAP), Sarbanes-Oxley (SOX), statutory Model Audit Rule (MAR), and System and Organization Controls 1 (SOC1) reporting. This internship will be a full-time (40 hours/week) program that will run for 8-11 months with two cohorts, one starting in January 2026 and the other May 2026. How you will make an impact: * Create and document results of control testing and review. * Provide research support, develop work programs, engagement plans and collaborate with audit team members. * Assess risk of financial processes, operational processes, and the supporting IT systems. * Document business processes dependent on financial data systems. * Analyze results of specific or general work requests. * Having direct contact with external audit firms for purposes of audit planning and remediation * Opportunity to do innovative work that means more to you and those we serve * Create greater care for our members, greater value for our customers, and greater health for our communities Minimum Requirements: * The ability to work 40 hours per week for the duration of the internship and work in-office at least once per week. * Actively pursuing a Bachelor's or Master's degree in either: Accounting, Finance, Business Information Systems, Management Information Systems, or a related program (MSA, MBA, MSIS, etc). Preferred Skills, Capabilities, and Experiences: * Excellent Problem-solving, Analytical, and Organizational skills * Excellent written and verbal communication skills * Excellent organization and time management skills * Ability to work in a team-based team environment * Skilled in Microsoft Office Suite with emphasis on Excel, Word, and Access * Excellent Communication skills, both written and oral * Excellent Problem-solving, Analytical, and Organizational skills * Excellent Public Speaking and Presentation skills Job Level: Non-Management Non-Exempt Job Family: ADM > Intern Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

Job Description: Quality Control & Receiving Associate The Quality Control & Receiving Associate is responsible for inspecting, verifying, and documenting incoming materials and finished goods to ensure compliance with company and customer specifications. This role plays a critical part in maintaining product quality, verifying supplier shipments, and supporting overall production efficiency in a secondary packaging manufacturing environment. What you'll do as a Quality Control & Receiving associate Receiving: Verify incoming shipments against purchase orders, packing slips, and invoices for accuracy in quantity, product type, and condition. Inspect raw materials, components, and packaging supplies for defects, damage, or non-conformance. Properly label and document received goods in the company's inventory system. Coordinate with purchasing and suppliers to resolve discrepancies, shortages, or damaged goods. Ensure materials are stored in compliance with safety, quality, and organizational standards. Quality Control: Perform in-process and final inspections of packaged products to verify compliance with quality standards and customer requirements. Check incoming materials (up to and including containers, labels, inserts, part numbers, etc.) for proper specifications, accuracy, and condition. Document inspection results, deviations, and corrective actions in accordance with company procedures. Work closely with production and purchasing teams to identify, communicate, and resolve quality issues in real time. Support corrective and preventive action processes (CAPA) for recurring or significant quality concerns. Assist with product testing, measurement, and verification using appropriate tools and equipment. General: Maintain accurate and organized records for audits, certifications, and traceability requirements. Follow all company safety, housekeeping, and compliance policies. Participate in training programs to stay current on quality and regulatory requirements. Support continuous improvement initiatives to enhance efficiency, quality, and customer satisfaction. What we're looking for Education & Experience: High school diploma or equivalent required; associate degree or technical certification in quality, manufacturing, or logistics preferred. Prior experience in quality control, receiving, or inventory management in a manufacturing environment (packaging experience a plus). Skills & Competencies: Strong attention to detail with the ability to identify defects and inconsistencies. Understanding of quality management systems and inspection tools, including calipers, Ability to read and interpret packing slips, purchase orders, and product specifications. Strong organizational skills with accurate record-keeping. Proficiency with Microsoft Office and ERP/inventory management systems preferred. Effective communication and problem-solving skills. Ability to work independently and collaboratively in a fast-paced production environment. Tool Reading Competencies Ability to read and interpret blueprints, and GD&T symbols Skilled in using calipers, micrometers, height gauges, and bore gauges Familiar with thread gauges, protractors, and alignment tools Accurate in documenting and reporting measurement results Physical Requirements: Ability to lift up to at least 50 lbs. Standing, walking, and moving materials throughout the shift. Manual dexterity and visual acuity to perform inspections. Job Type: Full-time

About Our Team At Tolco Corporation, we are the trigger sprayer experts. With a foundation of over 64 years of selling best-in-class cleaning tools, our major product categories focus on dispensing, including trigger sprayers, pumps, bottles and closures. We attribute our success to our dedicated team who strive to provide quality customer service and take pride in providing fast and efficient shipping. We often collaborate across teams to get the job done; however, we don't take ourselves too seriously. It is important for us to have fun too! About You The ideal candidate is a detail-oriented problem-solver with a strong commitment to quality. A proactive mindset, technical aptitude, and strong communication skills are essential to thrive in this role. If you take pride in ensuring products meet high standards and enjoy working in a structured, process-driven environment, we encourage you to apply. Job Summary The Quality Control Analyst ensures that all inbound and returned products meet Tolco's quality standards through systematic inspection, documentation, and testing. This role involves evaluating product performance, chemical resistance, output, and compliance with specifications, while also inspecting goods produced or assembled by Tolco as directed by the manager. This position reports to the Quality Control Manager. Job Responsibilities Perform timely inspections of inbound goods against Tolco's product specifications Select samples from the warehouse/receiving area and transport them (using non-motorized handcart) to the inspection station Conduct functional tests to verify proper operation, chemical resistance, output and performance Use testing equipment to measure product compliance Evaluate customer-returned products as directed by the QC Manager to determine root causes of defects or failures Inspect internally produced or assembled goods before outbound shipment to ensure compliance with quality standards Record test results and document inspection findings Maintain organized and up-to-date quality records in the Quality Control Master Specification Worksheet Requirements Education & Experience: Associates Degree in Quality Assurance Mgmt preferred, and/or minimum of 3+ years experience in quality control, inspection, or manufacturing Certifications: Quality Control/Inspection (i.e. CQT or CQI) preferred but not required Technical Skills: Basic computer skills, including proficiency in Microsoft 365, Google Suite and an ERP Physical Requirements: Ability to lift/move items up to 50 lbs and stand for extended periods of time Soft Skills: Detail-oriented, analytical, and able to follow standardized procedures Benefits and Other Important Information This is a full-time, on-site position 8am-5pm, Monday-Friday. Tolco offers a comprehensive benefits package, including medical, dental, vision, voluntary life insurance, 401k disbursements, paid vacation, and more. More About Tolco Tolco Corporation is a leading manufacturer of cleaning tools used in the Janitorial, Beauty & Barber, Animal Health, and Auto Detailing markets. Our major product categories focus on dispensing, which include trigger sprayers, pumps, bottles, and containers. Additionally, we offer over 1000 products, and carry items in the restroom care, floor & window cleaning, utility, and safety categories. Tolco is a third-generation family business operating out of Toledo, OH since 1961.

BEL GEO is hiring motivated, interns for our Construction Material Testing (CMT) department. As a QC/QA Field Technician, you'll conduct quality control and assurance tests on construction materials like soil, concrete, asphalt, and aggregates. This role ensures all work meets project specifications and industry standards. The work is mostly outdoors on active construction sites, with a mix of fieldwork (75%) and lab/office duties (25%). We provide a month of training and mentorship before you begin independent work. This internship is a great opportunity to gain practical experience in the geotech field. With additional experience and education, you could advance to a Senior Field Technician or Project Engineer. This role offers the possibility of a full-time job after the internship ends.

Job Details Entry Corporate Headquarters - Cleveland, OH Full Time $13.00 - $15.00 Hourly Day ABOUT US: Midwest Direct was founded in 1982 as a provider of mail presorting operations. Helping companies in a variety of industries with their personalization and direct mail service, our technology has advanced to the point where just one of our machines can sort up to 50,000 pieces per hour! Midwest Direct helps our clients efficiently create and deliver their print, mail and digital messages with the best audience data for targeted and accurate deliverability. When you add in our additional delivery channels, such as email, Informed Delivery, and online advertising, we average over two million messages a day delivered to mailboxes, inboxes and online. Midwest Direct is looking for a Warehouse Associate! **$500 Sign-On Bonus!** Job Duties Include: - Ensuring jobs are checked in promptly and correctly to guarantee that the items are able to be processed to meet our deadlines. - Preparing all Outbound Mail for outgoing shipment. Job Responsibilities: Operation of a Tow Motor is Prepare work orders for production by client or sub-client Verify piece counts supplied by customer to ensure shipments are complete Perform multi-point quality checks before product is released to production Check in all incoming mail jobs and verify counts Create work orders Validate mail tray accuracy Prepare pallets for outgoing shipment Wrap and weigh skids Communicate all issues, errors or questionable items with supervisor Place all jobs with issues on hold Unload inbound shipments Use pallet jack to move pallets of mail Schedule: Sunday, Monday, Wednesday, Friday, Saturday. OR Tuesday, Wednesday, Thursday, Saturday Sunday. 7am - 3:30pm Compensation: Starting rate: $13.00 - $15.00/hr Incentives provide the opportunity to earn up to $15.00 hourly! BENEFITS TO JOINING MIDWEST: - Weekly pay - Paid vacation and holidays - Attendance bonuses - Medical, Dental, Vision, & Life Insurance - 401k plans - Employee referral bonuses - Public transportation benefits Job Requirements: Able to lift up to 25-50 lbs. continuously Able to stand for long periods of time Able to read and write proficiently Able to be detail-oriented Able to operate a pallet jack Possess computer skills, with an emphasis on Excel and Google Possess basic mathematical aptitude Experience with tow motors and forklifts is REQUIRED! MUST be able to pass a criminal background check & drug test! Midwest Direct is proud to be an equal opportunity employer- and celebrate our employees' differences, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or Veteran status.