Quality technician jobs in Columbia, MO - 34 jobs

For more than 100 years, Modine has solved the toughest thermal management challenges for mission-critical applications. Our purpose of Engineering a Cleaner, Healthier World means we are always evolving our portfolio of technologies to provide the latest heating, cooling, and ventilation solutions. Through the hard work of more than 11,000 employees worldwide, our Climate Solutions and Performance Technologies segments advance our purpose with systems that improve air quality, reduce energy and water consumption, lower harmful emissions, enable cleaner running vehicles, and use environmentally friendly refrigerants. Modine is a global company headquartered in Racine, Wisconsin (U.S.), with operations in North America, South America, Europe, and Asia. For more information about Modine, visit modine.com. Position Description This position is responsible for conducting inspections to ensure quality or detect defects in chiller units. The Quality Technician is responsible for ensuring products, materials, and processes meet established standards. Key Responsibilities * Performs quality checks by station and performs final inspections * Inspects manufactured/fabricated materials to ensure compliance with standards and specifications * Records and maintains data and documentation of inspection results in physical and electronic documents * Collaborates with production team regarding quality issues * Proposes and initializes corrective actions with operations team * Conducts quality audits of manufacturing process to identify areas of improvement and ensuring compliance with regulations and company standards Required Education & Qualifications * 1+ Years manufacturing experience, preferably in quality * Familiarity with non-conformance action plans * Work well across multiple departments/people * Use good judgment in resolving problems and making independent decisions * Computer skill desirable in Microsoft Office Programs (excel, outlook, SAP, etc.) Modine is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law. Modine provides a competitive benefit package, which could include paid vacation, short term disability, 401(k), health, dental, vision, life insurance, flex spending benefits, tuition reimbursement, Health Savings Account and much more. Human Resources will provide more detail upon your hiring.

Full-time Description ThermAvant Technologies is seeking a full-time Manufacturing "Braze" Technician to join our growing Braze department. As a key member of our team, you will help develop and enhance our braze process and play an essential role in processing production parts through braze ovens. This position offers an exciting opportunity to contribute to a dynamic, fast-paced environment. Key Responsibilities: Prepare, instrument, and load parts into fixtures and braze ovens based on the provided production schedule. Perform quality checks during the braze process, including part dimensions, cleanliness, fit-up, and braze quality. Conduct routine maintenance on braze ovens and associated equipment. Identify process trends and nonconformities, providing feedback for continuous improvement. Assist in preparing metallurgical samples from the brazing process for analysis. Help achieve and maintain certifications and qualifications for all equipment and processes. Contribute to the establishment and preservation of documented procedures. Maintain up-to-date knowledge of brazing specifications relevant to the job function. Ensure attention to detail and quality while meeting production deadlines. Promote and maintain a safe and clean working environment. Participate in inspections, audits, and the resolution of non-conformities. Properly use shop tools, hand tools, and equipment required for brazing operations. Collaborate with others to maintain a positive and efficient team environment. Complete additional tasks as required or requested. Requirements Able to pass a background check High school diploma or equivalent, or 2+ years of relevant experience. Ability to read and interpret mechanical drawings and schematics. Familiarity with quality management systems such as AS9100 and ISO 9001:2008 a plus. Proficiency with basic computer applications (Word, Excel, email) and strong communication skills (both written and verbal). Exceptional attention to detail and manual dexterity. Ability to handle heavy materials (>50 lbs) when necessary. Experience with material handling equipment (overhead cranes, tow-motors, pallet jacks) is a plus. Experience with high-temperature ovens, brazing ovens, or clean room environments is a plus. Special Working Conditions/Job Characteristics: Full-time position (40 hours per week, Monday through Friday). Willingness to work overtime as needed. Physical ability to lift up to 50 pounds regularly. Experience with CNC machines, programming, or high-temperature ovens (e.g., braze or autoclave) is a plus. Benefits: 100% company-paid dental, vision, and health insurance. Paid holidays and paid time off. Why Join Us? If you have a strong attention to detail and a passion for quality manufacturing, we invite you to apply for this rewarding role. Join a company that values innovation, teamwork, and safety while providing opportunities for professional growth and development. Salary Description $18.00 - $25.00 Per hour

PharmaLogic is the fastest-growing SPECT & PET radiopharmaceutical solutions provider and contract development and manufacturing organization (CDMO) with radiopharmacies across North America. We are passionate about expanding the power of radiopharmaceutical technology to provide transformative diagnostic and therapeutic agents to patients from bench to bedside. PharmaLogic offers you an exceptional opportunity to join our dynamic team as a Pharmaceutical Production Technician! Hours for this role are 10:00pm to 6:00am. If you have a passion for nuclear medicine and want to make a significant contribution to patient care while working in a stimulating and dynamic environment, then this opportunity is for you. Role Summar y: As a Pharmaceutical Production Technician, you will play a vital role in the operation, production and QC of PET radiopharmaceuticals. The position involves maintenance and repairs of some equipment such as chemistry modules and analytical equipment. You will be expected to assist in facility maintenance, system repairs, PMs, and system modifications to increase your expertise and ensure system reliability. Job Responsibilities and Duties: 1. Operate cyclotron for PET production. 2. Perform maintenance and repairs on synthesis modules and analytical equipment. 3. Perform PET radiopharmaceutical production and Quality Control (QC) in cGMP environment. Responsible for routine production, packaging and shipping of radioisotopes. 4. Ensure compliance with all regulatory commitments and company policies and procedures including cGMP and radiation safety. 5. Maintain records to comply with FDA requirements. 6. Order parts and supplies for maintenance and production. 7. Clean and maintain production areas. Job Requirements │ Skills │ Education: • Academic background in chemistry, engineering, electronic technology; or completion of training at an advanced military electronics school; or an equivalent combination of education and experience. • Experience in electrical, mechanical engineering, medical equipment services or equivalent. Pharmacy tech certification a plus. • Experience working with ionizing radiation and radioactive equipment a preferred. • Experience troubleshooting, performing repairs and maintaining equipment. • Strong analytical, troubleshooting and customer service skills. • Working knowledge of cGMP environment and regulations. Come join our winning team and begin a fulfilling career with us by applying today. PharmaLogic is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status, or any other protected class. Benefits Include: 401(k) retirement benefit program Medical Dental care Disability insurance Employee assistance program Extended health care Life insurance On-site parking Paid time off Vision care

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Applies GMP/GLP in all areas of responsibility, as appropriate Applies the highest quality standard in all areas of responsibility Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Reviews and approves/rejects completed client laboratory reports and like records for accuracy, traceability, and completeness. Evaluates addressed deficiencies for clarification and for potential impact on compliance status. Works with staff to correct any noted deficiencies/inconsistencies. Assist with implementation and monitoring of quality systems and procedures (e.g. CAPA, change controls, trainings, etc.) Reviews protocols, procedures, data, reports, and other documents to ensure accordance with specified regulatory requirements, protocol, and/or project plan, methods, and SOPs. Keeps supervisor informed of significant issues or developments identified during quality assurance activities. Learn new tasks and remember the processes associated with this role. Ability to communicate with Scientific staff for resolving comments Ability to complete tasks in situations that have a speed or productivity quota. Communicates effectively with client staff members Performs other duties as assigned Qualifications Basic Minimum Qualifications : Bachelor's degree is required. A degree in a relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical science, or other directly related field or degree with comparable coursework is preferred. In some cases, experience in the relevant area may be used to substitute the Bachelor's degree. Authorization to work in the United States indefinitely without restriction or sponsorship Other Qualifications : Experience with reading and understandings protocols, SOPs, and technical guidelines. Ability to define and solve practical problems, present solutions, establish facts, and draw valid conclusions Additional Information Position is full-time, Monday-Friday, 8:00 a.m.-4:30 p.m. with additional hours, as needed. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. We offer excellent full-time benefits including : Comprehensive medical coverage, Life and disability insurance, 401(k) with company match, Paid holidays and vacation, Dental and vision options. Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. The Group also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Applies GMP/GLP in all areas of responsibility, as appropriate Applies the highest quality standard in all areas of responsibility Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration Reviews and approves/rejects completed client laboratory reports and like records for accuracy, traceability, and completeness. Evaluates addressed deficiencies for clarification and for potential impact on compliance status. Works with staff to correct any noted deficiencies/inconsistencies. Assist with implementation and monitoring of quality systems and procedures (e.g. CAPA, change controls, trainings, etc.) Reviews protocols, procedures, data, reports, and other documents to ensure accordance with specified regulatory requirements, protocol, and/or project plan, methods, and SOPs. Keeps supervisor informed of significant issues or developments identified during quality assurance activities. Learn new tasks and remember the processes associated with this role. Ability to communicate with Scientific staff for resolving comments Ability to complete tasks in situations that have a speed or productivity quota. Communicates effectively with client staff members Performs other duties as assigned Qualifications Basic Minimum Qualifications : Bachelor's degree is required. A degree in a relevant field such as chemistry, biochemistry, biology, chemical engineering, pharmaceutical science, or other directly related field or degree with comparable coursework is preferred. In some cases, experience in the relevant area may be used to substitute the Bachelor's degree. Authorization to work in the United States indefinitely without restriction or sponsorship Other Qualifications : Experience with reading and understandings protocols, SOPs, and technical guidelines. Ability to define and solve practical problems, present solutions, establish facts, and draw valid conclusions Additional Information Position is full-time, Monday-Friday, 8:00 a.m.-4:30 p.m. with additional hours, as needed. Candidates currently living within a commutable distance of Columbia, MO are encouraged to apply. We offer excellent full-time benefits including: Comprehensive medical coverage, Life and disability insurance, 401(k) with company match, Paid holidays and vacation, Dental and vision options. Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Job purpose The Quality Technician performs and documents routine field and laboratory testing/inspections as required by the Project Quality Management Plan and/or as directed by a Quality Manager. Duties and responsibilities Testing Concrete for Air Content, Slump, and Temperature. Making concrete cylinders/beams in the field for early or 28-day acceptance. Nuclear Gauge Density Testing on Soil and Aggregate bases. Using core drill to cut concrete cores on various pavements. Measuring, trimming, and capping concrete cores. Perform Concrete Plant Inspections Sample aggregates and soils at jobsites, concrete plants, and quarries. Break cylinders and cores for strength determination. Maintain and calibrate company owned testing equipment. Filling out, documenting, and submitting all reports that correlates with the above duties and responsibilities as required by the Owner. Be reliable, possess a good attitude and strong work ethic. Be a team player. Perform other duties as assigned. Qualifications Below qualifications are not required for hire but must be acquired within one year of hire date. MoDOT certifications for Concrete Field, Concrete Strength, Soil Denstity and/or Field Density and Aggregate Tech. Nuclear Density Gauge Safety and Hazmat/Transportation Training Certification. Railroad Safety Training. 30-hour OSHA training. Ability to deal effectively and tactfully with a wide variety of individuals in person, via telephone and in writing. Excellent customer relations skills. Ability to work independently and resolve practical problems, keeping all appropriate parties aware of issues or risks. Have a strong work ethic. Excellent verbal and written communication skills. Understand basic behavior-based safety programs and enforce company's safety policies. Must have and maintain a valid driver's license. Must be able to pull trailers and maintain a DOT medical examination card. Working conditions Outside environment, exposure to all weather conditions and temperature extremes. Site specific exposure to hazardous materials requiring proper use of Personal Protective Equipment. Noise levels are site specific and may be subject to PPE. Physical requirements 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 frequently required to stand; walk; use hands to handle/feel objects, tools, or controls; and reach with hands and arms. You are occasionally required to climb or balance and stoop or kneel. You must regularly lift and/or move up to 50 pounds. Specific vision abilities required by this job include distance vision, peripheral vision, depth perception, and the ability to adjust focus. The position requires that you will walk the construction site, climb ladders, climb stairs, and walk on uneven ground. Position will require employee to spend a large portion of their time on the project sites. Millstone Weber is an Equal Opportunity Employer and has long led the industry in training and hiring a diverse and inclusive workforce. To accomplish our goals of quality, innovation and continuous improvement, we are committed to partnering with employees and subcontractors who share our company values and seek to continually exceed the expectations of project owners. We strive to maintain a work environment that provides all employees with an opportunity to be successful without regard to race, creed, color, religion, sex, sexual orientation, gender identity, national origin, disabled Veterans and Vietnam Era Veterans, age, or physical/mental condition. As part of that policy, we adopt and support the Equal Opportunity Laws that are designed to promote the full realization of equal employment opportunity through a positive continuing program.

Our Draught Quality Technicians play a crucial role in ensuring the quality of our draught beer. They travel to bars and restaurants to maintain draft beer systems and clean lines on a set schedule, and they also are responsible for maintaining the draught equipment we own that is used for special events. They also assist with training bar and restaurant staff in proper pouring techniques, changing kegs, and making minor adjustments to keep the beer flowing the way it was intended to. The best person for this job is someone who doesn't mind getting their hands dirty and enjoys troubleshooting. This job involves local travel in a company-provided vehicle, and is perfect for the person who doesn't want to sit at a desk all day. Job Responsibilities Maintain a cleaning schedule wherein every draught beer line in the territory is cleaned at least every two weeks Maintain tap cleaning logs on a daily basis, check and date QC stickers with adherence to rigorous supplier guidelines Troubleshoot basic draught system problems and respond to trouble calls in a timely manner. Maintain product freshness and presentation through product rotation and equipment cleanliness and appearance Assist with draught system installations according to legal guidelines Maintain tools to perform specific tasks (spanner wrench, thermometers, tower wrench, etc.) Merchandise/install paper and permanent Point of Sale materials Ensure assigned Company vehicle is maintained to and clean

We are seeking an experienced Quality Control Technician to work in the company's materials testing lab. The successful candidate will be responsible for performing a variety of lab tests, ensuring that all testing is completed accurately and in compliance with legal and regulatory requirements. As a key member of our team, the Quality Control Technician will work closely with other departments and stakeholders to ensure the efficient and effective use of company resources. Responsibilities Perform a variety of lab tests on construction materials, including concrete, asphalt, and soil Analyze and interpret test results, and ensure that all testing is completed accurately and in compliance with legal and regulatory requirements Maintain lab equipment and supplies, and ensure that all lab-related activities are carried out in accordance with best practices and standards Collaborate with project managers and other stakeholders to ensure that lab testing aligns with project requirements and timelines Communicate lab-related information to stakeholders Identify and report any quality control issues or concerns Other duties as assigned Qualifications Associate's degree in chemistry, geology, or a related field 2+ years of experience in a quality control role, preferably in the construction industry Strong technical skills, with a deep understanding of lab testing processes and procedures Strong attention to detail and accuracy Strong organizational and time-management skills Ability to work effectively in a fast-paced, dynamic environment A commitment to promoting diversity, equity, and inclusion in the workplace Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)

As a Quality Control Technician, you will assist leadership in responding to company Quality Response Teams (QRTs) by maintaining all quality databases that include repair and QRT information. Complete Quality Department SOP training with existing and new Quality staff and facilitate estimates, scheduling and revised billing of QRTs. Essential Functions: Investigate all customer QRT concerns and provide research leadership. Document all discussions and e-mail history in the QRT database. Provide QRT feedback to Customer Service to resolve the quality issue. Enter Post-Ship Repairs. Enter a brief historical QRT description into the AS400 any time we have a QRT. Involve leadership in the investigation and resolution process, as needed. Initiate Error Reviews on all QRTs that were resolved by Credit or feedback. Learn all necessary department functions of prepress and finishing to expedite a Repair through the departments. Make follow up calls to the Customer and Sales, as assigned. Take revised job specs from the customer and route quote requests to the Estimating department. Work with the Scheduling department to provide the necessary information for customers needs. Communicate job instructions to Purchasing prior to orders arriving to ensure stock availability or possible options. Complete and maintain all required paperwork, records and documents for Repairs and QRT policies. Create and distribute reports to management. Must be pro-active in identifying situations early and alerting the CSR or Production with an accurate interpretation of the potential problem. Knowledge, Skills and Abilities Ability to handle multiple tasks and projects. Ability to remain organized and self-directed in a fast-paced environment. Ability to work in a team environment. Ability to interface with a variety of individuals or groups on a frequent basis. Ability to work with limited direction and supervision, while demonstrating good judgment and strict confidence. Ability to learn computer applications as necessary for the position. Must successfully complete any training or certification courses required to support or strengthen position. Ability to read, interpret and follow verbal and written instructions, work procedures and other related materials. Excellent verbal and written communication skills including strong customer service skills. Must communicate appropriate information accurately and clearly as needed. Demonstrated advanced proficiency with MS Word, Excel, Outlook and Windows based databases. Minimum Requirements: High School Diploma and two years' experience in print manufacturing operations or related function.

Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers' toughest challenges. While we continue updating the Solventum Careers Page and applicant materials, some documents may still reflect legacy branding. Please note that all listed roles are Solventum positions, and our Privacy Policy: *************************************************************************************** applies to any personal information you submit. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Job Description: Quality Engineer (Solventum) We are pleased to report that Solventum has successfully completed the sale of its Purification & Filtration (P&F) business to Thermo Fisher Scientific Inc. (Thermo Fischer). This is a significant milestone for the P&F business, allowing for the strategic investment and resources needed to sustain growth and deliver customer solutions. Please note that this position is scheduled to transfer to a local subsidiary of Thermo Fisher in your country. However, the position is in a country where the transfer of employees to Thermo Fisher is delayed until a later date. By joining Solventum during this transitional period, you will be able to work alongside an energized and mission-driven team who is experiencing this transition along with you. Until the transfer is complete, you will be employed by Solventum, and your employment is subject to all applicable terms and conditions as outlined in our employment agreement and company policies The Impact You'll Make in this Role As a Quality Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Providing product assurance engineering support for commercialized products including specification and design control, change management, risk management, investigations, and continuous improvement. Reviewing and approving IQ/OQ/PQ documents and validation documents to qualify and validate new equipment and processes. Participating in and leading customer audits, ISO 9001 audits, ISO 13485 audits, internal audits, and other activities to identify improvement opportunities. Providing quality assurance and control for products used in FDA regulated industries, including control of incoming materials, review of in-process tests and release tests and device history records. Working with manufacturing engineers and other personnel to solve product quality issues. Leading investigations, corrective action responses, trending and monitoring for nonconforming materials, complaints, and supplier issues. Interacting with Division quality personnel and outside suppliers to ensure product quality and performance. Driving quality improvement using engineering best practice, statistical techniques, and Lean Six Sigma methodologies. Your Skills and Expertise To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications: Bachelor's Degree or higher (completed and verified) from an accredited institution Additional qualifications that could help you succeed even further in this role include: Bachelor's degree or higher in Manufacturing/Industrial Engineering, Chemical Engineering, Mechanical Engineering, Statistics/Mathematics from an accredited institution Three (3) years of engineering experience in a private, public, government or military environment Experience with quality systems such as Quality Manuals, ISO-13485, 21 CFR Part 210, 211 and 820, metrology, calibration, auditing and supplier management Working knowledge of root cause analysis tools and techniques American Society for Quality, Certified Quality Engineer (CQE) certification or willingness to obtain Proficiency in the use of statistical and quality engineering tools such as exploratory data analysis, basic statistics, Gage R&R, Analysis of Variance, Failure Modes and Effects Analysis, Statistical Process Control and Capability, acceptance sampling, correlation and regression, and experimental design Excellent verbal and written communication skills Proficient in MS Office (Word, Excel, PowerPoint, Access) and writing/using data queries, extracts and analysis Skills including organization, resilience, collaboration, and curiosity. Work location: Onsite: Columbia, MO Travel: May include up to 5% domestic travel Relocation Assistance: is not authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Supporting Your Well-being Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope. Applicable to US Applicants Only:The expected compensation range for this position is $95,825 - $117,120, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: *************************************************************************************** of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers. Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain *****************. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains. Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly. Solventum Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with the terms.

Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers' toughest challenges. While we continue updating the Solventum Careers Page and applicant materials, some documents may still reflect legacy branding. Please note that all listed roles are Solventum positions, and our Privacy Policy: *************************************************************************************** applies to any personal information you submit. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Job Description: Quality Engineer (Solventum) We are pleased to report that Solventum has successfully completed the sale of its Purification & Filtration (P&F) business to Thermo Fisher Scientific Inc. (Thermo Fischer). This is a significant milestone for the P&F business, allowing for the strategic investment and resources needed to sustain growth and deliver customer solutions. Please note that this position is scheduled to transfer to a local subsidiary of Thermo Fisher in your country. However, the position is in a country where the transfer of employees to Thermo Fisher is delayed until a later date. By joining Solventum during this transitional period, you will be able to work alongside an energized and mission-driven team who is experiencing this transition along with you. Until the transfer is complete, you will be employed by Solventum, and your employment is subject to all applicable terms and conditions as outlined in our employment agreement and company policies The Impact You'll Make in this Role As a Quality Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: Providing product assurance engineering support for commercialized products including specification and design control, change management, risk management, investigations, and continuous improvement. Reviewing and approving IQ/OQ/PQ documents and validation documents to qualify and validate new equipment and processes. Participating in and leading customer audits, ISO 9001 audits, ISO 13485 audits, internal audits, and other activities to identify improvement opportunities. Providing quality assurance and control for products used in FDA regulated industries, including control of incoming materials, review of in-process tests and release tests and device history records. Working with manufacturing engineers and other personnel to solve product quality issues. Leading investigations, corrective action responses, trending and monitoring for nonconforming materials, complaints, and supplier issues. Interacting with Division quality personnel and outside suppliers to ensure product quality and performance. Driving quality improvement using engineering best practice, statistical techniques, and Lean Six Sigma methodologies. Your Skills and Expertise To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications: Bachelor's Degree or higher (completed and verified) from an accredited institution Additional qualifications that could help you succeed even further in this role include: Bachelor's degree or higher in Manufacturing/Industrial Engineering, Chemical Engineering, Mechanical Engineering, Statistics/Mathematics from an accredited institution Three (3) years of engineering experience in a private, public, government or military environment Experience with quality systems such as Quality Manuals, ISO-13485, 21 CFR Part 210, 211 and 820, metrology, calibration, auditing and supplier management Working knowledge of root cause analysis tools and techniques American Society for Quality, Certified Quality Engineer (CQE) certification or willingness to obtain Proficiency in the use of statistical and quality engineering tools such as exploratory data analysis, basic statistics, Gage R&R, Analysis of Variance, Failure Modes and Effects Analysis, Statistical Process Control and Capability, acceptance sampling, correlation and regression, and experimental design Excellent verbal and written communication skills Proficient in MS Office (Word, Excel, PowerPoint, Access) and writing/using data queries, extracts and analysis Skills including organization, resilience, collaboration, and curiosity. Work location: Onsite: Columbia, MO Travel: May include up to 5% domestic travel Relocation Assistance: is not authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Supporting Your Well-being Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope. Applicable to US Applicants Only:The expected compensation range for this position is $95,825 - $117,120, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: *************************************************************************************** of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers. Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain *****************. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains. Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly. Solventum Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with the terms.

Job Title: Quality Area Lead - 3rd Shift Hours: M-F 12:00AM to 08:30AM; Training will be held on day shift Pay: $34.91/hour + Shift Differential ($6.28/hr) while working nights TYPE: HOURLY Minimum Education and Experience: College Bachelor's degree preferred Minimum 3 years related work experience, preferably in a quality environment General Scope of Position: The Quality Lead role will have ownership of the performance of quality throughout the LIV area. They are required to lead autonomously, motivate and develop their team. This role is the business facing lead for the area, ensuring partnership across End to End Supply Chain operations. Job Skills/Tasks: Essential Functions: Accountable for performance of the following: Safety 100% completion of risk assessments, SQC audits, SBO's for direct reports. World class execution of 5S and GMP within their area. Team's execution to the f-tag program. Quality Lead Quality Technicians Report and review E-Incidents to suppliers Participate in Internal Auidt program Investigate MQI's with a cross functional team to prevent reoccurrence Communicate holds to planning Manage the rework area and instructions Utilizes SAP QM and Unilever specifications including PLM and JDA TNT system and support verification of use for quality purposes. Ensure all Area equipment validations are completed using IQ, OQ, PQ. Calibrations of all department equipment Owner of SOP and work instruction for Area to ensure updated regularly. Supports effort to complete and maintain internal and external audits and certifications. Responsible of traceability compliance and auditing to ensure compliance e.g includes annual mock recall exercises. Ensures proper onboarding of new hires in department. Oversee Cleaning and Disinfection execution on shift. Supports and participates in Quality Pillar activities for UMS program. Drives quality focused improvement activities, reducing quality losses. Utilizes advanced knowledge of category and technology details and requirements to support site innovation and changes. Supports the quality Digital agenda. Ensure all supply's are ordered in a timely manner. All other duties as assigned. Productivity Glidepath with area plan as well as overall factory plan. Build strategic plan to execution targets for their department and program. Utilization of shift handover checklist to ensure seamless communication across shifts. Participation in daily Planning meeting to ensure alignment to area strategy. Cost/Labor Manage area labor to budget. Complete department payroll Data Integrity Understand all quality data entry, and reporting. Ability to coach others on proper usage. Competencies: Skills Required: Ability to develop leaders. Strong sense of self-accountability and thrives in an autonomous environment. Flexible work schedule to ensure support across their teams of varying shifts. Verified and demonstrated technical skills in manufacturing operations. Proficient in Microsoft Office. Planning Understand and utilize data to drive decisions and align resources. Lead discussions and decision making. Manage multiple workstreams simultaneously. Leadership Ability to gain buy-in and motivate their area team as well as cross-functional team members. Execute performance escalation standards. Teamwork One Team mindset. Bias for Action. Drives for solutions. Personal Protective Equipment: Refer to department specific PPE assessment Promotional Progression: (List and Describe) This is a developmental role that could lead to increasing leadership within Unilever. In this role you will be challenged to develop your area leadership team and ensure performance across all shifts. This position will require thorough knowledge of the operations environment and experience developing teams. Why work for Unilever | Culture for Growth | Every Voice Matters | Global Reach | Strategy | Unilever | Unilever Global Website | Employment is subject to verification of pre-screening tests, which may include drug screening, physical and background check. *Any coverages for health insurance and retirement benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents #TER123 ------------------------------------ At Unilever, inclusion is at the heart of everything we do. We welcome applicants from all walks of life and are committed to creating an environment where everyone can thrive/succeed. All applicants will receive fair and respectful consideration, and we actively support the growth and development of every employee. Unilever is an Equal Opportunity Employer/Protected Veterans/Persons with Disabilities. For more information on your federal rights, please see Know Your Rights: Workplace Discrimination is Illegal Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check. If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at NA.Accommodations@unilever.com. Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment. #LI-DNP

ESSENTIAL DUTIES & RESPONSIBILITIES: include the following. Other duties may be assigned. Inspect product and processes at various stages of production process. Ensures continuous production of products is consistent with established standards by performing the following duties. 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Ensures that all incoming raw materials and packaging are inspected and meet specifications. • Samples raw materials to ensure inbound ingredients are in specification. • Pulls samples for retention program. • Conduct daily food safety audits in the facility to ensure GMP's are being adhered to and report deficiencies to QA Manager. • Conducts inspections and completes and/or verifies documentation required by our SQF program. • Conduct daily quality audits in the warehouse area to ensure compliance of storage requirements. • Conducts daily audits to ensure the facility complies with all FDA requirements. • Verify temperature and record keeping for the inbound refrigeration trailers. • Maintain accurate data files and track retention program. • Report findings and recommendations to key personnel as necessary. • Perform other duties as specified by QA Manager. • Perform related duties as assigned by supervisor. • Maintain compliance with all company policies and procedures. PROMOTE: • Safety & Quality per Parker expectations • Teamwork with all departments & staff • Red Zone support & accuracy • Chain of Command • Setting a good example • Following direction • Problem solving in a timely manner. Requirements Physical Requirements: • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions • 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 frequently required to stand; walk; use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; talk or hear; and taste or smell. The employee is occasionally required to sit. The employee must occasionally lift and/or move up to 50 pounds. • The work environment characteristics described here are representative of those an employee encounters while performing 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 frequently works near moving mechanical parts and is frequently exposed to extreme cold and extreme heat. The employee is occasionally exposed to wet and/or humid conditions and vibration. The noise level in the work environment is usually loud. • Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards Education and/or Work Experience Requirements: • High School graduate and limited experience in a production facility or 2 + years of experience working in a FDA food plant. Preferred: HACCP certified and / or SQF Certified. • Have the ability to read and interpret documents in English such as safety rules, operating and maintenance instructions, and procedure manuals. Have the ability to write routine reports and correspondence in English. Bi-lingual preferred. • Have the ability to work with mathematical concepts such as probability and statistical inference. • Have the ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. • Have the ability to enter and interpret data on Microsoft Excel and Microsoft Word documents • Have the ability to apply commonsense understanding to carry out instructions furnished in written, oral, or diagram form. • Excellent verbal and written communication skills, including ability to effectively communicate with internal and external customers Salary Description start 23.65 per hour full 23.90 per hour

American Plastics, headquartered in St. Louis, Missouri, is a leading designer and manufacturer of innovative plastic-injection molded products for the household & garage storage and commercial cleaning end-markets. We are searching for a Process Technician for our Jefferson City, MO location. This position will report to the Production Manager. Responsibilities Monitor and maintain standard cycle times and part quality Be able to understand and communicate the information provided within the job packet pertaining to specification sheet, standard routing, B.O.M.'s, scrap reports and quality requirements Be able to identify all resins used in molding operation including regrind and the associated usage percentage Must understand and operate the operator interface ‘CRT' screen on computer-controlled presses, including all screens required to control the process Must be able to establish a new process, do mold sets, Robot Programming and start a machine based upon settings in Mold Books/QR Code. Demonstrate a basic knowledge and understanding of hot runner systems, Valve Gates, and standard sprue molds Trouble shoot issues on Injection Molding machines and Robots. Other duties as assigned by Management Fixed Schedule: All (4) shifts A, B, C, D are scheduled on a 2/2/3. This schedule gives you a 3-day weekend every other week! The schedule pattern consists of four 12-Hour shifts who work two days in a row, get two days off and then work another three days, which results in only 14 working days each month! Requirements At least 18 years of age Eligible to work in the United States of America Pass a Pre-Employment Drug Screen & Authorize Background Check Must be able to work a 12-Hour Shift Knowledge of operating the following Injection molding machines a must, such as: Engel, Milacron, Battenfeld, UBE and HPM's Knowledge with Wittman and Servpro Robots preferred. Organized, detail oriented, team player with a sense of urgency Resourceful, with ability to apply critical problem-solving skills Effective Communication Skills Applicant must have 2 plus years' experience as a process tech in injection molding or similar process Follow departmental documentation procedures 5S and Lock Out Tag Out experience preferred Benefits: If you are interested in joining the American Plastics team and want to work in a fast-paced, progressive environment, we want to hear from you. We offer a competitive salary, full benefit package including medical/dental, 401k, and paid vacation.

QUALITY CONTROL TECHNICIAN (3rd Shift) By joining the Morris Packaging team, you will become part of one of the most exciting teams in the packaging industry. If you are looking for a great career that provides job satisfaction and professional advancement with a company that values YOU, join our team today! Our Quality Control Techs start out at $23/hour ($21/hour and $2 shift differential) plus comprehensive benefits! The Quality Control Technician position is an 8-hour shift Monday through Friday (10:30pm-6:30am) working in our state of the art, climate-controlled facility, with the opportunity for voluntary overtime and, at times, may require overtime beyond the normal workday. As a Quality Control technician, you will be responsible for ensuring compliance with implementing Morris Packaging's and customers quality standards, following quality control best practices, providing guidance, adhering to quality control policies, actively participating in resolving production and customer issues and offering support to all areas of production, safely, efficiently and accurately. Morris Packaging provides on-site training and certification, to support your success. Job duties Include: Monitor product quality of each department. Ensure deficiencies are caught and corrected. Report quality deficiencies and communicate those deficiencies to operators, department & shift leads, shift supervisors and other quality control technicians. Flag, document and quarantine defective material. This includes moving defective products to the designated area and ensuring all nonconforming material is tracked to the origination point of defect and recorded. Ability to take direction and follow the shift supervisor and/or shift lead requests. Maintain housekeeping standards and always work safely. Responsible for banding materials to pallet to ensure safety when moved. Ability to run the laboratory equipment as needed for testing. This includes computers, COF tester, micrometer, gloss meter, tear tester and all other in-house quality control equipment. Maintain positive working relationships with team members, production staff and visiting customers and suppliers. Conduct department cleaning procedures. Support training of quality control technicians. Required Qualifications: High School diploma or equivalent. Must be able to read standard measuring tape (imperial or metric). Ability to maintain, understand and follow quality, safety and SQF standards, policies and procedures. Ability to read and write English. Ability to communicate clearly with team members and production staff. Ability to understand and read a tape measure. Ability to differentiate between colors. Ability to prioritize and manage multiple tasks. Ability to receive, track and distribute materials, supplies and equipment. Ability to complete routine quality paperwork. Ability to read, sort, check, count and verify numbers. Ability to perform simple arithmetic. Manufacturing experience preferred. Work Environment: While performing the duties of this job, the employee will be primarily in our climate-controlled facility. The plant floor is subject to vibration and equipment noise leading to a loud environment. The employee is frequently exposed to moving mechanical parts and might also be exposed to outside conditions, tight spaces, cleaning solvents and heights. There is a moderate to high demand for tight deadlines. This position will experience moderate interruption in workflow, starting and stopping for product changeovers. Physical Demands: The physical demands here are representative of those that must be met by employees to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk and listen. The employee is required to see color variance between products, perform tasks requiring manual dexterity, stand for extended periods of time and walk extended distances. While performing the duties of this job: Continuous (6 or more hours per day) working at a computer terminal. Continuous (6 or more hours per day) standing and walking. Continuous (6 or more hours per day) talking, teaching and repetitive motion, hand/wrist movement. Intermittent (1 to 2 hours per day) bending, pushing, pulling, reaching, lifting, and grasping. Ability to move and lift objects, frequently 20-75 lbs. Ability to use lifting equipment. Good eyesight, normal hearing. Position Type/Expected Hours of Work: This is a full-time position. Days, nights and hours may vary depending on assigned shift and productions requirements. This position may require significant work hours beyond the normal workday based on the demands of the business cycle or customer volume of business. Morris Packaging offers a comprehensive benefits package to provide the protection you need today and in the future. Benefits may include but are subject to change: time off plans, medical coverages, bonus programs, disability coverages, company paid & voluntary life insurance, 401K plans with company match, & HSA contributions (when applicable). Equal Opportunity/ Affirmative Action Employer

Work Eligibility: Must be a U.S. Citizen or a permanent lawful resident of the U.S. Plans and directs activities concerned with the development, application, and maintenance of quality standards for processes, materials, and products. Assists quality personnel with daily quality requirements for production and provide support to other departments as required on quality issues. Preferred Educational Experience: Bachelors degree in Engineering field or equivalent work experience. Preferred Work Experience: Minimum of six (6) years experience in quality and manufacturing. Auditing experience preferred. Essential Functions: Ability to perform all safety critical functions. The product must be built to the designated specs approved and can not be deviated or substituted. The control, performance and tolerance are essential for the part to function so that it does not jeopardize public safety or it's compliance with government regulations. Must be able to recognize and call the critical characteristic symbols as listed on the blueprints. Develop and implement methods and standards of inspection, testing, and evaluation to meet customer requirements during the APQP process. Establish and maintain programs to evaluate the precision and accuracy of production, measuring, and test equipment (gage calibration) utilizing measurement system analysis process. Assist Purchasing with a qualified vendor base and work with them to ensure proper control/change process is followed. Devise sampling procedures and related forms / instructions for recording, evaluating, and reporting quality and reliability data. Performs Gauge R &Rs Perform SPC Analysis Assist the production teams on issues related to corrective and preventive actions. Participate on new product development teams to insure a smooth transition of new products to the manufacturing floor and completion of all quality documentation. Develop and implement methods and procedures for disposition of discrepant material. Provides assistance with customer quotations by evaluating quality specifications. Support Sales through customer visits on product quality issues required. Assist Purchasing in the development of a qualified vendor base and work with them to resolve quality issues. Go on technical reviews with customers. Interpret customer specific specifications-ID Critical characteristics, working knowledge of APQP. Understand PPAP requirements to customers and knowledge of SPC. Understand PFMEA control plans and process flow. MRB Delegation and Authority/Disposition Demonstrated working knowledge of AIAG Core Tools Follow all 6S & Safety Guidelines Safety Sort Straighten Scrub Standardize Sustain Non Essential Functions: Organize and implement quality audits, including resolution of non-conformance's. Supervise quality personnel as required by Quality Manager. Performs other duties as assigned. Understand zero PPM and zero defects. Project Timing Charts Qualifications and Desired Skills Organizational management skills Communications skills Work well with others Office equipment Computer skills Problem solving Analytical skills Time management Physical Requirements: Data entry 80% of the time sitting Some bending/stooping Lifting less than 35lbs Climate controlled environment Color perception and vision requirements AAP/EEO Statement: It is the policy of Orscheln Products to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law.

Purpose of the Role Responsible for ensuring production runs smoothly and generates a consistently suitable output of products that meet the quality and efficiency standards of ISO 9001. The individual understands the customer's needs and requirements and coordinates employee efforts and communications between management, engineering, and the production teams. Key Responsibilities and Duties Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams. Devising ways to improve the manufacturing process to ensure higher-quality goods. Devising, improving, and reviewing new specifications and procedures for products or processes, and training staff to use them. Setting the requirements for raw materials from suppliers and monitoring their compliance with company policies. Ensuring legal obligations are followed and ensuring compliance with regulatory bodies and with health and safety guidelines. Overseeing product development procedures to identify any deviations from quality standards. Inspecting the final output, comparing it to the requirements, and approving or rejecting the final products. Developing a comprehensive Quality Management System (QMS) in accordance with ISO 9001 Keeping accurate documentation and performing statistical analysis for the QMS. Requirements Required Competencies Education: Bachelor's degree in science or business-based programs or relevant experience Experience: Previous experience in production or manufacturing Skills Strong attention to detail, observation, organizational, and leadership skills. In-depth knowledge of quality control procedures and legal standards. Strong knowledge of mathematics, data analysis, and statistical methods. Excellent communication and listening skills. Good technical and IT skills.

's Quality Engineering & Assurance Team** Our Quality Engineering & Assurance team is the innovative engine at our company. We are a dedicated group of builders and problem-solvers responsible for the most critical, customer-facing platforms. Within this team, the Quality practice is not a downstream function but a fully integrated partner in development. Our mission is to embed quality into every stage of the lifecycle, and as a Quality Engineer, you will be on the front lines of this effort. **Position Overview** Are you a driven Quality Engineer passionate about building the future of testing? We are seeking a creative and hands-on QE to be a key contributor to our quality practice. This is an exciting opportunity to move beyond traditional QA and dive into the world of AI-driven testing, helping us build and maintain robust quality standards for our mission-critical intelligent applications that are redefining customer interaction. **Key Responsibilities** + Design, develop, and maintain test automation frameworks using Java and Python. Write clean, efficient, and scalable automation scripts for new features to ensure robust test coverage across all deliverables. + Perform API testing: Understand API concepts, develop and execute functional tests, interpret Swagger YAML files, and validate endpoints using Postman or Rest Assured automation frameworks. + Conduct database testing: Write and execute SQL queries to retrieve, update, and delete data, ensuring database integrity and reliability. + Own quality for assigned features and components: Collaborate with product managers and developers on requirements analysis, create detailed test cases, execute comprehensive test suites (functional, integration, regression), and provide final quality sign-off. + Track and report testing progress: Use tools such as JIRA, ADO, or ALM for defect logging and reporting, ensuring transparency of feature quality to the team and stakeholders. Also understanding of CI/CD concepts. + Implement and execute test plans for AI/ML applications: Support QA activities and certify the quality of AI-powered systems, including hands-on testing of chatbots for intent recognition, conversational flow, response accuracy, and edge case handling. + Leverage modern AI tools to enhance workflow: Utilize AI code assistants like GitHub Copilot to accelerate test script development and explore generative AI for tasks such as test data creation and bug report summarization. + Ensure AI reliability and fairness: Execute test cases to identify issues related to bias, fairness, and model robustness, contributing to the overall trustworthiness of AI systems. + Develop and maintain test automation scripts and frameworks using Java and Python. + Have proficiency with test and defect management tools, particularly JIRA or any similar tools. **Required Skills & Qualifications** + Bachelor's or Master's degree in Computer Science, Engineering, or a related technical field, or equivalent practical experience. + 0 - 1 years of professional experience in a Quality Assurance or Quality Engineering role. + Some hands-on experience developing and maintaining test automation scripts and frameworks using Java and Python. + Basic understanding of the Software Testing Life Cycle (STLC) and practical experience working in an Agile/Scrum environment. + A keen interest in or prior experience testing AI-powered applications, such as chatbots or other AI/ML-based systems. + Hands-on experience with the Hybrid Automation frameworks. + Familiarity with CI/CD concepts and tools (e.g., Jenkins, GitLab, GitHub Actions). + Exposure to performance testing tools (e.g., JMeter, Gatling). + Basic knowledge of cloud platforms (AWS, Azure, or GCP) and containerization (Docker) + A passion for learning and staying up to date with the latest trends in AI and software testing. **Location** New hires will be hired to the Cognizant office in **Plano, TX** , where you will work alongside other experienced Cognizant associates delivering technology solutions. Applicants must be willing to relocate to this major geographic area. While we attempt to honor candidate location preferences, business needs and position availability will determine final location assignment. **Start Date** New hires will start in **January 2026** . While we will attempt to honor candidate start date preferences, business need and position availability will determine final start date assignment. Exact start date will be communicated with enough time for you to plan effectively. **Salary and Other Compensation:** Applications are accepted on an ongoing basis. The annual salary for this position is $65,000.00 depending on experience and other qualifications of the successful candidate. This position is also eligible for Cognizant's discretionary annual incentive program, based on performance and subject to the terms of Cognizant's applicable plans. **Why Choose Us?** Cognizant delivers solutions that draw upon the full power and scale of our associates. You will be supported by high-caliber experts and employ some of the most advanced and patented capabilities. Our associate's diverse backgrounds offer multifaceted perspectives and fuel new ways of thinking. We encourage lively discussions which inspire better results for our clients. **Benefits** Cognizant offers the following benefits for this position, subject to applicable eligibility requirements: + Medical/Dental/Vision/Life Insurance + Paid holidays plus Paid Time Off + 401(k) plan and contributions + Long-term/Short-term Disability + Paid Parental Leave + Employee Stock Purchase Plan **Disclaimer** The hourly rate, other compensation, and benefits information is accurate as of the date of this posting. Cognizant reserves the right to modify this information at any time, subject to applicable law. **Work Authorization** Due to the nature of this position, Cognizant cannot provide sponsorship for U.S. work authorization (including participation in a CPT/OPT program) for this role. _Cognizant is always looking for top talent. We are searching for candidates to fill future needs within the business. This job posting represents potential future employment opportunities with Cognizant. Although the position is not currently available, we want to provide you with the opportunity to express your interest in future employment opportunities with Cognizant. If a job opportunity that you may be qualified for becomes available in the future, we will notify you. At that time you can determine whether you would like to apply for the specific open position. Thank you for your interest in Cognizant career opportunities._ Cognizant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

Job DescriptionDescription: ThermAvant Technologies is seeking a full-time Manufacturing "Braze" Technician to join our growing Braze department. As a key member of our team, you will help develop and enhance our braze process and play an essential role in processing production parts through braze ovens. This position offers an exciting opportunity to contribute to a dynamic, fast-paced environment. Key Responsibilities: Prepare, instrument, and load parts into fixtures and braze ovens based on the provided production schedule. Perform quality checks during the braze process, including part dimensions, cleanliness, fit-up, and braze quality. Conduct routine maintenance on braze ovens and associated equipment. Identify process trends and nonconformities, providing feedback for continuous improvement. Assist in preparing metallurgical samples from the brazing process for analysis. Help achieve and maintain certifications and qualifications for all equipment and processes. Contribute to the establishment and preservation of documented procedures. Maintain up-to-date knowledge of brazing specifications relevant to the job function. Ensure attention to detail and quality while meeting production deadlines. Promote and maintain a safe and clean working environment. Participate in inspections, audits, and the resolution of non-conformities. Properly use shop tools, hand tools, and equipment required for brazing operations. Collaborate with others to maintain a positive and efficient team environment. Complete additional tasks as required or requested. Requirements: Able to pass a background check High school diploma or equivalent, or 2+ years of relevant experience. Ability to read and interpret mechanical drawings and schematics. Familiarity with quality management systems such as AS9100 and ISO 9001:2008 a plus. Proficiency with basic computer applications (Word, Excel, email) and strong communication skills (both written and verbal). Exceptional attention to detail and manual dexterity. Ability to handle heavy materials (>50 lbs) when necessary. Experience with material handling equipment (overhead cranes, tow-motors, pallet jacks) is a plus. Experience with high-temperature ovens, brazing ovens, or clean room environments is a plus. Special Working Conditions/Job Characteristics: Full-time position (40 hours per week, Monday through Friday). Willingness to work overtime as needed. Physical ability to lift up to 50 pounds regularly. Experience with CNC machines, programming, or high-temperature ovens (e.g., braze or autoclave) is a plus. Benefits: 100% company-paid dental, vision, and health insurance. Paid holidays and paid time off. Why Join Us? If you have a strong attention to detail and a passion for quality manufacturing, we invite you to apply for this rewarding role. Join a company that values innovation, teamwork, and safety while providing opportunities for professional growth and development.