Quality engineer jobs in Topeka, KS - 81 jobs

Job Purpose Provide quality assurance, food safety, employee safety, and regulatory leadership to the facility by ensuring quality systems are communicated, implemented, and sustained. Ensure products, systems, and programs are consistent and meet both internal and external requirements. Essential Functions Oversee food safety program, quality standards, and legality of products manufactured in the facility Maintain the facility GFSI audit standard Ensure compliance with quality policies, procedures, cGMPs, and product specifications Preserve the integrity of the GFSI and facility quality systems through enforcement of the policies and procedures outlined in the quality/food safety manual Oversee Food Safety and HACCP teams, ensuring changes are reviewed in the facility as introduced and potential risks identified Monitor quality metrics and key performance indicators and recommend changes to meet standards Maintain and update the recall program, acting as the recall team leader Facilitate customer complaint process and plant deviation investigations, as well as implement corrective actions for continuous improvement Maintain supplier records ensuring compliance with regulations and guidelines Manage the facility's internal auditing program and verification and validation activities to ensure finished product meets established company quality and food safety standards Oversee the non-conforming product program for the facility, as well as implement corrective actions for continuous improvement Participate in new product development and commercialization process, reviewing all quality and food safety changes as they occur Oversee the development, implementation, and maintenance of the environmental, health, and safety (EHS) programs in the facility, e.g., safety manual, safety committee, safety auditing, etc. Preserve the integrity of the EHS system through enforcement of the policies and procedures outlined in the safety manual; re-evaluate programs and procedures comprising the safety manual whenever process or facility changes are made Evaluate and participate in employee accident investigations to ensure thorough root cause analysis is conducted; implement and ensure corrective actions are completed Review facility accident statistics, monitor trends, and provide recommendations on prevention strategies Provide guidance to the plant team on OSHA regulations Schedule, conduct, and oversee internal and external audits of the Quality, Food Safety, and EHS systems in the facility including all local, state, and federal regulatory agencies Maintain kosher program and other certifications (RSPO, Organic, Non-GMO) as required Ensure employees are trained adequately on food safety, GFSI, quality assurance concepts, regulatory requirements, and employee safety Prepare and manage departmental budgets Interview, select, and train quality and supervisory employees Directly manage QA Supervisor, Sanitation/Safety Supervisor, and QA administration (others as necessary) Keep apprised of industry best practices and developments in federal, state, and local regulations that impact facility quality, food safety, and EHS systems Perform other job-related duties as assigned Qualifications (Education/Experience) Bachelor's degree in Food Science or related degree preferred HACCP, PCQI, and OSHA certification preferred Minimum 5 years of progressive and demonstrated quality assurance and food safety management leadership experience in the food industry or manufacturing industry Proficient knowledge in food safety programs and systems: GFSI (BRC or SQF preferred), internal auditing, cGMPs, HACCP, FSMA, Sanitation Experience leading regulatory inspections Proven fiscal responsibility (financial planning, budgeting, financial analysis, variance reporting, etc.) Strong computer skills including experience with ERP systems and Microsoft Office Excellent skills in the areas of teamwork, motivation, decision making, relationship building, and coaching Strong verbal and written communication skills Ability to think critically and solve complex problems Ability to organize, manage multiple priorities, and maintain high attention to detail in a fast-paced environment RISE123 MON123

Science you can trust from concept to consumer. Since 1967, Deibel Laboratories has operated several private food testing facilities providing services in both Microbiology and Chemistry testing. We play an integral role in food and product safety for industry-leading producers, as well as family-run operations much like our own. Our lab location in Manhattan, KS is hiring a full-time Quality Manager. (40 hours/week plus benefits included). We offer a competitive salary based on knowledge and experience. This position includes full health benefits for self and family (employer pays for 90% of employee premiums and 50% of dependents on our base plan). Deibel also offers a self-funded dental plan, vision plan, and 401K option along with profit sharing. Check out our website to learn more about what we do at ******************* Compensation : $22 - $24 Hourly D.O.E. plus a competitive benefits package. Schedule: Sunday - Thursday from 9am - 5:30pm(Close) Required Skills/Abilities: The Quality Manager handles the “day to day” quality systems at the laboratory and trains lab staff on Quality SOPs, assigns certain tasks to lab Associates, and verifies conformance to the written program. This individual is ultimately in charge of implementing and maintaining the Quality Management System (QMS) at the site laboratory, for PM, QM, QC and Procedural SOPs. This individual will report to the Director of Quality. Responsible for the initial implementation and ongoing maintenance of new/existing Procedures or Accreditations within our Labs. Responsible for making the site Lab Manager, and the Director of Quality aware of any Non-Conformance incidents. Responsible for the day-to-day Quality activities, or for reviewing Quality Forms for compliancy to our written program. Responsible for day-to-day laboratory activities, where needed, to ensure client result quality and reliability are maintained. Education and Experience: Bachelor of Science, or similar is preferred 1-5 years of experience in a related compliancy field, such as ISO, Pharmaceutical or similarly (highly) regulated industry is preferred. Proficient in Microsoft Office Suite or related software. Physical Requirements: Occasional exposure to laboratory fumes, chemicals, and materials will occur when in the laboratory. Safety equipment of gloves, laboratory coat, and eyeglasses may need to be worn depending on the testing process. Extended time spent in a standing position. Ability to lift up to 50lbs occasionally and 10 - 15lbs repeatedly. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Deibel is committed to fostering a diverse and welcoming workplace with people of all types of backgrounds and experiences. SERVICE - QUALITY - TRANSPARENCY - PARTNERSHIP - EDUCATION - PROFESSIONALISM

Job Description McFarlane is a rapidly growing 50+ years old aviation firm that focuses on the design and manufacture of high-quality aircraft parts within the general aviation and commercial marketplace. We believe in providing better parts with superior “old-school” customer service. When you join the McFarlane team, you'll join a dedicated group of colleagues passionate about aviation, community, and the McFarlane way. Position Description: Quality Inspector How You Will Make an Impact: As a Quality Inspector, you will perform preliminary and in-process inspections of aircraft related components. To excel in this role, applicants should be able to show great attention to detail, possess strong organizational skills, and be able to demonstrate the ability to interpret approved data. When You Will Work: Monday through Friday, full-time position with flexible 1st shift hours. Operational Duties: Perform preliminary, in-process and final dimensions inspections Demonstrate the ability to interpret approved data sch as engineering drawings and specifications. Documenting inspection results by completing logs and reports Communicate with production, engineering and quality team Inspecting aircraft components to verify correct finish, configuration or other measurable or observable characteristics Performing and recording first article inspections in accordance with standards Establish quality standards for products according to company procedures Read blueprints and specifications to ensure that products meet production standards Recommend necessary adjustments and changes to production processes Use instruments such as micrometer screw gauges, CMM and RAM optical to measure products Accept and reject finished products and discuss inspection results with the production team Perform inspections at random to assess product quality Qualifications: Preferred minimum 3 years aerospace manufacturing experience Knowledge of FAA regulatory requirements and processes Experience using handheld measuring and testing devices (e.g.; digital multimeter, caliper, micrometers, radius gages, etc.) Demonstrated ability to use computer programs such as Microsoft office products Must read, write and understand the English language Ability to read and comprehend technical manuals Experience working in a fast pace environment Previous experience using continuous improvement/lean tools such as; Six Sigma, 5-S, Lean Manufacturing, etc. to drive improvement A strong customer-oriented mindset with the ability to adapt and be flexible Ability to work with a team and independently Physical Requirements In this position you must be able to stand and occasionally sit Must be capable of regular, reliable and timely attendance Ability to lift up to 20 to 40 lbs. Excellent visual acuity Working Conditions Clean and climate-controlled facility Safe and casual work environment Non-union environment Education Requirements High School Diploma/GED McFarlane Aviation is an equal opportunity employer committed to fostering an inclusive, innovative environment with the best employees- so we welcome applications from everyone, to celebrate a diverse mix of experiences, backgrounds, and identities. Please get in touch if you'd like to discuss any reasonable adjustments to your application, in order that we can accommodate and support you in the recruitment process. If you want to work for a company where who you are is valued and respected, we'd love to hear from you.

McFarlane is a rapidly growing 50+ years old aviation firm that focuses on the design and manufacture of high-quality aircraft parts within the general aviation and commercial marketplace. We believe in providing better parts with superior “old-school” customer service. When you join the McFarlane team, you'll join a dedicated group of colleagues passionate about aviation, community, and the McFarlane way. Position Description: Quality Inspector How You Will Make an Impact: As a Quality Inspector, you will perform preliminary and in-process inspections of aircraft related components. To excel in this role, applicants should be able to show great attention to detail, possess strong organizational skills, and be able to demonstrate the ability to interpret approved data. When You Will Work: Monday through Friday, full-time position with flexible 1st shift hours. Operational Duties: Perform preliminary, in-process and final dimensions inspections Demonstrate the ability to interpret approved data sch as engineering drawings and specifications. Documenting inspection results by completing logs and reports Communicate with production, engineering and quality team Inspecting aircraft components to verify correct finish, configuration or other measurable or observable characteristics Performing and recording first article inspections in accordance with standards Establish quality standards for products according to company procedures Read blueprints and specifications to ensure that products meet production standards Recommend necessary adjustments and changes to production processes Use instruments such as micrometer screw gauges, CMM and RAM optical to measure products Accept and reject finished products and discuss inspection results with the production team Perform inspections at random to assess product quality Qualifications: Preferred minimum 3 years aerospace manufacturing experience Knowledge of FAA regulatory requirements and processes Experience using handheld measuring and testing devices (e.g.; digital multimeter, caliper, micrometers, radius gages, etc.) Demonstrated ability to use computer programs such as Microsoft office products Must read, write and understand the English language Ability to read and comprehend technical manuals Experience working in a fast pace environment Previous experience using continuous improvement/lean tools such as; Six Sigma, 5-S, Lean Manufacturing, etc. to drive improvement A strong customer-oriented mindset with the ability to adapt and be flexible Ability to work with a team and independently Physical Requirements In this position you must be able to stand and occasionally sit Must be capable of regular, reliable and timely attendance Ability to lift up to 20 to 40 lbs. Excellent visual acuity Working Conditions Clean and climate-controlled facility Safe and casual work environment Non-union environment Education Requirements High School Diploma/GED McFarlane Aviation is an equal opportunity employer committed to fostering an inclusive, innovative environment with the best employees- so we welcome applications from everyone, to celebrate a diverse mix of experiences, backgrounds, and identities. Please get in touch if you'd like to discuss any reasonable adjustments to your application, in order that we can accommodate and support you in the recruitment process. If you want to work for a company where who you are is valued and respected, we'd love to hear from you.

**_What Application Development & Maintenance contributes to Cardinal Health_** Information Technology oversees the effective development, delivery, and operation of computing and information services. This function anticipates, plans, and delivers Information Technology solutions and strategies that enable operations and drive business value. Application Development & Maintenance performs configuration or coding to develop, enhance and sustain the organization's software systems in a cross-functional team environment through adherence to established design control processes and good engineering practices. This job family programs and configures end user applications, systems, databases and websites to achieve the organization's internal needs and externally-facing business needs. Application Development & Maintenance partners with business leaders, investigates user needs and conducts regular assessments, maintenance and enhancements of existing applications. The SAP Software Engineer focused on Data Conversions, Data Quality, and Reporting is responsible for designing, developing, and maintaining data solutions that ensure data integrity and enable effective business intelligence. The role combines technical skills in data migration and ETL processes with an understanding of data governance and reporting tools. **_What is expected of you and others at this level_** + Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects + May contribute to the development of policies and procedures + Works on complex projects of large scope + Develops technical solutions to a wide range of difficult problems + Solutions are innovative and consistent with organization objectives + Completes work; independently receives general guidance on new projects + Work reviewed for purpose of meeting objectives + May act as a mentor to less experienced colleagues **_Responsibilities_** + Design and execute data conversion strategies for SAP implementations and upgrades, including data extraction, transformation, and loading (ETL) from legacy systems into SAP. + Utilize SAP data migration tools such as SAP Data Services, LSMW, and Migration Cockpit to perform data loads and conversions. + Develop and maintain technical specifications, data mapping documents, and transformation rules. + Collaborate with business and technical teams to gather data requirements and ensure seamless data flow across systems. + Establish and maintain data quality frameworks to ensure the accuracy, consistency, and integrity of master and transactional data in SAP. + Perform data profiling, cleansing, and validation to identify and resolve data discrepancies before and after migration. + Define and monitor data quality metrics and key performance indicators (KPIs). + Work with business data stewards to correct data quality issues and promote data governance policies and standards. + Design, develop, and implement reporting solutions, dashboards, and analytical models using SAP technologies like SAP Analytics Cloud (SAC), SAP BW/4HANA, or SAP Fiori. + Translate business needs into technical specifications for reports and ad-hoc queries. + Optimize report performance and data extraction processes for efficiency. + Provide support and training to end-users on reporting tools to enable data-driven decision-making **_Qualifications_** + Bachelor's Degree in related field preferred or equivalent work experience preferred + Proven experience in SAP Data Conversions, migrations and ETL processes. + Proficiency with SAP data tools such as SAP Data Services, SAP BW/HANA or SAP Analytics Cloud + Strong knowledge of SQL, data modelling and database concepts + Experience with SAP modules and data structures (e.g., Master Data, Financials, Supply Chain, OTC, PTP processes). + Excellent analytical, problem solving and communication skills + Ability to work both independently and collaboratively with cross-functional teams **Anticipated salary range:** $94,900 - $135,600 **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 01/20/2026 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

Last date to apply: We are continuously accepting applications Are you a seasoned Supplier Development Engineer/Supplier Quality Engineer with a solid background in quality assurance within a manufacturing setting, ideally in the heavy equipment industry? Husqvarna Construction is a part of Husqvarna AB. We are a world leader in the construction and stone industries. Our extensive construction product range includes machines, diamond tools and all accessories that you need for cutting, sawing and drilling, as well as polishing floors. We are located in Olathe, Kansas. Check us out at ********************************** We are looking for a candidate with demonstrated expertise in supplier development engineering to join our team in Olathe, KS. As our Supplier Quality Engineer, you will play a critical role in ensuring that all purchased materials meet our rigorous quality standards. Your work will support the success of our Olathe assembly facility by driving quality assurance from established suppliers and cultivating new supplier relationships that align with our production goals. What You'll Do: Process Assurance * Collaborate with new product development teams to provide supplier quality planning and risk assessment. * Define Advanced Part Quality Planning (APQP) requirements for new parts and oversee supplier APQP processes, including Production Part Approval Process (PPAP). * Actively participate in project meetings, engineering reviews, and manufacturing pilots to ensure quality standards are maintained from design to production. Supplier Qualification & Development * Partner with Sourcing to assess, select, and improve supplier performance to meet our quality benchmarks. * Conduct comprehensive Supplier Quality Audits, implement corrective actions, and educate suppliers on our quality assurance standards and best practices. Quality Deviation Management * Oversee the disposition and cost recovery of non-conforming materials, working closely with Quality Control on fault classification and escalation. * Develop and implement incoming inspection plans and facilitate root cause analysis and corrective actions (8D), ensuring effective solutions are validated. * Report key quality metrics, including PPM (Parts Per Million) reject rates and quality issues, to the Global Supplier Quality Engineering (SQE) Manager. Continuous Improvement Initiatives * Contribute to product and process improvement by identifying supplier quality risks and recommending preventive actions. * Partner with design teams to enhance component manufacturability and quality, aligning with best practices for continuous improvement. Key Skills and Knowledge: * Solid expertise in supplier quality assurance, auditing practices, and quality management systems. * Proficient in MS Office and familiar with measurement systems, assembly procedures, and mechanical drawings. * Practical knowledge of machinery operation, quality auditing, and improvement tools. Qualifications: * Bachelor's degree required, with 3-5 years of relevant experience in manufacturing or purchasing. * Certified Supplier Quality Professional (ASQ) preferred. Working Conditions: * Exposure to diverse manufacturing environments and approximately 20% travel, primarily local/domestic (within 3 hours). We Offer: * A competitive salary. * A full benefits package, including medical/dental/vision insurance, at date of hire. * A 401(k) with matching and no vesting. * An employee purchase discount on Husqvarna products. * An education assistance program. * Paid parental leave. * . . . and more! If you're passionate about elevating supplier quality and have a track record of success in manufacturing environments, especially within the heavy equipment industry, we want to hear from you. Join us in driving excellence in supplier quality to support the continued success of our Olathe assembly facility! Husqvarna is an Equal Employment Opportunity employer committed to providing equal opportunity in all of our employment practices, including selection, hiring, assignment, re-assignment, promotion, transfer, compensation, discipline and termination. Husqvarna prohibits discrimination, harassment and retaliation in employment based on race; color; religion; national origin; gender; sexual orientation; pregnancy; age; disability; service member status; or any other category protected by federal, state, or local law.

Last date to apply: We are continuously accepting applications Are you a seasoned Supplier Development Engineer/Supplier Quality Engineer with a solid background in quality assurance within a manufacturing setting, ideally in the heavy equipment industry? Husqvarna Construction is a part of Husqvarna AB. We are a world leader in the construction and stone industries. Our extensive construction product range includes machines, diamond tools and all accessories that you need for cutting, sawing and drilling, as well as polishing floors. We are located in Olathe, Kansas. Check us out at ********************************** We are looking for a candidate with demonstrated expertise in supplier development engineering to join our team in Olathe, KS. As our Supplier Quality Engineer, you will play a critical role in ensuring that all purchased materials meet our rigorous quality standards. Your work will support the success of our Olathe assembly facility by driving quality assurance from established suppliers and cultivating new supplier relationships that align with our production goals. What You'll Do: Process Assurance Collaborate with new product development teams to provide supplier quality planning and risk assessment. Define Advanced Part Quality Planning (APQP) requirements for new parts and oversee supplier APQP processes, including Production Part Approval Process (PPAP). Actively participate in project meetings, engineering reviews, and manufacturing pilots to ensure quality standards are maintained from design to production. Supplier Qualification & Development Partner with Sourcing to assess, select, and improve supplier performance to meet our quality benchmarks. Conduct comprehensive Supplier Quality Audits, implement corrective actions, and educate suppliers on our quality assurance standards and best practices. Quality Deviation Management Oversee the disposition and cost recovery of non-conforming materials, working closely with Quality Control on fault classification and escalation. Develop and implement incoming inspection plans and facilitate root cause analysis and corrective actions (8D), ensuring effective solutions are validated. Report key quality metrics, including PPM (Parts Per Million) reject rates and quality issues, to the Global Supplier Quality Engineering (SQE) Manager. Continuous Improvement Initiatives Contribute to product and process improvement by identifying supplier quality risks and recommending preventive actions. Partner with design teams to enhance component manufacturability and quality, aligning with best practices for continuous improvement. Key Skills and Knowledge: Solid expertise in supplier quality assurance, auditing practices, and quality management systems. Proficient in MS Office and familiar with measurement systems, assembly procedures, and mechanical drawings. Practical knowledge of machinery operation, quality auditing, and improvement tools. Qualifications: Bachelor's degree required, with 3-5 years of relevant experience in manufacturing or purchasing. Certified Supplier Quality Professional (ASQ) preferred. Working Conditions: Exposure to diverse manufacturing environments and approximately 20% travel, primarily local/domestic (within 3 hours). We Offer: A competitive salary. A full benefits package, including medical/dental/vision insurance, at date of hire. A 401(k) with matching and no vesting. An employee purchase discount on Husqvarna products. An education assistance program. Paid parental leave. . . . and more! If you're passionate about elevating supplier quality and have a track record of success in manufacturing environments, especially within the heavy equipment industry, we want to hear from you. Join us in driving excellence in supplier quality to support the continued success of our Olathe assembly facility! Husqvarna is an Equal Employment Opportunity employer committed to providing equal opportunity in all of our employment practices, including selection, hiring, assignment, re-assignment, promotion, transfer, compensation, discipline and termination. Husqvarna prohibits discrimination, harassment and retaliation in employment based on race; color; religion; national origin; gender; sexual orientation; pregnancy; age; disability; service member status; or any other category protected by federal, state, or local law.

COME JOIN OUR JOURNEY! When you join TT, you join our global community of visionaries, creators, and achievers dedicated to engineering and manufacturing electronic solutions enabling a safer, healthier and more sustainable world. Simply put, we are a global manufacturer with a passion for engineering advanced electronics that benefit our planet and people for future generations. We are committed to having a positive impact on the world through a culture built around safety, transparency, collaboration, and positive relationships. Our teams are fueled by performance and expertise, leading the charge in innovation, efficiency and delivering world-class customer service. Be part of the journey. Role Overview and Responsibilities This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e., "Green Card Holder"), Political Asylee, or Refugee. Introduction The Quality Technician plays a critical role in maintaining site-wide quality control by managing all non-conforming material, coordinating third-party source inspections, and performing timely inspections on returned goods. This position ensures proper containment and documentation of quality issues, prepares and supports materials for external inspections, and provides quick assessments of returned items to facilitate accurate and timely customer responses. The technician partners closely with Quality, Operations, and Supply Chain to resolve issues, maintain accurate quality records, and uphold all procedural and regulatory requirements. Key Responsibilities Manage and process all non-conforming material, including identification, segregation, documentation, and disposition. Coordinate and facilitate third-party source inspections, ensuring required materials, documentation, and quality records are prepared and available. Perform timely inspections on returned goods (RMA), including visual, mechanical, or dimensional checks to support quick evaluation and customer response. Maintain accurate records for NCRs, source inspections, RMAs, and other quality-related data in accordance with internal procedures. Support material flow by resolving quality holds quickly and escalating issues when needed to prevent delays or quality escapes. Collaborate with Quality Engineers, Operations, and Supply Chain to investigate issues, verify corrective actions, and support continuous improvement activities. Follow established quality procedures, work instructions, and regulatory/ITAR requirements to ensure compliance and audit readiness. Other duties, as assigned or required. Qualifications, Skills and Attributes Core Requirements Exceptional attention to detail with strong observational and analytical skills to identify quality issues accurately and consistently. Proficiency with inspection tools and equipment, including calipers, micrometers, gauges, and other precision measurement instruments. Working knowledge of quality systems and methodologies, such as AS9100, ISO standards, Lean Manufacturing, and root-cause analysis tools. Ability to read and interpret engineering drawings, blueprints, specifications, and technical documentation with a high level of accuracy. Strong communication and interpersonal skills, with the ability to collaborate effectively across Quality, Operations, Engineering, and Supply Chain. Advanced computer proficiency, including Microsoft Office Suite, quality management software (QMS), and data analysis tools within a manufacturing or regulated environment. Ability to perform the essential functions of the job with or without reasonable accommodation, in accordance with ADA requirements. Desireable Skills and Experience High school diploma or equivalent required; additional technical, vocational, or trade school training in quality control, manufacturing, engineering, or a related field strongly preferred. Five or more years of experience in quality inspection, manufacturing, electronics, or a regulated production environment; experience working within AS9100 or aerospace/defense quality systems is highly advantageous. Demonstrated ability to accurately use and read precision measurement tools, including but not limited to calipers, micrometers, feeler gauges, height gauges, and X-ray or other non-destructive inspection equipment. Strong understanding of inspection techniques, non-conformance handling, and documentation requirements in a high-mix, high-reliability manufacturing environment. Competence in interpreting engineering drawings, specifications, and technical data, including GD&T, preferred. Proficiency in computer-based quality systems, including QMS platforms, ERP systems, and Microsoft Office Suite. This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e., "Green Card Holder"), Political Asylee, or Refugee. TT Electronics does not accept any unsolicited resumes from third parties. Any resumes submitted by a third party for this or any other position will not be subject to any recruitment fees if hired. Solving Technology Challenges for a Sustainable World We want the very best people in our TT family across the globe - so we welcome applications from everyone, to celebrate a diverse mix of experiences, backgrounds and identities. We are committed to equality of opportunity for all and you can rest assured that TT Electronics takes positive steps to ensure we are an inclusive business, that will welcome and support you, from your initial application to wherever your career takes you! Please get in touch if you'd like to discuss any reasonable adjustments to your application, in order that we can accommodate and support you in the process. If you want to work for a company where who you are is valued and respected, we'd love to hear from you. #WeAreTT #BeMeAtTT

As an Advanced Mfg Engineer II here at Honeywell, you will play a crucial role in ensuring the quality and efficiency of our manufacturing operations. You will be responsible for developing and implementing strategies to optimize production processes, driving continuous improvement initiatives, and collaborating with cross-functional teams to achieve operational excellence. With your expertise and leadership, you will contribute to the growth and success of our organization. In this role, you will impact our manufacturing operations by optimizing production processes and driving continuous improvement initiatives. You will contribute to increased efficiency, reduced costs, and improved quality in our manufacturing operations. Your expertise will help us stay at the forefront of advanced manufacturing technologies and ensure that we deliver innovative and high-quality products to our customers. Your contributions will directly impact our bottom line and help us maintain our position as a global technology leader. At Honeywell, our people leaders play a critical role in developing and supporting our employees to help them perform at their best and drive change across the company. Help to build a strong, diverse team by recruiting talent, identifying, and developing successors, driving retention and engagement, and fostering an inclusive culture. YOU MUST HAVE • Bachelor's degree from an accredited institution in a technical discipline such as science, technology, engineering, mathematics • Proven experience in advanced manufacturing, process optimization, and lean manufacturing principles • Strong knowledge of manufacturing technologies, such as automation, robotics, and additive manufacturing WE VALUE • Advanced degrees in Engineering such as EE (Electrical Engineering), ME (Mechanical Engineering) • Experience with data analysis and statistical process control • Excellent problem-solving and decision-making skills • Expertise in implementing advanced manufacturing technologies and processes • Strong project management skills • Able to read technical drawings and documentation (Electronics & Mechanical) • Knowledge of using Six sigma/quality Tools and APQP (PFMEA, Control plan, SPC MSA, etc.) • Familiarity with Pick and place machines for surface mounted technology • AOI/AXI understanding • Knowledge of conformal coating process • Experience with modern circuit card production equipment BENEFITS OF WORKING FOR HONEYWELL In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays .For more Honeywell Benefits information visit: ******************************* The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Posting updated 10/24/2025 Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. citizen, U.S. permanent resident, or have asylum or refugee status in the U.S. Key Responsibilities Lead and oversee advanced manufacturing processes to ensure quality, efficiency, and productivity Develop and implement strategies to optimize production processes and drive continuous improvement Collaborate with crossfunctional teams to identify and implement advanced manufacturing technologies Analyze production data and metrics to identify areas for improvement and implement corrective actions Provide technical expertise and guidance to manufacturing teams Ensure compliance with safety regulations and industry standards Manage and allocate resources effectively to meet production targets

As an Advanced Mfg Engineer II here at Honeywell, you will play a crucial role in ensuring the quality and efficiency of our manufacturing operations. You will be responsible for developing and implementing strategies to optimize production processes, driving continuous improvement initiatives, and collaborating with cross-functional teams to achieve operational excellence. With your expertise and leadership, you will contribute to the growth and success of our organization. In this role, you will impact our manufacturing operations by optimizing production processes and driving continuous improvement initiatives. You will contribute to increased efficiency, reduced costs, and improved quality in our manufacturing operations. Your expertise will help us stay at the forefront of advanced manufacturing technologies and ensure that we deliver innovative and high-quality products to our customers. Your contributions will directly impact our bottom line and help us maintain our position as a global technology leader. At Honeywell, our people leaders play a critical role in developing and supporting our employees to help them perform at their best and drive change across the company. Help to build a strong, diverse team by recruiting talent, identifying, and developing successors, driving retention and engagement, and fostering an inclusive culture. Key Responsibilities * Lead and oversee advanced manufacturing processes to ensure quality, efficiency, and productivity * Develop and implement strategies to optimize production processes and drive continuous improvement * Collaborate with crossfunctional teams to identify and implement advanced manufacturing technologies * Analyze production data and metrics to identify areas for improvement and implement corrective actions * Provide technical expertise and guidance to manufacturing teams * Ensure compliance with safety regulations and industry standards * Manage and allocate resources effectively to meet production targets YOU MUST HAVE * Bachelor's degree from an accredited institution in a technical discipline such as science, technology, engineering, mathematics * Proven experience in advanced manufacturing, process optimization, and lean manufacturing principles * Strong knowledge of manufacturing technologies, such as automation, robotics, and additive manufacturing WE VALUE * Advanced degrees in Engineering such as EE (Electrical Engineering), ME (Mechanical Engineering) * Experience with data analysis and statistical process control * Excellent problem-solving and decision-making skills * Expertise in implementing advanced manufacturing technologies and processes * Strong project management skills * Able to read technical drawings and documentation (Electronics & Mechanical) * Knowledge of using Six sigma/quality Tools and APQP (PFMEA, Control plan, SPC MSA, etc.) * Familiarity with Pick and place machines for surface mounted technology * AOI/AXI understanding * Knowledge of conformal coating process * Experience with modern circuit card production equipment BENEFITS OF WORKING FOR HONEYWELL In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays .For more Honeywell Benefits information visit: ******************************* The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Posting updated 10/24/2025 Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. citizen, U.S. permanent resident, or have asylum or refugee status in the U.S.

At Kalmar, we are moving goods in critical supply chains around the world. As the forerunner in sustainable material handling equipment and services, we set the industry benchmark for a zero-emission future. We are driven by teamwork, innovation, and taking ownership to deliver results. With our global reach and local expertise, our success starts with a strong focus on the customer, ensuring their needs guide our daily work. We are dedicated to respecting others and fostering an inclusive culture where all voices are heard, empowering us to succeed together. With us, your work has an impact. Your work moves the world! Join us and take your career to the next level Purpose of the Position The Industrial Engineer increases production and operational efficiency through people,process, and technology. This role designs, develops, tests, and evaluates integrated systemsthat optimize manufacturing performance, including human factors, quality control,inventory control, logistics, material flow, and cost efficiency. What are your key responsibilities: * Conduct time studies and motion studies to establish standard work and improve * productivity. * Solve quality issues and support root cause analysis to prevent recurrence. * Lead and support major and minor process improvement and capital projects. * Conduct and facilitate kaizen events and continuous improvement initiatives for both production and non-production areas. * Train operations and management personnel on lean tools, process documentation, and problem-solving techniques. * Develop and maintain production standard work documentation. Perform material flow analysis and create PFEP (Plan for Every Part) to optimize logistics * and inventory management. * Design and update production layouts using AutoCAD for optimal space and workflow efficiency. * Utilize CATIA for fixture, lifting device, and ergonomic tooling design. * Perform process and design FMEA to identify and mitigate potential risks. * Support implementation of new technologies, production software, and digital tools to enhance manufacturing capabilities. * Collaborate cross-functionally with engineering, quality, and production to ensure manufacturability and cost efficiency. * Support the development and integration of electrical systems and complex control systems used in modern terminal tractors. * Apply understanding of CANbus systems, wiring, and electrical schematics in troubleshooting and process optimization. * Assist in the introduction and validation of new product configurations and technologieson the production line. * Lead layout and efficiency studies to continuously improve flow, safety, and productivity in manufacturing operations. What we offer you: "People who move together" * Purpose that drives change: You'll have a direct impact on Kalmar's future and contribute to solutions that transform global trade, creating environmental and operational breakthroughs. * Rewards that count: You'll have development opportunities to grow and we prioritise work-life balance, providing flexible working hours and a hybrid work model tailored to meet your needs. * Competitive Benefits: You will have comprehensive healthcare options, matching 401K, performance based annual bonus system, 3 weeks paid time off and 11 holidays. * People who move economies: You'll collaborate with a global team, build strong relationships, solve challenges, celebrate wins, and connect with colleagues and clients in an open, sustainable culture. * Safety that moves us forward: Beyond physical safety, you'll benefit from the stability of a long-standing company, established in the 1940s, offering strong job security and a reliable foundation for your career. What you bring to the role: Education * Bachelor's degree in Industrial Engineering, Manufacturing Engineering, or related field, or equivalent experience. Experience Minimum of 5 years of relevant industrial or manufacturing engineering experience, preferably in a vehicle or heavy equipment environment. Competencies * Strong analytical and problem-solving skills with hands-on experience in process improvement. * Proficiency in AutoCAD, CATIA, and related design software. * Working knowledge of CANbus systems and electrical controls. * Experienced in lean manufacturing principles, kaizen facilitation, and project leadership. * Strong communication and leadership skills. * Proficient with Google Workspace tools (Docs, Sheets, Slides, Forms, etc.). * Highly organized and detail-oriented. * Capable of working independently and cross-functionally in a fast-paced environment. * Flexible and willing to support projects requiring overtime or weekend work as needed Ready to elevate your career? Apply today! Please submit your resume/CV today for consideration! About Kalmar Kalmar (Nasdaq Helsinki: KALMAR) is moving goods in critical supply chains around the world, with the vision to be the forerunner in sustainable material handling equipment and services. The company offers a wide range of industry shaping heavy material handling equipment and services to ports and terminals, distribution centres, manufacturing and heavy logistics. Headquartered in Helsinki, Finland, Kalmar operates globally in over 120 countries and employs approximately 5,200 people. In 2024, the company's sales totalled approximately EUR 1.7 billion. ********************

Job Description MGP Ingredients is a leading supplier of premium distilled spirits and food ingredient solutions. Its Distilling Solutions segment provides bourbons, whiskeys, ryes, gins, and vodkas to craft and multinational brands. MGP's own Branded Spirts business is growing following the 2021 acquisition of Luxco, a top spirits producer, bottler, supplier, and importer as well as the 2023 acquisition of Penelope Bourbon, known for its wide range of uniquely blended expressions. Ingredient Solutions delivers nutritional, functional wheat- and pea-based ingredients aligned with consumer trends. The company operates in locations across the Midwestern U.S., and overseas in Northern Ireland and Mexico. THE OPPORTUNITY As the Distillery Process Engineer (Biofuel), you will be responsible for enhancing product quality, safety, and manufacturing efficiency by addressing and resolving daily process challenges. Drive sustainable improvements in cost-effectiveness and product performance through the optimization of manufacturing processes, leveraging capital projects, statistical analysis, designed experiments, and procedural changes. Lead continuous improvement initiatives at the site, utilizing tools such as Zero-Based Analysis (ZBA), GAP analysis, and time studies. Collaborate with cross-functional teams to solve problems and develop new products. Oversee the startup of new products and equipment, including supervising installation, troubleshooting initial production issues, ensuring new processes and products meet requirements, and documenting and transferring them to production. WHAT YOU WILL BE DOING: DISTILLERY OPERATIONS 35% • Oversee daily operations at the Atchison facilities within the Distillery operations to ensure system performance, availability, and reliability targets are consistently met. • Provide troubleshooting and technical support as needed to address operational issues. • Monitor system performance for deviations from targets and offer guidance on corrective actions. • Develop and maintain standard operating procedures to ensure consistent and efficient plant operations. ENGINEERING 30% • Maintain and create new piping and instrumentation diagrams, as well as other flow diagrams, to ensure accurate process documentation. • Support the implementation of expense and capital projects, providing necessary technical documentation and oversight. • Lead the site's continuous improvement initiatives, including managing and updating the GAP analysis and ZBA program. QUALITY 15% • Troubleshoot quality issues and implement corrective actions to maintain high standards of product quality. SAFETY 13% • Provide technical support and expertise for MGP Safety Up and individual safety subcommittee activities. • Monitor and support SEM (Safety, Environment, and Maintenance) suggestions to enhance safety practices. • Participate in incident investigations and assist in the implementation of corrective actions. SHIFT SUPERVISION 2% • Serve as a relief shift manager when necessary to ensure uninterrupted plant operations. Managing hourly employees and ensure the consistent implementation of plant directives to maintain smooth production facility operations. WHO WE ARE LOOKING FOR: Bachelor's of Science in Chemical Engineering (required). 5+ years ethanol plant experience with deep knowledge of milling, cooking, fermentation, distillation and dryhouse operation process technologies, 2+ years of project management experience. Experience using Microsoft Office (Excel, Word, PowerPoint, and Outlook). Experience with AutoCAD and SAP preferred but not required. Strong leadership, coaching and interpersonal skills. Excellent verbal and written communication skills Good problem solving and project management skills Detail-oriented, collaborative, safety-focused, and ready to grow. Frequent exposure to plant environments (wet floors, noise, temperature variations) Must be comfortable with physical tasks like climbing, maneuvering in tight spaces, and occasional lifting If the above speaks to you, we're excited to learn more about you! At MGP, we know that our people are our greatest strength. With different perspectives and unique ways of thinking, our employees are as varied as our products. We believe that inclusivity strengthens the organization and champions a company culture that is evolving to reflect all of us. Culture results from our behaviors, our personal commitment, our curiosity, how we collaborate, and the ways we courageously share our perspectives and expect others to do the same. Each of us can make a difference by fostering thinking and actions that empower us to connect, belong and grow together. Compensation is competitive and is commensurate with experience. MGP offers exceptional medical, dental, vision, short and long-term disability, life insurance, 401(k) Match and PTO. All successful candidates for this position will be required to submit to a criminal background check and drug test.

MGP Ingredients is a leading supplier of premium distilled spirits and food ingredient solutions. Its Distilling Solutions segment provides bourbons, whiskeys, ryes, gins, and vodkas to craft and multinational brands. MGP's own Branded Spirts business is growing following the 2021 acquisition of Luxco, a top spirits producer, bottler, supplier, and importer as well as the 2023 acquisition of Penelope Bourbon, known for its wide range of uniquely blended expressions. Ingredient Solutions delivers nutritional, functional wheat- and pea-based ingredients aligned with consumer trends. The company operates in locations across the Midwestern U.S., and overseas in Northern Ireland and Mexico. THE OPPORTUNITY As the Distillery Process Engineer (Biofuel), you will be responsible for enhancing product quality, safety, and manufacturing efficiency by addressing and resolving daily process challenges. Drive sustainable improvements in cost-effectiveness and product performance through the optimization of manufacturing processes, leveraging capital projects, statistical analysis, designed experiments, and procedural changes. Lead continuous improvement initiatives at the site, utilizing tools such as Zero-Based Analysis (ZBA), GAP analysis, and time studies. Collaborate with cross-functional teams to solve problems and develop new products. Oversee the startup of new products and equipment, including supervising installation, troubleshooting initial production issues, ensuring new processes and products meet requirements, and documenting and transferring them to production. WHAT YOU WILL BE DOING: DISTILLERY OPERATIONS 35% • Oversee daily operations at the Atchison facilities within the Distillery operations to ensure system performance, availability, and reliability targets are consistently met. • Provide troubleshooting and technical support as needed to address operational issues. • Monitor system performance for deviations from targets and offer guidance on corrective actions. • Develop and maintain standard operating procedures to ensure consistent and efficient plant operations. ENGINEERING 30% • Maintain and create new piping and instrumentation diagrams, as well as other flow diagrams, to ensure accurate process documentation. • Support the implementation of expense and capital projects, providing necessary technical documentation and oversight. • Lead the site's continuous improvement initiatives, including managing and updating the GAP analysis and ZBA program. QUALITY 15% • Troubleshoot quality issues and implement corrective actions to maintain high standards of product quality. SAFETY 13% • Provide technical support and expertise for MGP Safety Up and individual safety subcommittee activities. • Monitor and support SEM (Safety, Environment, and Maintenance) suggestions to enhance safety practices. • Participate in incident investigations and assist in the implementation of corrective actions. SHIFT SUPERVISION 2% • Serve as a relief shift manager when necessary to ensure uninterrupted plant operations. Managing hourly employees and ensure the consistent implementation of plant directives to maintain smooth production facility operations. WHO WE ARE LOOKING FOR: Bachelor's of Science in Chemical Engineering (required). 5+ years ethanol plant experience with deep knowledge of milling, cooking, fermentation, distillation and dryhouse operation process technologies, 2+ years of project management experience. Experience using Microsoft Office (Excel, Word, PowerPoint, and Outlook). Experience with AutoCAD and SAP preferred but not required. Strong leadership, coaching and interpersonal skills. Excellent verbal and written communication skills Good problem solving and project management skills Detail-oriented, collaborative, safety-focused, and ready to grow. Frequent exposure to plant environments (wet floors, noise, temperature variations) Must be comfortable with physical tasks like climbing, maneuvering in tight spaces, and occasional lifting If the above speaks to you, we're excited to learn more about you! At MGP, we know that our people are our greatest strength. With different perspectives and unique ways of thinking, our employees are as varied as our products. We believe that inclusivity strengthens the organization and champions a company culture that is evolving to reflect all of us. Culture results from our behaviors, our personal commitment, our curiosity, how we collaborate, and the ways we courageously share our perspectives and expect others to do the same. Each of us can make a difference by fostering thinking and actions that empower us to connect, belong and grow together. Compensation is competitive and is commensurate with experience. MGP offers exceptional medical, dental, vision, short and long-term disability, life insurance, 401(k) Match and PTO. All successful candidates for this position will be required to submit to a criminal background check and drug test.

• Validation engineer with experience in equipment, HVAC, utility and process qualification within a pharmaceutical industry. Previous plant experience is recommended. Background in aseptic processing, microbiology, environmental monitoring, chemistry, and production is recommended. The additional resources are requested for a total of fourteen (14) weeks starting in December 2017 and ending March 2018 to support Winter Shutdown changes. Hours can involve weekend or night shifts. Validation activities including writing system impact assessments, oversight of engineering during shutdown activities, execution of installation qualification, operational qualification, performance qualification, and summarizing qualification results/drafting qualification report summaries. The support staff must act in accordance with plant safety requirements, training and procedures. POSITION RESPONSIBILITIES • Schedules and executes validations/qualifications per Standard Operating Procedures (SOPs) and regulatory guidelines. • Coordinates and communicates all testing with affected functional groups and evaluates test results. • Executes equipment, facility, utility and computer system, Automated Process Control validation studies to include protocol preparation, scheduling, protocol execution, analyze data and compose a final report. • Oversee and assist Engineers and/or Technicians with their assigned projects. • Provide technical expertise to define approaches and execution of system validation activities in accordance with cGMP, cGXP, CFR 21 Parts, 11, 210 and 211, EU Annex 11, ICH Q7, Q8 and Q9, and other applicable regulations, procedures and industry guidance. • Thorough understanding of risk based validation, industry standards and best practices for validation. ORGANIZATIONAL RELATIONSHIPS • Will interact with Shutdown stakeholders: Engineering, Operations, Quality, Safety, Planning, Contractors, etc. • Weekly/daily meeting attendance as required. • Will participate in team led by Pfizer group leaders. EDUCATION AND EXPERIENCE • Education: BS/BA degree in science, engineering, manufacturing technology or closely related field or combination of education and work experience • Experience: Recommended minimum of 4 years pharmaceutical validation experience TECHNICAL SKILLS REQUIREMENTS • Knowledge of ICH and other regulatory guidelines; demonstrated ability to interpret and apply these guidelines to document writing PHYSICAL POSITION REQUIREMENTS • Logistics: Requires contractor to be on-site weekly with travel home every other weekend • Must be able and willing to work beyond office hours which may include weekends. • Requires routine sitting, standing, walking, listening and talking • Acute mental and visual attention at all times • Handle multiple projects while managing frequent interruptions • Requires moderate lifting or moving up to 25 pounds (lbs Additional Information Anuj Mehta ************

Responsibilities: * Review and evaluate Quality Documents, ensuring that all documents are applicable to current standards & procedures and properly represent current manufacturing processes and procedures. * Ensure procedures are being followed for the following processes: * Creation of Manufacturing Inspection Reports (MIR) for all parts and assemblies. * First Article Inspections (FAI) * In Process Inspections * Internal, Customer, Supplier and other third-party audits * Final Inspection Reports * Inspection and receipt of all incoming parts and material (raw material, hardware, supplies, and parts returning from outside processing). * Review and approval of vendor certifications and inspection processes. * Generate and complete "Corrective Action Reports" (CAR) in a timely manner; also ensure that the corrective actions are incorporated back into the Manufacturing Process Plans (MPP) and Manufacturing Inspection Reports (MIR) * Lead quality initiatives including any actions or audits required. * Establish inspection training programs and growth opportunities that appropriately reach each person within quality. The goal is to improve skill sets and the ability to be cross-functional within the quality assurance organization. * Take the lead in understanding "form, fit, and function" of products and parts that we manufacture and assemble. Identify 'grey area" questions and work with all departments, customers, and sister companies to identify solutions and outcomes that are satisfactory to all parties. * Follow up on corrective actions with verification and validation. Resolve quality and process issues. * Enhance and improve methods for inspection, testing, sampling, and training. * Assist in other areas or perform other duties as required by business demands. * Maintains safe and clean work environment; maintaining compliance with established policies and procedures * Perform other duties as assigned by supervision.

**_What Industrial Engineering contributes to Cardinal Health_** Engineering is responsible for performing research and analyses to develop design options for components, products, systems and processes. Industrial Engineering is responsible for enhancing / developing processes, layout and associated tools. Identifies, analyzes and implements new or existing technology to optimize business processes. Designs process improvements to reduce cost, cycle time, improve quality and/or increase throughput. Directs external resources / contractors as required. The Principal Industrial Engineer supports Pharmaceutical Supply Chain Operations in the areas of capital project planning and management, capacity planning, operational process change, and overall distribution center operating layout optimization. The position will also support deployment of new process and automation solutions, facilitate new building designs and layouts changes. Additional responsibilities include partnering with Operations leaders, deploying capital project investments for Pharma Supply Chain Operations, and overseeing project implementation and adoption to realize improvements. **_Responsibilities_** + Drive process engineering initiatives including conceptual operational designs, layout-change scenarios, and innovative automation solutions. Work closely with business operations partners to iterate on solutioning to optimize results. Bring modernization concepts to Operations through material handling and engineering external partnerships. + Works closely with Pharmaceutical Supply Chain Operations Vice Presidents, and site leaders to manage capital projects planned within the buildings. Develops capital budget priorities, establishes preliminary budgets,business case justifications, and formalizes all capital requests for budgeted, approved, or newly scoped projects. + Leads multifunctional teams of stakeholders and contributors to deliver large complex projects on time and under budget.Coordinates with other functional groups including Corporate Real Estate,field operations, Security, Information Technology, Inventory, Quality & Regulatory, Sales,and EH&S to ensure efforts are aligned, and coordinated as projects are developed and analyzed. + Integrated team members supporting operations leadership teams to ensure that capital projects and infrastructure are deployed, coordinated, managed, and maintained to drive building performance expectations. This role also manages and executes small construction projects independent of Corporate Real Estate / Construction including all cage and vault construction resulting from expansion or relocation needs. **_Qualifications_** + Bachelor's Degree in related field or relevant work experience, preferred + 4-6 years of experience in Operations, project and budgetary management, capital investment analysis and deployment, leading complex projects with multi-functional teams, preferred + Experience with automation solutions, facility design, material handling systems, integrated warehouse controls and execution applications, preferred + Experience with AutoCAD and other software applications to drive warehouse design and concepting, preferred + Strong Leadership skills, Strong scheduling and organizational skills + Excellent technical problem-solving capability + High level of initiative - Team player + Willing and transparent communicator + Proficient with Microsoft Office Suite + Excellent written and verbal communication skills + Moderate travel to other facilities for projects and supervision of equipment installation (25%, up to 50% during specific deployment activities and project implementations) **_What is expected of you and others at this level_** + Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects + May contribute to the development of policies and procedures + Works on complex projects of large scope + Develops technical solutions to a wide range of difficult problems + Solutions are innovative and consistent with organization objectives + Completes work; independently receives general guidance on new projects + Work reviewed for purpose of meeting objectives + May act as a mentor to less experienced colleagues **Anticipated salary range:** $94,900 - $135,600 **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 3/13/2026 *if interested in opportunity, please submit application as soon as possible. The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

COME JOIN OUR JOURNEY! When you join TT, you join our global community of visionaries, creators, and achievers dedicated to engineering and manufacturing electronic solutions enabling a safer, healthier and more sustainable world. Simply put, we are a global manufacturer with a passion for engineering advanced electronics that benefit our planet and people for future generations. We are committed to having a positive impact on the world through a culture built around safety, transparency, collaboration, and positive relationships. Our teams are fueled by performance and expertise, leading the charge in innovation, efficiency and delivering world-class customer service. Be part of the journey. Role Overview and Responsibilities This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e., "Green Card Holder"), Political Asylee, or Refugee. Introduction The Quality Technician plays a critical role in maintaining site-wide quality control by managing all non-conforming material, coordinating third-party source inspections, and performing timely inspections on returned goods. This position ensures proper containment and documentation of quality issues, prepares and supports materials for external inspections, and provides quick assessments of returned items to facilitate accurate and timely customer responses. The technician partners closely with Quality, Operations, and Supply Chain to resolve issues, maintain accurate quality records, and uphold all procedural and regulatory requirements. Key Responsibilities * Manage and process all non-conforming material, including identification, segregation, documentation, and disposition. * Coordinate and facilitate third-party source inspections, ensuring required materials, documentation, and quality records are prepared and available. * Perform timely inspections on returned goods (RMA), including visual, mechanical, or dimensional checks to support quick evaluation and customer response. * Maintain accurate records for NCRs, source inspections, RMAs, and other quality-related data in accordance with internal procedures. * Support material flow by resolving quality holds quickly and escalating issues when needed to prevent delays or quality escapes. * Collaborate with Quality Engineers, Operations, and Supply Chain to investigate issues, verify corrective actions, and support continuous improvement activities. * Follow established quality procedures, work instructions, and regulatory/ITAR requirements to ensure compliance and audit readiness. * Other duties, as assigned or required. Qualifications, Skills and Attributes Core Requirements * Exceptional attention to detail with strong observational and analytical skills to identify quality issues accurately and consistently. * Proficiency with inspection tools and equipment, including calipers, micrometers, gauges, and other precision measurement instruments. * Working knowledge of quality systems and methodologies, such as AS9100, ISO standards, Lean Manufacturing, and root-cause analysis tools. * Ability to read and interpret engineering drawings, blueprints, specifications, and technical documentation with a high level of accuracy. * Strong communication and interpersonal skills, with the ability to collaborate effectively across Quality, Operations, Engineering, and Supply Chain. * Advanced computer proficiency, including Microsoft Office Suite, quality management software (QMS), and data analysis tools within a manufacturing or regulated environment. * Ability to perform the essential functions of the job with or without reasonable accommodation, in accordance with ADA requirements. Desireable Skills and Experience * High school diploma or equivalent required; additional technical, vocational, or trade school training in quality control, manufacturing, engineering, or a related field strongly preferred. * Five or more years of experience in quality inspection, manufacturing, electronics, or a regulated production environment; experience working within AS9100 or aerospace/defense quality systems is highly advantageous. * Demonstrated ability to accurately use and read precision measurement tools, including but not limited to calipers, micrometers, feeler gauges, height gauges, and X-ray or other non-destructive inspection equipment. * Strong understanding of inspection techniques, non-conformance handling, and documentation requirements in a high-mix, high-reliability manufacturing environment. * Competence in interpreting engineering drawings, specifications, and technical data, including GD&T, preferred. * Proficiency in computer-based quality systems, including QMS platforms, ERP systems, and Microsoft Office Suite. * This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e., "Green Card Holder"), Political Asylee, or Refugee. TT Electronics does not accept any unsolicited resumes from third parties. Any resumes submitted by a third party for this or any other position will not be subject to any recruitment fees if hired. Solving Technology Challenges for a Sustainable World We want the very best people in our TT family across the globe - so we welcome applications from everyone, to celebrate a diverse mix of experiences, backgrounds and identities. We are committed to equality of opportunity for all and you can rest assured that TT Electronics takes positive steps to ensure we are an inclusive business, that will welcome and support you, from your initial application to wherever your career takes you! Please get in touch if you'd like to discuss any reasonable adjustments to your application, in order that we can accommodate and support you in the process. If you want to work for a company where who you are is valued and respected, we'd love to hear from you. #WeAreTT #BeMeAtTT

MGP Ingredients is a leading supplier of premium distilled spirits and food ingredient solutions. Its Distilling Solutions segment provides bourbons, whiskeys, ryes, gins, and vodkas to craft and multinational brands. MGP's own Branded Spirts business is growing following the 2021 acquisition of Luxco, a top spirits producer, bottler, supplier, and importer as well as the 2023 acquisition of Penelope Bourbon, known for its wide range of uniquely blended expressions. Ingredient Solutions delivers nutritional, functional wheat- and pea-based ingredients aligned with consumer trends. The company operates in locations across the Midwestern U.S., and overseas in Northern Ireland and Mexico. THE OPPORTUNITY As the Distillery Process Engineer (Biofuel), you will be responsible for enhancing product quality, safety, and manufacturing efficiency by addressing and resolving daily process challenges. Drive sustainable improvements in cost-effectiveness and product performance through the optimization of manufacturing processes, leveraging capital projects, statistical analysis, designed experiments, and procedural changes. Lead continuous improvement initiatives at the site, utilizing tools such as Zero-Based Analysis (ZBA), GAP analysis, and time studies. Collaborate with cross-functional teams to solve problems and develop new products. Oversee the startup of new products and equipment, including supervising installation, troubleshooting initial production issues, ensuring new processes and products meet requirements, and documenting and transferring them to production. WHAT YOU WILL BE DOING: DISTILLERY OPERATIONS 35% * Oversee daily operations at the Atchison facilities within the Distillery operations to ensure system performance, availability, and reliability targets are consistently met. * Provide troubleshooting and technical support as needed to address operational issues. * Monitor system performance for deviations from targets and offer guidance on corrective actions. * Develop and maintain standard operating procedures to ensure consistent and efficient plant operations. ENGINEERING 30% * Maintain and create new piping and instrumentation diagrams, as well as other flow diagrams, to ensure accurate process documentation. * Support the implementation of expense and capital projects, providing necessary technical documentation and oversight. * Lead the site's continuous improvement initiatives, including managing and updating the GAP analysis and ZBA program. QUALITY 15% * Troubleshoot quality issues and implement corrective actions to maintain high standards of product quality. SAFETY 13% * Provide technical support and expertise for MGP Safety Up and individual safety subcommittee activities. * Monitor and support SEM (Safety, Environment, and Maintenance) suggestions to enhance safety practices. * Participate in incident investigations and assist in the implementation of corrective actions. SHIFT SUPERVISION 2% * Serve as a relief shift manager when necessary to ensure uninterrupted plant operations. Managing hourly employees and ensure the consistent implementation of plant directives to maintain smooth production facility operations. WHO WE ARE LOOKING FOR: * Bachelor's of Science in Chemical Engineering (required). * 5+ years ethanol plant experience with deep knowledge of milling, cooking, fermentation, distillation and dryhouse operation process technologies, 2+ years of project management experience. * Experience using Microsoft Office (Excel, Word, PowerPoint, and Outlook). * Experience with AutoCAD and SAP preferred but not required. * Strong leadership, coaching and interpersonal skills. * Excellent verbal and written communication skills * Good problem solving and project management skills * Detail-oriented, collaborative, safety-focused, and ready to grow. * Frequent exposure to plant environments (wet floors, noise, temperature variations) * Must be comfortable with physical tasks like climbing, maneuvering in tight spaces, and occasional lifting If the above speaks to you, we're excited to learn more about you! At MGP, we know that our people are our greatest strength. With different perspectives and unique ways of thinking, our employees are as varied as our products. We believe that inclusivity strengthens the organization and champions a company culture that is evolving to reflect all of us. Culture results from our behaviors, our personal commitment, our curiosity, how we collaborate, and the ways we courageously share our perspectives and expect others to do the same. Each of us can make a difference by fostering thinking and actions that empower us to connect, belong and grow together. Compensation is competitive and is commensurate with experience. MGP offers exceptional medical, dental, vision, short and long-term disability, life insurance, 401(k) Match and PTO. All successful candidates for this position will be required to submit to a criminal background check and drug test.

• Validation engineer with experience in equipment, HVAC, utility and process qualification within a pharmaceutical industry. Previous plant experience is recommended. Background in aseptic processing, microbiology, environmental monitoring, chemistry, and production is recommended. The additional resources are requested for a total of fourteen (14) weeks starting in December 2017 and ending March 2018 to support Winter Shutdown changes. Hours can involve weekend or night shifts. Validation activities including writing system impact assessments, oversight of engineering during shutdown activities, execution of installation qualification, operational qualification, performance qualification, and summarizing qualification results/drafting qualification report summaries. The support staff must act in accordance with plant safety requirements, training and procedures. POSITION RESPONSIBILITIES • Schedules and executes validations/qualifications per Standard Operating Procedures (SOPs) and regulatory guidelines. • Coordinates and communicates all testing with affected functional groups and evaluates test results. • Executes equipment, facility, utility and computer system, Automated Process Control validation studies to include protocol preparation, scheduling, protocol execution, analyze data and compose a final report. • Oversee and assist Engineers and/or Technicians with their assigned projects. • Provide technical expertise to define approaches and execution of system validation activities in accordance with cGMP, cGXP, CFR 21 Parts, 11, 210 and 211, EU Annex 11, ICH Q7, Q8 and Q9, and other applicable regulations, procedures and industry guidance. • Thorough understanding of risk based validation, industry standards and best practices for validation. ORGANIZATIONAL RELATIONSHIPS • Will interact with Shutdown stakeholders: Engineering, Operations, Quality, Safety, Planning, Contractors, etc. • Weekly/daily meeting attendance as required. • Will participate in team led by Pfizer group leaders. EDUCATION AND EXPERIENCE • Education: BS/BA degree in science, engineering, manufacturing technology or closely related field or combination of education and work experience • Experience: Recommended minimum of 4 years pharmaceutical validation experience TECHNICAL SKILLS REQUIREMENTS • Knowledge of ICH and other regulatory guidelines; demonstrated ability to interpret and apply these guidelines to document writing PHYSICAL POSITION REQUIREMENTS • Logistics: Requires contractor to be on-site weekly with travel home every other weekend • Must be able and willing to work beyond office hours which may include weekends. • Requires routine sitting, standing, walking, listening and talking • Acute mental and visual attention at all times • Handle multiple projects while managing frequent interruptions • Requires moderate lifting or moving up to 25 pounds (lbs Additional Information Anuj Mehta ************