Quality engineer jobs in Lexington, KY - 120 jobs

Developing operating process plans to machine or assemble parts for assigned area of the Powertrain department Leading, planning, procurement, installation, trial, and launching of engine/transmission machining or assembly lines Creating and maintaining schedule and budget for assigned area Develop / improve standard tools and benchmarks Lead and participate in cross functional working groups across local facility and corporate departments to achieve project goals Visualize activity plans and schedules to facilitate quick consensus building to secure project priorities. Analyze critical manufacturing issues and clearly communicate root cause and countermeasure plans to stakeholders Requirements: Automotive pre-production or manufacturing engineering experience Automation experience including specification, tooling/jig design, equipment procurement, and installation 3D CAD experience (Catia or Delmia) Programmable Logic Controller (PLC) familiarity skills Design for Manufacturing / Simultaneous Engineering experience Internal Logistics experience including route planning, simulations and analysis, packaging, and automation Quality Process Set Up [containment, repeatability, nondestructive inspection] Project management skills including scheduling, budgeting, coordinating, problem solving, and reporting Willing to relocate and work in Office in Georgetown KY Ability to work up to 55 hours a week

The Quality Manager is responsible for leading all quality systems within the manufacturing operation to ensure consistent product quality, compliance, and continuous improvement. This role drives quality strategy, develops and maintains effective processes, and partners closely with operations to reduce defects, improve efficiency, and strengthen accountability across the plant.

The Manager, Data Quality, is responsible for overseeing the full data management lifecycle and operational workflow of Company Entity Management (CEM) for company and contact data within Dodge Construction Network's (Dodge) master data ecosystem. This role leads both onshore and offshore teams to ensure the accuracy, completeness, and standardization of company entities that power Dodge's products, customer experiences, and analytics. The Manager will define and execute the end-to-end operating model for CEM including the development of Standard Operating Procedures (SOPs), establishing KPIs, designing quality and governance frameworks, and defining requirements for automation and human-in-the-loop workflows. This role drives continuous improvement by refining processes, enhancing data sourcing and enrichment, evaluating automation outputs, and collaborating closely with cross-functional partners across Product, Engineering, and Operations. This leader must bring strong people management and project management skills, an analytical mindset, and have experience working in scalable data operations environments. This is a full-time position and reports directly to the Director of Data Acquisition. **_Preferred Location_** + This is a remote, home-office-based role, and candidates located in the continental United States will be considered. + For this position, there is a preference to hire in the Central and Eastern Time Zone; however, candidates in other areas/time zones would be considered as well. **_Travel Requirements_** Expected travel is minor for this role. **_Essential Functions_** + Design, maintain, and improve company and contact entity workflows, SOPs, SLAs, and quality standards + Define and track KPIs for team efficiency, business impact, financial stewardship, and client satisfaction + Oversee entity creation, updates, merges, conflict resolution, and exception handling + Partner with automation, engineering, and data science to integrate and optimize human-in-the-loop and machine-assisted processes + Analyze performance patterns to identify automation gaps, reduce manual interventions, and continuously improve processes + Lead, mentor, and develop CEM team members + Establish performance expectations, work allocation, and capacity planning + Manage relationships with third party data providers and offshore vendors + Collaborate closely with Engineering, Product, Sourcing, and Sales to align CEM standards with business and platform needs + Participate in roadmap discussions, attribute model design, and classification/taxonomy updates **_Education Requirement_** Bachelor's degree in Information Systems, Data Analytics, Supply Chain Management, Computer Science, Engineering, Operational Management, or related technical fields or equivalent education and work experience. **_Required Experience, Knowledge and Skills_** + 7+ years of experience in data operations, master data management, digital operations, or business transformation + 2+ years managing teams + Proven experience managing both onshore and offshore teams + Experience with SQL and/or Python programming + Advanced problem solving and data driven decision making capabilities + Proven record of managing external vendor relationships + Ability to translate technical concepts into actional business insights for non-technical stakeholders + Experience with automation tools, scraping frameworks, and data pipelines + Exposure to data operations utilizing machine learning and data enrichment techniques + Proficiency in data governance, KPI management, and quality assurance + Strong project management skills, including planning, prioritization, and execution of change management + Excellent written and verbal communication skills for presenting strategies, reporting performance metrics, and building relationships with stakeholders **_Preferred Experience, Knowledge and Skills_** + Data Visualization tools such as AWS Quicksight, PowerBI, Tableau + Knowledge of construction industry or content workflows a plus + Experience with salesforce a plus + Familiarity with cloud-based data environments + Familiarity with Jira/Confluence **_About Dodge Construction Network_** Dodge Construction Network exists to deliver the comprehensive data and connections the construction industry needs to build thriving communities. Our legacy is deeply rooted in empowering our customers with transformative insights, igniting their journey towards unparalleled business expansion and success. We serve decision-makers who seek reliable growth and who value relationships built on trust and quality. By combining our proprietary data with cutting-edge software, we deliver to our customers the essential intelligence needed to excel within their respective landscapes. We propel the construction industry forward by transforming data into tangible guidance, driving unparalleled advancement. Dodge is the catalyst for modern construction. **_Salary Disclosure_** Dodge Construction Network's compensation and rewards package for full time roles includes a market competitive salary, comprehensive benefits, and, for applicable roles, uncapped commissions plans or an annual discretionary performance bonus. **_For this role, we are only considering candidates who are legally authorized to work in the United States and who do not now or in the future require sponsorship for employment visa status._** **_A background check is required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job and consistent with all federal state and local ordinances._** **_Reasonable Accommodation_** **_Dodge Construction Network is committed to recruiting, hiring, and promoting people with disabilities. If you need an accommodation or assistance completing the online application, please email_** **_***************************_** **_._** **_Equal Employment Opportunity Statement_** **_Dodge Construction Network is an Equal Opportunity Employer. We are committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. All employment decisions shall be based on merit, qualifications, and business needs without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, pregnancy, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law._** \#LI-Remote \#LI-CS1 \#DE-Remote \#DE-2026-22

**Collaborate with Innovative 3Mers Around the World** Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. **This position provides an opportunity to transition from other private, public, government or military experience to a 3M career.** **The Impact You'll Make in this Role** As a Manufacturing Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by: + Develop and implement improvements related to safety, quality, service, and productivity. + Work closely with production and maintenance teams to perform troubleshooting activities and resolve equipment/downtime issues. + Identify improvement opportunities requiring capital expenditure; establish justification and manage projects to completion. + Actively participate in the day-to-day operations, EHS activities, MOC process change management, OEE analysis, and resolution of gaps in performance + Initiate and lead Continuous Improvement projects. Use project management tools to convey objectives, timelines, obstacles, and next steps. + Effectively troubleshoot defects and variation, perform root cause analysis, and apply problem solving skills. + Develop process standards and other documentation supporting the operation. + Provide engineering support for assigned areas including occasional availability on nights/weekends. **Your Skills and Expertise** To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: + Bachelor's degree or higher in a science or engineering discipline (completed and verified prior to start) from an accredited institution. + Two (2) years of experience in a manufacturing environment in aprivate, public, government or military environment **.** Additional qualifications that could help you succeed even further in this role include: + Experience in a Manufacturing Engineer role (specifically with process equipment). + Experience leading multi-functional teams through complex projects from planning to completion. + Experience developing and managing capital budgets and project completion within time and cost projections. + Excellent problem solving and analytical skills. Experience with CI, Six Sigma, and Lean. + Strong interpersonal, organizational and communication skills + Strong data analysis skills including Excel, Minitab, and SQL querying experience. + Experience presenting ideas in PowerPoint. + Knowledge of robots, camera/scanner vision systems, and PLC programming + Self-motivated, team player **Work location: On-site, Cynthiana, KY** **Travel: May include up to 10% domestic/international** **Relocation Assistance: May be 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** 3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope. **Chat with Max** For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting Applicable to US Applicants Only:The expected compensation range for this position is $98,413 - $120,282, 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: **************************************************************** Good Faith Posting Date Range 07/03/2025 To 08/02/2025 Or until filled All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M. Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M. Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties. Pay & Benefits Overview: https://**********/3M/en\_US/careers-us/working-at-3m/benefits/ 3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law. **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.** **3M 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 3M 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. At 3M we apply science in collaborative ways to improve lives daily as our employees connect with customers all around the world. Learn more about 3M's creative solutions to global challenges at ********** or on Twitter @3M or @3MNews. 3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law.

Job Description Standards Engineer Georgetown, Kentucky, United States On Site Contract | Full Time $45-$48 per hour Benefits Begin Day 1 Paid Time Off Paid Holidays Position Overview Reliance One, Inc. is seeking a Standards Engineer to support the development, maintenance, and implementation of facility and construction standards. This role plays a critical part in ensuring engineering standards align with industry best practices, regulatory requirements, and operational needs across multiple disciplines. Responsibilities Develop, review, and update facility and construction standards and specifications related to mechanical, electrical, civil, and architectural systems Collaborate with design, planning, manufacturing, and project teams to complete standards and specifications Monitor industry trends, global manufacturing trends, and current/past building issues; update standards as needed Manage multiple standards concurrently to ensure timely completion Provide guidance and interpretation of standards to internal engineering and project teams Document, track, and maintain records related to standards and specifications Required Qualifications Bachelor's degree in Engineering (Mechanical, Electrical, Industrial, or related field) 5-10 years of relevant engineering experience Proven experience in standards development, engineering implementation, or quality assurance (5+ years preferred) Strong knowledge of industry codes and standards, including ASTM, ASHRAE, IBC, NFPA, and related regulations Excellent analytical, communication, and organizational skills Ability to work collaboratively in a cross-functional team environment Intermediate proficiency with Microsoft Office Proficiency in AutoCAD, Bluebeam, or other PDF editing software Equal Employment Opportunity (EEO) Statement Reliance One, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, disability status, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make: As a Validation Engineer, you will play a key role in supporting the qualification and validation activities that ensure our manufacturing processes and equipment meet rigorous regulatory and quality standards. Your expertise will help maintain compliance with cGMP and industry guidelines, contributing to the reliable production of safe and effective pharmaceutical products. You will collaborate closely with cross-functional teams to execute validation protocols and ensure smooth technology transfers. Responsibilities: Develop, execute, and review validation protocols for equipment, processes, and utilities in a GMP manufacturing environment. Support installation, operational, and performance qualification (IQ/OQ/PQ) activities to ensure equipment and systems meet design specifications. Assist in the development and maintenance of validation documentation, including protocols, reports, and traceability matrices. Collaborate with manufacturing, quality, engineering, and other stakeholders to ensure validation requirements are met. Participate in risk assessments and change control processes related to validation activities. Support continuous improvement initiatives for validation strategies and documentation. Ensure compliance with cGMP, GAMP5, and regulatory expectations throughout the validation lifecycle. Communicate validation status and issues effectively through written reports and verbal updates. Assist in training team members on validation procedures and standards. Qualifications: Minimum Qualifications: BS in engineering, related degree, or equivalent experience 4 years of related experience, or 3 years with a Master's degree Preferred Qualifications: Previous work experience in a GMP manufacturing environment Working knowledge of cGMP, GAMP5, and regulatory requirements Experience working with nasal spray products, devices, or related drug-delivery systems Effective oral and written communication skills Technical writing experience including SOPs, maintenance PMs, user requirement specifications, design qualifications, and traceability matrices supporting regulatory agency inspections or audits. # LI-Onsite

Full-time Description Excel Engineering is seeking a team-oriented, highly motivated Validation Engineer for our Lexington, Kentucky area. We offer full-service Engineering Consulting services in the US and abroad. Since 1990, Excel Engineering has differentiated its services from that of its competition by providing engineering solutions to achieve our clients' business objectives. We are seeking a Validation Engineer to support projects, technical transfers, and ongoing validation maintenance including, but not limited to, the following major disciplines: Facilities, Utilities, and Equipment (FUE) Qualification Computerized Systems Validation (CSV) Cleaning Validation Sterilization Validation Materials Validation Process Validation Primary Responsibilities Develop, execute, and review validation deliverables including Validation Plans and Reports, User Requirements Specifications, Risk Assessments, Design Qualification, Installation Qualification, Operational Qualification, Performance Qualification, Standard Operating Procedures, and Validation Maintenance packages. Perform data collection, analysis, and resolve deviations or non-conformances identified during validation activities. Author SOP updates and revisions related to processes, equipment and system modifications. Maintain compliance with company policies, cGMPs, regulatory requirements, and safety protocols. Operate and program instruments (e.g., temperature/humidity dataloggers) for controlled temperature/humidity chamber qualifications (e.g., lyophilizers, warehouses, sterilizers, incubators). Collaborate with engineering, quality, manufacturing, and regulatory teams to ensure successful project execution. Requirements Education and Experience Bachelor's degree in science, engineering or other related technical field from an ABET Accredited Institution such as Chemical Engineering, Mechanical Engineering, Computer Engineering, or Electrical Engineering. Cumulative GPA of 3.0 or higher on a 4.0 Scale. 5+ years of related experience. Qualifications Experience applying cGMP principles to equipment, facility, utility, laboratory, and computer systems. Experience supporting commissioning and qualification of major capital projects or facility start-ups. Engineer in Training (EIT) registration or ability to obtain such is highly preferred. Ability to write and speak in the English language. Willingness to travel up to 10% of the time. Additional Skills Applicable to the Role Excellent interpersonal skills, as well as verbal and written communications. Ability to work collaboratively with individuals at all levels in the organization in a team environment. Knowledge of relevant technical software. Knowledge of MS Office software products: Word/Excel/Outlook. We offer a competitive salary and benefits package. Excel Engineering is focused on cultivating a high performing culture where a service oriented approach, continuous improvement, and goal orientation are valued. If you enjoy working in a fast paced, challenging and rewarding environment, Excel Engineering is for you! Excel Engineering is an Equal Opportunity Employer. Applicants will receive consideration for employment regardless of their race, color, religion, national origin, sex, sexual orientation, disability, age, veteran status, marital status, or status with regard to public assistance. In our commitment to diversity, equity, and inclusion, we strongly encourage applicants from populations that are underrepresented in the engineering field to apply. For applicants who need an accommodation to apply, please contact human resources at ********************.

**_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 (***************************************************************************************************************************

Business: Pharma Solutions Department: Facilities, Maintenance & Engineering Reporting to the Engineering Manager, the Manufacturing Process Engineer serves as subject-matter-expert and provides real-time, process engineering support to the manufacturing process. This position is responsible for design, project management, and implementation of new and existing systems, utilities and equipment, and ensures Quality, Compliance, and improved OTIF for all products produced at the manufacturing facility in Lexington, Kentucky. Reporting Structure This position reports to the Engineering Manager. Key Responsibilities: * Designs and project manages changes, improvements, new systems and or equipment. * Prepares Change Control Records (CCRs), Design Specifications, User Requirements Specifications, System Specifications, Design documents, Drawings, and Validation Documents for improvement, planned and corrective maintenance and system or process improvements * Leads/assists in Continuous Improvement Projects, including identification of opportunities, researches literature and vendors, prepares and presents proposals, develops and executes projects, and closes projects, all following appropriate change control methodologies * Represents Technical Subject Matter Expert (SME) in teams assembled to specify, install, troubleshoot and maintain systems, equipment and processes * Supports day-to-day production and maintenance activities * Provides training support as required. * Develops and or modifies SOPs for the Processes and Equipment. * Participates in deviation investigations to identify root causes and define corrective and preventive actions (CA/PA). * Creates and maintains drawings and sketches. * Manages Technical Publications Library to ensure the relevant manuals, specifications, design information for all of our facilities, utilities, equipment and products are on hand * Primary/First Line responsibility for operation and maintenance of the Validated Systems to maintain production capability required. * Primary/First Line responsibility for enhancements and upgrades of manufacturing related systems to maintain production capability. Qualifications: * Bachelor's degree in Mechanical, Electrical, or Chemical Engineering * Minimum 3-5 years of pharmaceutical manufacturing/maintenance experience required (parenteral/sterile filling experience preferred) * Expertise in troubleshooting production equipment/systems * Ability to work flexible schedule to support 24-hour operation (requires assignment on shift for 4 shift rotating days off schedule) * PC literate with standard office application (Word, Excel, PowerPoint) competency * Experience with maintenance and administration of both Windows-based and industrial (e.g., PLC) computer networks. * Experience with Allen-Bradley ControlLogix and Siemens PLCs; experience with HMI software applications; experience with automating processes and equipment * Knowledge and understanding of cGMPs including FDA, PMDA, and EU regulations; knowledge of cGMP validation requirements and techniques; experience with commissioning and validation protocol development and execution. * Knowledge and experience in cGMP CA/PA, root-cause analysis, risk assessment and investigation tools and techniques.

The Injection Mold Pilot Engineer will play a pivotal role in the Pilot group, which is responsible for the successful launch of new products. This position entails leading the process setup and validation for new models, ensuring manufacturability and compliance with company standards, and driving continuous improvement projects during product launches. Responsibilities + Lead the process setup and validation for new models, including mold trials, DOE (Design of Experiments), capability studies, and full production handoff. + Collaborate closely with product design and tool designers to ensure parts and molds are manufacturable and compliant with company standards. + Develop and document standardized molding processes for each new tool to ensure consistency and repeatability. + Work with tooling vendors and internal toolrooms to oversee new mold fabrication, testing, and modification. + Conduct mold acceptance trials (T0/T1/T2) and provide feedback for tooling optimization. + Establish robust process parameters for new tools and products. + Coordinate with cross-functional teams including Design, Quality, Production, Tooling, Supply Chain, and Customers. + Train production staff and technicians on new processes to ensure successful scale-up and long-term stability. + Support the standardization of mold designs, components, and processing methods across new product lines. + Drive continuous improvement projects during new product launches to reduce cycle time, improve yield, and enhance manufacturability. + Assist launch team with various process preparation tasks including process documentation, prototype event parts preparation, and customer documentation. Essential Skills + 3+ years of experience with injection mold startup/setup. + Ability to read part drawings, such as AutoCAD and Catia. + Strong communication and project management skills, with the ability to coordinate schedules between multiple teams/groups such as design, tooling, production, suppliers, and customers. + Experience in automotive manufacturing, process improvement, mechanical engineering, and plastic injection. + Proficiency in lean manufacturing, product development, and project management. Additional Skills & Qualifications + Experience with new product development and process setup. + Knowledge of APQP/PPAP. + Proficiency in Six Sigma. + Experience with tooling design, PLC programming, and Microsoft Excel. Work Environment The work environment is an automotive manufacturing setting. The facility experiences hot conditions in the summer and cooler temperatures in the winter. All proper personal protective equipment (PPE) is required on the manufacturing floor, including steel-toed boots, eyewear, and ear plugs. Work hours are on the first shift from 7 AM to 4 PM, with approximately 200 people employed at the plant. Job Type & Location This is a Contract to Hire position based out of Georgetown, KY. Pay and Benefits The pay range for this position is $31.25 - $36.06/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Georgetown,KY. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Quality Technician / Quality Inspector Full-Time | 2nd Shift | On-site The Quality Technician supports the Quality Department by ensuring products and processes meet internal standards and customer expectations. This role performs audits, inspections, and documentation activities to maintain compliance with quality management systems and promote continuous improvement. Essential Duties & Responsibilities Perform receiving and dock audits on finished goods and raw materials based on quality concerns or routine sampling. Conduct process audits within the organization as requested. Ensure FIFO and 5S procedures are followed throughout the department. Perform in-process inspections to verify correct dimensions, material tolerances, and overall product quality. Sort nonconforming products and report results to the Quality team. Track daily scrap and submit reports to Quality leadership. Recommend and help train temporary staff for sorting tasks as needed. Immediately report any nonconformance issues. Document and submit discrepancies to Quality leadership. Assist with preparation, packaging, and labeling of trial shipments. Contribute to internal and external audits as needed. Perform all inspections and audits according to established procedures. Qualifications Minimum Education & Experience High school diploma, GED, or equivalent. 12 years of experience in a manufacturing or production environment. Knowledge, Skills & Abilities Ability to operate hand jacks, scales, and measuring equipment. Strong attention to detail and ability to work independently. Effective communication and problem-solving skills. Computer Skills Proficiency in Office 365 or similar software. Experience with RF scanners. Familiarity with ERP systems (JDE preferred). Certificates / Licenses Valid drivers license. Supervisory Responsibilities None. Physical Demands & Work Environment Frequent standing, walking, reaching, and use of hands. Occasional sitting, stooping, kneeling, crouching, or crawling. Ability to lift and move up to 25 lbs regularly. Exposure to moving mechanical parts; moderate noise level. Ability to work independently with minimal supervision. Must work on-site 100% of the time. Schedule 2nd shift position. Overtime may be required based on production needs.

This is a high-impact opportunity for a skilled Process Engineer with a background in plastics and injection molding. In this role, you'll lead efficiency initiatives, manage capital projects, and support continuous improvement across multiple manufacturing facilities. Ideal for a hands-on engineer who thrives in dynamic environments, this position offers both technical leadership and cross-functional collaboration across production, quality, and maintenance teams. Key Responsibilities Drive process improvements to enhance quality, efficiency, and throughput in manufacturing operations Lead capital projects, including scoping, budgeting, scheduling, and execution Apply Lean, Six Sigma, and Total Quality Management (TQM) methodologies to solve operational challenges Conduct root cause analyses and lead corrective action implementation Collaborate closely with production, maintenance, and quality departments Develop and maintain process documentation and conduct training sessions for plant teams Provide technical support and leadership for plastics and injection molding operations across multiple sites Ensure ongoing compliance with safety and operational standards Qualifications Bachelor's degree in Engineering or equivalent work experience 4-7 years of experience in manufacturing or process engineering roles Required: Plastics industry background and hands-on injection molding experience Required: Experience managing capital projects within a plant setting Preferred: Familiarity with extrusion systems, plastic processing equipment, and mechanical systems Experience training operators or technicians is a plus Strong communication, analytical, and problem-solving skills Willing and able to travel up to 60% Please Do Not Apply If You: Have frequent job changes without demonstrated career progression Lack hands-on experience in plastics manufacturing or injection molding Have not supported or managed capital projects in an industrial setting Do not have experience in manufacturing environments Have misrepresented or unverifiable credentials Interview Process Recruiter Interview Hiring Manager Interview Final Panel Interview (Onsite) Offer Benefits & Perks Medical, Dental, Vision, and Life Insurance Retirement Plan Paid Time Off Signing Bonus (negotiable) Full Relocation Package (if applicable)

Donaldson is committed to solving the world's most complex filtration challenges. Together, we make cool things. As an established technology and innovation leader, we are continuously evolving to meet the filtration needs of our changing world. Join a culture of collaboration and innovation that matters and a chance to learn, effect change, and make meaningful contributions at work and in communities. The Manufacturing Engineer II role, evaluates and introduces process and product modifications, standards and improvements through knowledge of manufacturing equipment and processes, while increasing product quality, output and cost effectiveness for the corporation. This role is based out of Frankfort, IN and would require this individual to be on site regularly. Role Responsibilities: * Monitors and modifies equipment to ensure safety and efficiency in the production line. * Implements corrective actions. * Reviews and verifies accuracy of existing procedures and bill of materials. * Negotiates final design to ensure manufacturability and product requirements. Conducts testing and evaluation of products and processes. * Conducts studies for process and product improvements. * Develops analyses and testing procedures to anticipate any potential process or product failure. * Conducts studies to improve plan layout, production line efficiency and production line control. * Contributes to product failure mode and effects analyses. * Manages product or process development projects. * Collaborates on technical program objectives and product specifications that meet marketing and manufacturing needs. * Recommends and employs new equipment. * Provides technical support to developers to ensure manufacturability of developed products and processes. Minimum Qualifications: * Associate's degree and 4+ years of experience in engineering (Manufacturing or Mechanical preferred) or Bachelor's degree in Engineering, Computer Science, or related field and 2+ year of experience in engineering (Manufacturing or mechanical preferred) Preferred Qualifications: * 5+ years prior experience in a manufacturing environment. * Working knowledge of Lean Manufacturing tools and techniques * Experience with AutoCAD and/or SolidWorks * Working knowledge of Allen Bradley PLC's and their programming * The ability to direct, motivate, and provide clear direction in a production work environment. * Proven ability to troubleshoot mechanical/electrical and controls systems in an operational environment. * Proven project management skills including delivery of results on time and within budget through dynamic and creative thinking. * Excellent communication and analytical skills and proven ability to work effectively in cross-functional teams at all levels of the organization. Key words: Manufacturing, Engineering, AutoCAD, SolidWorks, Mechanical Employment opportunities for positions in the United States may require use of information which is subject to the export control regulations of the United States. Hiring decisions for such positions are required by law to be made in compliance with these regulations. Applicants for employment opportunities in other countries must be able to meet the comparable export control requirements of that country and of the United States. Donaldson Company has been made aware that there are several recruiting scams that are targeting job seekers. These scams have attempted to solicit money for job applications and/or collect confidential information, Donaldson will never solicit money during the application or recruiting process. Donaldson only accepts online applications through our Careers | Donaldson Company, Inc. website and any communication from a Donaldson recruiter would be sent using a donaldson.com email address. If you have any questions about the legitimacy of an employment opportunity, please reach out to ******************************* to verify that the communication is from Donaldson. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

Job Description Ventek Solutions (Ventek) is a leading manufacturer specializing in engineered shape molded foam components, protective packaging, and multi-material assembly solutions. The organization helps customers address complex challenges in product protection, component light-weighting, insulation, and design simplification. Ventek's services span a variety of industries, including construction, automotive, electronics, medical, and more. Ventek Solutions leverages creative design, thoughtful engineering, and meticulous program management to deliver customized solutions. Ventek operates 8 plants in the US and Mexico with corporate headquarters in Charleston, SC. Position Summary We are seeking an experienced Quality Tech 1 - 3rd shift 10pm - 6:30 am Mon - Friday Join our dynamic team as a Quality Technique Specialist, where your expertise will play a critical role in ensuring our products and services meet the highest standards of excellence. As a Quality Technique Specialist, you will be at the forefront of implementing and refining quality assurance processes, driving continuous improvement, and ensuring compliance with industry regulations. **Key Responsibilities:** - Develop, implement, and maintain quality assurance protocols and procedures. - Conduct thorough inspections and tests to ensure product compliance with specifications and standards. - Analyze data to identify areas for improvement and recommend effective quality enhancements. - Collaborate with cross-functional teams to resolve quality-related issues and implement corrective actions. - Document COA's COC's as required - Must know which measurement and test equipment(M&TE) tools are appropriate for various task and how to assess tool accuracy and precision; understand the concept of standards traceability for M&TE> - Train and mentor team members on best quality practices and continuous improvement methodologies. **Qualifications:** - Proven experience in quality assurance or a similar role. - Strong understanding of quality control methodologies and tools. - Excellent analytical and problem-solving skills. - Effective communication skills, with the ability to collaborate with diverse teams. - Proficiency in using relevant software and tools for quality management. - Quality certification (e.g., Six Sigma, ISO) is a plus. **Benefits:** - Competitive salary and performance-based bonuses. - Comprehensive health, dental, and vision insurance. - Opportunities for professional development and growth. - Collaborative and innovative work environment. - Flexible working hours and a generous vacation policy. If you are passionate about quality techniques and are eager to contribute to a forward-thinking organization, we encourage you to apply for this exciting opportunity. Join us and be a part of a team that values quality and strives for excellence in everything we do.

Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers. This position provides an opportunity to transition from other private, public, government or military experience to a 3M career. The Impact You'll Make in this Role As a Manufacturing Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by: Develop and implement improvements related to safety, quality, service, and productivity. Work closely with production and maintenance teams to perform troubleshooting activities and resolve equipment/downtime issues. Identify improvement opportunities requiring capital expenditure; establish justification and manage projects to completion. Actively participate in the day-to-day operations, EHS activities, MOC process change management, OEE analysis, and resolution of gaps in performance Initiate and lead Continuous Improvement projects. Use project management tools to convey objectives, timelines, obstacles, and next steps. Effectively troubleshoot defects and variation, perform root cause analysis, and apply problem solving skills. Develop process standards and other documentation supporting the operation. Provide engineering support for assigned areas including occasional availability on nights/weekends. Your Skills and Expertise To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications: Bachelor's degree or higher in a science or engineering discipline (completed and verified prior to start) from an accredited institution. Two (2) years of experience in a manufacturing environment in a private, public, government or military environment. Additional qualifications that could help you succeed even further in this role include: Experience in a Manufacturing Engineer role (specifically with process equipment). Experience leading multi-functional teams through complex projects from planning to completion. Experience developing and managing capital budgets and project completion within time and cost projections. Excellent problem solving and analytical skills. Experience with CI, Six Sigma, and Lean. Strong interpersonal, organizational and communication skills Strong data analysis skills including Excel, Minitab, and SQL querying experience. Experience presenting ideas in PowerPoint. Knowledge of robots, camera/scanner vision systems, and PLC programming Self-motivated, team player Work location: On-site, Cynthiana, KY Travel: May include up to 10% domestic/international Relocation Assistance: May be 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 3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope. Chat with Max For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting Applicable to US Applicants Only:The expected compensation range for this position is $98,413 - $120,282, 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: ******************************************************************* Faith Posting Date Range 07/03/2025 To 08/02/2025 Or until filled All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M.Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M.Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.Pay & Benefits Overview: https://**********/3M/en_US/careers-us/working-at-3m/benefits/3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law. 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. 3M 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 3M 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.

Business: Pharma Solutions Department: Facilities, Maintenance & Engineering Reporting to the Engineering Manager, the Manufacturing Process Engineer serves as subject-matter-expert and provides real-time, process engineering support to the manufacturing process. This position is responsible for design, project management, and implementation of new and existing systems, utilities and equipment, and ensures Quality, Compliance, and improved OTIF for all products produced at the manufacturing facility in Lexington, Kentucky. Reporting Structure This position reports to the Engineering Manager. Key Responsibilities: • Designs and project manages changes, improvements, new systems and or equipment. • Prepares Change Control Records (CCRs), Design Specifications, User Requirements Specifications, System Specifications, Design documents, Drawings, and Validation Documents for improvement, planned and corrective maintenance and system or process improvements • Leads/assists in Continuous Improvement Projects, including identification of opportunities, researches literature and vendors, prepares and presents proposals, develops and executes projects, and closes projects, all following appropriate change control methodologies • Represents Technical Subject Matter Expert (SME) in teams assembled to specify, install, troubleshoot and maintain systems, equipment and processes • Supports day-to-day production and maintenance activities • Provides training support as required. • Develops and or modifies SOPs for the Processes and Equipment. • Participates in deviation investigations to identify root causes and define corrective and preventive actions (CA/PA). • Creates and maintains drawings and sketches. • Manages Technical Publications Library to ensure the relevant manuals, specifications, design information for all of our facilities, utilities, equipment and products are on hand • Primary/First Line responsibility for operation and maintenance of the Validated Systems to maintain production capability required. • Primary/First Line responsibility for enhancements and upgrades of manufacturing related systems to maintain production capability. Qualifications: • Bachelor's degree in Mechanical, Electrical, or Chemical Engineering • Minimum 3-5 years of pharmaceutical manufacturing/maintenance experience required (parenteral/sterile filling experience preferred) • Expertise in troubleshooting production equipment/systems • Ability to work flexible schedule to support 24-hour operation (requires assignment on shift for 4 shift rotating days off schedule) • PC literate with standard office application (Word, Excel, PowerPoint) competency • Experience with maintenance and administration of both Windows-based and industrial (e.g., PLC) computer networks. • Experience with Allen-Bradley ControlLogix and Siemens PLCs; experience with HMI software applications; experience with automating processes and equipment • Knowledge and understanding of cGMPs including FDA, PMDA, and EU regulations; knowledge of cGMP validation requirements and techniques; experience with commissioning and validation protocol development and execution. • Knowledge and experience in cGMP CA/PA, root-cause analysis, risk assessment and investigation tools and techniques.

**_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 (***************************************************************************************************************************

Job DescriptionQuality Technician / Quality Inspector Full-Time | 2nd Shift | On-site The Quality Technician supports the Quality Department by ensuring products and processes meet internal standards and customer expectations. This role performs audits, inspections, and documentation activities to maintain compliance with quality management systems and promote continuous improvement. Essential Duties & Responsibilities Perform receiving and dock audits on finished goods and raw materials based on quality concerns or routine sampling. Conduct process audits within the organization as requested. Ensure FIFO and 5S procedures are followed throughout the department. Perform in-process inspections to verify correct dimensions, material tolerances, and overall product quality. Sort nonconforming products and report results to the Quality team. Track daily scrap and submit reports to Quality leadership. Recommend and help train temporary staff for sorting tasks as needed. Immediately report any nonconformance issues. Document and submit discrepancies to Quality leadership. Assist with preparation, packaging, and labeling of trial shipments. Contribute to internal and external audits as needed. Perform all inspections and audits according to established procedures. QualificationsMinimum Education & Experience High school diploma, GED, or equivalent. 12 years of experience in a manufacturing or production environment. Knowledge, Skills & Abilities Ability to operate hand jacks, scales, and measuring equipment. Strong attention to detail and ability to work independently. Effective communication and problem-solving skills. Computer Skills Proficiency in Office 365 or similar software. Experience with RF scanners. Familiarity with ERP systems (JDE preferred). Certificates / Licenses Valid drivers license. Supervisory Responsibilities None. Physical Demands & Work Environment Frequent standing, walking, reaching, and use of hands. Occasional sitting, stooping, kneeling, crouching, or crawling. Ability to lift and move up to 25 lbs regularly. Exposure to moving mechanical parts; moderate noise level. Ability to work independently with minimal supervision. Must work on-site 100% of the time. Schedule 2nd shift position. Overtime may be required based on production needs.

Job Title: Process EngineerJob Description Provide technical support to maintain safety and improve and optimize manufacturing operations and processes within the manufacturing facility. This role involves maintaining safe working practices while improving conversion costs, directly impacting competitiveness and profitability. Responsibilities * Maintain safety as the number one priority in daily responsibilities, responding to production crew needs, and developing and implementing process improvements for quality, waste, and productivity improvement. * Investigate causes of ongoing process, quality, production efficiency, and high waste problems. Develop solutions using problem-solving techniques. * Train machine operators on new equipment installations, modifications, and new operating procedures. * Maintain standard operating conditions system ensuring consistent manufacturing equipment processing conditions. * Work with plant BPI resources to ensure technical support resources are always available to production. * Collaborate with manufacturing supervisors, production crews, and maintenance to troubleshoot manufacturing problems and develop corrective actions. * Participate in the evaluation of projects and waivers to aid in effective scheduling and necessary product development coverage to minimize machine downtime and high waste. * Facilitate equipment modifications with plant project engineering to increase machine productivity and reduce waste. * Initiate and document procedures to safely increase machine productivity and reduce waste while maintaining product quality per customer expectations. * Supervise engineering co-op students depending on experience and workload, including performance evaluations, training, and directing activities. Essential Skills * Manufacturing engineering * Process improvement * Process engineering * Troubleshooting * Manufacturing process validation * Continuous improvement * Investigation and analysis * Six Sigma Additional Skills & Qualifications * Bachelor's degree in Engineering (Chemical, Electrical, Mechanical, or Industrial) with 1+ years of experience. * Hands-on manufacturing/process engineering experience working on floor with equipment. * Equipment troubleshooting skills. * Experience with roto presses or printing/lamination equipment, flexo/digital printing. * Experience with SPC/mini-tab. * Knowledge of equipment having air flow, Six Sigma. * Professional development classes in communication, conflict resolution, problem-solving skills, statistical process control, and advanced uses of software packages. * Strong interpersonal and communication skills, both oral and written. * Strong analytical and problem-solving skills. * General knowledge of flexible packaging products, including desired properties and quality standards. * Solid computer skills including Microsoft Word, Excel, Outlook, SharePoint, and the ability to quickly learn job-specific software. * Strong knowledge of processes used to manufacture and convert flexible packaging, especially blown film, metallization, flexographic printing, extrusion coating, adhesive laminating, and slitting/winding operations. Work Environment The role is based in a clean, climate-controlled manufacturing environment. The facility includes large equipment for printing/lamination involving rollers and roto presses. The team is small, consisting of only one other Process Engineer. Job Type & Location This is a Permanent position based out of Shelbyville, KY. Pay and Benefits The pay range for this position is $85000.00 - $110000.00/yr. Health, dental, vision, 401k, PTO/holiday pay Workplace Type This is a fully onsite position in Shelbyville,KY. Application Deadline This position is anticipated to close on Jan 27, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.