Reliability engineer jobs in Indiana

Job Title: DevOps Support Engineer (Service Reliability Engineer) Industry: Pharmaceutical JOB DESCRIPTION: Theoris is seeking a Service Reliability Engineer (SRE) Consultant to provide day-to-day support, monitoring, troubleshooting, and issue resolution for the MD3 infrastructure. The consultant will work alongside and under the technical direction of client staff, focusing on ensuring the reliability and performance of enterprise vendor applications hosted in AWS and a proprietary Kubernetes platform. The ideal candidate is proactive, self-sufficient, and comfortable working in an ambiguous environment. This role requires collaborating with vendors, driving deployments, and contributing to ongoing support as applications move through deployment cycles and into production. RESPONSIBILTIES: Continuously monitor the health and performance of the MD3 infrastructure, including data observations, HPC, and LiveDesign tasks. Utilize monitoring tools such as ServiceNow, Splunk, and Grafana to detect and respond to incidents in real-time. Perform regular job queue checks and maintenance activities. Monitor the MD3 dashboard and community chats/channels for issues or alerts. Diagnose, troubleshoot, and resolve technical issues related to the MD3 infrastructure. Collaborate with DevOps engineers and technical teams to resolve incidents. Document and communicate root cause analyses and resolution steps. Develop and implement automation scripts to streamline monitoring and troubleshooting. Identify areas for improvement in the infrastructure and propose solutions to enhance reliability. Participate in post-incident reviews to address monitoring and support gaps. Work closely with the DevOps team to align with business goals and research needs. Provide updates on incidents and resolutions to stakeholders. Participate in regular standups and scrums to discuss ongoing issues. Build and share bi-weekly reports on MD3 infrastructure status and performance. Develop and maintain knowledge articles for the help desk (ServiceNow) and user FAQs. Ensure documentation is up-to-date and easily accessible for the support team and end-users. Establish SLAs based on current ITSM practices for incident and problem resolution. Ensure all incidents and problems are addressed within defined SLAs. Performance Optimization: Fine-tune applications and infrastructure to meet performance benchmarks. Capacity Planning: Anticipate growth needs to scale infrastructure and optimize resource utilization. Create and maintain runbooks for critical alerts. REQUIREMENTS: Experience working with AWS-hosted vendor applications and Kubernetes platforms. Strong background in monitoring, troubleshooting, and supporting cloud-based infrastructures. Proficiency with monitoring tools such as ServiceNow, Splunk, and Grafana. Experience collaborating with DevOps engineers and technical teams. Ability to develop automation scripts to improve support workflows. Excellent communication and collaboration skills. Self-sufficient, proactive, and comfortable in ambiguous environments. Experience working in agile environments and participating in standups and scrums. Experience working with enterprise vendor applications and customized deployments. Background in performance tuning and capacity planning. Familiarity with help desk knowledge management and incident response SLAs. About Theoris: Our goal is to Fuel Your Career! As a Theoris team member, you join a culture based on people-centered values and an environment that fosters both personal and professional growth. We build long-term relationships with our clients and our consultants. With over 30 years of building strong relationships in the industry, we're uniquely positioned to make the right connections. This knowledge is used to find the right job placement. Our recruiting teams are experts dedicated to the information technology and engineering staffing space and are highly respected by our client base. Best-In-Class-Benefits We are in the people business; treating people right is our ONLY priority. Theoris Services consultants are full-time employees with full benefits, including: Robust Health Insurance 401(k) plan PTO accrual Paid holidays Excellent cash-based referral program

Looking to speed the progress of your engineering career? Join a market a leader in ingredient manufacturing that is investing in people, plant and technologies. Ready to make your application Please do read through the description at least once before clicking on Apply. About the Role Our Sr. Reliability Engineer role is fundamentally important to Primient plant operations. We list "Safety" first in our values because our greatest priority is caring for our people and the environment. Your development will be enhanced by working alongside expert colleagues in a highly collaborative team environment. You'll also join our structured development program: the Engineering Ladder. As your skills and experience grow, so will your responsibilities and impact. QUALIFICATIONS BS in Mechanical Engineering or a related engineering field. Experience in a Chemical Process Safety or Combustible Dust setting preferred. About You We are looking for engineers who strive for excellence and are eager for more responsibility: 7+ years of manufacturing engineering experience 3+ year working in a reliability engineering role (preferred) Background in rotating or fixed equipment, seals, piping, pumps, fans, blowers, and material handling equipment (preferred) Deep understanding of CMMS functions as they relate to cost tracking, predictive / preventive care, and maintenance processes. xevrcyc (preferred) Strong project management skills. Strong written and verbal communication skills, and attention to detail Key responsibilities: Sr. Reliability Engineer Work Capital projects both large (>$1m) and small ($

Operations Engineer - Pharmaceutical Manufacturing | Noblesville, IN Day Shift | Mon-Fri Onsite | Direct Hire | Full Benefits Day 1 We're representing a global manufacturer in the pharmaceutical industry that's experiencing significant growth and facility expansion. This new Operations Engineer role is ideal for someone who thrives at the intersection of manufacturing, quality, and engineering. You'll take ownership of quality events, root cause investigations, and process reliability improvements, ensuring consistent production performance in a regulated environment. What You'll Do Lead investigations for deviations, non-conformances, and CAPAs Manage process and reliability improvement projects to reduce recurring issues Partner with Quality, Production, and Engineering to drive accountability and compliance Author and review SOPs, Batch Records, and Change Controls Support regulatory and internal audits Analyze production data to identify trends and improvement opportunities What We're Looking For Bachelor's degree in Engineering or Life Sciences (advanced degree a plus) 2+ years of experience in pharmaceutical or related manufacturing environment Strong understanding of cGMP and aseptic or cleanroom operations Experience with root cause analysis and problem-solving tools (5 Whys, Fishbone, etc.) Project management and technical documentation skills Lean/Six Sigma certification or exposure preferred Hands-on, team-oriented approach in a fast-paced setting Why You'll Love It Here Global stability with strong local growth and investment Mission-driven work with direct impact on patient health Collaborative, team-focused culture and real advancement potential Competitive compensation, full benefits Day 1, and generous paid time off Interested? Let's connect. This is an excellent opportunity to join a growing pharmaceutical operation and make an immediate impact on production reliability, quality, and overall process excellence.

Johnson Service Group (JSG) is currently looking for a Process Engineerwho will be responsible for developing and optimizing continuous production and manufacturing processes to achieve the output, quality, and cost goals of the organization. Collect production data and apply standard scientific and statistical methods to analyze, document, and diagram production processes. Identify process bottlenecks and devises solutions to resolve. Recommend changes or upgrades to equipment, work methods, or other aspects of the process to improve efficiency and utilization of resources including labor, energy, and raw materials. This is a contract hire role with a food manufacturer in Plymouth IN Pay $55/hour Primary Responsibilities Evaluate and improve processes in manufacturing systems. Continuous review of existing processing equipment and procedures for relevance and efficiency, formulate solutions when shortfalls are noted. Maintain reliable and safe manufacturing systems while improving production rates, efficiencies, yields, costs, and changeovers. Work with Sales, R&D, Purchasing, Production and Quality to ensure successful conversion of small-scale pilot plant process to commercially viable production. Create and maintain master recipes and control recipes in the systems (SAP/WinCC). Provide technical input for recipe management and equipment selection from initial recipe development to scale-up to commercial production. Improve manufacturing process capability and production capacity while maintaining and improving quality standards. Develop and implement systems that optimize all phases of manufacturing process. Project Leader to improve quality and efficiency of manufacturing process. Perform new ingredient testing. Collect, record, transcribe data and publish report. Work with Production, QA, R & D and Maintenance groups to review records and data to find root causes of non-conforming production and develop corrective actions. Provide suggestions during incident investigations (e.g., Customer Complaint, product defect). Provide input, when necessary, on Food Safety, GMP and HACCP. Provide engineering and/or technical support for all factory floor systems, to include working with maintenance department to help troubleshoot and resolve known issues (including but not limited to PLC control system). Participate or lead in validation and commissioning of new and modified equipment. Develop, implement, and document novel and creative solutions to complex problems with various system dynamics. Formal Education Required BS in Food Engineering, Chemical Engineering or related engineering or science discipline. Specific Experience And Key Knowledge Requirements 10 years' experience in a food manufacturing environment. Special Skills And Abilities Required Excellent computer skills in a Microsoft Windows environment, SAP and other software systems. Knowledge and /or specialized training in HACCP, GMPs and SQF. Knowledge of Aseptic (HTST) Processing Systems and requirements. Knowledge of HMI, SCADA and data archiving systems. Knowledge of troubleshooting Ladder Logic Programming or PLC control programming. Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies. Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law. #D400

We are seeking a motivated professional to join our Manufacturing Engineering team, combining Industrial Engineering expertise with Continuous Improvement principles. This role focuses on optimizing production systems to improve safety, quality, efficiency, and overall throughput. Key Responsibilities: Design and implement efficient manufacturing processes, layouts, and workflows. Develop and standardize labor processes and improve operational flow. Lead Lean and CI initiatives including 6S, standardized work, and kaizen events. Analyze production data to identify improvement opportunities and cost savings. Support process automation, equipment utilization, and manufacturing transformation projects. Prepare reports, metrics, and financial justifications for new processes. Qualifications: Bachelor's degree in Industrial Engineering or related field (preferred). Hands-on experience in manufacturing and continuous improvement. Strong analytical, project management, and communication skills. Proficiency in Microsoft Office and CAD tools. Adaptable, collaborative, and effective in fast-paced environments.

The Science Team at Pride Health supporting the Pharmaceutical Industry that has an opening for Process Development Engineer in Indianapolis, IN! The Process Development Engineer plays a vital role in maintaining, troubleshooting, and optimizing equipment reliability in a regulated pharmaceutical manufacturing environment. Responsibilities include performing preventive, predictive, and corrective maintenance on mechanical, pneumatic, hydraulic, and control systems, ensuring compliance with cGMP standards and safety protocols. Additional Details: Contract Length: 6 months with the possibility of extension Pay range: $27 to $ 57/hour on W2 as per your experience Schedule: Flexibility with Schedules Must-Have : GMP maintenance experience: Minimum 3 years Pharmaceutical experience: Minimum 4-5 years Strong background in process systems within regulated environments (pharma, food & beverage, or healthcare-related). Key Responsibilities: Execute process and equipment maintenance activities in compliance with cGMPs, SOPs, and safety standards. Design, implement, and optimize production processes for improved efficiency and reliability. Troubleshoot and resolve issues in mechanical, electrical, pneumatic, and PLC-controlled systems. Develop and maintain accurate documentation, including Maintenance and Calibration Records, in line with GMP requirements. Support validation and qualification activities (IQ/OQ/PQ) for equipment and process changes. Collaborate with Quality, Engineering, and Production teams to ensure equipment reliability and compliance. Participate in continuous improvement initiatives and support root cause investigations. Maintain a safe and compliant work environment following OSHA and site-specific safety protocols. Support audits and inspections by regulatory agencies and internal quality teams. Qualifications 3-5+ years of experience in process or mechanical engineering within pharmaceutical, biotech, or regulated manufacturing industries. Strong understanding of cGMP principles and regulated environments. Proficiency in process troubleshooting, data analysis, and root cause investigations. Ability to interpret technical drawings, P&IDs, and engineering documentation. Excellent communication, analytical, and problem-solving skills. Comfortable working in confined spaces, at heights, and around chemicals. Hands-on experience with hand tools, power tools, and diagnostic instruments. Must be authorized to work in the United States. Russell Tobin offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors. APPLY NOW! About Us Russell Tobin is a leading minority-owned professional and technical recruitment and staffing advisory organization. We are comprised of specialized practices focusing on a variety of skill sets and industries. Having a depth and breadth of industry expertise, our subject matter experts are able to provide tailored and swift sourcing solutions to fulfill client hiring needs. In other words, we connect top talent with companies. We are the staffing arm of the Pride Global network, a minority-owned integrated human capital solutions firm, with additional offerings in vendor management, payroll programs, and business process optimization. As a certified minority-owned business, Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics. #LI-JR1

Job title: Principal Project Engineer ( Blending & Packaging Systems) Permanent About the role The Principal Project Engineer, Blending & Packaging is responsible for leading the engineering oversight and execution of two major packaging systems, one related to blending systems and one for composite can and tub packaging lines. This role spans the full lifecycle of project delivery, including front-end engineering, design development, construction, commissioning, and validation. The engineer will serve as the technical lead and integrator across cross-functional teams and external partners to ensure successful implementation aligned with strategic production goals. Responsibilities Project Oversight: Lead and coordinate engineering activities for two major packaging proposals, ensuring alignment with long-term production and expansion strategies. Design & Integration: Oversee development of process and packaging line layouts, equipment specifications, and automation architecture. Ensure integration of mechanical, electrical, and control systems across vendors. Construction & Commissioning: Support and guide construction planning, installation, and commissioning phases. Ensure readiness for validation and production ramp-up. Validation & Compliance: Lead validation strategy and execution in compliance with FDA, GMP, and internal quality standards. Ensure documentation and traceability across all phases. Stakeholder Engagement: Collaborate with internal teams (R&D, Supply Chain, Manufacturing, and Quality) and external engineering partners to ensure project milestones are met. Documentation & Change Control: Manage engineering documentation, change requests, and project records in accordance with document control systems. Continuous Improvement: Identify opportunities for process optimization, risk mitigation, and cost savings throughout the project lifecycle. Develop detailed project plans, including timelines, budgets, and resource allocation. Lead option analysis and packaging planning efforts. Work in partnership with engineering and construction partner firms to execute all phases of execution including commissioning. Conduct inspections and quality control checks to ensure the integrity and durability of packaging projects. Identify and mitigate potential risks associated with packaging projects. Prepare and maintain project documentation, including reports, drawings, and specifications. Identify opportunities for process improvements and implement best practices in packaging engineering. Required Skills: Bachelor's degree in Mechanical, Electrical, Packaging, or Industrial Engineering or related field. Minimum of 7 years of experience in packaging engineering in an FDA-regulated environment. Understanding of FDA, cGMP, ASTM, and ISO guidelines. Strong leadership, project management, and organizational skills. Proficiency in engineering software and tools (e.g., Revit, Autodesk Construction Cloud, Procore, AutoCAD, Civil 3D). Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Knowledge of building design and construction methods, materials, and regulations. Deep understanding of packaging engineering principles and practices. Works effectively with cross-functional teams and stakeholders. Ensures accuracy and thoroughness in all project-related activities. Flexible and able to adapt to changing project requirements and priorities. Manage stakeholders across the company gaining alignment and consensus around scope, costs, and schedule. Deliver Factory of the Future for in scope processes and products.

Compal is a world-leading manufacturer of diverse products, including notebook PCs, smart devices, and automotive electronics. Is this the next step in your career Find out if you are the right candidate by reading through the complete overview below. Engineers have the opportunity to work on cutting-edge projects xevrcyc and see their designs brought to life on a large, global scale.

Standard Work and Process Doc Development Safety and Manufacturing CNC Programming Development Entry Level Mistake Proofing related to Safety and Quality Control Plan, PFMEA, SFMEA and Risk Assessments Cycle Time Studies Standard Cost Review

Process and Automation Engineer Domestic & International Travel: Yes, 30-50% Contract Type: 6-Month Contract-to-Hire Company: Brooksource Engineering (On-site at a pharmaceutical manufacturing client) Compensation: $65/hour ++ Position Overview As a Process and Automation Engineer, you will focus on defining, validating, and optimizing high-speed assembly and packaging processes for pharmaceutical products. This role emphasizes mechanical systems, process characterization, and regulatory compliance while supporting major capital projects for new product launches and capacity expansions. You will collaborate with OEMs and internal teams to ensure robust process design, seamless equipment integration, and adherence to qualification standards (IO/OQ/PQ). Key Responsibilities Process Design & Optimization: Develop and refine process flows for automated assembly and packaging lines, ensuring throughput, reliability, and quality. Equipment Integration Oversight: Partner with OEMs to confirm mechanical and process requirements are met during design and installation. Engineering Studies & Characterization: Define and execute studies to characterize unit operations, establish operating ranges, and validate process capability. Risk Analysis & Mitigation: Apply FMEA and other risk assessment tools to identify and mitigate process and patient risks. Qualification & Validation: Lead or support Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities for new equipment and processes, ensuring compliance with cGMP and regulatory standards. Performance Analysis: Use statistical methods and process data to identify bottlenecks, optimize cycle times, and improve efficiency. Documentation & Compliance: Author and maintain process documentation, including SOPs, process flow diagrams, validation protocols, and qualification reports. Continuous Improvement: Drive Kaizen and OPEX initiatives to enhance process reliability and reduce cost of goods. Mentorship: Provide guidance to junior engineers on process validation strategies and best practices. Minimum Qualifications Process Engineering Expertise: Experience in mechanical assembly processes, high-speed packaging systems, and process optimization. Capital Project Delivery: Proven ability to support large-scale process implementation projects in regulated environments. Validation Knowledge: Hands-on experience with IO/OQ/PQ protocols and execution. Preferred Qualifications Familiarity with cGMPs, commissioning, and qualification processes. Experience with DOE, GR&R, and statistical analysis for process improvement. Understanding of automation systems and their impact on process performance. B.S./M.S. in Mechanical, Chemical, or Industrial Engineering (or equivalent experience). Additional Information Travel: Up to 25% on average, with peaks exceeding 50% during major project phases.

At IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry. We are looking for a talented CQV Engineer II to join our team at our office located in _____________. In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS clients. You will also follow IPS and client standards and requirements, overall good industry practices for C/Q/V services, and regulatory requirements. You may also perform standalone commissioning services for non-FDA-regulated clients. Additional Responsibilities Write C/Q/V documents following established standards and templates, including but not limited to the following: Commissioning Forms C/Q/V Protocols and Summary Reports Standard Operating Procedures Impact Assessments Specifications (URS/FRS/DDS) FATS/SATs Perform field/site activities including, but not limited to, the following: Attend and witness FATs and SATs as a representative of IPS clients. Execution of commissioning forms and witnessing of vendor start-up and testing. Execution of C/Q/V protocols. Walkdown and verification of system drawings (P&IDs, as-builts, etc.) Compile data and prepare reports for completed C/Q/V activities including ETOPs, protocol data packages, etc. Assist in deviation investigation and resolution of problems and issues encountered during field execution activities. Work with the Project Delivery department or CM for start-up and vendor testing. Witness and troubleshoot as required. Primary responsibilities include C/Q/V of equipment and systems, including CSV and automation, supporting pharmaceutical, biotech, and medical device industries. Read, understand, and utilize the IPS Best Practices and SOPs for the delivery of compliance services Perform work to meet IPS budget requirements and quality standards. Provide consistent, complete, and timely feedback and reports to IPS project leaders, project managers, or management, of project status and issues, as requested. Come join our dynamic team that creates world-class designs for our clients, and propel your career to new horizons! Qualifications & Requirements Bachelor of Science in Engineering. 2+ years of relevant work experience. This is an entry-level position. Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA. Preferred Qualifications Experience in writing and execution of PFC, FC, IQ, OQ, and PQ forms/protocols for GMP Utilities, Equipment, Systems, and Software. General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validation processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA. Context & Safety This position will have up to 100% travel to the site, or as required by the assigned project. You may be assigned to a client site for an extended period. Overnight travel or staying in the city of the client's location is possible depending on the assignment. Travel will be per the IPS Travel Policy, client-specific travel policy, or project-specific travel plan. You may visit active construction sites and will be required to take site safety training and adhere to site safety rules. This position is a safety-sensitive position. The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas. All interviews are conducted either in person or virtually, with video required. About Us IPS, a Berkshire Hathaway company, is a global leader in technical consulting, architecture, engineering, procurement, construction management, commissioning, qualification, and validation services for technically complex facilities. Integration is how we think and work. It requires the ability to unite existing and emerging technologies into a process that reliably delivers products and accelerates speed to market. That end-to-end mindset allows us to be agile and anticipate challenges as we move projects toward operational readiness. IPS applies design and delivery expertise, client-side experience, and supplier-side insight to every project. We infuse our curiosity, our passion, and our commitment to partnership in delivering solutions at any scale. We meet our clients where they are and get them to where they need to go. That's only possible when we care as much as our clients do. Specialties Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV, and Staffing Services. All qualified applicants will receive consideration for employment at IPS without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. IPS is proud to be an affirmative action and equal opportunity employer. Connect With Us! If you do not meet the qualifications for this specific role, but would like to submit your resume for general consideration, please click here!

What Makes a Honda, is Who makes a Honda Honda has a clear vision for the future, and it's a joyful one. We are looking for individuals with the skills, courage, persistence, and dreams that will help us reach our future-focused goals. At our core is innovation. Honda is constantly innovating and developing solutions to drive our business with record success. We strive to be a company that serves as a source of “power” that supports people around the world who are trying to do things based on their own initiative and that helps people expand their own potential. To this end, Honda strives to realize “the joy and freedom of mobility” by developing new technologies and an innovative approach to achieve a “zero environmental footprint.” We are looking for qualified individuals with diverse backgrounds, experiences, continuous improvement values, and a strong work ethic to join our team. If your goals and values align with Honda's, we want you to join our team to Bring the Future! Job Purpose Utilize engineering methods to engage in continuous improvement activities, while improving SQDCM (Safety, Quality, Cost, Delivery, Morale, Environment) characteristics. Key Accountabilities Root cause identification and countermeasure for complex problems Data analysis for identification of improvement activities Completion of studies (project/plant characteristic impacts) Work closely with other engineering groups to develop solution and implement countermeasures Manage projects (Mass production) Develop processes from drawing Work with production team to understand new processes Work with counterparts in other North American plants to understand change points Data analysis/trend identification Maintaining/achieving production targets (budgets/efficiency/quality/delivery) Qualifications/Experience/Skills Minimum Educational Qualifications: Bachelor's degree in engineering field or equivalent related experience Minimum Experience: Prefer intern or co-op experience (1-2 terms) or related work experience at two years Other Job-Specific Skills: Strong continuous improvement mindset; MS office; problem solving/decision making skills; project management capabilities Working Conditions Shift rotation when needed and weekend work when needed What differentiates Honda and make us an employer of choice? Total Rewards: Competitive Base Salary (pay will be based on several variables that include, but not limited to geographic location, work experience, etc.) Paid Overtime Regional Bonus (when applicable) Industry-leading Benefit Plans (Medical, Dental, Vision, Rx) Paid time off, including vacation, holidays, shutdown Company Paid Short-Term and Long-Term Disability 401K Plan with company match + additional contribution Relocation assistance (if eligible) Career Growth: Advancement Opportunities Career Mobility Education Reimbursement for Continued Learning Training and Development programs Additional Offerings: Tuition Assistance & Student Loan Repayment Lifestyle Account Childcare Reimbursement Account Elder Care Support Wellbeing Program Community Service and Engagement Programs Product Programs Honda is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, veteran status, or any other protected factor.

LHH Recruitment Solutions is seeking for a client a Continuous Improvement Engineer Experience Level: Mid-Senior (6+ years) Preferred Certification: Six Sigma (Green Belt or higher) LHH Recruitment Solutions is partnering with a client to find a highly skilled Continuous Improvement Engineer who will drive operational excellence and efficiency across processes. The ideal candidate will leverage proven methodologies, data-driven insights, and a collaborative approach to identify opportunities for improvement, implement sustainable solutions, and foster a culture of continuous improvement. Key Responsibilities Analyze current processes to identify inefficiencies and develop actionable improvement plans. Lead cross-functional projects focused on process optimization, cost reduction, and quality enhancement. Utilize Lean and Six Sigma principles to design and implement process improvements. Develop and maintain performance metrics to monitor progress and ensure sustainability of improvements. Facilitate workshops and training sessions to promote continuous improvement culture across teams. Collaborate with stakeholders to align improvement initiatives with business objectives. Prepare detailed reports and presentations for leadership on project outcomes and ROI. Qualifications Experience: Minimum 6 years in process improvement, operational excellence, or related roles. Education: Bachelor's degree in Engineering, Operations Management, or related field (Master's preferred). Certifications: Six Sigma Green Belt or higher strongly preferred; Lean certification is a plus. Proven track record of leading successful improvement projects in manufacturing, supply chain, or service environments. Strong analytical skills with proficiency in data analysis tools. Excellent communication and stakeholder management skills. Benefits Medical, Dental, and Vision PTO 401k

An exciting career awaits you At MPC, we're committed to being a great place to work - one that welcomes new ideas, encourages diverse perspectives, develops our people, and fosters a collaborative team environment. E&M Electrical Reliability Engineer Overview The primary role of the Electrical Reliability Engineer is to provide technical expertise in the support of pipeline station equipment across Marathon Pipe Line (MPL). The major role of the position is to provide technical support to projects and department initiatives. Other major roles include the development of specifications, MOC approvals and Region Supervisory and Technician support and liaison. This position reports to the Electrical Reliability Engineering Manager with no indirect report requirements. The Engineer serves as a mentor to the L&SE engineers Responsibilities Provide technical input on project requirements and potential solutions. Provide electrical engineering leadership on project development, design and electrical issues. Will be assigned to Technical Design Reviews (typically on Level 2+ projects) to ensure appropriate application of the standards and resolve design conflicts of the standards. L&SE completes Level 0 and 1 project designs without the need for the specialists to provide direction. Perform MOC Evaluations for assigned projects. Research issues and make engineered recommendations on equipment design. Provide electrical input to TAPRoot investigations Provide input on standard development act as owner/SME of assigned standards. Project close out support - Review as built drawings for completeness as a part of Intelex close-out MOC closeouts Develop standard detail drawings Provide ArcFlash, Hazardous Area Classification, and ETAP reviews on large projects. Develop the programing requirements for Motor Protection and Feeder Protection relays and provide training to specialists. Owner of all station ETAP models. L&SE owns Rectifier and Block valve ETAP documentation and maintenance Help identify where Electrical generator plans are needed and PIF the ideas. Participate as an SME on MPC/Industry Communities of Practice. Provide SME for commercial development/special projects, due diligence reviews, joint interest maintenance activities. Work with third parties including contactors, engineering consultants, manufacturer reps, equipment vendors, the local utilities, inspectors and other pipeline companies as necessary Research and evaluate manufacturers for the purchase of equipment. Research, evaluate, and specify equipment to assure equipment is fit for purpose. Assist Electrical Reliability Manager with setting budgets and goals for upcoming years. Assist other Electrical SMEs with the planning and execution of electrical PMs as necessary Maintain Technical Competency and have working knowledge of the following equipment: Low and medium voltage electrical equipment including Switchgear MCCs VFDs Transformers Motors MV circuit breakers and transrupters MV substation equipment MV cables Conduit, cable tray and other raceways Overhead and underground power distribution systems Possess and maintain working knowledge of the following industry standards NFPA 70 (NEC) National Electrical Code NFPA 70E Electrical Safety in the Workplace NFPA 70B Electrical Equipment Maintenance Program OSHA 1910 Subpart S: Electrical API RP 500 Recommended Practice for Classification of Locations for Electrical Installations at Petroleum Facilities Classified as Class I, Division 1 and Division 2 Occasionally backfill for the Electrical Reliability Manager or other electrical specialists. Identify individual career objectives and develop a plan to achieve career objectives. Qualifications Education: minimum of Bachelor's degree in Electrical Engineering Indianapolis preferred but open to other locations Technical Experience: Five (5) years or more of pipeline operations, engineering or maintenance experience seem to provide the experience needed. A Professional Engineering License is desired but not required. Leadership: Display ability to make technical judgments and decisions is required Good Communication skills: written and oral Interpersonal skills: being able to relate to various people and groups and maintain positive relationships Strategic thinking Experience in working around electrical parts and the construction of them, such as hands-on experience with mechanical and electrical equipment and project leader experience. This experience will arm the engineer with the ability to judge critical paths. Facilitate change as required by department and company goals. Be willing to embrace new technology and other initiatives. Travel Requirement: 10 - 15% #LS #mpl As an energy industry leader, our career opportunities fuel personal and professional growth. Location: Indianapolis, Indiana Additional locations: Job Requisition ID: 00019669 Location Address: 10722 E County Road 300 N Education: Employee Group: Full time Employee Subgroup: Regular Marathon Petroleum Company LP is an Equal Opportunity Employer and gives consideration for employment to qualified applicants without discrimination on the basis of race, color, religion, creed, sex, gender (including pregnancy, childbirth, breastfeeding or related medical conditions), sexual orientation, gender identity, gender expression, reproductive health decision-making, age, mental or physical disability, medical condition or AIDS/HIV status, ancestry, national origin, genetic information, military, veteran status, marital status, citizenship or any other status protected by applicable federal, state, or local laws. If you would like more information about your EEO rights as an applicant, click here. If you need a reasonable accommodation for any part of the application process at Marathon Petroleum LP, please contact our Human Resources Department at ***************************************. Please specify the reasonable accommodation you are requesting, along with the job posting number in which you may be interested. A Human Resources representative will review your request and contact you to discuss a reasonable accommodation. Marathon Petroleum offers a total rewards program which includes, but is not limited to, access to health, vision, and dental insurance, paid time off, 401k matching program, paid parental leave, and educational reimbursement. Detailed benefit information is available at ***************************** hired candidate will also be eligible for a discretionary company-sponsored annual bonus program. Equal Opportunity Employer: Veteran / Disability We will consider all qualified Applicants for employment, including those with arrest or conviction records, in a manner consistent with the requirements of applicable state and local laws. In reviewing criminal history in connection with a conditional offer of employment, Marathon will consider the key responsibilities of the role.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. The position is responsible for working with Contract Manufacturer(s) (CM) and Original Equipment Manufacturer (OEM) to support, supply, quality, and continuous process improvement of delivery devices, sub-assemblies, and components that are supplied to Lilly packaging and manufacturing sites. The Lead Engineer ensures that equipment is in-control, compliant, and capable of meeting customer needs, while also driving associated continuous improvement effort. Additionally, the Lead Process Engineer serves as the technical leader for the engineering team and leads project prioritization and strategic continuous improvement planning while also training and mentoring the CMO Process Engineers within their assigned scope of CMs. Key Objectives/ Deliverables: Obtain technical expertise of equipment and processes in area of responsibility. This includes clear understanding of equipment flow chart/process flow document, and critical process parameters for the process. Develop and provide training, technical oversight and mentorship to CMO process engineers. Provide program management support for CMO process engineers across multiple sites to evaluate reliability improvement projects, replicate across similar lines in the platform network and the shutdown management of those projects. Work with external companies and project teams to develop product and process improvements. Evaluate scope and business cases for proposed capital improvement projects. Lead prioritization of process and product changes necessary to maintain, sustain and improve the manufacturing process. Ensure Technical Stewardship projects to improve device design are prioritized within the Process Team agenda. Support/lead the resolution of escalated manufacturing related issues, including deviations, investigations and evaluation of manufacturing data and supply chain coordination issues. Utilize formal problem-solving techniques, including Root Cause Analysis, to resolve equipment issues. Support the timely completion of documentation and process updates resulting from local and global procedural changes, audits, complaint investigations, documentation reviews, product reviews, process reviews and equipment reviews. Develop effective and productive working relationships with colleagues at CM sites. Define and mitigate technical and patient risks, including use of FMEA Minimum Requirements: Minimum 3 years engineering experience in automated assembly equipment Root Cause Analysis, Investigation and Problem Solving skills Strong communication, teamwork, and networking skills Training, coaching and mentoring experience Proven ability to organize and prioritize multiple tasks Strong attention to detail Additional Preferences: Dry device assembly experience preferred Experience with DOE and statistical methods as applied to engineering studies and reports Experience in capital project delivery and project management scheduling and budgeting processes Experience working with 3rd party suppliers, specifically Original Equipment Manufacturers (OEM's) and Contract Manufacturers (CM's) Education Requirements: BS in an Engineering or Engineering related field Other Information: Ability to travel 25% on average with peak over 50% for a few months at a time Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $64,500 - $167,200 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Major Tool & Machine (MTM) takes great pride in the talented people that come to work here. We offer market leading pay, benefits, optional 4/10 work schedule, quarterly bonus potential and a culture focused on employee engagement. Our work is essential to the world as we provide CNC machining, manual and robotic welding, engineering, program management, inspection, assembly and cleanroom services on a large scale projects to our customers in the Space, Defense, Energy, Nuclear, and Commercial Industries. Whether you are looking for a place to put your current strong skills to work in a more challenging, purpose filled environment, or you ultimately want long term professional growth and advancement opportunities, this could be the place for you. We are seeking a high caliber Process Engineer. In this role, you will prepare estimates and quote new jobs for RFQs and develop work order material and new manufacturing processes for new product launches, based on customer requirements. Duties: Complete estimates using VISUAL Manufacturing. Obtain material, subcontract and sublet quotations from materials department as necessary. Conduct contract review of technical requirements versus quotation and coordinate order acknowledgment with CFT Leader. Complete quality planning for projects. Maintain part hierarchy and drawing/revision number documentation. Provide technical support for manufacturing, material and subcontract/sublet contracting. Complete disposition, root cause analysis and corrective actions as necessary for non-conformances. Create fixture and process drawings as necessary Review and disposition Engineering Change Requests Conduct job release and post job review meetings. Participate in performance improvement activities with manufacturing personnel. Review Customer Change Requests, evaluate cost and delivery impact. Notify Sales and incorporate as necessary. Maintain electronic job folder. Requirements: Bachelor's Degree in Mechanical or Industrial Engineering, Mechanical Engineering Technology, or related field preferred. Prior Engineering experience developing new manufacturing processes for new product launches. The ideal candidate will have a strong background in machining, blueprint reading, and GD&T. 3D modeling experience preferred. Strong computer literacy, written and verbal communication, and project management skills are required. ABOUT US Major Tool & Machine (MTM) was founded in 1946, starting with only four employees to support the commercialization of the jet engine following World War II. Today, MTM is a contract manufacturer in Indianapolis, Indiana with a 600,000+ sq ft. manufacturing facility, 400+ skilled employees, best-in-industry business and quality systems, and project management expertise. Located for easy access on the east side of downtown Indianapolis, we are short commute away from most any place in the counties surrounding Indianapolis. Major Tool is a Precinmac company, a portfolio of businesses across the US and Canada that provide similar machining, fabrication and other manufacturing services to customers who provide critical services in turn in their various industries. Our Precinmac values are Trust, Gratitude, Action, Excellence and Growth, with a commitment to live these out daily in our workplaces. Benefits Excellent Benefits including three health insurance plan options - with a base plan option requiring ZERO employee paid premium. Dental and vision plans have very reasonable employee premiums. Participants in our health insurance have the onsite clinic available at no additional charge for medical services. All employees can access the mental health services provided in the clinic, For HDHP health insurance options, we contribute to your health savings account (HSA) and offer other flexible spending account (FSA) options. We support your retirement goals with a 401k company match. In addition to work schedule options we provide immediate Paid Time Off (PTO) availability and 10 paid Holidays, Along with in house training programs, we offer educational assistance for coursework that will support your career growth at Major Tool, We care about the health of our employees and provide a tobacco free facility, onsite fitness center and wellness events, short and long term disability and life insurance coverage fully paid. We are proud to be an Equal Opportunity Employer. We follow all applicable non-discrimination laws relating to employment, including candidates with disability or veteran status.

Martinrea is a diversified global automotive supplier, engaged in the design, development and manufacturing of metal parts, assemblies and modules, complex fluid management systems and aluminum products. We employ approximately 15,000 skilled and motivated people at manufacturing, engineering and technical centers in Canada, the United States, Mexico, Brazil, Germany, Slovakia, Spain and China. Our business strategy leverages world-class technologies, motivated and talented people, and high-quality products. We aim to be the best automotive parts supplier in the world in the products and services we provide our customers. Are you tired of driving out of town for work? Do you want to make a difference in your community and have a greater work life balance? Martinrea North Vernon; part of the Fluids Division of Martinrea, is currently seeking an experienced Process Engineer. Join our team and stop living to work; work to live with Martinrea North Vernon. Job Summary: The Process Engineer position provides professional guidance, leadership, and training to other personnel; is responsible for, but not limited to, planning and coordinating new manufacturing projects; improving manufacturing processes, layouts, and tooling. Required Minimum Qualifications: University education in engineering and/or technical field preferred Engineering in a manufacturing field Three (3) to five (5) years of OEM manufacturing and support experience (automotive industry preferred). Critical Success Factors: Excellent attendance Work with management to report and monitor process compliance Collaborate and communicate effectively across different organizational levels, functions, and businesses. Highly proficient with the full Microsoft Office suite (Excel, Word, Access, PowerPoint, Outlook and Visio). Excellent communication skills (English written and oral). Excellent time management and work organizational (prioritization) skills. Excellent analytical and problem solving skills to resolve new and unique problems. Ability to grasp modern technology quickly Responsibilities: Responsible for creating, maintaining and implementing product Process Flows and Process FMEA's in coordination with quality documents (Control Plans) by following QA-WI-051 " Documentation Requirements" Participate in APQP and compliance with the program Gate Review processes. Tooling/Equipment Sourcing and Acceptance Criteria Tooling/Equipment Run-Off Approval Mistake proofing Identification and Tracking Mistake proofing validation Set-Up Instructions Monitors project development, approval, and implementation schedules and timelines/Ghantt Charts Attends builds at customer assembly plant Familiarity with Ford/GM/Chrysler change processes AutoCAD Supports timely completion of all Internal and External customer complaints Working Conditions Office Environment Plant Floor (PPE required) Effort/Physical Demands Constant communication with employees, peers, and management Overtime as required Health and Safety Responsibilities Must work in accordance with Health and Safety regulations, Company Rules, Plant Rules, policies and procedures Must use or wear equipment, protective devices or certain clothing as required by the company Other Duties: This is not designed to contain a comprehensive list of duties and responsibilities required for this job. Duties and responsibilities may change at any time with or without notice Disclaimer: This job description does not constitute a contract of employment.

Working at Freudenberg: We will wow your world! Responsibilities: Analyze existing manufacturing and operational processes to identify areas for improvement. Design, develop, and implement process enhancements that improve quality, reduce waste, and increase throughput. Collaborate with cross-functional teams including Operations, Quality, Maintenance, and Engineering to drive continuous improvement initiatives. Develop and maintain process documentation including work instructions, process flow diagrams, and standard operating procedures. Monitor process performance using KPIs and data analytics; recommend corrective actions as needed. Support capital projects and equipment upgrades by providing process input and validation. Lead root cause analysis and problem-solving efforts for process-related issues. Ensure compliance with safety, environmental, and regulatory standards in all process changes. Train and mentor operations staff on new processes and improvements. Qualifications: Bachelor's degree in Engineering (Mechanical, Industrial, Chemical, or related field). 3+ years of experience in process engineering or manufacturing environment. Strong analytical and problem-solving skills. Proficiency in process mapping, Lean, Six Sigma, or other continuous improvement methodologies. Experience with data analysis tools and manufacturing software (e.g., ERP, MES). Excellent communication and collaboration skills. Ability to manage multiple projects and priorities in a fast-paced environment. Communication & Collaboration: Communicates clearly and concisely, while engaging proactively with colleagues at all levels of the organization. Value for Customers: Anticipates, understands and meets internal/external customers' needs and expectations. Develops solutions based on a customer centric approach. Innovation: Drives and supports innovative ideas, while taking informed risks to seek and develop new or improved solutions. Drive & Execution: Proactively identifies what needs to be done and takes action. Explores new ways and pursues new opportunities. The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law. Freudenberg-NOK General Partnership

Satellite Suites is looking for a motivated Manufacturing Engineer to join our team. In this role, you'll take ownership of designing, developing, and improving our production processes, implementing new manufacturing equipment, and working in a cross functional team to ensure we maintain high standards of safety, quality, and efficiency. You'll also play a key role in shaping the future of our Suites product line and drive innovation across the organization. We're seeking someone who thrives on problem-solving, has a passion for process improvement, and wants to make a real impact on both our products and our team. Why Join Us? Innovate & Lead: Be a key player in designing and implementing cutting-edge processes. Your work will directly contribute to our success. Collaborative Team: Work alongside talented engineers, production experts, and leaders. We foster a supportive, team-driven environment. Professional Growth: We value learning and development. You'll have opportunities to grow, both in technical skills and leadership. Key Responsibilities: Design, develop, and implement manufacturing processes for current and future product lines. Continuously analyze and improve production systems to reduce waste and boost efficiency. Lead and manage engineering projects from concept through completion, ensuring timely delivery. Collaborate with cross-functional teams to troubleshoot and resolve design or production challenges. Drive cost-saving initiatives while maintaining high quality and safety standards. Prepare, review, and maintain technical documentation including drawings, reports, and specifications. Stay current on new technologies and industry best practices to innovate and enhance product designs. Qualifications: Education: Bachelor's degree in Mechanical Engineering, Automotive Engineering, or a related field. Experience: Minimum 5 years of experience in vehicle or trailer design, manufacturing, or related industries. Technical Skills: Proficiency in CAD software (AutoCAD, SolidWorks) and understanding of electrical systems. Preferred Certifications: SolidWorks, Lean Six Sigma. Technology Skills: Experience with MS Office, Sage X3 is a plus. Soft Skills: Strong problem-solving abilities, excellent communication skills, and a collaborative team player. Physical Requirements: Ability to lift up to 25 pounds regularly and up to 50 pounds occasionally, with extended periods of standing or walking. What We Offer: Competitive Compensation Comprehensive Benefits including health, dental, and retirement plans with profit sharing. Career Development Opportunities Dynamic, Innovative Work Environment