Support all Manufacturing Engineering functions for North America powertrain battery tray/frame, casting, components, engine, and transmission programs. Their primary role of this function is to participate within an Engineering team to develop and launch processes that meet all objectives for safety, quality, delivery, and cost for both new model (NM), non-new model (NNM), and adaptation programs. Main responsibilities include: Perform assessments for process changes and related investment requirements for cost studiesUnderstand engineering scope definition, Requests for Quotes (RFQ’s), sourcing, technical evaluations, design, manufacturing, and installation of air/mist/coolant collectors and filtrationSupport and prioritize the Non-New Model (NNM) powertrain programs requests and ensure that approved programs are completed on time and within budgetSupport all New Model (NM) program’s facilities aspects including site preparation and machine installationSupport flow activities on programs ensuring successful implementation and tracking of the Iron Triangle (Scope, Timing, and Cost)Participate in the implementation of Stellantis Production Way (SPW) methodology, supporting all activities including deployment of advanced SPW tools and guide systematic root cause problem solving methods to attack risksDevelopment/improvement of process and equipment standards related to facilities infrastructure.Support manufacturing plants located in Dundee and Trenton, Michigan, Kokomo, Indiana, and Saltillo, Mexico; transmission plants in Kokomo and Tipton, Indiana; and casting plants in Toledo, Ohio, Kokomo, Indiana, and Etobicoke, Ontario in conjunction with Global Center of Competency initiativesDrive standardization across plants in all regions

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.Organization and Position OverviewLilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact.The HVAC Engineer is the site Subject Matter Expert (SME) for site HVAC (GMP and non GMP) and the ancillary systems associated within the facilities. During the project phase, the HVAC Engineer will be a key player in the cross functional project team in charge of the construction, commissioning, qualification, start-up and operational readiness of all HVAC systems. During the day-to-day operation, the HVAC Engineer will be responsible for effectively, reliably, and cost effectively operating the site’s HVAC (GMP and non-GMP) and ancillary systems associated within the facilities, maintaining all these systems in a state of compliance, in-control, and fit for use, capable of meeting all site needs. The HVAC Engineer will also be responsible for driving continuous improvement initiatives and local capital investment.Be the SME with a deep technical expertise in all systems (GMP and non-GMP HVAC and ancillary systems associated within their facilities), understanding their applications in pharmaceutical manufacturing, understanding flow charts and process parameters, and awareness of industry trends.Ensure the assigned processes are aligned with Industry and Lilly StandardsSupport risk assessment exercises using the different tools available (e.g. FMEA)Engage in teams, committees, or other groups and/or individually to achieve the departmental, site and/or company goalsInitial project asset delivery phase and future local capital investment:Lead or engage in projects/changes for all the systems ncluding Design, verification activities (IV/OV/PQ), as user representative for capital projects or delivery agent for local projects.Develop the proper documentation (URs, Specification, test cases, etc..) to demonstrate that systems are properly installed, qualified and started up and that remains in a controlled stateContribute to the process resource assessment, capital plans, expense budgets, and prioritize appropriateDaily Support for operations:Monitor utility systems and maintain KPI’s to assure that they are operating properly, in compliance with requirements.Provide written instructions for the proper way to operate and maintain the equipment and process to assure that the system operates within the controlled parametersImplement efficient and effective maintenance and reliability techniques,Apply problem solving skills by leading equipment failures troubleshooting, demonstrating RCA lead investigator proficiency and guide operations personnel in the resolution of process issues.Provide customer consultation and notifications on issues that involve utilities areas assignedAssure that all necessary items are identified on the proper tracking systems, and make sure that items are completed by the required dateProvide technical assistance as necessary to maintenance, and operations personnelSupport internal and external inspections and investigations (including Quality and HSE)Maintain efficient communications with appropriate site customer groupsProficiency with the Trackwise and CAPA systemsBasic Requirements:Bachelor’s degree in Engineering (prefer ME, MET, EE, Chem E)5+ years of experience in HVAC/Utilities and their use in a manufacturing setting, pharma preferred.Additional Preferences: Previous start up experience for new site HVAC systemsExperience with Building Management SystemsUnderstanding energy reduction techniques used in HVAC systemsPrevious equipment commissioning experienceEngineering experience with manufacturing plant utilitiesProject management experienceExperience with maintenance and computerized maintenance management systems (CMMS)Previous experience with deviation and change management systems including TrackwiseExcellent interpersonal, written and verbal communication skillsKnowledge of cGMPDemonstrated high level of understanding of engineering concepts, 1st principles, and engineering functional standardsStrong technical capability and ability to train and mentor othersOther Information:Initial location at Lilly Technology Center, Indianapolis.Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.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 (https://careers.lilly.com/us/en/workplace-accommodation) 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), enAble (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 - $167,200Full-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

Support all Manufacturing Engineering functions for North America powertrain battery tray/frame, casting, components, engine, and transmission programs. Their primary role of this function is to participate within an Engineering team to develop and launch processes that meet all objectives for safety, quality, delivery, and cost for both new model (NM), non-new model (NNM), and adaptation programs. Main responsibilities include: Perform assessments for process changes and related investment requirements for cost studiesUnderstand engineering scope definition, Requests for Quotes (RFQ’s), sourcing, technical evaluations, design, manufacturing, and installation of air/mist/coolant collectors and filtrationSupport and prioritize the Non-New Model (NNM) powertrain programs requests and ensure that approved programs are completed on time and within budgetSupport all New Model (NM) program’s facilities aspects including site preparation and machine installationSupport flow activities on programs ensuring successful implementation and tracking of the Iron Triangle (Scope, Timing, and Cost)Participate in the implementation of Stellantis Production Way (SPW) methodology, supporting all activities including deployment of advanced SPW tools and guide systematic root cause problem solving methods to attack risksDevelopment/improvement of process and equipment standards related to facilities infrastructure.Support manufacturing plants located in Dundee and Trenton, Michigan, Kokomo, Indiana, and Saltillo, Mexico; transmission plants in Kokomo and Tipton, Indiana; and casting plants in Toledo, Ohio, Kokomo, Indiana, and Etobicoke, Ontario in conjunction with Global Center of Competency initiativesDrive standardization across plants in all regions

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.Organization and Position OverviewLilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact.The HVAC Engineer is the site Subject Matter Expert (SME) for site HVAC (GMP and non GMP) and the ancillary systems associated within the facilities. During the project phase, the HVAC Engineer will be a key player in the cross functional project team in charge of the construction, commissioning, qualification, start-up and operational readiness of all HVAC systems. During the day-to-day operation, the HVAC Engineer will be responsible for effectively, reliably, and cost effectively operating the site’s HVAC (GMP and non-GMP) and ancillary systems associated within the facilities, maintaining all these systems in a state of compliance, in-control, and fit for use, capable of meeting all site needs. The HVAC Engineer will also be responsible for driving continuous improvement initiatives and local capital investment.Be the SME with a deep technical expertise in all systems (GMP and non-GMP HVAC and ancillary systems associated within their facilities), understanding their applications in pharmaceutical manufacturing, understanding flow charts and process parameters, and awareness of industry trends.Ensure the assigned processes are aligned with Industry and Lilly StandardsSupport risk assessment exercises using the different tools available (e.g. FMEA)Engage in teams, committees, or other groups and/or individually to achieve the departmental, site and/or company goalsInitial project asset delivery phase and future local capital investment:Lead or engage in projects/changes for all the systems ncluding Design, verification activities (IV/OV/PQ), as user representative for capital projects or delivery agent for local projects.Develop the proper documentation (URs, Specification, test cases, etc..) to demonstrate that systems are properly installed, qualified and started up and that remains in a controlled stateContribute to the process resource assessment, capital plans, expense budgets, and prioritize appropriateDaily Support for operations:Monitor utility systems and maintain KPI’s to assure that they are operating properly, in compliance with requirements.Provide written instructions for the proper way to operate and maintain the equipment and process to assure that the system operates within the controlled parametersImplement efficient and effective maintenance and reliability techniques,Apply problem solving skills by leading equipment failures troubleshooting, demonstrating RCA lead investigator proficiency and guide operations personnel in the resolution of process issues.Provide customer consultation and notifications on issues that involve utilities areas assignedAssure that all necessary items are identified on the proper tracking systems, and make sure that items are completed by the required dateProvide technical assistance as necessary to maintenance, and operations personnelSupport internal and external inspections and investigations (including Quality and HSE)Maintain efficient communications with appropriate site customer groupsProficiency with the Trackwise and CAPA systemsBasic Requirements:Bachelor’s degree in Engineering (prefer ME, MET, EE, Chem E)5+ years of experience in HVAC/Utilities and their use in a manufacturing setting, pharma preferred.Additional Preferences: Previous start up experience for new site HVAC systemsExperience with Building Management SystemsUnderstanding energy reduction techniques used in HVAC systemsPrevious equipment commissioning experienceEngineering experience with manufacturing plant utilitiesProject management experienceExperience with maintenance and computerized maintenance management systems (CMMS)Previous experience with deviation and change management systems including TrackwiseExcellent interpersonal, written and verbal communication skillsKnowledge of cGMPDemonstrated high level of understanding of engineering concepts, 1st principles, and engineering functional standardsStrong technical capability and ability to train and mentor othersOther Information:Initial location at Lilly Technology Center, Indianapolis.Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.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 (https://careers.lilly.com/us/en/workplace-accommodation) 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), enAble (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 - $167,200Full-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

The Supplier Quality Engineer will strive to meet plant metrics by driving the suppliers defects back to the supplier and having them correctly root cause the issue and provide permanent corrective actions.Work alongside Resident Engineering and the rest of the plant quality and manufacturing teams to meet plant metrics of Warranty, FTC, FTQ, Cost, throughput, and the other various Quality goals. Drive team success by clarifying expectations and minimizing political hurdles. Demonstrate commitment to delivering results and champion achievements. Exhibit a willingness to do things differently and consistently translate ideas into actions that deliver results. Possess strong interpersonal skills with the ability to work in a team environment. Display effective communication skills to support meetings at all levels of the company, including senior leadership. Specific Roles & Responsibilities: Verify out of spec condition reported from plant floor Generate report of out of spec condition and contact vendor Work with production floor and finance to gather related costs associated with supplier non-conformances (NCT or SCAP) Lead or support containment of supplier pass-thru defects to vehicle assembly plants Lead and manage communication with suppliers for part returns, investigations and their reporting. Write and manage potential non-conforming tickets, 3CPRs and GIMs. Daily management of supplier table for part dispositions. Communication with production floor for notification of material defects and clean points. Follow up and verify supplier counter measures in accordance with SPW philosophy. Develop S&P matrix (for assigned suppliers) Process PPAPs on time on parts from CNs, New Supplier or Forever Requirements and provide objective evidence to approve or reject the PPAP. Quantify the Cost recovery of supplier issues. Keep up to date withthe Quality Commitment 7 information to show in the Leadership meeting. Prioritize proactive engagement with corporate supplier quality and suppliers for process improvements in accordance with S&P matrix. Review and approve proactive 8 Stage projects with supplier and corporate supplier quality. Complete QA Matrix and Kaizen projects to meet plant metrics. Pursue supplier visits to represent the plant'sinterest andwork towards guaranteeing quality parts.

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.Organization and Position OverviewLilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact.The HVAC Engineer is the site Subject Matter Expert (SME) for site HVAC (GMP and non GMP) and the ancillary systems associated within the facilities. During the project phase, the HVAC Engineer will be a key player in the cross functional project team in charge of the construction, commissioning, qualification, start-up and operational readiness of all HVAC systems. During the day-to-day operation, the HVAC Engineer will be responsible for effectively, reliably, and cost effectively operating the site’s HVAC (GMP and non-GMP) and ancillary systems associated within the facilities, maintaining all these systems in a state of compliance, in-control, and fit for use, capable of meeting all site needs. The HVAC Engineer will also be responsible for driving continuous improvement initiatives and local capital investment.Be the SME with a deep technical expertise in all systems (GMP and non-GMP HVAC and ancillary systems associated within their facilities), understanding their applications in pharmaceutical manufacturing, understanding flow charts and process parameters, and awareness of industry trends.Ensure the assigned processes are aligned with Industry and Lilly StandardsSupport risk assessment exercises using the different tools available (e.g. FMEA)Engage in teams, committees, or other groups and/or individually to achieve the departmental, site and/or company goalsInitial project asset delivery phase and future local capital investment:Lead or engage in projects/changes for all the systems ncluding Design, verification activities (IV/OV/PQ), as user representative for capital projects or delivery agent for local projects.Develop the proper documentation (URs, Specification, test cases, etc..) to demonstrate that systems are properly installed, qualified and started up and that remains in a controlled stateContribute to the process resource assessment, capital plans, expense budgets, and prioritize appropriateDaily Support for operations:Monitor utility systems and maintain KPI’s to assure that they are operating properly, in compliance with requirements.Provide written instructions for the proper way to operate and maintain the equipment and process to assure that the system operates within the controlled parametersImplement efficient and effective maintenance and reliability techniques,Apply problem solving skills by leading equipment failures troubleshooting, demonstrating RCA lead investigator proficiency and guide operations personnel in the resolution of process issues.Provide customer consultation and notifications on issues that involve utilities areas assignedAssure that all necessary items are identified on the proper tracking systems, and make sure that items are completed by the required dateProvide technical assistance as necessary to maintenance, and operations personnelSupport internal and external inspections and investigations (including Quality and HSE)Maintain efficient communications with appropriate site customer groupsProficiency with the Trackwise and CAPA systemsBasic Requirements:Bachelor’s degree in Engineering (prefer ME, MET, EE, Chem E)5+ years of experience in HVAC/Utilities and their use in a manufacturing setting, pharma preferred.Additional Preferences: Previous start up experience for new site HVAC systemsExperience with Building Management SystemsUnderstanding energy reduction techniques used in HVAC systemsPrevious equipment commissioning experienceEngineering experience with manufacturing plant utilitiesProject management experienceExperience with maintenance and computerized maintenance management systems (CMMS)Previous experience with deviation and change management systems including TrackwiseExcellent interpersonal, written and verbal communication skillsKnowledge of cGMPDemonstrated high level of understanding of engineering concepts, 1st principles, and engineering functional standardsStrong technical capability and ability to train and mentor othersOther Information:Initial location at Lilly Technology Center, Indianapolis.Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.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 (https://careers.lilly.com/us/en/workplace-accommodation) 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), enAble (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 - $167,200Full-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

Resident Engineer acts within the Chief Engineering team to coordinate product actions between Indiana Transmission Plant, Kokomo Casting Plant, Kokomo Transmission Plant and the Product Release Center and Product Validation Center. Activities involve coordination with suppliers, as well as Vehicle Assembly Plants and Module Integrators. Collaborate with Master-Black-Belt coach to execute Shainin studies to establish root cause and identify solutions for over-target conditions Job responsibilities include but not limited to: Engineering Changes/Design Requirements: Pilot BuildsProduction Evaluation RunsProcess Deviation Approvals Process Change Requests and validationDesign Model Year Build CardsAdherence to design standards and Bill of MaterialProvide technical direction to employees regarding root cause analysis, issue resolution and establish corrective actions serving as the Subject Matter Expert (SME) within the manufacturing facilityInterpret released engineering designs, specifications, materials and standards for hourly and salary personnelCommunicate with design engineering on the “best practice” to design for manufacturingLead teams to identify risks/hazards associated with product designs, processes, applications, applying lessons learned, and assist in the generation of PFMEA's and associated control plansIdentify Error and Mistake Proofing opportunities for identified human errorsIdentify components for traceability throughout the manufacturing processInterface with model responsible engineers to facilitate launch of new programs with highest quality standards and performance Warranty/Car Plant/Functional Audit Findings: Troubleshoot to determine cause of failure and implement countermeasuresWork with Test Garage personal to prevent possible failuresProvide product training to salary and non-salary plant personnelReview competitive benchmarkingServe as the Voice of the CustomerDevelop inspection standards and best methods for performing inspection FTC/FTQ: Assist manufacturing engineering with process variation reductionReduce plant cost by assisting in scrap reduction, obsolescence reduction, acceptable rework procedures, etc.Provides supervision necessary to perform, administer or direct rework/repair methods and processes in compliance with engineering standards

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.Organization and Position OverviewLilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact.The HVAC Engineer is the site Subject Matter Expert (SME) for site HVAC (GMP and non GMP) and the ancillary systems associated within the facilities. During the project phase, the HVAC Engineer will be a key player in the cross functional project team in charge of the construction, commissioning, qualification, start-up and operational readiness of all HVAC systems. During the day-to-day operation, the HVAC Engineer will be responsible for effectively, reliably, and cost effectively operating the site’s HVAC (GMP and non-GMP) and ancillary systems associated within the facilities, maintaining all these systems in a state of compliance, in-control, and fit for use, capable of meeting all site needs. The HVAC Engineer will also be responsible for driving continuous improvement initiatives and local capital investment.Be the SME with a deep technical expertise in all systems (GMP and non-GMP HVAC and ancillary systems associated within their facilities), understanding their applications in pharmaceutical manufacturing, understanding flow charts and process parameters, and awareness of industry trends.Ensure the assigned processes are aligned with Industry and Lilly StandardsSupport risk assessment exercises using the different tools available (e.g. FMEA)Engage in teams, committees, or other groups and/or individually to achieve the departmental, site and/or company goalsInitial project asset delivery phase and future local capital investment:Lead or engage in projects/changes for all the systems ncluding Design, verification activities (IV/OV/PQ), as user representative for capital projects or delivery agent for local projects.Develop the proper documentation (URs, Specification, test cases, etc..) to demonstrate that systems are properly installed, qualified and started up and that remains in a controlled stateContribute to the process resource assessment, capital plans, expense budgets, and prioritize appropriateDaily Support for operations:Monitor utility systems and maintain KPI’s to assure that they are operating properly, in compliance with requirements.Provide written instructions for the proper way to operate and maintain the equipment and process to assure that the system operates within the controlled parametersImplement efficient and effective maintenance and reliability techniques,Apply problem solving skills by leading equipment failures troubleshooting, demonstrating RCA lead investigator proficiency and guide operations personnel in the resolution of process issues.Provide customer consultation and notifications on issues that involve utilities areas assignedAssure that all necessary items are identified on the proper tracking systems, and make sure that items are completed by the required dateProvide technical assistance as necessary to maintenance, and operations personnelSupport internal and external inspections and investigations (including Quality and HSE)Maintain efficient communications with appropriate site customer groupsProficiency with the Trackwise and CAPA systemsBasic Requirements:Bachelor’s degree in Engineering (prefer ME, MET, EE, Chem E)5+ years of experience in HVAC/Utilities and their use in a manufacturing setting, pharma preferred.Additional Preferences: Previous start up experience for new site HVAC systemsExperience with Building Management SystemsUnderstanding energy reduction techniques used in HVAC systemsPrevious equipment commissioning experienceEngineering experience with manufacturing plant utilitiesProject management experienceExperience with maintenance and computerized maintenance management systems (CMMS)Previous experience with deviation and change management systems including TrackwiseExcellent interpersonal, written and verbal communication skillsKnowledge of cGMPDemonstrated high level of understanding of engineering concepts, 1st principles, and engineering functional standardsStrong technical capability and ability to train and mentor othersOther Information:Initial location at Lilly Technology Center, Indianapolis.Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.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 (https://careers.lilly.com/us/en/workplace-accommodation) 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), enAble (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 - $167,200Full-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

Engineering Group Lead E-Motor The UPEEngineering Group Leadis responsible for leading Manufacturing Engineering functions for Kokomo Indiana area powertrain/propulsion programs. Their primary role is to guide their Engineering team to develop and launch processes that meet all objectives for safety, quality, delivery, and cost Emotor manufacturing including stator and rotor assembly. Main responsibilities include: Perform assessments for process changes and related investment requirements for cost studies Oversee engineering scope definition, Requests for Quotes (RFQ’s), sourcing, technical evaluations, design, manufacturing, and installation of manufacturing equipment of electric hairpin stators and rotor assembly equipment.Manage all New Model (NM) program’s facilities aspects including site preparation and machine installation Lead activities on programs ensuring successful implementation and tracking of the Iron Triangle (Scope, Timing, and Cost) Lead their team in the implementation of Stellantis Production Way (SPW) methodology, supporting all activities including deployment of advanced SPW tools and guide systematic root cause problem solving methods to attack risks Development/improvement of process and equipment standards related to manufacturing engineering specifically for electric hairpin stator and rotor assembly.Lead industrialization for process design and installation of electric motor hairpin Stator and Rotor line manufacturing lines in Kokomo Indiana.Drive standardization across plants in all regions Lead procurement, design, build, install, qualification and launch of facilities and process supporting equipment and infrastructure Support Stellantis Production Way initiatives

Overview: Join Benevis: A Leader in Compassionate Dental Care At Benevis, we are dedicated to delivering superior dental services. We are actively seeking an Endodontist or a General Dentist with significant endodontic experience to enhance our team. In this role, you will utilize your specialized skills in complex root canal treatments, upholding the highest standards of patient care. Diagnosing and treating dental issues related to tooth pulp and roots, you'll employ advanced techniques and technology.Responsibilities: Your Role:Perform advanced root canal treatments.Diagnose and treat issues related to tooth pulp and roots.Collaborate with a team committed to exceptional dental care. Qualifications: We expect you to have: DDS/DMD from a dental education program accredited by the Commission on Dental Accreditation (CDA) Completed an Endodontic Residency accredited by the CDA OR significant endodontic experience A valid dentistry license in the state of practice (or eligibility for licensure). Other certifications as required - CPR/BLS, DEA, etc. Our Offer: Competitive CompensationNever any Lab Fees401(k) Retirement Plan with Company matchFlexible Work Schedule: Offering part-time and moonlighting roles with variable schedule choices, perfect for professionals available for one or more days a month. Professional Growth: CE opportunities through ADA Accredited Continued Education Recognition Program (C.E.R.P).Immigration Sponsorship: VISA and Green Card sponsorship where applicable.Join Us in Our Mission: Be part of a team where each day brings a chance to make a significant impact on the lives of the patients we serve. At Benevis, you're not just joining a company; you're becoming part of a family that values teamwork, respect, and the power of a smile. LI-Onsite We are an equal opportunity employer and do not discriminate based on race, color, creed, religion, sex, national origin, age, citizenship, disability, sexual orientation, or any other characteristic protected by federal, state, or local law . #LI-Onsite LI-Onsite LI-Onsite #LI- Onsite