Electrical Engineer jobs at Johnson & Johnson - 184 jobs

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* **Job Function:** R&D Product Development **Job Sub** **Function:** R&D Electrical/Mechatronic Engineering **Job Category:** Scientific/Technology **All Job Posting Locations:** Cincinnati, Ohio, United States of America **Job Description:** **About Surgery** Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that's reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world. Your contributions will help effectively treat some of the world's most prevalent conditions such as obesity, cardiovascular disease and cancer. Patients are waiting. Your unique talents will help patients on their journey to wellness. Learn more at *******************/medtech We are searching for the best talent for a **Staff Engineer, Controls and Automation** . _This role will be based in Cincinnati, OH and will work a Flex/Hybrid schedule with 3 days per week on-site_ . Relocation assistance may be available on a case-by-case basis. **Purpose** : The Staff Engineer, Controls and Automation will serve as a key technical contributor with respect to controls and automation of manufacturing lines for our new product development teams. Our team of scientists, engineers, and technical specialists are in the forefront of technology in the medical device industry, and we put this same passion into all we do, including our manufacturing lines. As a key member of this group, you will be making vital contributions bringing advanced Controls, Automation, Vision Systems, and SCADA/MES systems to life to deliver lifesaving medical devices to market thereby improving patient care through innovation. This role provides an opportunity to develop exciting new manufacturing systems delivering medical devices to the market. **You will be responsible for** : + Leads Automation and Controls strategy from concept with equipment vendor through IQ/OQ/PQ at the production plant. This includes working with vendors to deliver robust solutions with respect to all Rockwell/Allen Bradley PLCs, HMIs, Cognex/Keyence Vision Systems, and any MES/SCADA systems. + The individual will guide the Product Development Team through automation specifications, requirements and validations of the entire manufacturing lines as well as providing guidance for TMV and GR&R issues related to automation. + Collaborate with external suppliers and internal partners to deliver advanced automated manufacturing lines with outstanding metrics such as minimal downtime and minimal scrap. + Participate in multi-functional discussions and design reviews, including product manufacturing at multiple scales (modeling, lab, pilot and manufacturing) + Individual will have strong foundation in automation engineering, PLC/HMI programming, and control systems. + Ability to design, troubleshoot, and validate GxP-compliant automated equipment. + Proficiency in electrical schematics, wiring diagrams, and P&IDs. + Familiarity with ISA-95 / PERA architectures for IT/OT integration. + Prior experience in medical devices, pharmaceutical, or other GxP-regulated industries. + Strong documentation skills for validation protocols and QMS alignment. + Experience leading FAT, SAT, and commissioning of automated equipment. + Exposure to digital twin / data collection systems (e.g., WinCC, Ignition historian). + Cross-functional collaboration with Quality, Manufacturing, and IT. + Travel to manufacturing suppliers and manufacturing base up to 30%. **Qualifications / Requirements** : + Minimum of a Bachelor's Degree is **required** ; Advanced Degree _strongly preferred_ . Electrical Engineering, Computer Science, Mechatronics, or Mechanical Engineering field of study required. + At least 8+ years relevant controls/automation engineering experience **required** ( _6+ with Advanced Degree_ ). + Experience in developing and validating test methods on an automated production line. + Successful experiences in launching new automation lines delivering products to market. + Excellent communication, collaboration and influencing skills + Demonstrated ability to deliver project outcomes in an ambiguous environment + Requires experience managing self-directed work teams + This position is based in Cincinnati, Ohio and requires up to 30% travel both domestic and international. **Preferred Technical Skills** : PLC/HMI + Experience programming PLCs. (Preferably Allen Bradley) + RSLogix / Studio 5000 (ControlLogix, CompactLogix) + FactoryTalk View SE/ME (HMI design and distributed systems) + FactoryTalk Directory and Active Directory Integration + Knowledge of Stratix switch configuration (VLANs, QoS, NAT, IGMP snooping) + Experience with ThinManager-managed thin clients + Experience programming Human Machine Interface (HMI). + Proven problem-solving and troubleshooting skills with respect to electrical hardware and software. + Proficiency in AutoCAD Electrical or EPLAN for reading, updating and troubleshooting equipment schematics + Servo motion control (Kinetix, Siemens drives, or equivalent) + Safety systems: GuardLogix, CIP Safety, ISO 13849/IEC 62061 familiarity + Networking: PERA architectures, Stratix managed switches, IGMP/VLAN configurations, cybersecurity hardening. Machine Vision + Experience programming and developing vision systems in both Cognex and Keyence. + Cognex VisionPro / In-Sight Explorer: Vision tool development, defect detection, TestRun + Keyence (XG-X, CV-X, LM series): Measurement applications, vision inspection, light micrometer programming + Integration of vision systems into Rockwell PLCs and SCADA MES/SCADA + Experience developing MES/Scada systems, Ignition experience a plus. + Ignition (Inductive Automation): Tag configuration, scripting, database integration, historian setup + Siemens Opcenter (MES): Recipe management, track-and-trace, electronic batch records, equipment integration + Experience and knowledge of network and database design for production systems: + Industrial EtherNet/IP and Profinet communications + SQL / MS SQL database integration for historians, MES, and analytics + OPC-UA or MQTT connectivity and gateway concepts Data Acquisition + Experience and knowledge of network and database design. + Industrial Ethernet/IP and Profinet communications + SQL / MSSQL database integration for historians and MES + OPC-UA connectivity Robotics + Experience with FANUC/UR programming, debugging, path optimizing, and operating industrial and/or collaborative robots. + Applying robotics for assembly, handling, or inspection in a production environment. + Programming and operating collaborative robots, + Performing quality control AI/ML + Designing, developing, and deploying AI models and systems by collecting and preparing data, writing code, and implementing algorithms. + Responsibilities include creating scalable machine learning pipelines, optimizing model performance, and integrating AI solutions into production environments. Networking + Design, implement, and maintain a company's production network infrastructure to ensure it is secure, stable, and performs efficiently. Key duties include installing and configuring network hardware like routers and switches, troubleshooting network issues, managing network security. + Ability to design, review, and maintain production network architectures in alignment with IT/OT cybersecurity standards. + Familiarity with: + Network hardware configuration (routers, managed switches) + Network segmentation, VLANs, QoS, and secure remote access + Collaboration with corporate IT on ISA-95 / PERA aligned architectures Additional Qualifications + Experience successfully taking a manufacturing line through IQ/OQ/PQ. + Certifications & Regulatory Knowledge + GAMP 5: Experience with validation and lifecycle documentation (URS, FRS, IQ/OQ/PQ, risk assessments) + 21 CFR Part 11 & Part 820: Understanding of electronic records, audit trails, and FDA compliance + Certified Automation Professional (CAP) - ISA or equivalent (preferred) + Rockwell Automation Certification (e.g., ControlLogix Programmer, FactoryTalk SE) + Ignition Gold Certification (preferred) + Siemens Opcenter or MES integration training (preferred) + Cognex Certified Vision Professional (CCVP) or A3 CVP - Basic/Advanced + Keyence Vision / Measurement certification (vendor training acceptable) Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please contact us via *******************/contact-us/careers or contact AskGS to be directed to your accommodation resource. \#LI-Hybrid **Required Skills:** **Preferred Skills:** Analytical Reasoning, Calibration Procedures, Customer Service, Engineering, Goal-Oriented, Problem Solving, Process Oriented, Project Management, Research and Development, Robotic Automation, SAP Product Lifecycle Management, Smart Systems, Technical Research, Technical Troubleshooting, Technical Writing, Technologically Savvy, Versatility **The anticipated base pay range for this position is :** $109,000.00 - $174,800.00 Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation -120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado -48 hours per calendar year; for employees who reside in the State of Washington -56 hours per calendar year Holiday pay, including Floating Holidays -13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave - 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave - 80 hours in a 52-week rolling period10 days Volunteer Leave - 32 hours per calendar year Military Spouse Time-Off - 80 hours per calendar year For additional general information on Company benefits, please go to: *********************************************

**Job Title:** Electrical Engineer **About the Job** Join a global network that powers how Sanofi delivers - seamlessly, purposefully, and at scale. In Manufacturing & Supply, you'll help reimagine how life-changing treatments reach people everywhere, faster. **Our Team/ Overview** Sanofi is an innovative global healthcare company with one purpose: to pursue scientific miracles to improve lives. Our team strives to transform the practice of medicine, connecting our science to communities in meaningful ways. Within our Sanofi Manufacturing & Supply Ambition, we're minimizing the environmental impact of our products and activities across our value chain while adapting our business to environmental changes, and strengthening the resilience of healthcare systems. The Electrical Engineer will work under the Site Sustainability Lead to assist in developing and executing site electrical reliability and sustainability programs aligned with Sanofi Planet Care strategies and site business needs. The Electrical Engineer is responsible for developing and executing site programs involving the reliability and performance of the Site's Electrical infrastructure. The position supports site infrastructure projects, day to day electrical troubleshooting, electrical design calculations and upkeep of electrical documentation on all electrical systems serving Swiftwater site. **About Sanofi:** We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system - and innovative pipeline - enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives. **Main Responsibilities:** **Electrical Systems** + Key stakeholder for the life-cycle management of electrical assets. This includes being the liaison for electrical equipment / system modifications and Preventative Maintenance (PM) review/modification, to improve operation, uptime and efficiency. Provide electrical support to manufacturing equipment, identifying and managing electrical projects and assist with coordination of electrical repair during shutdowns. + Liaison with the Engineering department to review all new projects for electrical needs. This will include such things as design calculations, developing maintenance plans, and project commissioning activities. + Through individual contribution and/or leading teams, coordinate all electrical changes with CAD team, reconcile electrical changes within existing electrical drawings, reviewing final electrical drawings and approving them within drawing management system. + Ensure compliance with regulatory requirements and good documentation practices are followed to track all work and make data analysis efficient. + Support a strong Maintenance Safety Culture that encourages taking the right amount of time to perform each task safely. + Work with Site Engineering to develop and manage the Electrical Engineering Standards. **Site Sustainability** + Develops and executes sustainability programs aligned with Sanofi Planet Care strategies. Works collaboratively within Engineering and across departments to ensure operational efficiency and to identify and implement projects to reduce the environmental footprint of the site. + Ensures programs are aligned with HSE management systems. Contributes to ISO 50001and site sustainability audits + Participates in Sustainability COP network **Related KPIs & Metrics** + Planet Care Metrics (CO2, Energy, Water) + 2030 Energy Project Roadmap + Area maintenance spend (budget, headcount, parts, services) + Deviations and discards due to maintenance issues + HSE Compliance (wastewater, air emissions, ISO50001, ISO14001) + HSE performance (injury rates, near misses, pSIFs) **About You** **Education & Experience & Certifications** **Requirements** + BS in Electrical Engineering required with 0-5 years of experience. + Proficient in reading and interpreting associated electrical drawings. + Authorized to work in the US for any employer without requiring sponsorship, now or in the future. **Preferred Experience** + Technical experience in construction, predictive and preventative maintenance, troubleshooting, and operation of electrical distribution systems at a large industrial site. + Experience with power distribution equipment including medium voltage switchgear, transformers, relays, generators, automatic transfer switches, UPS, low voltage switchgear, and industrial building distribution. + Ability to lead small projects as a project manager. + Stakeholder & people management - Cross-functionally in a matrix organization **Key Involvement in Decision-Making Process** **Key Roles (D,A,I)** D: Provide Utilities/Sustainability review/expertise for projects A: Develops and manages the Sustainability roadmap including identification of projects I: Delivers the ISO 50001 program elements to maintain certification A: Capital Project Endorsement/Approvals A: Tier 3 Project Management & Delivery D: Project Engineering & Project Standards A: Project Sourcing & 3rd Party Contractor Management **Why Choose Us?** + Bring the miracles of science to life alongside a supportive, future-focused team. + Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally. + Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. + Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. \#GD-SP \#LI-SP \#LI-Onsite \#vhd **Pursue** **_progress_** **, discover** **_extraordinary_** Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video (************************************************** and check out our Diversity Equity and Inclusion actions at sanofi.com (************************************************************************ ! _US and Puerto Rico Residents Only_ Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. _North America Applicants Only_ The salary range for this position is: $75,000.00 - $108,333.33 All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK (********************************************************************************************************* . Global Terms & Conditions and Data Privacy Statement (*************************************************************** Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting ************** or via our movie We are Sanofi (***************************** As an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live. All in for Diversity, Equity and Inclusion at Sanofi - YouTube (************************************************

Job Description Diality is a medical device company focused on developing solutions to improve lives impacted by kidney disease. Diality offers the Moda-flx Hemodialysis System, a user-friendly, mobile, and connected hemodialysis system designed to maximize clinical flexibility and ease-of-use for both clinical and non-clinical users. The Moda-flx Hemodialysis system combines flow rate capabilities of conventional in-center dialysis devices with a fully integrated reverse osmosis (RO) water filtration system to provide a broad range of prescriptions and meet the needs of any professional dialysis care setting. The Staff Electrical Engineer will be responsible for troubleshooting system issues for hemodialysis devices. Responsibilities include assessing system complaints, performing root cause analysis, conducting tests and providing resolutions; creating and reviewing documentation and related drawings; designing electrical components, circuits or sub-systems of moderate difficulty; Additionally, the role involves planning and coordinating detailed phases of electrical and systems engineering activities for the assigned project, and participating sub-system integration, verification and troubleshooting. Responsibilities: Lead investigations into complex technical issues or failures related to hardware/software sub-components. Diagnoses and proposes solutions for electrical system issues. Directs the application of existing principles and guides development of new policies and ideas within the function. Understands and works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors. Exhibits advanced wide-ranging experience, using in-depth professional knowledge, acumen, concepts, and company objectives to develop, resolve complex models and procedures. Conducts engineering activities for all aspects of electrical design to ensure product features, performance and quality are met within the cost budget and delivered on time. Identifies and specifies electronic subsystems and boards. Strategizes and develops verification and validation test plans to ensure product requirement specifications are met. Coordinates testing activities with internal teams and external partners to ensure V&V testing deliverables are met. Documents and analyze design requirements for implementation. Designs, models, simulates and tests complex electronic circuits, subsystems and systems. Create schematic drawings, guides PCB layout, generates BOMs and build packages, and coordinates with contract manufacturer on board fabrication and assembly. Supports system integration and troubleshooting, verification and validation, including safety, EMC and reliability. Applies Apply advanced problem-solving techniques, such as root cause analysis (RCA) and failure mode and effects analysis (FMEA), to identify underlying causes and implement robust corrective actions. Works with production to ensure manufacturability and testability of electrical designs. Ensures all the design activities and documents meet the regulatory and QMS requirements. Required Skills & Abilities Proficient with electronic circuits design, including power, analog and digital components and applications. Proficient with EDA tools to do schematics and layout design. Proficient with lab instruments to do measurement and troubleshooting. Strong problem-solving skills with the ability to conceptualize and develop innovative engineering solutions to complex technical challenges. Understanding of design for manufacturability and reliability, with full product life cycle experience. Excellent communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and stakeholders at all levels of the organization. Proven ability to drive results and meet project timelines and milestones while maintaining high standards of quality and compliance. Show high initiative and collaboration, be self-motivated, and have ability to act independently on technical matters. Education & Experience Bachelor's degree in science or engineering. Minimum 8 years of related experience or 6 years and a Master's degree Knowledge of FDA QSR, ISO 13485, ISO 60601, ISO 14971, experience with test and troubleshooting of electrical safety and EMC is a plus. Experience in hemodialysis/hydraulic electrical system design, familiar with motor driver design, sensor signal processing is a plus. Experience with project or technical management is a plus.. Travel Willingness to travel domestically as needed (up to 10%) primarily to visit vendors and attendance at select conferences. Physical Requirements Sustained periods of time standing and sitting in a laboratory Sitting at a desk utilizing a computer Some lifting of

Job Type: Full-Time About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them. Description: We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Electrical Infrastructure - Sr. Automation & Controls Engineer to join our team. In this role, you will be responsible for the management and execution of all Engineering activities related to the building electrical systems, including generators, transformers, switchgear, motor control centers & switchboards, UPS and other down-stream equipment. Key duties involve troubleshooting problems, performing repairs and ensuring equipment reliability to provide essential utility services. Provide operational support, complex troubleshooting, and optimization for automation equipment, directing and coordinating activities to improve reliability, and applying advanced engineering principles to the design and implementation of new equipment. Key Responsibilities: * Regular and predictable onsite attendance and punctuality. * Direct more complex group projects - identify, propose and champion creative and constructive solutions articulating the business value created. Monitor and communicate progress on all projects within the assigned portfolio to successfully deliver project scope, timeline and budget objectives. Maintain a "state of control" over systems by assuring maintenance of as-built drawings, system documentation and EX rating management. * Troubleshoot control and instrumentation systems to resolve complex equipment issues. Provide engineering expertise and technical guidance to maintenance to perform repairs, design changes, or other corrections as a result of troubleshooting or performance evaluation. Estimates project budgets and resource requirements. * Mentor peers and site resources on automation and control systems facility utility systems. Provide training and technical supervision to instrumentation and electrical personnel as well as Flow technicians for automation control systems throughout the site. * Develop test plans, implementation plans, and project timelines for various projects. * Write functional requirements/specifications documents. * Support the design, specification, installation, startup and validation of building electrical distribution equipment from medium voltage services to equipment MCC. Partner with Engineering lead of process control systems, electrical systems and instrumentation for capital and upgrade projects. Ensure site specifications, standards and cGMP compliance to expectations are met and that good engineering practices are followed. Coordinate with other engineers, project managers, and suppliers to ensure a complete and timely design and implementation. * Identify continuous improvement activities related to building electrical infrastructure, automation control systems throughout the site and champion solutions aligned with site and department metrics, Business Objectives and Strategy. Identify areas of opportunity to improve equipment and component reliability. * Review electrical equipment thermography study, interpret data & determine if action needs to be taken based on findings from study. * Update single line drawings, panel schedules, & control diagrams. * Review time current curves, determine best circuit breakers/ fuses for implementing based on equipment being used to reduce arc-flash, ensure transformers are protected correctly and reduce false motor overload trips Qualifications: We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them: * Bachelor's Degree in Engineering * In lieu of a bachelor's degree, an additional four years of experience is required in the areas of engineering below. * Experience with network and system administration of Microsoft based systems. * Demonstrated computer skills, including but not limited to, MS Excel, Word, PowerPoint, and Project. * Proven ability to simultaneously manage multiple projects and initiatives. * Demonstrated successful communication and negotiation skills to manage conflicting and/or multiple demands, including ability to present to various level within an organization. * Demonstrated ability to apply analytical skills to identify problems; recognizes symptoms, causes, and alternate solutions and makes timely sound decisions even under risk and uncertainty. * Willingness to travel to external domestic and international supplier sites (typically less than 10% of the time). * Provide engineering expertise and technical guidance when necessary, including off-shift on-call support rotation. * 6+ years of experience in power distribution systems (utility to MCC/PP), process control systems, variable frequency drives (VFD) and automated control systems, preferably in the chemical, food, or pharmaceutical industries. Preferred Qualifications: * Programming/troubleshooting Allen-Bradley Programmable Logic Controllers * Experience supporting Building Utility Systems * AutoCAD What We Offer*: * Annual performance bonus, commission, and share potential * Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute * A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries * 3 personal days (prorated based on hire date) * 11 company paid holidays * Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits * Employee discount program * Wellbeing rewards program * Safety and Quality is a top organizational priority * Career advancement and growth opportunities * Tuition reimbursement * Paid maternity and parental leave * Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms. Recruiters: Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma. Equal Opportunity Employer: Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law. #LI-KJ1 Location: Columbus, OH, US, 43228 Nearest Major Market: Columbus

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to win in self-care. Description Overview Scope of the Role Experience Required Benefits We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more about Total Rewards at Perrigo. We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo Nearest Major Market: Eau Claire

Introduction to role The Senior Automation Controls Engineer - Facilities & Engineering is responsible for leading and managing the technical aspects of facilities and process automation/controls, including development and validation, engineering projects, and capital investments within a pharmaceutical organization. This role involves providing expert technical guidance, overseeing complex projects, and ensuring that all systems and processes meet regulatory requirements and support operational efficiency. Accountabilities Leadership and Oversight: Lead technical teams and provide guidance on facilities and process automation/controls, including development and validation activities, engineering solutions, and capital projects. Mentor and support junior engineers and other technical staff in development of cross functional support for automated systems. Collaborate with cross-functional teams to align engineering and project activities with organizational goals. Facilities Management: As asset owner, oversee the maintenance and operation of automation/control systems and equipment within the site including critical facilities/utilities, laboratories, production areas, and administrative spaces. Develop and implement strategies for facility automation/controls improvements and upgrades to enhance operational efficiency and compliance. Ensure automation/controls systems adhere to health, safety, and environmental regulations. Validation Management: Lead the development and execution of validation strategies, protocols, and documentation for site systems, equipment, and processes with focus on assets associated with automation/controls. Ensure that validation activities meet regulatory requirements (e.g., FDA, EMA) and internal standards. Manage complex validation projects, including protocol design, execution, and reporting. Automation/ Controls Oversight: Oversee automation/controls programs to ensure the reliability of systems including electrical components, software environments, and automated field devices. Develop and implement maintenance and inspection programs for critical equipment. Ensure automation/controls engineering procedures and processes comply with industry standards and regulatory requirements. Engineering Leadership: Lead engineering projects related to the design, installation, and commissioning of systems and equipment. Ensure engineering activities adhere to Good Manufacturing Practices (GMP) and other relevant regulations. Develop and implement preventive and predictive maintenance programs to enhance equipment reliability. Capital Projects Management: Manage all aspects of capital projects, including automation/controls systems upgrades, expansions, and new installations. Develop project plans, budgets, and schedules; monitor progress and ensure projects are completed on time and within budget. Coordinate with internal stakeholders, external contractors, and vendors to achieve project objectives and compliance. Documentation and Reporting: Prepare and review comprehensive documentation for qualification/validation, engineering procedures and work instructions, and capital projects. Generate detailed reports on project status, validation results, project activities, and asset ownership/maintenance work. Ensure that documentation is accurate, complete, and compliant with regulatory requirements. Compliance and Safety: Ensure all facilities, systems, and processes comply with regulatory requirements and industry standards. Develop and enforce safety protocols and emergency response plans. Conduct regular audits and inspections to ensure compliance and address any issues promptly. Continuous Improvement: Identify and implement process improvements to enhance efficiency, reduce costs, and improve system reliability. Stay current with industry trends, technological advancements, company guidance, and regulatory changes to ensure best practices are applied. Essential Skills/Experience Bachelor's degree in Engineering, Electrical Engineering preferred, or a related engineering field; Master's degree preferred. 7-10 years of experience in automation/controls software and equipment systems, with background in qualification/validation, facilities engineering, and capital projects. Significant experience in a pharmaceutical or regulated industry is preferred. Extensive knowledge of GMP, FDA regulations, and other relevant compliance requirements. Proven experience in leading complex automation/controls processes, asset ownership, engineering projects, and capital investments. Strong project management skills with experience in budgeting, scheduling, and resource allocation. Excellent analytical, problem-solving, and communication skills. Ability to manage multiple priorities and work effectively under pressure. Working Conditions: Office and on-site facilities environment, with occasional travel to various company sites or off-site locations. May require occasional evening or weekend work to address urgent issues or project needs. Desirable Skills/Experience Cell Therapy Experience When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. AstraZeneca is a place where every day brings new challenges. We lead from the front to ensure everyone's voice is heard on site while building trust and respect with our teams. Our adaptable nature allows us to draw on diverse expertise across functions to overcome obstacles. We champion ideas from anyone on our site with a drive to see things through. Our supportive team environment ensures we succeed together by looking out for each other. With opportunities for growth beyond your role in a stable company committed to eliminating emissions by 2025, AstraZeneca is where you can make a real impact. Ready to take on this exciting challenge? Apply now! The annual base pay for this position ranges from $$132,900 - $199,351. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Date Posted 26-Jan-2026 Closing Date 12-Feb-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

What you will do Johnson Controls is searching for a Principal Electronics Engineer to be located at the R&D facility in Westford, MA. In this role you will be responsible for designing electronic analog & digital hardware for new fire alarm products as well as supporting existing product lines. Work may include analog design, embedded system designs, small signal and instrumentation circuitry, switch mode power supplies, front panel user interfaces, audio amplifiers, peer-to-peer networking, linear power supplies, sensors and detectors, and fiber optics. In addition, research new technology that can be used within these products. This position is in Westford, MA, and you will be required to be on-site 3 days a week. How you will do it Work on analog and digital design and analysis Work on microcontroller and embedded system design Work with other organizations to conceive, develop, and release new products to production Work in a team environment to generate creative solutions to product needs Possibly lead small cross-functional teams of less senior engineers (typ. electrical & mechanical), being responsible for costing, scheduling, and meeting design requirements Work closely with Product Management to determine product specifications Understand how to design equipment to meet agency certifications (UL, ULC, CE, FCC) What you will need Bachelor's Degree in Electrical/Electronic Engineering 8-12 years of experience in electronics design related to analog, power, audio, or embedded products/systems Low-current analog design Discrete electronic component-level knowledge and experience Experience with electronic CAD (schematic capture, circuit simulation, or related) Ability to work well with others in a team environment that spans multiple countries Experience transitioning products to manufacturing Preferred Power supply design, microprocessors and embedded system design Experience with Data Acquisition systems and lab equipment automation Some mechanical design support experience Experience with optics/physics would be a plus HIRING SALARY RANGE: $97,000 - 135,000 (Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, location and alignment with market data.) This role offers a competitive Bonus plan that will take into account individual, group, and corporate performance. This position includes a competitive benefits package. For details, please visit the About Us tab on the Johnson Controls Careers site at ***************************************** Johnson Controls International plc. is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, genetic information, sexual orientation, gender identity, status as a qualified individual with a disability or any other characteristic protected by law. To view more information about your equal opportunity and non-discrimination rights as a candidate, visit EEO is the Law. If you are an individual with a disability and you require an accommodation during the application process, please visit here.

Job DescriptionDescription: We are seeking a hands-on Automation & Controls Engineer to support, troubleshoot, and improve a wide range of manufacturing equipment in a regulated pharmaceutical environment. This role is ideal for mechanically inclined problem-solvers who enjoy being on the production floor, working directly with machines, controls, and electrical systems - not behind a desk. Job Type: Full-Time Location: Hauppauge, NY Works Hours: Monday - Friday, 8:00AM - 4:00PM Pay Range: $90,000 - $140,000 per year, depending on experience Start Date: ASAP What makes this role exciting: A true automation playground - work hands-on with a wide variety of manufacturing equipment, controls platforms, and technologies in a complex pharmaceutical environment. Real impact, real machines - you'll diagnose, fix, and improve equipment that directly supports production, quality, and reliability - not abstract or purely digital systems. High visibility & ownership - your expertise will be relied on across maintenance, engineering, and operations, with meaningful input into equipment improvements and upgrades. Constant learning & challenge - no two days look the same; you'll be exposed to diverse machinery, evolving technology, and new technical challenges. Hands-on engineering - ideal for mechanically curious problem-solvers who prefer being on the floor, working with equipment, over desk-only work. Why Join CPC? At CPC, you'll be part of a team that has set the standard in pharmaceutical development and contract manufacturing since 1971, helping bring high-quality OTC, dietary supplement, and prescription products to market faster and safer than ever. We pride ourselves on quality as a core value, innovative problem-solving, and a collaborative culture where everyone plays a role in advancing formulation and manufacturing excellence. CPC offers an inclusive, respectful workplace with opportunities to grow your skills and career while working with cutting-edge technologies and serving leading global brands. With a commitment to employee success, competitive benefits, and a culture built on teamwork and integrity, CPC is a place where your contributions truly make an impact. Requirements: Responsibilities: In this role, you will: Troubleshoot and resolve PLC, electrical, and control system issues across a wide range of manufacturing equipment to minimize downtime and improve reliability. Design, implement, and optimize machine control systems, including PLCs, HMIs, servos, and electrical components. Own automation documentation and standards, maintaining current PLC/HMI programs, electrical drawings, and equipment documentation. Collaborate closely with maintenance, engineering, and operations teams to execute repairs, improvements, change control, and equipment qualification. Mentor and guide mechanics and technicians, promoting safe work practices, strong troubleshooting skills, and first-time-right execution. Education & Experience: Bachelor's Degree in Electrical Engineering, Automation Engineering, or a related engineering discipline. Minimum 3 years of progressive experience supporting and improving automated manufacturing equipment. Skills, Knowledge & Abilities: Mechanically curious and systems-oriented thinker Comfortable working directly on equipment in a production environment Enjoys variety, challenge, and continuous learning Practical, hands-on problem solver - not purely theoretical Hands-on experience with PLC, HMI, and servo systems (Allen-Bradley, Siemens, Mitsubishi) Experience troubleshooting electrical control panels, sensors, drives, and actuators AutoCAD or similar electrical drafting experience preferred Working knowledge of OSHA and NEC requirements

We are seeking a hands-on Automation & Controls Engineer to support, troubleshoot, and improve a wide range of manufacturing equipment in a regulated pharmaceutical environment. This role is ideal for mechanically inclined problem-solvers who enjoy being on the production floor, working directly with machines, controls, and electrical systems - not behind a desk. Job Type: Full-Time Location: Hauppauge, NY Works Hours: Monday - Friday, 8:00AM - 4:00PM Pay Range: $90,000 - $140,000 per year, depending on experience Start Date: ASAP What makes this role exciting: A true automation playground - work hands-on with a wide variety of manufacturing equipment, controls platforms, and technologies in a complex pharmaceutical environment. Real impact, real machines - you'll diagnose, fix, and improve equipment that directly supports production, quality, and reliability - not abstract or purely digital systems. High visibility & ownership - your expertise will be relied on across maintenance, engineering, and operations, with meaningful input into equipment improvements and upgrades. Constant learning & challenge - no two days look the same; you'll be exposed to diverse machinery, evolving technology, and new technical challenges. Hands-on engineering - ideal for mechanically curious problem-solvers who prefer being on the floor, working with equipment, over desk-only work. Why Join CPC? At CPC, you'll be part of a team that has set the standard in pharmaceutical development and contract manufacturing since 1971, helping bring high-quality OTC, dietary supplement, and prescription products to market faster and safer than ever. We pride ourselves on quality as a core value, innovative problem-solving, and a collaborative culture where everyone plays a role in advancing formulation and manufacturing excellence. CPC offers an inclusive, respectful workplace with opportunities to grow your skills and career while working with cutting-edge technologies and serving leading global brands. With a commitment to employee success, competitive benefits, and a culture built on teamwork and integrity, CPC is a place where your contributions truly make an impact. Requirements Responsibilities: In this role, you will: Troubleshoot and resolve PLC, electrical, and control system issues across a wide range of manufacturing equipment to minimize downtime and improve reliability. Design, implement, and optimize machine control systems, including PLCs, HMIs, servos, and electrical components. Own automation documentation and standards, maintaining current PLC/HMI programs, electrical drawings, and equipment documentation. Collaborate closely with maintenance, engineering, and operations teams to execute repairs, improvements, change control, and equipment qualification. Mentor and guide mechanics and technicians, promoting safe work practices, strong troubleshooting skills, and first-time-right execution. Education & Experience: Bachelor's Degree in Electrical Engineering, Automation Engineering, or a related engineering discipline. Minimum 3 years of progressive experience supporting and improving automated manufacturing equipment. Skills, Knowledge & Abilities: Mechanically curious and systems-oriented thinker Comfortable working directly on equipment in a production environment Enjoys variety, challenge, and continuous learning Practical, hands-on problem solver - not purely theoretical Hands-on experience with PLC, HMI, and servo systems (Allen-Bradley, Siemens, Mitsubishi) Experience troubleshooting electrical control panels, sensors, drives, and actuators AutoCAD or similar electrical drafting experience preferred Working knowledge of OSHA and NEC requirements

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. Position Brand Description: The Process Control Engineer provides automation support for manufacturing operations in accordance with appropriate GMP and safety guidelines. This support includes change control implementation, deviation investigation, routine automation computer system support activities, and off hours automation computer system support. The Process Control Engineer also leads non-routine automation computer system support activities, delivers engineering projects to the business, is able to utilize first principles in delivery of these solutions, and can recommend new control strategies for the various chemical processes utilized in manufacturing operations. Key Objectives/Deliverables: Manufacturing Operations Automation Support Provide frontline automation technical support to manufacturing operations for process control system software and platforms. Ability to configure process control systems and troubleshoot computer system software. Provide a high level of data mining and analysis to identify improvements in the manufacturing process. Design and implement automation related changes to manufacturing operations. Lead investigation of automation related deviations. Perform system support activities (e.g. system backups, performance monitoring, password maintenance, etc.) Provide off hours automation support to operations. Perform all work in a manner consistent with Lilly policies, procedures, and standards. Ability to work in a safe manner and ensure safety of others. Provide engineering solutions to the business Automation design and delivery of new process units. Provides project management and technical leadership to projects. Oversight of specialists and/or contractors assisting in the delivery of automation solutions. Utilizes S88 and fundamental engineering principles in the delivery of automation solutions. Is responsible for ensuring that life-cycle plans are developed and executed for automation systems. Provide recommendations on new control strategies/technologies Research and maintain familiarity with various control strategies/technologies. Research and maintain familiarity with chemical processes utilized in pharmaceutical manufacturing. Mentor Technicians, Specialists, and Engineers Mentor specialists in technical and professional development. Basic Requirements: Bachelor of Science in Engineering. Minimum 2 years of industrial experience. Experience with Distributed Control Systems (DeltaV). Additional Preferences: Ability to configure process control systems and troubleshoot computer hardware. Experience working in a regulated environment, preferably pharmaceutical or chemical manufacturing for 2+ years. Previous experience with manufacturing deviation and change control processes. Understanding of S88. Familiar with control theory. Teamwork and interpersonal skills. Good written and oral communication skills. Attention to detail. Additional Information: Able to provide 24 hours per day, 7 days per week on-call support approximately 1 week per month. Tasks require entering manufacturing and laboratory areas which require wearing appropriate PPE. 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 $66,000 - $171,600 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

Senior Power Electronics Engineer Who we are… We are a team of scientists, engineers, technicians, and innovators dedicated to changing the world by developing medical isotopes to treat and eradicate cancer. We believe in building an environment where collaboration, curiosity, and camaraderie thrive. We also enjoy darts, cornhole, ping-pong, chili cook-offs, and other fun events that make our company a community where we make a life, not just a living. Who you are… You love details and precision. You find enjoyment in solving puzzles, designing and mapping systems, and building efficient circuitry. Words that describe you are focused, curious, and collaborative. What you can expect to work on… The Power Electronics Engineer role at Niowave has responsibility over design, implementation and integration of accelerator power systems. These systems are varied and include critical accelerator subsystems like the cathode heater, the electron gun tuners, etc. This position will also involve support to cryogenics, RF, and high voltage subsystems and some involvement in circuits that enable or control specialized accelerator systems like RF and beam loss detectors. Design, implement and maintain accelerator power systems including controlled heaters and tuners. Consult with controls engineers on the proper power layout for normal-conducting beamline magnets and beamline diagnostics. Interface with nuclear engineers concerning the design and operation of the x-ray conversion target. Be part of the team designing the concept, architecture, and components of future systems. Conduct optimization work on existing systems, perform measurements and validation tests Confirm system capabilities by designing testing methods What you need to succeed… Bachelor's degree in the fields of electrical engineering, specifically power electronics and circuits 5+ years of power electronics experience. Experience designing, building and testing systems. Broad understanding of power electronics/circuitry technology. Regularly engages in mentoring multiple team members in all aspects of RF Engineering. Expert level analytical and problem-solving skills; Organizational and project management skills for self and teams. Embrace and model the Niowave Values of Teamwork, Courage, Integrity, and Upright Zeal. Understand how to integrate into a new team/organization - appreciate the history of current state, know how and when to make suggestions, as well as using just the right pace to reach the improved future state. Understand their own communication and learning styles, can assess others' styles, and is able to find the right path to connect the two. Great to have… Master's or Doctorate degree in the fields of electrical engineering, power electronics, circuits, etc. 8+ years of power electronics related experience. 5+ or more years of experience with power electronics and accelerators in a research or production environment. Experience leading teams to complete large projects. 2+ years' experience of direct supervisory experience of five or more people. Work Environment… Full-time position. The company's standard operating hours are Monday thru Friday 6a - 6p with production related activities requiring 24/7/365 shifts. This position will have regular working hours during M - F with an expectation of adjusting to meet technical objectives and to meet with staff working outside of the standards operating hours as needed. Niowave has multiple locations within the Lansing area. Travel between locations is expected in the role. Please provide a cover letter specifically describing the nature of your technical expertise.

Soaring above the ordinary, the IMPACT Fly Team is a powerhouse of innovation, precision, and technical mastery. As Major Project Automation & Controls Technicians, you're the architects of efficiency-engineering smarter systems, optimizing workflows, and tackling high-stakes challenges with finesse. Whether troubleshooting on-site or designing groundbreaking solutions, this elite squad is always ready to fly in, fix, and revolutionize. Ready to take your expertise to the next level? Because IMPACT is more than a name-it's a mission. What we offer Competitive salary Paid vacation/holidays/sick time - 10+ days of vacation first year Comprehensive benefits package including 401K, medical, dental, and vision care - Available day one Extensive product and on the job/cross training opportunities With outstanding resources Encouraging and collaborative team environment Dedication to safety through our Zero Harm policy Check us Out: A Day in a Life at Johnson Controls: What you will do As a senior level team member of the iMPACT Fly Team, you will be responsible for traveling 75-100% of the time to and assisting JCI Customers at all levels of building automation system programming, checkout and commissioning. This will include validating hardware and software commissioning activities for building automation systems. You will need to apply your advanced HVAC & Building Automation experience to work on assigned projects. You will work directly on multiple project teams to assist the Project Managers and Field Technicians. How you will do it Loads system-level controller software Performs advanced commissioning and system diagnostics from system-level controllers to end devices (such as: sensors, actuators, etc.) and completes all required commissioning documentation Keeps management and JCI contractor or customer informed of job progress and issues Calibrates systems requiring basic electronic test equipment Completes administrative tasks including but not limited to time sheets, expense reports, and on-site documentation Documents changes and provides information for as-built documentation Communicates with the JCI contractor or customer upon arrival and before leaving the work site Follows all safety standards and attends required safety training. High degree of regard to employee and subcontractor safety. What we look for Advanced computer skills (Metasys preferred) Advanced knowledge of electrical testing and commissioning tools Strong documentation acumen Good communication and listening skills Advanced knowledge of mechanical HVAC systems Low voltage/120-volt wiring skills preferred A valid driver's license, with no major or frequent traffic violations HIRING HOURLY RANGE: $31- $42 (Hourly rate to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.) This position includes a competitive benefits package. For details, please visit the Employee Benefits tab on our main careers page at *************************************** Johnson Controls International plc. is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, genetic information, sexual orientation, gender identity, status as a qualified individual with a disability or any other characteristic protected by law. To view more information about your equal opportunity and non-discrimination rights as a candidate, visit EEO is the Law. If you are an individual with a disability and you require an accommodation during the application process, please visit here.

Soaring above the ordinary, the IMPACT Fly Team is a powerhouse of innovation, precision, and technical mastery. As Major Project Automation & Controls Technicians, you're the architects of efficiency-engineering smarter systems, optimizing workflows, and tackling high-stakes challenges with finesse. Whether troubleshooting on-site or designing groundbreaking solutions, this elite squad is always ready to fly in, fix, and revolutionize. Ready to take your expertise to the next level? Because IMPACT is more than a name-it's a mission. What we offer Competitive salary Paid vacation/holidays/sick time - 10+ days of vacation first year Comprehensive benefits package including 401K, medical, dental, and vision care - Available day one Extensive product and on the job/cross training opportunities With outstanding resources Encouraging and collaborative team environment Dedication to safety through our Zero Harm policy Check us Out: A Day in a Life at Johnson Controls: What you will do As a senior level team member of the iMPACT Fly Team, you will be responsible for traveling 75-100% of the time to and assisting JCI Customers at all levels of building automation system programming, checkout and commissioning. This will include validating hardware and software commissioning activities for building automation systems. You will need to apply your advanced HVAC & Building Automation experience to work on assigned projects. You will work directly on multiple project teams to assist the Project Managers and Field Technicians. How you will do it Loads system-level controller software Performs advanced commissioning and system diagnostics from system-level controllers to end devices (such as: sensors, actuators, etc.) and completes all required commissioning documentation Keeps management and JCI contractor or customer informed of job progress and issues Calibrates systems requiring basic electronic test equipment Completes administrative tasks including but not limited to time sheets, expense reports, and on-site documentation Documents changes and provides information for as-built documentation Communicates with the JCI contractor or customer upon arrival and before leaving the work site Follows all safety standards and attends required safety training. High degree of regard to employee and subcontractor safety. What we look for Advanced computer skills (Metasys preferred) Advanced knowledge of electrical testing and commissioning tools Strong documentation acumen Good communication and listening skills Advanced knowledge of mechanical HVAC systems Low voltage/120-volt wiring skills preferred A valid driver's license, with no major or frequent traffic violations HIRING HOURLY RANGE: $31- $42 (Hourly rate to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.) This position includes a competitive benefits package. For details, please visit the Employee Benefits tab on our main careers page at *************************************** Johnson Controls International plc. is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, genetic information, sexual orientation, gender identity, status as a qualified individual with a disability or any other characteristic protected by law. To view more information about your equal opportunity and non-discrimination rights as a candidate, visit EEO is the Law. If you are an individual with a disability and you require an accommodation during the application process, please visit here.

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. Lilly 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 Engineer - Automation Engineering will work as a member of the Automation Engineering Department at Eli Lilly, Foundry. The engineer will provide automation support for one or more operating areas across site and/or for capital projects. Process Automation is core to delivering a right first time facility start up and continued support of ongoing manufacturing operations into the future. The Engineer is also responsible for the productivity and mentorship of the employees with the purpose of ensuring that reliable and compliant control applications and systems are used in the manufacturing at Foundry. Additionally, the Senior Principal Engineer as a key technical expert with partners to influence and implement within the process control organization and across functional disciplines to support the process control technical agenda, business plan priorities, and compliance objectives. In the project delivery phase and startup phase of the project (startup expected 2025 to 2028), automation engineering roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up. Key Objectives/Deliverables: • Technical Leadership • Mentor process control team, including design, controls philosophy, implementation and commissioning • Process control work implementation and coordination • Develop and implement the Automation Engineering Project Plan. Operational Excellence • Technically lead and oversee the work of Site Area leads and System Integrators and review Functional Requirements, Design Specifications, automation hardware, application software, Test Specifications. • Lead/Participate in design reviews and Site system hardware reviews, attend equipment and software FATs • Lead a team of automation engineers supporting commissioning • Provide periodic status updates to Project Management • Devise functional requirements and process control strategies for control systems in collaboration with Automation System Administrators to ensure all required hardware, instrumentation and controls are accounted for • Perform Automation Engineering activities including design, tuning and troubleshooting of control loops, devices and hardware • Implement and support electronic systems (such as plant historians) used to capture process automation related production data • Maintain the validated state of the site control system hardware in line with Lilly quality standards including the development and execution of validation strategies and associated documentation • Automation support for capital projects including new product introductions • Promote the use of automation to improve productivity, operational efficiency and compliance • Develop a ‘network' of corporate contacts and leveraging corporate expertise when needed • Perform Site support that will include shift rotation to provide continuous support of day to day activities Organizational Capability • In coordination with automation and compliance consultants, set and reinforce standards for appropriate rigor in automation work products. • Demonstrated initiative, good planning and organizational skills, ability to prioritize tasks, commitment to task completion and timelines. • Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement • Demonstrated ability to influence peers and business partners • Good written and verbal communication skills for both technical and non-technical audiences • Knowledge of GMP, regulatory requirements, computer system validation Basic Requirements: • Minimum B.S. in Engineering and experience in Automation Engineering, preferably in major pharmaceutical manufacturing. • A minimum of 2+ years working experience in Biopharma engineering, operations, or manufacturing. Additional Preferences: • Experience in design, development, commissioning and qualification of highly automated greenfield manufacturing sites utilizing SCADA, DCS, BMS controller and hardware, valves, motors, control panels, and Warehouse and Robotics systems (DeltaV, Rockwell, Johson Controls, Fanuc, Rosemount, Fisher etc). • Experience in facilitating and driving decision-making at an organizational level. • For Internal Lilly employees - LRL/Product Research Development experience preferred Other Information: Initial location at Lilly Technology Center, Indianapolis. Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly 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

Keene, NH - location Estimated duration: 6 to 9 months Responsibilities • Support design reviews, debug, acceptance and validation activities for equipment being developed by external suppliers. • Support decommissioning of equipment at Keene site and recommissioning at Southington site. • Support Keene production as needed. Candidate level: • Engineer at E2, E3 or Senior. Open to principal level. Qualifications: • 4+ years' experience in a medical device manufacturing environment. • Strong preference for assembly automation systems experience. • Validation experience: IQ, OQ, PQ and TMVs • Automation control systems background - PLCs, HMIs, Vision systems, Servos & Robots. • Familiarity with standard MS Office tools. • Good verbal and written communication skills. Additional desired qualifications - not mandatory: • Fundamental knowledge of statistical analysis - specifically GR&Rs & Process Capability. • Allen -Bradley/Rockwell Automation programming experience: Studio5000, RSView ME/SE. • Siemens S7 programming experience. • Staubli/EPSON/ABB robot experience

Zoetis is the world's largest Manufacturer and Supplier of Animal Pharmaceuticals. Looking for your chance to work for the #1 Animal Health company in the world? Zoetis is looking for the next amazing colleague to join our family. Does working in a safe and fast-paced manufacturing environment in an exceptionally clean facility, using high tech products sound like your dream job? Our Lincoln facility has received the prestigious Star Safety Award through the OSHA Voluntary Protection Program which sets us apart from other manufacturing businesses in the Lincoln area. Benefits Include: 4 weeks accrued paid vacation and 13 paid holidays. 401(k) match with company profit sharing. Tuition reimbursement and Student Loan repayment program. Great Health, personal, and family benefits starting day 1. Position Responsibilities Looking for a detail-focused Engineer who takes pride in a job well-done... Own: We're not an army...you'll have a chance to learn and take individual responsibility for your processes. Our team supports Allen-Bradley, Andover Continuum, Emerson Delta V, GE Proficy, Honeywell Experion and Micromax, and Rockwell. Your background and skillset will allow you to grow into an expert; and to be treated and respected as one. Build knowledge and collaborate with fellow highly motivated experts. As a subject-matter expert, you will help make decisions about equipment, scheduling and improvements that ultimately help all of us succeed. Strategize: Plan and support Capital expansion. Our site has re-invested 100's of millions of dollars over the past decade. We're growing and you'll grow with us. Customer focus: Work cross-functionally with multiple teams to diagnose and correct issues as they arise. Growth: Develop additional skills...grow yourself with exposure to new platforms and new requirements. We're CFR21-Part 11, ISPE cGAMP and Zoetis Validation compliant. Learn new technologies as our rapidly growing site continues to expand to support the world's needs. Education and Experience You'll need to have: Bachelor's in Engineering, Computer Science or equivalent 2 years of experience with Process Engineering controls, PLC's, installing and maintaining computer and network systems in a manufacturing environment. Installing, maintaining, repairing, and administrating computer systems. Computer programming language (example VB.NET and Python) Basic Networking understanding. Even Better if you have: Experience in Active Biological Ingredient, Active Pharmaceutical Ingredient, or Drug Product manufacturing. Technical Skills and Competencies Required If you know what Siemens, Allen Bradley or CLICK all have in common then you've already got some of the experiences that we're looking for. If not, fear not...we'd love to teach you if you love to learn. Physical Position Requirements Our team works in a variety of conditions from laboratories to farm operations...but everyone needs to: SAFELY work in an industrial environment, Be able to keyboard for extended periods of time...sitting, standing, your choice, Occasionally lift up to 50 lbs....never more, Occasionally work in areas that may be hot, cold, stinky, noisy, ultra-clean, or require additional PPE. May be exposed to temperature variations, prolonged standing, or walking. Full time RegularColleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume. Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at ********************************** to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at ********************** site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

Job Title Global Controls Engineer - Automation The actual location of this job is in Greenwood, SC. Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza AG as a Global Controls Engineer - Automation and help shape the future of life sciences through cutting-edge automation solutions. This role offers the chance to work on global projects that impact multiple continents, driving innovation and efficiency across our manufacturing sites. What you will get An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. A variety of benefits dependent on role and location. The full list of our global benefits can be found here: *************************************** What you will do Develop, replicate, and support global automation systems across sites in Belgium, France, US, Mexico, China, Japan, and India. Apply advanced PLC/SCADA/Simotion expertise to global initiatives, focusing on software development and validation. Design and execute test plans to ensure software reliability and compliance. Lead commissioning activities and support validation of control systems. Collaborate with R&D and production site automation teams to align strategies and solutions. Provide accurate time estimates for control software development tasks. Drive continuous improvement and contribute to environmental and health safety initiatives. What we are looking for Bachelor's degree required in Electrical Engineering, Mechatronics, Computer Science, Mechanical Engineering, or Robotics. Master's degree preferred. Minimum of 4 years of experience in a manufacturing environment with a focus on automation required. Strong skills in PLC/SCADA systems and software development processes required. Ability to work independently and collaboratively in a global team setting. Excellent project management, communication, and organizational skills. Open to mentorship and professional growth opportunities. About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values-Collaboration, Accountability, Excellence, Passion, and Integrity-reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

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. Position Brand Description: The Process Control Engineer provides automation support for manufacturing operations in accordance with appropriate GMP and safety guidelines. This support includes change control implementation, deviation investigation, routine automation computer system support activities, and off hours automation computer system support. The Process Control Engineer also leads non-routine automation computer system support activities, delivers engineering projects to the business, is able to utilize first principles in delivery of these solutions, and can recommend new control strategies for the various chemical processes utilized in manufacturing operations. Key Objectives/Deliverables: Manufacturing Operations Automation Support Provide frontline automation technical support to manufacturing operations for process control system software and platforms. Ability to configure process control systems and troubleshoot computer system software. Provide a high level of data mining and analysis to identify improvements in the manufacturing process. Design and implement automation related changes to manufacturing operations. Lead investigation of automation related deviations. Perform system support activities (e.g. system backups, performance monitoring, password maintenance, etc.) Provide off hours automation support to operations. Perform all work in a manner consistent with Lilly policies, procedures, and standards. Ability to work in a safe manner and ensure safety of others. Provide engineering solutions to the business Automation design and delivery of new process units. Provides project management and technical leadership to projects. Oversight of specialists and/or contractors assisting in the delivery of automation solutions. Utilizes S88 and fundamental engineering principles in the delivery of automation solutions. Is responsible for ensuring that life-cycle plans are developed and executed for automation systems. Provide recommendations on new control strategies/technologies Research and maintain familiarity with various control strategies/technologies. Research and maintain familiarity with chemical processes utilized in pharmaceutical manufacturing. Mentor Technicians, Specialists, and Engineers Mentor specialists in technical and professional development. Basic Requirements: Bachelor of Science in Engineering. Minimum 2 years of industrial experience. Experience with Distributed Control Systems (DeltaV). Additional Preferences: Ability to configure process control systems and troubleshoot computer hardware. Experience working in a regulated environment, preferably pharmaceutical or chemical manufacturing for 2+ years. Previous experience with manufacturing deviation and change control processes. Understanding of S88. Familiar with control theory. Teamwork and interpersonal skills. Good written and oral communication skills. Attention to detail. Additional Information: Able to provide 24 hours per day, 7 days per week on-call support approximately 1 week per month. Tasks require entering manufacturing and laboratory areas which require wearing appropriate PPE. 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 $66,000 - $171,600 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

Role: Hardware Engineer (Testing) Duration: 6+ Months BGV will be done for the selected candidates. · Automotive experience with 5-10 Years of experience in hardware(HW) testing domain · Strong hardware debugging, understanding of HW and Tools · Strong Communication · Bachelor's degree · Responsibilities include all tasks related with validation test development and timing plans to meet program/project objectives. · Generate a detailed testing schedule and procedure and State of Requirements (SOR) to quote and develop a new tester as required. · Responsible to execute validation testing and maintain the test equipment and ensure that the equipment calibration is current. · Develop a new testing procedure to resolve a new failure and/or chronic issue for continuous Improvement. · Implement the test plan and develop, find and quote equipment for the internal and test lab. · Execute the buildup and implementation of test stands and associated hardware and software required for the validation. · Create test procedures and work instructions for lab technician to perform testing. · Record, analyze and document the test results in a formal document and prepare final test reports. · Create test setups and fixtures design to properly operate, monitor, and orient the product while under test. · Interact with external test facilities for the execution of validation testing if required. · Complete validation report with analyzing failures and identify countermeasures. · Maintain equipment calibration. Please respond with your word resume and requested details: Full Name : Work Authorization: Contact Number : Email ID : Skype ID: Current location: Willing to relocate : Rate/hr : Additional Information All your information will be kept confidential according to EEO guidelines.