Automation Engineer jobs at Novo Nordisk

Embedded Test Engineer Are you ready to develop the future of retail? As the world's leader in IoT and data technologies for commerce, our mission is to help retailers and brands use digitalization to become more efficient, more intelligent, and more sustainable-and in doing so, enable more positive commerce. VusionGroup is a fast-growing, fast-paced retail tech company. We believe that by thinking big and working together as one team-agile thinkers, tech makers, and change agents-we can build the largest retail IoT platform in the world. Job Description We build. We create impact. At VusionGroup, we're proud to offer innovative products that meet the needs of our customers. To help us continue expanding our offerings, we're in search of an Embedded Test Engineer to test our IoT solutions. In this role, you will design and execute test plans for embedded systems, performing both manual and automated testing. You'll develop and maintain automated test scripts to improve efficiency and validate hardware-software integration for seamless operation. Develop Validation Test Plans: Design and develop comprehensive validation test plans for firmware and hardware, electronic components, PCBs, and complete systems to ensure compliance with design specifications and industry standards. Test Documentation: Create and maintain clear, comprehensive, and detailed documentation of test procedures, results, and defects for future reference and continuous improvement. Perform Functional Testing: Conduct functional, environmental, and stress testing on electronic systems to verify performance and durability across a variety of real-world scenarios. Analyze Test Results: Collect, analyze, and interpret test data to identify potential issues with functionality, reliability, or performance. Work with design and engineering teams to resolve identified issues. Documentation: Prepare detailed reports of validation results, including pass/fail criteria, root cause analysis of failures, and recommendations for design or process improvements. Prototype & Pilot Testing: Validate prototypes and production units to identify any design issues before mass production. Support Failure Analysis: Investigate and analyze failure modes, root causes, and implement corrective actions to prevent future issues. Collaboration: Work closely with cross-functional teams to ensure alignment on testing strategies, product improvements, and release schedules. Qualifications Qualifications we're looking for. Experience: 3+ years of experience in embedded systems testing/ electronics validation, testing, and troubleshooting. Experience with embedded firmware test and hardware debugging (oscilloscopes, logic analyzers, multimeters etc.) Experience with microcontrollers, processors, and programable logic devices. Hands-on experience with manual and automated tests. Skills: Excellent problem-solving skills with a focus on attention to detail. Strong communication skills and ability to work collaboratively in a fast-paced environment. Abilities: Ability to work collaboratively with cross-functional teams (Mechanical Engineering, Industrial Engineering, etc.) Education: Bachelor's degree in Electrical Engineering, Computer Science, or a related technical field. Preferred Qualifications: Experience in scripting languages like Python for test automation. Familiarity with PCB design software and embedded systems testing is a plus. We innovate. We help communities thrive. VusionGroup has an international presence in 19 countries. In joining us, you'll be part of a globally distributed team of intellectually curious, committed, and collaborative co-workers. The work is fast paced, challenging, and ambitious. Here, you will feel valued for your contributions as we reinvent modern commerce-together. We feel supported. You will too. VusionGroup is a place where people feel safe, happy, and respected. We offer programs and benefits to support you in whatever comes next in your life, including: Generous paid time off (PTO): 35 days PTO to enable work/life integration and promotes a culture of trust. Health & Wellness: Eligibility for healthcare benefits begin day one, plus retirement savings plans. Financial future: While retirement savings plans vary by country, we help you plan for your future. Family-First Support: Navigate family challenges with our assistance, securing time for both your loved ones and self-care. Hybrid work: Find your balance with two days working from home, three days in the office, plus the freedom to work anywhere for up to two weeks a year. Time off to volunteer and give back to your community. Career Growth: E-learning opportunities and workshops, and global mobility potential Commute benefits: up to $100/month per employee for commuting expenses. Philanthropy: Our company matches employee donations up to $500 per year for causes close to your heart. Additional Information All your information will be kept confidential according to EEO guidelines.

Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients-including DoD, DOE, and municipalities-through robust logistics and continuous investment in people, technology, and infrastructure. We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, dioxins/furans, radiochemicals, and more. Job Description Eurofins Environment Testing is seeking a Senior Analyst to join our team! The Senior Analyst will have previous experience with HR/MS instrumentation in a production, laboratory setting. The Senior Analyst prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins' Quality Assurance programs and SOP's. The Senior Analyst is responsible for maintaining instrumentation; tuning and calibrating instrument daily; analyzing quality control and client samples; reviewing and assembling data in an efficient manner with a high degree of quality; evaluating current organizational and analytical systems; diagnosing complex problems and offering solutions with a high degree of independence; suggesting and implementing improvements to maximize quality and productivity; acting as technical resource for internal problems and projects; assisting in "brainstorming" client problems and projects; training new employees in all aspects of instrumentation; researching new and emerging technologies. Essential Duties and Responsibilities: * Applies GMP/GLP in all areas of responsibility, as appropriate * Demonstrates and promotes the company vision * Regular attendance and punctuality * Perform routine and advanced maintenance on the instrumentation * Tune and calibrate instrumentation * Analyze samples and associated QC * Review, work up, and assemble all supporting data * Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC department * Perform additional responsibilities (i.e., audit, verification, etc.) with minimal supervision * Evaluate current analytical system performance and recommend corrective action to enhance efficiency and productivity * Train other departmental analysts in procedures related to operations listed in the above * Search technical literature for scientific information relative to improving analytical or operational performance * Understand and use LIMS * Make working calibration standards * Use word processor on PC * Monitor and change gas cylinders * Review and amend departmental methods when required, either as part of yearly review or when an analytical change to the method is made * Conducts all activities in a safe and efficient manner * Performs other duties as assigned Qualifications Basic Minimum Qualifications * 5+ year HR/MS experience in a production laboratory * At least 5 years experience related to performing extractions and/or instrumental chromatographic analyses utilizing wet chemical and chromatographic techniques) in a wide variety of matrices encountered in environmental testing. * Bachelor's degree in chemistry, biology, physics or related degree concentration * Authorization to work in the United States indefinitely without restriction or sponsorship * Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Skills and Abilities * Exceptional technical skills, including logical thinking and deductive reasoning; good work habits (e.g., cleanliness, efficiency, carefulness, effective organizational skills); * High accuracy in recording and transcribing data; * Personal maturity and sense of responsibility; * Good written and oral communication skills; * Ability to learn new methods and techniques; * Willingness to follow instructions and comply with company policies; * Consciousness of, and a positive attitude toward, quality control and safety procedures; * Good understanding of chemical principles; * Accurate management of numbers, both by hand and using a calculator; * Set up and perform nonroutine standardized tests with minimal supervision; * Demonstrated versatility, flexibility, and efficiency; * Effective use of time while managing multiple priorities; * Above satisfactory reasoning ability; * Self-motivated to improve technical skills and operations; * Superior leadership, organizational, and communication skills; * Lead a project to a satisfactory conclusion on time; * Consult with clients on work performed for them; * Problem solving skills; * Function under high stress levels; multitask; * See cause-and-effect relationships; * Retain large amounts of information Additional Information Compensation Range: $80,000 - $120,000 per year depending on level of experience and qualifications. Position is full-time, and exempt from overtime pay. Candidates must be available to work the following shift: * Monday - Friday, 8:00am to 5:00pm and any additional hours needed Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR 6.151 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients-including DoD, DOE, and municipalities-through robust logistics and continuous investment in people, technology, and infrastructure. We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, dioxins/furans, radiochemicals, and more. Job Description Eurofins Environment Testing is seeking a Senior Analyst to join our team! The Senior Analyst will have previous experience with HR/MS instrumentation in a production, laboratory setting. The Senior Analyst prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins' Quality Assurance programs and SOP's. The Senior Analyst is responsible for maintaining instrumentation; tuning and calibrating instrument daily; analyzing quality control and client samples; reviewing and assembling data in an efficient manner with a high degree of quality; evaluating current organizational and analytical systems; diagnosing complex problems and offering solutions with a high degree of independence; suggesting and implementing improvements to maximize quality and productivity; acting as technical resource for internal problems and projects; assisting in “brainstorming” client problems and projects; training new employees in all aspects of instrumentation; researching new and emerging technologies. Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrates and promotes the company vision Regular attendance and punctuality Perform routine and advanced maintenance on the instrumentation Tune and calibrate instrumentation Analyze samples and associated QC Review, work up, and assemble all supporting data Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC department Perform additional responsibilities (i.e., audit, verification, etc.) with minimal supervision Evaluate current analytical system performance and recommend corrective action to enhance efficiency and productivity Train other departmental analysts in procedures related to operations listed in the above Search technical literature for scientific information relative to improving analytical or operational performance Understand and use LIMS Make working calibration standards Use word processor on PC Monitor and change gas cylinders Review and amend departmental methods when required, either as part of yearly review or when an analytical change to the method is made Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Basic Minimum Qualifications 5+ year HR/MS experience in a production laboratory At least 5 years experience related to performing extractions and/or instrumental chromatographic analyses utilizing wet chemical and chromatographic techniques) in a wide variety of matrices encountered in environmental testing. Bachelor's degree in chemistry, biology, physics or related degree concentration Authorization to work in the United States indefinitely without restriction or sponsorship Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Skills and Abilities Exceptional technical skills, including logical thinking and deductive reasoning; good work habits (e.g., cleanliness, efficiency, carefulness, effective organizational skills); High accuracy in recording and transcribing data; Personal maturity and sense of responsibility; Good written and oral communication skills; Ability to learn new methods and techniques; Willingness to follow instructions and comply with company policies; Consciousness of, and a positive attitude toward, quality control and safety procedures; Good understanding of chemical principles; Accurate management of numbers, both by hand and using a calculator; Set up and perform nonroutine standardized tests with minimal supervision; Demonstrated versatility, flexibility, and efficiency; Effective use of time while managing multiple priorities; Above satisfactory reasoning ability; Self-motivated to improve technical skills and operations; Superior leadership, organizational, and communication skills; Lead a project to a satisfactory conclusion on time; Consult with clients on work performed for them; Problem solving skills; Function under high stress levels; multitask; See cause-and-effect relationships; Retain large amounts of information Additional Information Compensation Range: $80,000 - $120,000 per year depending on level of experience and qualifications. Position is full-time, and exempt from overtime pay. Candidates must be available to work the following shift: Monday - Friday, 8:00am to 5:00pm and any additional hours needed Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Company description: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR 6.151 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Contract: 3 months Automation Engineer Write, edit, review, and approve lifecycle documentation for computerized systems. URS, FRS, CDS, CS, ERES assessments, IA, IOQ • Use both Veeva and Kneat to do the above • Integrate equipment with DeltaV and PI historian using OPC, EtherNet/IP, PI interfaces and PI connectors • Execute IQs and IOQs in Kneat on DeltaV

As a Lab Automation Engineer in Bio-product Research and Development, you will be responsible for identifying automation opportunities, assessing available technologies, and for implementing automation technologies across different laboratory areas. The ability to thrive in a team environment while seeking to leverage use of the automation tools available is a must. The scientist/engineer is also responsible for working collaboratively with a wide array of scientists, engineers and automation experts from many disciplines, leading / supporting organization initiatives, and providing internal influence on the use of automation in a laboratory setting. Responsible for design and implementation of key automation aspects of laboratory equipment Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. Contribute to the completion of projects, manage own time on agreed targets, develop plans for own projects and leads small project teams. Demonstrate good planning, organizing, time management and team participation skills Mentor and guide junior staff and serve as a technical trainer, whenever necessary Clearly communicate progress and issues to peers Requirements Bachelor's and/or master's degree in engineering, life sciences or related field At least 3 years' experience/ knowledge with automated systems, including programming and improving complex systems Familiarity with at least one computer coding language (such as Python, Java, C#, HTML), understanding in version control systems (like GitHub or GitLab) is a plus Able to independently contribute through development and optimization of automation technologies preferred. Able to oversee implementation of automation technologies with third parties through technical skills and project management principles Must be able to work productively in an interdisciplinary team environment Experience with Hamilton, Scinomix, Tecan or similar automated laboratory platforms preferred Good oral and written communication, problem-solving, and analytical skills Ability to influence and educate other scientists and engineers to use automation technologies as part of implementation Proficiency using PC and Microsoft Office tools Excellent organizational and time management skills Strong attention to detail GMP and Good Documentation Practice Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes) Basic skills with EXCEL and PowerPoint Experience with and tolerance for high levels of challenge and change Experience with project management including capturing project requirements and deliverables, timeline development, stakeholder management and communications

The scope of this role is to provide direct coordination and integrated Automation Support within Global Robotics Asset Portfolio to ensure the outputs required are developed and delivered, inclusive of delivery to sites in Indianapolis, Raleigh Durham NC, Concord NC, Alzey Germany, and potentially other future sites. Highly versed in Allen Bradley Rockwell Controls including Studio5000 and FactoryTalk SE applications. (Required) Experience with FANUC Robotic systems desired but not required Experience in Commissioning and Qualification, asset delivery, validation activities and cGMP regulations. Experience delivering and/or troubleshooting automated applications within the pharmaceutical industry. Work with client Platform owner and Robotic application integration to troubleshoot, shakedown, and oversee Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT). Troubleshoot system issues found during production and help identify and implement solutions. Evaluate production metrics and historian data to identify issues, recommend and help implement improvements. Ability to travel to client production sites up to 25%+ (1-2 weeks per month as needed by the project Demonstrated ability to effectively work independently and to take initiative especially within a complex network environment Previous automated assembly equipment validation experience Strong documentation management and technical writing skills Contribute to the completion of projects, manage own time on agreed targets, develop plans for own projects and leads small project teams Demonstrate good planning, organizing, time management and team participation skills Modify moderately complex to highly complex control logic that requires a degree of scientific and/or manufacturing process expertise Clearly communicate progress and issues to peers Must be willing to work onsite in Indianapolis, IN Must be willing to travel to multiple sites Must have 5+ years of experience as an Automation Engineer (pharmaceutical environment experience highly preferred) Bachelor's Degree or equivalent required Proficiency using PC and Microsoft Office tools Outgoing personality with a strong ability to communicate effectively with peers in clear, concise terms Ability to work as part of a team Strong problem-solving and critical thinking skills Excellent organizational and time management skills Strong attention to detail GMP/Validation practices Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes) Basic skills with EXCEL and PowerPoint Strong interpersonal skills and clear communication capabilities Experience with and tolerance for high levels of challenge and change Responsible for installing, maintaining, and troubleshooting automated utility, processing, filing, inspection, and packaging equipment Contribute technical content to validation protocols on automation systems and perform execution of protocols Requirements Highly versed in Allen Bradley Rockwell Controls including Studio5000 and FactoryTalk SE applications. (Required) Experience with FANUC Robotic systems desired but not required Experience in Commissioning and Qualification, asset delivery, validation activities and cGMP regulations. Experience delivering and/or troubleshooting automated applications within the Pharmaceutical industry. Work with client's Platform owner and Robotic application integration to troubleshoot, shakedown, and oversee Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT). Troubleshoot system issues found during production and help identify and implement solutions. Evaluate production metrics and historian data to identify issues, recommend and help implement improvements. Ability to travel to client's production sites up to 25%+ (1-2 weeks per month as needed by the project Demonstrated ability to effectively work independently and to take initiative, especially within a complex network environment Previous automated assembly equipment validation experience Strong documentation management and technical writing skills

Participate in developing and documenting User Stories, including testing estimates and validation tests. Develop automated tests for features developed in-sprint. Perform desk checks and code reviews. Develop, document, and maintain the test strategy and test scenarios. Partner with the developers to ensure all areas of the application are fully tested and issues are clearly logged and prioritized consistently. Partner with developers to find technical solutions for test automation. Manage the defect log and ensure issues are resolved, including validation of the fix. Certify software functionality for new Production releases. Work with Integration Build teams to manage dev, QA, and production release of the software. Provide exploratory testing to understand the feature and how it is implemented, to find additional or unexpected behavior, and to refine and define additional test cases for the feature. QUALIFICATIONS Bachelors degree in computer science or equivalent experience. Minimum 7 years of industry experience, preferably in an Agile development environment. 5+ years of Java and Javascript development experience. Experience with test toolsets/frameworks - Cucumber/Gherkin, Selenium web driver, Maven. Experience with automated testing tools - Selenium Webdriver with JavaScript and Java. Experience working with databases and various data formats and related technologies for testing. Experience with defect tracking tools (JIRA). Experience with source control versioning systems (Git, Stash, Source tree.). Experience in API automation testing using JAVA Springboot. Experience in writing SQL queries. Knowledge in Couchbase database queries. Experience with Splunk. Experience in manual testing. Knowledge in CI/CD processes and tools preferably Jenkins. Knowledge in Couchbase database queries. Experience with Version control tools - Jenkins, Maven, Git, Grunt. Ability to work independently with an aptitude for detailed work and follow-up activities. Experience in heavy traffic eCommerce applications.

Participate in developing and documenting User Stories by providing the test strategy and automation estimates Develop, document, and maintain the test strategy and test scenarios Build and execute unit, component, acceptance, integration, load, security, scalability, usability, and platform tests Conducts code reviews to ensure consistency, quality, and reusability of test automation artifacts Partner with the developers to ensure all areas of the application are fully tested and to find technical solutions for test automation Build and manage automated test suites and ensure execution through various environments, CI-CD pipelines and to be used by NOC teams. Regularly execute, maintain and upkeep automated test suites and analyze the results to identify the cause for failures. Create defects for issues found with appropriate details and ensure issues are resolved, including validation of the fix, and required automation updates Present appropriate results to sign off on software functionality for new Production releases Work with cross teams and release management team to manage dev, QA, and production release of the software Perform exploratory testing to understand the feature and how it is implemented, to find additional or unexpected behavior, and to refine and define additional test cases for the feature Contribute to the QA automation framework using industry standard tools and approaches Leverage and enhance coding standards and best practices for automated QA code Participate in analyzing Major Incidents and Emergency Change controls to identify opportunities to automate software quality test cases to reduce or eliminate those

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description The Quality Assurance (QA) Engineer will be responsible for bridging technical operations and quality assurance. Valuable in high throughput, regulated labs, and are key to preventing quality failures through proactive risk and process management. This role involves monitoring lab processes, conducting audits, analyzing data to identify potential issues, and driving continuous improvement initiatives to minimize errors and ensure data integrity. Key Responsibilities & Duties * Quality Management System (QMS): Participate in the maintenance and improvement of the QMS. Help ensure that procedures are compliance with regulatory standards (e.g. CLIA, CAP, FDA, ISO 15189). Identify and investigate non-conformances. Assist in developing technical SOPs and work instructions. * Auditing and Compliance: Provide technical documentation for audits and inspections. Ensure all validation and qualification documentation is complete and audit ready. Plan and conduct internal audits of laboratory operations, processes, and systems to assess compliance with established quality standards and regulations. Support external audits and inspections from regulatory agencies. * Corrective and Preventive Actions (CAPA): Conduct technical root cause analyses for system-related failures or deviations. Help develop and implement Action Plans. * Process Improvement: Identify areas for process improvement and lead continuous improvement activities. Utilize Lean Six Sigma or other quality tools to identify inefficiencies. Develop and maintain process maps, value stream maps and other visual tools to identify bottlenecks and opportunities. Collaborate with lab operations and IT to improve workflows and reduce errors. Develop and use statistical analysis and quality control charts to monitor trends and recommend solutions for enhanced quality and efficiency. Assist in the development and refinement of quality metrics and dashboards. * Training: Assist in the development and delivery of quality assurance training programs for laboratory staff to ensure adherence to quality protocols and procedures. * Collaboration: Work closely with lab management, technical directors, and other cross-functional teams to integrate process improvements and quality requirements into daily operations and new process development. Contribute to the evolution of a proactive quality culture, aligned with our service vision and mission Qualifications * Education: Bachelor's degree in a chemical, biological, physical, laboratory science or related science or engineering field. * Experience: 3+ years of experience in a Quality Engineering or Process Improvement preferable in a regulated laboratory or healthcare setting. * Regulatory Knowledge: Thorough understanding of industry-specific quality standards and regulations (e.g., ISO 15189, CAP, CLIA, FDA, etc.). * Technical Skills: Proficiency with Laboratory Information Management Systems (LIMS), statistical analysis software, and Microsoft Office (especially Excel for data analysis). Experience with Lean Six Sigma, Statistical Process Control, Value Stream Mapping, Root Cause Analysis, CAPA, etc. is key toward process improvement role. * Problem-Solving: Strong analytical and problem-solving abilities with experience in root cause analysis. * Communication: Excellent written and verbal communication skills, with the ability to present data and reports to diverse stakeholders. * Attention to Detail: Meticulous attention to detail and a high level of accuracy in all documentation and processes. * Work Environment: Ability to work independently and collaboratively in a fast-paced, deadline-driven laboratory environment, which may involve working with potential biohazards or wearing personal protective equipment (PPE). Additional Information Compensation: * $90,000-$110,000 per year Schedule: * Monday - Friday 8:00am-4:30pm What we offer: * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is a global leader in analytical testing, operating over 950 labs in 60 countries with 65,000 employees. EAG Laboratories, part of Eurofins, offers advanced services in analytical chemistry, microscopy, surface analysis, and engineering sciences-including failure analysis, product reliability, and ATE testing. We support clients across the product lifecycle, from R&D to manufacturing. Serving diverse industries, EAG delivers expert insights and tailored solutions. Our engineers and scientists collaborate with clients to solve complex challenges and deliver actionable results. We foster a growth mindset, empowering individuals to drive success while meeting evolving technological and business needs. EAG's Engineering Sciences lab provides test, engineering, and reliability services to a broad spectrum of technology-based sectors. We are proud to support our clients who range from startup stages to Fortune 500 global industry leaders. Our engineering staff succeed within a challenging but inspiring world of innovation; helping to support our clients research, develop, understand, and refine technologies that shape consumer electronics, medical device, automotive, military, aerospace, and manufacturing industries, just to mention a few. We demonstrate a hands-on approach to technical expertise by utilizing leading-edge methods and tools to attain insight that fuel engineering. If you enjoy being immersed in technology, dreaming about the future, tackling challenges head-on, problem-solving through teamwork, flexing your technical abilities and taking pride in accomplishments, then join us to live this every day. We are looking for a ATE Test Engineer with proven experience in developing and supporting complex mixed-signal silicon SoC products. The ideal candidate will develop and oversee SoC test strategy, interact with manufacturing partners, define, and implement ATE programs and own the product from design, initial samples all the way through high volume production ramp. The candidate should have working knowledge of DUTs such as PMIC, ADC/DAC, FPGA, SoCs, and RF devices, etc. We welcome mid level candidates to apply! If you have some knowledge working knowledge, we'd like to consider you! Local SF Bay Area candidates are encouraged to apply. This role is subject to the International Traffic in Arms Regulations (ITAR) therefore all accepted applicants must be U.S. Persons as defined by ITAR: U.S. Person is a U.S. Citizen, U.S. Permanent Resident (i.e., "Green Card Holder"), Political Asylee, or Refugee. Key Responsibilities: Lead cross-functional test development initiatives, collaborating with design, product, and manufacturing teams to ensure robust test coverage and yield optimization. Mentor junior engineers and technicians, providing guidance on test strategy, debug techniques, and professional development. Drive continuous improvement in test methodologies, documentation standards, and team workflows. Represent the ATE team in technical reviews, program meetings, and customer interactions. Foster a culture of technical excellence, accountability, and innovation within the test engineering group. Qualifications Strong academic and technical background in electrical engineering or related degrees. BS and master's will be considered. Proven experience leading ATE test development projects from concept to production. Demonstrated ability to mentor and develop junior engineers, with a track record of building high-performing teams. Strong interpersonal and communication skills, with the ability to influence cross-functional stakeholders. Experience in strategic planning and resource management within an engineering environment. Ability to identify and implement process improvements that enhance team efficiency and product quality. 1+ years of experience releasing complex SoC/silicon products to high volume manufacturing. Working knowledge of high-speed protocols like PCIe, Ethernet, Infiniband, DDR, NVMe, USB, etc. Hands-on experience with high-speed mixed signal SoC test program/hardware development on multiple high-speed test platforms. Collaboration with design team to define test strategy, create and own test plan. Tester platform selection, design, and development of ATE hardware for wafer sort and final test. Familiar with high-speed load board design techniques. Proven track record of implementing ATE patterns to optimize tester resources and minimize ATE test time while maintaining product quality. Strong knowledge and development of DFT techniques implemented in silicon that provide maximum defect and parametric device coverage - SCAN, MEMBIST, SerDes and other functional tests. Skilled in control interfaces - I2C, I3C, SPI, MDIO, JTAG etc. Expertise in production test of high speed SerDes operating at 16Gbps and higher. Experience with micro-controller and FPGA designs. Skilled in ATE programming, silicon/ATE bring-up, bench-ATE correlation and debug. Experience with lab equipment including protocol analyzers, oscilloscopes, RF SA, VNA, and ICE. Experience with using Advantest 93k ATE, Teradyne UltraFlex/J750 platforms. Proficiency in, at least, one modern programming language such as C/C++, Python. Professional attitude with ability to execute on multiple tasks with minimal supervision. Strong team player with good communication skills to work alongside a team of high caliber engineers. Entrepreneurial, open-mind behavior and can-do attitude. Fluent in data processing using high level programming languages. Familiarity with modern databases. We encourage you to apply even if your experience is not a 100% match with the position. We are looking for someone with relevant skills and experience, not a checklist that exactly matches the job description. We want to help you grow and in return, you help us grow into a stronger, more inclusive organization. Physical Requirements: Must be able to remain in a stationary position up to 50% of the time. Ability to continuously operate a personal computer or lab equipment for extended periods of time (4 or more hours). Ability to operate a keyboard and other lab equipment, use a telephone, access file cabinets and other items stored at various levels, including overhead Ability to communicate clearly and understandably ensure an accurate exchange of information in normal conversational distance, over the telephone, and in a group setting. Ability to handle small and fragile devices with tweezers and /or fingers. Require close distance visual acuity with or without correction (Glasses, Contacts, etc.) Must be willing and able to wear PPE such as hard-hat, steel-toed shoes, safety glasses, laboratory coat and/or any other devices or equipment that is required. Learn new tasks, remember processes, maintain focus, complete tasks independently, make timely decisions in the context of a workflow, ability to communicate with visitors, ability to complete tasks in situations that have a speed or productivity quota. Ability to move equipment or items up to 50 lbs. The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. We will consider reasonable accommodations for qualified individuals with disabilities. If you have a disability or special need, we would like to know how we can better accommodate you. Additional Information Compensation is aligned with market standards for the region and tailored to individual qualifications and experience. What It's Like to Work Here: Teamwork: experience what being a part of the Eurofins-EAG family feels like. Be inspired by your leaders, be encouraged by your teammates and be supported in all parts of your journey while you work with us. Learning & Development: take on career development programs and goal setting to create big possibilities for your career and life. Develop within the company; be mentored and grown as a leader. Diversity & Authenticity: we work hard to embrace diversity and inclusion and encourage everyone to bring their authentic selves to work every day. Benefits & Perks to Foster Work/Life Balance: ✓ Medical, Dental and Vision Coverage ✓ 401k Company Matching ✓ Paid Time Off ✓ Wellness Program ✓ Education Assistance ✓ …and more! If you enjoy being immersed in technology, tackling problems head-on, finding solutions through teamwork, and taking pride in accomplishments, join us today! Eurofins EAG Laboratories is an equal opportunity employer and prohibits discrimination, harassment, and retaliation in all of our employment practices. Eurofins EAG Laboratories recruits, hires, trains, promotes and administers all employment-related matters based on an individual's qualifications, abilities, and efforts. Applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, citizenship status, sexual orientation, gender identity and/or expression, pregnancy, genetic information, disability, military and/or protected veteran status, and/or any other category protected by applicable federal, state, or local law. Eurofins EAG Laboratories is a Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer If you enjoy being immersed in technology, tackling problems head-on, finding solutions through teamwork, and taking pride in accomplishments, join us today! Check out our other EAG Laboratories opportunities: EAG Careers Eurofins USA Material Sciences is a Disabled and Veteran Equal Employment Opportunity employer.

Job Title: Electrical Infrastructure - Sr. Automation & Controls Engineer 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 3% 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. Location: Columbus, OH, US, 43228 Nearest Major Market: Columbus

The technician will be responsible for the quality and performance of the primary product line. The ideal candidate will have experience in both mechanical and electrical testing and assembly, due to the functionality of the products. The technician will be a part of the production cycle and will be responsible for production processing, building sensor systems, and overseeing the maintenance and operation of equipment. The technician will also perform tasks such as machining and assembling different components for the sensor system. The ideal candidate is a self\-motivated individual that sees the bigger picture when making and testing products. The candidate will also possess a strong attention to detail, the ability to work under the pressure of changing deadlines while maintaining the standard of quality and craftsmanship of the product. "}},{"field Label":"Skills","uitype":110,"value":"Skills and Qualifications Associate's Degree in Automotive Technology, CNC machinery or related field 2 years of experience in a related role Familiarity with the following tools and technologies (but not limited to): MATLAB SolidWorks or other 3D CAD software LabView Testing Software"}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"30142516","FontFamily":"Verdana, Geneva, sans\-serif","job OtherDetails":[{"field Label":"City","uitype":1,"value":"San Diego"},{"field Label":"State\/Province","uitype":1,"value":"CA"}],"header Name":"Test Engineer","widget Id":"2**********0118069","is JobBoard":"false","user Id":"2**********0043003","attach Arr":[],"custom Template":"3","is CandidateLoginEnabled":false,"job Id":"2**********0883031","FontSize":"12","location":"San Diego","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"fmv6cf7fa801b223c4cbf901e9c0ed9658cc2"}

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 03-Nov-2025 Closing Date 30-Dec-2025 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.

Summary/objective Performs diverse and complex technical assignments. This position is responsible for specific project work related to any number of tasks affecting the outcome of component integrity. Defines the requirements of new test equipment and is often responsible for the design, layout, and fabrication of custom test equipment. Essential Functions Executes work assignments in a prototype, test and/or quality environment. Demonstrates a proficiency with creating and following processes, procedures and techniques. Performs calculations and conducts moderate analysis. Compiles and organizes technical data, prepares reports, and provides recommendations. Creates and maintains standard documentation related to processes and procedures. Applies troubleshooting and diagnostic skills to resolve routine and complex problems. Maintains testing equipment. Full proficient usage of equipment and machinery. Identify and resolve routine and moderately routine problems. Plans activities within specific guidelines to meet deadlines. Conducts tests and/or experiments leading to improvements of current products and development of new ones. Develops, plans and investigates practical problems involving the full use of company products in diverse manufacturing processes to conform to company requirements. Conducts independent analysis of operating conditions and specifications proposed and requested by company. Competencies Analytical and problem-solving skills. Excellent interpersonal, written, and oral communication skills. Models the Niowave Values of Teamwork, Courage, Integrity, and Upright Zeal. Understands how to integrate into a new team/organization - appreciates 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. Understands their own communication and learning styles, can assess others' styles, and is able to find the right path to connect the two. Required Education and Experience Minimum of an associate's degree or equivalent in technical or mechanical engineering 4 years of experience with the following: Comprehension and execution of mechanical assembly drawings and bill of materials. Comprehension and execution of general schematics such as P&ID and electrical. General safety procedures and practices in an industrial work environment. Industry/Manufacturing experience (non-routine/production related) Preferred Education or Experience Project management Knowledge of electrical systems Experience with equipment, tools etc. used with chemistry and/or radioactive processes Technical writing Work Environment Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel objects, tools or controls; reach with hands and arms; climb stairs; talk and hear; wear safety glasses, goggles, gloves, and Tyvek suit; handle chemicals, solutions, and/or radioactive materials. Ability to lift or move products and supplies, up to 50 pounds. Position Type/Expected Hours of Work/Travel Full-time position. 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 work outside of the standards operating hours as needed. Niowave has multiple locations within the Lansing area. Travel between locations is expected in the role. Other duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

The Automation Engineer is responsible for overseeing and optimizing automation systems to improve production efficiency and reduce operational costs. This position involves designing, integrating, and implementing advanced hardware and software solutions within pharmaceutical manufacturing facilities. Essential Functions: Develop Control Systems based on coordination with OEM, in order to automate upstream and downstream processing equipment, including Mixers, Coaters, Pouches, Cartoners, Packaging Lines, Laboratory equipment, facility systems, stability Chambers, BMS, CIP (Clean in Place) and SIP (Steam in Place), Water System Controls, Tablet Press, Fluid Bed Dryers, Granulators, Vision System etc. Perform programming, qualification and validation of digital process automation systems. Provide 24x7 on-call Automation Support, including technical support and troubleshooting functions. Perform formal systems acceptance testing, including software simulation and hardware and equipment acceptance in pharmaceutical manufacturing facilities. Properly complete documentation for accurate recordkeeping, according to the Engineering Department's procedures, Assist with updating departmental procedures; monitor equipment, and ensure preventative maintenance is being done, handle calibration monitoring, engineering analysis. Assist with training coworkers on using equipment. Read, understand, verify and develop P&ID, Engineering Layout, Engineering Drawings and Engineering documents. Implement projects according to Good Automated Manufacturing Practice (GAMP) guide for validation of automated systems in pharmaceutical manufacture. Handle logistics and coordination of electrical construction activities as per engineering standards, vendor development, with the various departments like manufacturing, QA, QC, R&D for the engineering and Validation Aspects; maintain VMP and other GMP documents, Support Process Validation and Development Studies. Coordinate and ensure Safety Aspects. Perform hands on field installation, operational start-up, calibration, and commissioning activities. Support Change Control Management, updating documentation for client, including test plans and production implementation. Apply batch coding standards to automation process, including design of batch operations, unit procedures, and procedural recipe components to aforementioned processes. Additional Responsibilities: Assists with engineering projects and performs other duties as assigned. Education: Bachelors Degree (BA/BS) Electrical Engineering or Related Field - Required Masters Degree in Electrical Engineering or Related Field - Preferred Experience: 3 Years of Experience working with hydraulics, pneumatics, programmable logic controllers, electrical circuits, electrical machinery and human-machine interfaces within industrial and manufacturing plant, food or pharmaceutical processing facilities. Skills: Proficient with MS Office. - Intermediate Proficiency with Computer Aided Design Software (Autocad), Proficiency with MS Project Software - Advanced Technical writing skills. - Advanced Oral and written communication skills. - Advanced Must be able for follow direction and execute assigned work independently, after initial training is completed. - Advanced Ability to work both independently and in conjunction with a team - Advanced Specialized Knowledge: Fully comprehend, verify, and develop P&ID, Engineering Layout, Electrical/Controls Diagram, Engineering Drawings and Engineering documents, HMI, SCADA, VFD and PID Controller Programming Project Management The base salary for this position ranges from $95,000 to $110,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.

The Automation Engineer's primary role is to work under supervision and coordinating installation, troubleshooting and assist in maintaining automated processes and facility related equipment. Essential Functions: * Responsible for troubleshooting, servicing and repairing of computerized systems and robotic devices that are designed to reduce human interaction, such as robotic assembly devices and computer-controlled building air-conditioning systems with guidance from his/her supervisor. * Help perform hands on field installation, operational start-up, calibration, and commissioning activities under close supervision. * Support field technician, bench technician, robotics technician, production support technician and maintenance technician. * Help improve and monitor automation processes for optimum cost efficiency of production under close supervision. * Support installation and troubleshooting control systems to automate upstream and downstream processing equipment, including Mixers, Coaters, Pouchers, Cartoners, Packaging Lines, Laboratory Equipment, Facility Systems, Stability Chambers, BMS, CIP (Clean in Place) and SIP (Steam in Place), Water System Controls, Tablet Press, Fluid Bed Dryers, Granulators, Vision System. * Read, understand, verify and draft for approval P&ID, Engineering Layout, Engineering Drawings and Engineering documents and understand Electrical Schematics and wiring. * Assist in monitoring automated systems, help isolate problems and help perform repairs under close supervision. * Work under supervision to assist with the following: design, program, simulate and test automated machinery and processes in order to complete exact tasks; assist with design, upgrade, and troubleshoot new and existing PLC control systems based on company guidelines; assist with performing field commissioning based on project requirements;assist with execution of automation projects, hardware and software implementation, executing its qualification and validation. Assist with training coworkers on use of equipment. * Assist in providing 24x7 on-call Automation Support, including technical support and troubleshooting functions. * Knowledge of PLC and HMI programming such as Rockwell, Seimens systems.

The Automation Engineer is responsible for overseeing and optimizing automation systems to improve production efficiency and reduce operational costs. This position involves designing, integrating, and implementing advanced hardware and software solutions within pharmaceutical manufacturing facilities. Essential Functions: * Develop Control Systems based on coordination with OEM, in order to automate upstream and downstream processing equipment, including Mixers, Coaters, Pouches, Cartoners, Packaging Lines, Laboratory equipment, facility systems, stability Chambers, BMS, CIP (Clean in Place) and SIP (Steam in Place), Water System Controls, Tablet Press, Fluid Bed Dryers, Granulators, Vision System etc. * Perform programming, qualification and validation of digital process automation systems. Provide 24x7 on-call Automation Support, including technical support and troubleshooting functions. * Perform formal systems acceptance testing, including software simulation and hardware and equipment acceptance in pharmaceutical manufacturing facilities. * Properly complete documentation for accurate recordkeeping, according to the Engineering Department's procedures, Assist with updating departmental procedures; monitor equipment, and ensure preventative maintenance is being done, handle calibration monitoring, engineering analysis. Assist with training coworkers on using equipment. * Read, understand, verify and develop P&ID, Engineering Layout, Engineering Drawings and Engineering documents. * Implement projects according to Good Automated Manufacturing Practice (GAMP) guide for validation of automated systems in pharmaceutical manufacture. * Handle logistics and coordination of electrical construction activities as per engineering standards, vendor development, with the various departments like manufacturing, QA, QC, R&D for the engineering and Validation Aspects; maintain VMP and other GMP documents, Support Process Validation and Development Studies. Coordinate and ensure Safety Aspects. * Perform hands on field installation, operational start-up, calibration, and commissioning activities. * Support Change Control Management, updating documentation for client, including test plans and production implementation. * Apply batch coding standards to automation process, including design of batch operations, unit procedures, and procedural recipe components to aforementioned processes. Additional Responsibilities: * Assists with engineering projects and performs other duties as assigned.

The Automation Engineer's primary role is to work under supervision and coordinating installation, troubleshooting and assist in maintaining automated processes and facility related equipment. Essential Functions: Responsible for troubleshooting, servicing and repairing of computerized systems and robotic devices that are designed to reduce human interaction, such as robotic assembly devices and computer-controlled building air-conditioning systems with guidance from his/her supervisor. Help perform hands on field installation, operational start-up, calibration, and commissioning activities under close supervision. Support field technician, bench technician, robotics technician, production support technician and maintenance technician. Help improve and monitor automation processes for optimum cost efficiency of production under close supervision. Support installation and troubleshooting control systems to automate upstream and downstream processing equipment, including Mixers, Coaters, Pouchers, Cartoners, Packaging Lines, Laboratory Equipment, Facility Systems, Stability Chambers, BMS, CIP (Clean in Place) and SIP (Steam in Place), Water System Controls, Tablet Press, Fluid Bed Dryers, Granulators, Vision System. Read, understand, verify and draft for approval P&ID, Engineering Layout, Engineering Drawings and Engineering documents and understand Electrical Schematics and wiring. Assist in monitoring automated systems, help isolate problems and help perform repairs under close supervision. Work under supervision to assist with the following: design, program, simulate and test automated machinery and processes in order to complete exact tasks; assist with design, upgrade, and troubleshoot new and existing PLC control systems based on company guidelines; assist with performing field commissioning based on project requirements;assist with execution of automation projects, hardware and software implementation, executing its qualification and validation. Assist with training coworkers on use of equipment. Assist in providing 24x7 on-call Automation Support, including technical support and troubleshooting functions. Knowledge of PLC and HMI programming such as Rockwell, Seimens systems. Education: Bachelors Degree (BA/BS) Automation Technology, Electrical Engineer, Mechanical or Mechatronics Program - Required Master Degree (MS/MA) Electrical or Mechanical Engineer, Electrical & Electronics Engineer - Preferred Experience: 1-3 years or more in Experience working with hydraulics, pneumatics, programmable logic controllers, electrical circuits, electrical machinery and human-machine interfaces within industrial and manufacturing plant, food or pharmaceutical processing facilities Experience in Electrical and Mechanical Engineer & Electronics Engineer. Skills: Good math and analytic skills are essential to understand automated systems and isolate problems. - Intermediate Workers are expected to become proficient with various instruments and hand tools, such as electrical millimeters. - Intermediate Specialized Knowledge: Fully comprehend, verify, and develop P&ID, Engineering Layout, Engineering Drawings and Engineering documents. Basic knowledge of PLC programming. Understanding of control system such as Sensor, Electrical wiring, pneumatic components. Licenses: Certifications and credentials from Electronics Technicians Association and the Manufacturing Skill Standards Council are preferable.-Upon Hire-Preferred Certification of Automation systems- Preferred The base salary for this position ranges from $65,000 to $80,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.

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. 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