Automation Engineer jobs at Novo Nordisk - 157 jobs

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. We are seeking a detail-oriented QA Engineer to join our Pharmaceutical Quality Assurance. In this role, the Quality Assurance Engineer plays a key role in maintaining FDA and cGMP compliance for OTC pharmaceutical manufacturing operations. This position supports quality systems, investigations, and process improvements to ensure consistent product quality. Work Schedule: Monday - Friday 8:00 AM - 4:30 PM JOB QUALIFICATIONS: Bachelor's degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related field 2-5+ years of experience in Quality Assurance within pharmaceutical or OTC manufacturing Strong knowledge of cGMP, FDA regulations, and quality systems Experience with deviation investigations, CAPA management, and change control Familiarity with OTC drug manufacturing and labeling requirements Excellent written and verbal communication skills Strong attention to detail and documentation skills Ability to work cross-functionally in a regulated environment POSITION RESPONSIBILITIES: Ensure compliance with FDA regulations (21 CFR Parts 210, 211), cGMPs, and company quality systems Review and approve batch records, deviations, investigations, CAPAs, and change controls Provide quality oversight for manufacturing, packaging, labeling, and testing operations Investigate nonconformances, deviations, and complaints, and lead root cause analyses Support internal audits, FDA inspections, and third-party regulatory audits Review and approve SOPs, protocols, validation documents, and quality records Collaborate with Manufacturing, QC, Regulatory, and Engineering teams to resolve quality issues Ensure proper implementation of process validation, cleaning validation, and equipment qualification Monitor quality metrics and support continuous improvement initiatives Provide QA guidance and training to manufacturing and support staff Support product releases and ensure documentation accuracy and completeness PHYSICAL REQUIREMENTS: Work safely and follow all OSHA regulations and company safety policies and procedures Works frequently in a lab environment, handling of chemicals. Employees are required to wear eye protection and lab coats while in the lab area. Ability to frequently lift and/or move up to 25 lbs. Ability to occasionally lift and/or move up to 35 lbs. Ability to regularly stand, sit, and walk to perform tasks BENEFITS: PLD is a proud employer offering many corporate benefits, including: Medical and Dental Benefits Vision 401K with employer match Group Life Insurance Flex Spending Accounts Paid Time Off and Paid Holidays Tuition Assistance Corporate Discount Program Opportunities to Flourish Within the Company PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

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.

Our Automation Engineer supports, develops, and maintains automated systems used in pharmaceutical manufacturing. This role ensures that production equipment, control systems, and digital infrastructure operate reliably, efficiently, and in compliance with cGMP and regulatory standards. The engineer collaborates with cross‑functional teams to troubleshoot issues, implement improvements, and support new system installations or upgrades. Operates within legal and regulatory compliance, ensuring systems are maintained and operational within site and regulatory requirements. Capable of following procedures, documenting work as/when performed and maintaining a clean/organized workplace supporting site compliance and quality standards. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is an onsite role in Bloomsbury, New Jersey; Monday - Friday 6 AM - 2:30 PM. What the Automation Engineer Does Each Day: Provides technical skills and expertise to support operations, ensuring automated manufacturing equipment operates efficiently, including network configuration and integration principles, and the ability to work effectively with IT Supports constant operations by trouble shooting machines, monitoring PLC issues, performing root cause analysis on complex issues, and executing improvements Investigates automation incidents and problems to prevent recurrence including the development and implementation of corrective actions Design and implementation of equipment and facilities related controls including PLC coding (Allen-Bradley/Siemens), HMI and SCADA systems Evaluates automated and information technology systems, and develops strategies to optimize and ensure quality and stability of automation systems through future expansion, replacement, or upgrade Efficient use of different software tools and computer applications including but not limited to Microsoft Office, PLC programming software, electrical schematic design software, HMI programming software, SCADA systems and industrial networks (Allen-Bradley/Siemens) Effectively and accurately handles most technical questions and objections for assigned products Maintains appropriate documentation for equipment and processes including change control, drawings, manuals, and validation Streamlines workflows and develop automated laboratory processes and instrumentation systems, including collecting and documenting requirements, developing concepts, design, testing/validation, implementation, and training Recognizes priorities and takes action; makes productive use of time Understands and adheres to policies and procedures Software validation, data integrity, GAMP 5 and 21 CFR part 11 experience Operating and troubleshooting of Fanuc Robotics Our Most Successful Automation Engineer Has: Experience in aseptic processing preferred Experience with FDA, GMP, and ISO standards preferred Must possess the ability to work effectively with all levels of organization Demonstrated ability to build and maintain strong business and collaborative relationships, internally and externally Must possess excellent interpersonal, communication, and writing skills, ability to analyze technical issues, define/solve problems, establish project plans, and draw valid conclusions Ability to think analytically and systematically Aseptic Operator Qualification and Process Simulation Proficient in technical writing and current computer usage (Word, Excel, PowerPoint, etc.) Good working knowledge of regulatory guidance as it pertains to APIs and injectable drug products Minimum Requirements for this Role: Bachelor's degree in electrical engineering, Mechanical Engineering, or another related field, with 5+ years' experience in a manufacturing environment Experience working with PLCs, HMIs, Robotics (Fanuc, Staubli), and SCADA systems, preferably Rockwell or Siemens platforms Equipment/Instrument Calibration principles Proven ability to adapt and manage effectively in fast paced, changing environment 18+ years of age Able to successfully complete a drug and background check Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas Benefits of Working at Quva: Set, full-time, consistent work schedule Comprehensive health and wellness benefits including medical, dental and vision 401k retirement program with company match 17 paid days off plus 8 paid holidays per year Occasional weekend and overtime opportunities with advance notice National, industry-leading high growth company with future career advancement opportunities The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions Range: $85,993 - $134,364 Annually About Quva: Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.” California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

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

7,000 Diseases - 500 Treatments - 1 Rare Pharmacy PANTHERx is the nation's largest rare disease pharmacy, and we put the patient experience at the top of everything that we do. If you are looking for a career in the healthcare field that embraces authentic dedication to patient care, you don't need to look beyond PANTHERx. In every line of service, in every position and area of expertise, PANTHERx associates are driven to provide the highest quality outcomes for our patients. We are seeking team members who: Are inspired and compassionate problem solvers; Produce high quality work; Thrive in the excitement of the ever-challenging environment of modern medicine; and Are committed to achieving superior health outcomes for people living with rare and devastating diseases. At PANTHERx, we know our employees are the driving force in what we do. We cultivate talent and encourage growth within PANTHERx so that our associates can continue to explore their interests and expand their careers. Guided by our mission to provide uncompromising quality every day, we continue our strategic growth to further reach those affected by rare diseases. Join the PANTHERx team, and define your own RxARE future in healthcare! Location: Pittsburgh, PA (Hybrid) Classification: Exempt Status: Full-Time Reports to: Manager, Quality Assurance Business Purpose As a member of our IT Quality Assurance team, the QA Engineer will design and execute test plans to ensure the highest quality software products for our specialty pharmacy customers, relying on a strong technical knowledge of software quality assurance and emerging AI-driven testing methodologies. This role requires excellent communication and problem-solving skills with the ability to think critically to evaluate and analyze software applications. This position will be responsible for evangelizing and executing QA policies and procedures, adhering to QA standards, and monitoring the QA process to ensure a high quality of deliverables. Responsibilities Develops test plans and executes test cases based on business requirements. Tests across multiple platforms and applications on mobile and desktop. Monitors the QA process to ensure the highest quality of deliverables. Follows comprehensive QA processes and procedures. Analyzes and evaluates QA results. Provides a voice during team meetings and scrum ceremonies. Writes SQL queries to set up and validate test data. Communicates QA results to stakeholders. Develops and implements automated testing. Ability to leverage AI-powered testing tools and frameworks to enhance test coverage and efficiency. Implements machine learning models for predictive defect analysis and risk-based testing. Utilizes AI-driven test case generation and optimization techniques. Required Qualifications Bachelor's degree in computer science, Information Technology, or a related field. Minimum of two (2) years of experience in software quality assurance. Knowledge of software testing processes and methodology. Excellent problem-solving and troubleshooting skills. Excellent verbal and written communication skills. Basic understanding of AI concepts and their application in software testing. Familiarity with AI-driven software tools (e.g., Claude, Copilot). Preferred Qualifications Two (2) years of experience in a software QA role. Two (2) years of experience testing mobile applications. Experience testing SMS. Experience in the pharmacy industry Experience using proprietary project and issue tracking software (Azure DevOps, JIRA, etc.). Experience using test management systems (Azure Test Plans, TestRail, etc.) Experience in developing and implementing automated testing using a scripting language (C# preferred) and Selenium. Experience with AI-based visual testing and intelligent defect prediction tools. Work Environment This position operates in a home or professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Physical Demands While performing the duties of this job, the employee is regularly required to sit, see, talk, or hear. The employee frequently is required to stand; walk; use hands and fingers to handle or feel; and reach with hands and arms. Visual acuity is necessary for tasks such as reading, or working with various forms of data on a screen for extended periods. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job. Benefits: Hybrid, remote and flexible on-site work schedules are available, based on the position. PANTHERx Rare Pharmacy also affords an excellent benefit package, including but not limited to medical, dental, vision, health savings and flexible spending accounts, 401K with employer matching, employer-paid life insurance and short/long term disability coverage, and an Employee Assistance Program! Generous paid time off is also available to all full-time employees, as well as limited paid time off for part-time employees. Of course we offer paid holidays too! Equal Opportunity: PANTHERx Rare Pharmacy is an equal opportunity employer, and does not discriminate in recruiting, hiring, promotions or any term or condition of employment based on race, age, religion, gender, ethnicity, sexual orientation, gender identity, disability, protected veteran's status, or any other characteristic protected by federal, state or local laws.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of . Key Responsibilities: Execute and document validation activities (IQ, OQ, PQ, PPQ), including risk assessments and periodic reviews. Support the full Validation Life Cycle-from design through revalidation and continuous improvement. Collaborate with internal and external teams to ensure new systems meet cGMP and validation requirements. Maintain and update validation-related documentation (SOPs, Change Controls, CAPAs, Deviations). Assist in investigations and resolution of deviations involving equipment, systems, and processes. Provide validation support during audits and ensure inspection readiness Key Qualifications: Bachelor's degree in engineering, life sciences, or related field 2-5 years of validation experience in a GMP-regulated environment. Cross- Functional Communication Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

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. 67081 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.

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 26-Jan-2026 Closing Date 12-Feb-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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.

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

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.

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 $90,000 to $100,000 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. 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.

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

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

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

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