Validation Engineer Salary in North Carolina, USA

Job DescriptionAbout This RoleThe Manufacturing Engineer III designs, specifies, installs, commissions and validates new process equipment, provides engineering technical support and troubleshooting for assigned process equipment and a GMP biological manufacturing area such as Cell Culture, Harvest or Purification. The incumbent would support technology transfer of new processes into the facility, provide project engineering support as required for new process equipment installations and modifications to existing process equipment and have the ability to manage medium engineering projects with little direction. In addition, they would develop validation protocols, oversee validation testing and final report approvals. This role will work with and provide some direction to contractors and participate in and lead multi-function teams to implement change and improvements on existing processes.What You'll DoResponsible for supporting manufacturing operations by troubleshooting process equipment system issues and identifying improvements. Update preventative maintenance job plans, equipment standards, drawings and specifications as necessary.Identify and lead process equipment related projects, including technology transfers, capital projects, and modifications. Provide input & guidance to Tech Transfer and area efforts, provide technical evaluations of process equipment including validation requirements for change controls and associated action plans. Author and approve Trackwise generated workflows (change controls, deviations, CAPAs) for equipment/automation related changes, impact assessments, review automation protocols, and attend related meetings. Coordinate process equipment/cleaning validation protocols (development, management, tracking) including time spent on manufacturing floor. Specifically design and develop validation protocols, provide expertise to associated equipment and automation design / modifications, support FAT (Factory Acceptance Testing), equipment startup, & commissioning efforts, as required. Who You AreYou are an experienced process equipment engineer who likes to troubleshoot and investigate improvements to increase site operations and passionate about learning new technologies and working in a cross-functional environment. You are accountable for achieving milestones in equipment projects, involving frequent internal and external communication. As a representative of the Manufacturing Engineering organization, your role carries the weight of potential delays and extra resource allocation if errors occur in your decisions or recommendations. Your commitment lies in delivering accurate and timely results, ensuring efficient processes to prevent setbacks.QualificationsBachelor's degree in engineering or other highly technical discipline Minimum of 2 years of experience in manufacturing, engineering or validation, preferably in a biologics drug substance environment.Experience with bioreactor, centrifugation, chromatography and/or viral/ultra-filtration unit operations preferredPractical knowledge and application of GMP regulations and guidelines (ISPE, USP, PIC/S, Annex, ICH, etc.). Competency in DeltaV, MS Word, MS Excel, MS Power Point and MS Project. Excellent organization, time management, oral and written communication skills. Ability to work on-site.Ability to work rotating shifts/on-call, extended coverage support and weekends as needed.Additional InformationWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. PDN-9c35fe64-618d-4864-acff-2470a13668c7

Medical Device Client is seeking a Manufacturing Engineer in Cary, IL!Duration: 18 MonthsPay Rate Range: $46.66/hr. - $50.00/hr. Description/Comment:Provides engineering support to a manufacturing process, project, or function. Evaluates manufacturing outcomes and implements continuous improvements and cost efficiencies. Supports NPI and new equipment/process introductions. This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. Roles typically require a university degree, or an extensive amount of practical knowledge gained through experience. Job requires an understanding and application of procedures and concepts of own discipline. The job requires the ability to make judgements based on practice and previous experience. This job typically requires a degree or equivalent.Top Skills:- Automation problem solving- Mechanical aptitudeAdditional Job Details: Support the installation, validation, and production ramp up of a custom automation line for the high-volume manufacture of medical devices. Provide technical, engineering, validation, and documentation support. What you will do As a consultant in Manufacturing Engineering: you will provide technical and engineering support to implement a new high speed, automated medical device assembly line. This is a significant investment in our site, and critical to achieve our business goals. Responsibilities include: * Support engineering and project management in FAT, installation, and commissioning of the new assembly line. * Support development of the process FMEA and control plan for the new assembly process. * Complete process validations including VP, URS, IQ, OQ, PQ and associated documentation. * Develop appropriate supporting documentation, SOPs and work instructions compliant with Good Manufacturing Practices (GMP). * Collaborate with product and manufacturing engineering, equipment vendors, maintenance technicians and operations leadership to troubleshoot process and equipment issues. * Support line performance monitoring and lead practical problem solving (PPS) projects to remediate systemic issues.All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Job DescriptionAbout This RoleThe Engineer III Manufacturing designs, specifies and installs new equipment and provides engineering technical support and troubleshooting for assigned process equipment and area assets. Develops validation protocols, oversees validation testing and drafts final reports. Provides project engineering as required for new processing equipment installations and modifications to existing equipment. What You'll DoSupport Manufacturing operations by troubleshooting issues and identifying equipment system improvements. Update standards, drawings and specifications as necessary.Identify and lead equipment related projects, including technology transfers, capital projects, and modifications. Complete project management tracking of deliverables for metrics & reporting. Provide input & guidance to Tech Transfer and project / area efforts, provide technical evaluations of validation requirements for core change controls & associated action plans. Author sections of Validation-related reports & project plans, approve Trackwise-generated workflows (deviations, global change controls) for equipment / automation-related changes, review automation protocols, & attend related meetings. Coordinate Equipment/Cleaning Validation Protocols (development, training, management, tracking) - includes time spent on production floor. Specifically design & develop validation protocols, provide expertise to associated equipment & automation design / modifications, support FAT (Factory Acceptance Testing), equipment startup, & commissioning efforts, as required. Who You AreYou are accountable for achieving milestones in equipment projects, involving frequent internal and external communication. As a representative of the Manufacturing Engineering organization, your role carries the weight of potential delays and extra resource allocation if errors occur in your decisions or recommendations. Your commitment lies in delivering accurate and timely results, ensuring efficient processes to prevent setbacks.QualificationsBachelor's degree in engineering or other highly technical discipline Practical knowledge and application of GMP and EMA regulations. 2-4 years of experience in manufacturing, preferably in a pharmaceutical or biotech environment.Competency in Process Controls and Distributed Controls Systems, MS Word, MS Excel, MS Power Point and MS Project. Excellent oral and written communication skills. Ability to work rotating shifts, extended shifts and weekends as needed. Experience with either Fill Finish, Isolator (Bausch and Stroebel) and Lyophilizer technologies preferred.Additional InformationWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. PDN-9c4413ce-fa24-4acf-b2e6-1e5c9627734b

Job Description About This RoleThe Automation Engineer III provides 24/7 process controls/automation technical site support to the Biogen 900 Davis drive, NC manufacturing site. In addition, this role manages multiple small OPEX/CAPEX projects and continuous improvement initiatives that support the site from initial conception to final closure. The Automation Engineer III prioritizes between supporting the site and managing their assigned projects and tasks.What you'll doSystem Design and ImplementationSpecify, design, develop, install, commission, and qualify process control and automation solutions in direct support of commercial and clinical manufacturing operations.Collaborate with cross-functional teams to understand process requirements and develop control system specifications.Configure and program Supervisory Control and Data Acquisition (SCADA), Programmable Logic Controllers (PLC), and Human-Machine Interface (HMI) systems.Instrumentation and Control System IntegrationSpecify and select appropriate instrumentation for process monitoring and control.Integrate various control systems and devices to ensure seamless communication and coordination.Troubleshoot and resolve issues related to control system integration.Validation and ComplianceEnsure all automation systems comply with regulatory requirements, including cGMP (current Good Manufacturing Practice) standards.Participate in validation activities, including writing and executing validation protocols.Maintain documentation in accordance with industry and company standards.Provide technical assistance to site quality systems through investigations, control system assessments, and corrective/preventative support to ensure a compliant GMP workplace.Work with the Site Quality units to ensure deviations and CAPAs are completed ensuring due dates are met in a timely manner.Continuous ImprovementIdentify opportunities for process optimization, reliability improvement, and cost reduction through automation.Implement changes to enhance system performance and reliability.Stay abreast of industry trends and emerging technologies to recommend improvements.Troubleshooting and MaintenanceProvide technical support diagnosing and resolving automation systems issues in a timely manner.Develop and implement preventive maintenance procedures for control systems.Participate in on-call rotation for technical issues.Possible night shift support when/if needed in the future.Collaboration and CommunicationCollaborate with cross-functional teams, including process engineers, validation specialists, and maintenance teams.Provide training to operations and maintenance personnel on control system functionalities.Operating expense and small capital projects supportPrepare project estimates for control/automation design, equipment, installation, labor, materials, and other related costs. Prepare project forecasts and schedules and tracks costs.Concurrently manage and execute or participate as a team member on multi-disciplined automation and controls capital and operating expense projects from inception to project completion in support of site operations insuring safety, regulatory compliance, company standards, operational requirements and business needs are met.Ensure selection of new control system equipment and instrumentation assuring it meets all regulatory requirements and all instrumentation is correct for the intended use.Perform a lead role with site technical departments to develop standards for control systems and instrumentation for new and existing equipment.Who You AreA self- starter and self-motivated individual who drives results and leads change. You are very organized and thrive working in a dynamic environment where strong technical knowledge and execution are required.QualificationsBachelors degree, preferably in Electrical, Computer or Chemical Engineering or a related discipline.2-4 years hands on experience in process control/automation, preferably in the pharmaceutical industry.Experience with Rockwell PLCs and HMIs, Wonderware System Platform/ Archestra, SQL databases management, Networking and Communication protocols, Microsoft Server configuration and administration.Experience with validation processes and documentation: Writing user requirements, system functional/design documents, and test protocols experience.Must be willing to participate in an on-call rotation and possible shift coverage.Understands risks and associated controls with working in electrically classified areas.Preferred QualificationsSiemens PLCs and HMIs experience is a plus.Manufacturing Execution Systems experience is a plus.Pharmaceutical environment including regulatory requirements associated with 21 CFR Part 11 and supporting validation of control system equipment experience.Additional InformationWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. PDN-9c4413d5-18b3-4c4a-928c-50c3ff2f273e

Job DescriptionAbout This RoleThe Engineer III, Automation maintains and troubleshoots all process control system hardware and software (DeltaV DCS system) in support of the biopharmaceutical manufacturing process. Leads pre-planning change control meeting and facilitates change control approval process for new control strategies in support of new products and processes. Creates software life cycle design/validation documents, executes software validation, supports install/commissioning/manufacturing release of software changes. Supports tech transfers, SME lead on capital automation projects and performs Responsible Engineering (RE) duties across multiple Manufacturing Unit Operations. Troubleshoots process control systems and supports manufacturing operations through an 24/7 on-call rotation with some assistance.What You'll DoManage change controls and configure software for process improvements or new equipment. This includes configuring existing code and developing new control strategies for new and existing processes introduced into the facilities.Validate and test software. Create and execute software testing scripts utilizing GAMP 5 principles and internal compliance procedures.Troubleshoot software and hardware that comprises the DeltaV systems.Review and approve process automation reports (PARs)Lead automation functional change control planning meetings.Manage variable project arrival rate and prioritize these projects to maintain uninterrupted manufacturing operations.Who You AreYou have a combination of technical expertise, strong problem-solving skills, and effective communication abilities. You are adept at maintaining and troubleshooting process control systems while also demonstrating leadership in change control processes and software validation. Additionally, you are capable of managing various engineering projects and allocating tasks accordingly.QualificationsBachelors Degree in a relevant scientific/or technical discipline.2-4 years relevant experience.Comprehensive knowledge of DeltaV distributed control system.Experience implementing DeltaV software changes and supporting within production environmentsWorking knowledge of cGMP and GAMP guidelines.Preferred QualificationsBiotechnology or batch pharmaceutical experience production experience.Experience in Biotechnology Manufacturing specific areas: Cell Culture, Chromatography, Centrifugation, Ultrafiltration, CIP\SIP.Additional InformationWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. PDN-9c4617b1-8b17-4667-8a5c-b98ba27e223f

Infosys is seeking an Quality Assurance EngineerAs a QA Engineer you will act as a validation and quality assurance expert and review the functionality of existing systems. You will conduct requirement analysis, define test strategy & design and lead execution to guarantee superior outcomes. You will also be required to design an optimal test environment to simulate real-time scenarios. You will have the opportunity to collaborate with some of the best talent in the industry to create innovative high quality and defect-free solutions to meet our clients' business needs. You will be part of a learning culture, where teamwork and collaboration are encouraged, excellence is rewarded, and diversity is respected and valued.Required Qualifications:• Bachelor's degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education.• At least 1+ years of Information Technology experience and QA KnowledgeU.S. citizens and those authorized to work in the U.S. are encouraged to apply. We are unable to sponsor at this time.• Candidate must be located within commuting distance of Dallas Tx, or be willing to relocate to the area. • This position may require travel in the US and Canada• Experience with Testing strategies and Test Execution• Knowledge and experience with full SDLC lifecyclePreferred Experience:• Experience with Lean / Agile development methodologies• At least 1 years of experience in test strategy and test Design• 1+ yrs. of exp in Java/Python.• Exposure in Mobile and TV Apps testing.• Exposure in API Automation and QA process.• Good in communication and articulation• Team contribution and zeal to learn to technologiesThe job entails sitting as well as working at a computer for extended periods of time. Should be able to communicate by telephone, email or face to face. Travel may be required as per the job requirements. About UsInfosys is a global leader in next-generation digital services and consulting. We enable clients in more than 50 countries to navigate their digital transformation. With over four decades of experience in managing the systems and workings of global enterprises, we expertly steer our clients through their digital journey. We do it by enabling the enterprise with an AI-powered core that helps prioritize the execution of change. We also empower the business with agile digital at scale to deliver unprecedented levels of performance and customer delight. Our always-on learning agenda drives their continuous improvement through building and transferring digital skills, expertise, and ideas from our innovation ecosystem.Visit www.infosys.com to see how Infosys (NYSE: INFY) can help your enterprise navigate your next.Infosys is an equal opportunity employer, and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, spouse of protected veteran, or disability.

Job DescriptionAbout This RoleThe Automation Technical Authority Team within the Global Engineering function is looking to hire an Automation Engineer. This engineer is accountable for assisting in Capital Project planning and execution. This role effectively contributes and adds value to all stages of the asset's lifespan, ensuring standards, specifications, strategic approach to manage the lifecycle of the asset ensure optimal performance, efficiency, and longevity. This role will provide guidance on technical projects and engineering/automation teams. This Automation Engineer will leverage industry-leading subject matter capabilities within the Automation discipline to create an aligned strategic technical direction for Biogen PO&T site & external development and manufacturing operations, drive cost effectiveness, productivity, and compliance.This is a hybrid role to be based at our office in Research Triangle Park, NC. What You'll Do Participate in functional activities to support the Design, Development and Deployment of automated control systems, including: Capital Project Planning and Management, Control System Design, PLC/HMI/DCS configuration and FAT/SAT TestingSupport on the Commissioning and Validation of automated control systems, including: Installation, Operational, and Performance Qualifications and site turnover and support.Help to develop / maintain / improve Automation strategy and develop / maintain / improve Automation best practices, standards and specifications, accordingly; contribute to cross functional discussions; drive innovation, cost effectiveness and speed to execution in Automation throughout BiogenWho You Are You should have a solid understanding of manufacturing process and utility automation related to your assigned subject matter expertise. You should have experience working on projects with increasing complexity, taking on more responsibility as appropriate, and would have demonstrated an ability to work collaboratively with cross-functional teams to deliver results. You have demonstrated capability to develop and execute automation and CSV on projects / project opportunities that are generally considered to be of medium complexity, which are projects that have relatively moderate risk, few stakeholders, and relatively simple regulatory requirements, but with less stringent timelines.Qualifications Bachelor's degree in a relevant scientific or technical discipline and 3-5 years of experience in Biotech, Pharma or equivalent life science industry. A Master's degree and equivalent experience may also be considered.Demonstrated experience in AutomationExcellent leadership, people management, organization, communication, and inter-personal skills are requiredAbility to work in multi-disciplinary teams, with an emphasis on project design and execution.Strong communication and presentation skillsBackground in the successful design, development, installation, commissioning and turnover of process automation systems involving: instrumentation, electrical control panels, PLC/HMI/SCADA or DCS programming and Historian configurationTechnical experience with Emerson DeltaV, Rockwell ControlLogix PLCs and FactoryTalk View HMI/SCADA, Siemens Simatic S7 PLCs and WinCC HMI/SCADA and Pi Data HistorianExperience with the Installation, Commissioning and Qualification of automated control systems to follow cGMP, GAMP, and quality requirementsAdditional InformationWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. PDN-9c481d4c-1313-4656-980e-862b567b6c1f

We are seeking a US based Electronics Application Engineer. This role involves collaborating with Digital Engineering ECAD Platform and R&D teams to design, develop, and enhance electronic components and systems. The ideal candidate will be a problem solver who thrives in a fast-paced environment and is passionate about delivering practical and innovative solutions.Responsibilities:Collaborate with the ECAD Platform team to support deployment, evolution, and issue resolutions of ECAD Digital Engineering Applications such as Cadence, Sigrity, Altar Pollex, etc. Be familiar with the E2E ECAD design flow including core tools and customization.Work closely with Product Owners, R&D teams, and Business representatives to identify, document, and manage business requirements and use cases. Challenge and translate R&D business requirements into structured technical requirements (functional view).Contribute to the ECAD Platform Roadmap in close collaboration with the ECAD Product Owner.Understand E2E business processes, document and maintain specifications and process flows for application development, and identify potential gaps between the business process and the solutions. Influence technical direction.Assist R&D teams in the design and development of system level solutions.Provide coaching to business users in the functional use of the solutions and offer business support.Oversee verification and validation of solutions, Electronics systems and sub-systems, and drive user acceptance test.Stay updated on industry trends, technologies, and competitor products.Facilitate and lead ECAD Application Proof of Concepts with R&D teams.Provide training and support to users on new developments and products. QualificationsBachelor's or Master's degree in Electrical engineering, Electronics Engineering, or a related field.Demonstrated experience in electronic design and application development.Utilize knowledge of electronics HW design and simulation systems or products to support R&D project teams. Collaborate with cross-functional peers for the development of new offers or evolution of existing offers.Proficiency in Power Electronics, including design, component selection, and testing.Understanding of manufacturing processes of PCB/PCBA, Integrated Circuits, etc.Proficiency in simulation software such as Matlab, Simulink, PSpice, etc.Advanced understanding of EMC testing and design mitigation techniques.Exceptional problem-solving skills and the ability to work effectively in cross-functional teams.Strong communication skills, both verbal and written.Ability to manage multiple projects simultaneously and meet deadlines.Familiarity with the Agile product management process and experience with Cybersecurity is preferred. Why us?At Schneider Electric we're committed to creating a workplace that gives you not just a job but a meaningful purpose in joining our mission to bring energy and efficiency to enable life, progress and sustainability for all.We believe in e mpowering our team members to reach their full potential, fostering a sense of ownership in their work.We embrace inclusion as a fundamental value, ensuring that every voice is heard and valued. We value differences, and welcome people from all walks of life. We believe in equal opportunities for everyone, everywhere.If you want to be part of a company where your contributions truly matter, where you are empowered to make a difference and where inclusivity is valued, we would love to hear from you.Discover your M eaningful, Inclusive and Empowered career at Schneider Electric.€34.2bn global revenue +12% organic growth 135 000+ employees in 100+ countries #1 on the Global 100 World's most sustainable corporationsYou must submit an online application to be considered for any position with us. This position will be posted until filledSchneider Electric aspires to be the most inclusive and caring company in the world, by providing equitable opportunities to everyone, everywhere, and ensuring all employees feel uniquely valued and safe to contribute their best.We mirror the diversity of the communities in which we operate and we 'embrace different' as one of our core values. We believe our differences make us stronger as a company and as individuals and we are committed to championing inclusivity in everything we do. This extends to our Candidates and is embedded in our Hiring Practices.You can find out more about our commitment to Diversity, Equity and Inclusion here and our DEI Policy hereSchneider Electric is an Equal Opportunity Employer. It is our policy to provide equal employment and advancement opportunities in the areas of recruiting, hiring, training, transferring, and promoting all qualified individuals regardless of race, religion, color , gender, disability, national origin, ancestry, age, military status, sexual orientation, marital status, or any other legally protected characteristic or conduct.We are seeking a US based Electronics Application Engineer. This role involves collaborating with Digital Engineering ECAD Platform and R&D teams to design, develop, and enhance electronic components and systems. The ideal candidate will be a problem solver who thrives in a fast-paced environment and is passionate about delivering practical and innovative solutions.Responsibilities:Collaborate with the ECAD Platform team to support deployment, evolution, and issue resolutions of ECAD Digital Engineering Applications such as Cadence, Sigrity, Altar Pollex, etc. Be familiar with the E2E ECAD design flow including core tools and customization.Work closely with Product Owners, R&D teams, and Business representatives to identify, document, and manage business requirements and use cases. Challenge and translate R&D business requirements into structured technical requirements (functional view).Contribute to the ECAD Platform Roadmap in close collaboration with the ECAD Product Owner.Understand E2E business processes, document and maintain specifications and process flows for application development, and identify potential gaps between the business process and the solutions. Influence technical direction.Assist R&D teams in the design and development of system level solutions.Provide coaching to business users in the functional use of the solutions and offer business support.Oversee verification and validation of solutions, Electronics systems and sub-systems, and drive user acceptance test.Stay updated on industry trends, technologies, and competitor products.Facilitate and lead ECAD Application Proof of Concepts with R&D teams.Provide training and support to users on new developments and products.

The devices we make at SEL are embedded in the power grid. They prevent blackouts. They make outages safer and shorter in duration; they add cybersecurity, automation, and communication. They use cutting-edge technologies and operate at speeds that push other pieces of the grid to go faster. As a Power System Protection Engineer in Engineering Services, you'll provide solutions and services that help our customers protect and control critical electrical infrastructure and power systems worldwide.As a Protection Engineer, a typical day might include the following:Serve as technical lead and actively participate in complex project conceptual and detail design, execution, development, and support activities crossing multiple projects in power system protection and related SEL products. Lead project teams to resolve customer concerns and foster customer satisfaction.Training and assisting customers with the creation, design, configuration, validation, installation, commissioning and operation of automation and/or protection systems.Mentor and develop professional staff. May supervise as necessary.Developing technical proposals for customers.Completing and implementing assigned work within agreed upon scope, schedule and budget to a high level of quality and safety.Preparing and maintaining detailed design documents, reports, checklists, test reports, and deliverables.This job might be for you if:You have a B.S. in Electrical Engineering or relevant disciplineYou have 5+ years relevant application experience with electric power systems, industry practices, and protection area practices and philosophies (System protection, protective relays and their applications, settings, and testing)You have demonstrated ability to lead and supervise project teamsYou have knowledge of electric power system protection and control, integration and/or automation and communications applications.You have experience with electric power system design, studies, information and communication technology and protective relay applicationsYou are willing to travel about 25%You have excellent writing, documentation, and speaking skillsLocation:This position is located in Charlotte, NC, a vibrant and bustling metropolis located in the heart of North Carolina. As one of the fastest-growing cities in the United States, it seamlessly blends its rich history with a modern and dynamic atmosphere. With an eclectic culinary scene, charming neighborhoods, and a warm southern hospitality, Charlotte exudes a unique charm that captivates residents and visitors alike.Competitive pay. Superior benefits. Inspiring work. People are at the core of our company and we hire employee-owners. We welcome you to learn more about how we support employees.We're 100% employee owned. Retirement benefits include an employer funded stock ownership plan (ESOP) and personal 401K options.We offer top tier medical, prescription, dental, vision, life, and disability insurance.We recognize the importance of a healthy life balance and offer: 10 paid holidays, annual vacation accrual starting at 12 days, 9 paid sick days, and paid family and medical leave that covers 90% of your pay.We foster growth and development of our employees through avenues such as STEM courses, apprenticeships, tuition assistance, and engineering development programs. Ask our team about other benefits including wellness, fertility, adoption, and flexible spending benefits.Salary Information$90,00 - $130,000 per year. We are open to reviewing additional candidates with more or less experience and the pay range may differ if filled at a different level. Our pay ranges are determined by job, responsibility, and location. We base our starting pay offer and title on location and job-related factors such as candidate experience, training, knowledge, and skills.Communication with Applicants We communicate with all applicants. If you do not receive a response about your application, please check your SPAM filter or reach out to us at [email protected] is an Equal Opportunity Employer: Vets/Disabled.

Job DescriptionAbout This RoleThe Sr. Engineer II, Instrumentation and Controls provides engineering technical support and troubleshooting for Manufacturing Process / Utilitiy Equipment and Laboratory Analytical instrumentation. Participates in multi-functional teams to implement changes and improve on existing processes. This position partners with other teams including Utilities, Manufacturing, Process Engineering, Maintenance, and others to measure, target and improve reliability of all assets. Supports design, specification, installation, commissioning, and qualification of new equipment including URS and protocol writing and executions. Support technical development of I&C Maintenance Technicians and junior engineers. The role requires the knowledge / use of multiple control systems (Centralized Building Management System, PLC, DeltaV) for troubleshooting and improvement.What You'll DoTroubleshoot site operation issues and identify system improvements.Update standards, drawings, and specifications.Develop validation protocols and provide expertise in equipment and automation design/modifications.Author deviations, CAPA's, and change control records in a GMP environment.Configure Instrumentation & Control (I&C) systems, including utilities, process and laboratory instrumentation, control system hardware, and software.Support capital and operational expenditure projects, including scoping, modifications, design reviews, change controls, construction support, commissioning, and validation.Source and supervise I&C contractors.Oversee lifecycle management for I&C systems and equipment, implement upgrades and continuous improvements.Provide interim supervision and training of I&C technicians.Represent the department in cross-functional/global teams to address issues, implement change, and improve processes.Maintain personal training, goal development/completion, investigations, compliance workflow activities, and progress tracking.Provide engineering and validation support for utility systems.Collaborate with other groups as a representative of the facilities engineering team.Complete work tasks with oversight from the Facilities Engineering manager.Coach and mentor junior Facilities Engineering staff.Contribute to the completion of milestones associated with specific equipment projects or deliverables.Who You AreYou are a proactive problem-solver with a strong background in Instrumentation & Control systems. You are adept at troubleshooting, eager to improve existing systems, and capable of developing and updating technical documentation. You enjoy leading and collaborating with cross-functional teams, manage contractors, and mentor junior staff. You are an expert in Critical Risk Analysis and have a track record of successful project delivery.QualificationsBS in Electrical, Chemical, Mechanical or related engineering field.7 years transferrable experience.Practical knowledge of the application of FDA GMP and EMA regulations.Prior experience with variety of control systems & HMI's and the ability to program/configure these systems.Ability to read and understand electrical drawings and instrumentation datasheets/schematics.Experience with enterprise/IT systems.Demonstrates excellent oral and written communication skills.Competency in Microsoft Office Suite.May be asked to work extended shifts or weekends.Additional InformationWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. PDN-9c52297d-c8cc-4836-86cb-7c68dd4bfea0