NewSoftware Development Engineer JobotSoftware Development EngineerCary, NC$65–$80 / hourDevelopers at this level are building greater independence, taking ownership of small to medium-sized work items, and strengthening their core engineering skills across multiple application layers, including user interfaces, services, APIs, and data. Our teams include professionals across software engineering, product development, clinical informatics, research, and healthcare technology who share a commitment to reducing complexity and improving outcomes for patients and providers.
NewSustaining Engineer LINCOLN TECHNOLOGY SOLUTIONS, Inc.Sustaining EngineerCary, NC$95,000–$115,000Full timeJob descriptionLincoln Technology Solutions (LTS) is seeking a highly driven and technically strong Sustaining Engineer to support customer issue resolution, product reliability investigations, production engineering support, and electrical design activities across LTS display and control platforms. This role is best suited for an engineer who is comfortable working closely with Quality while maintaining technical ownership of engineering investigations, root cause analysis, corrective actions, reliability concerns, and production issue resolution.
NewValidation Engineer Performance ValidationValidation EngineerRaleigh, North CarolinaPerformance Validation is seeking a full-time Level 2 Validation Engineer/Specialist to join our team in Raleigh, NC The Level II Validation Engineer/Specialist reports directly to the Site Manager and will be assigned to one or more project teams headed by a Project Leader. We are a 100% employee owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, and North Carolina, and we support clients throughout the US and overseas.
Validation Engineer Zp Group LlcValidation EngineerClayton, NC$75–$84 / hourKeywords: Validation Engineer, CQV, Commissioning, Qualification, Validation, GMP, FDA, EU Annex 1, IQ, OQ, PQ, Sterile Manufacturing, Fill Finish, Aseptic Processing, Equipment Qualification, Pharmaceutical Manufacturing, Biotechnology, CAPA, Risk Assessment, Process Validation. The Validation Engineer will support CQV activities for a sterile fill-finish manufacturing facility, with responsibility for qualification and validation efforts across Material Handling, Inspection, Wash & Sterilization, Formulation, and Filling systems.
6245 - Solution Prep Principal CQV Engineer / Lead Validation Engineer Verista6245 - Solution Prep Principal CQV Engineer / Lead Validation EngineerApex, North CarolinaThe ideal candidate will have strong experience across the CQV lifecycle, including authoring validation documentation, supporting equipment startup and commissioning activities, coordinating vendor testing, and ensuring systems achieve operational readiness. This role will focus on solution preparation, buffer preparation, and media preparation unit operations, supporting commissioning, qualification, and validation activities to ensure systems are designed, installed, tested, and qualified in compliance with cGMP and regulatory expectations.
Validation Engineer Validation & Engineering Group, IncValidation EngineerHolly Springs, NCValidation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. The role demands deep technical expertise across the full validation lifecycle — including URS development, FAT/SAT execution, and Computer System Validation (CSV) — as well as hands-on experience with systems and controls integration.
6242 - Upstream Principal CQV Engineer / Lead Validation Engineer Verista6242 - Upstream Principal CQV Engineer / Lead Validation EngineerHolly Springs, North CarolinaThe nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice.
6243 - Downstream Principal CQV Engineer / Lead Validation Engineer Verista6243 - Downstream Principal CQV Engineer / Lead Validation EngineerHolly Springs, North CarolinaThe nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice.
6244 - CIP (Clean-in-Place) CQV Engineer / Lead Validation Engineer Verista6244 - CIP (Clean-in-Place) CQV Engineer / Lead Validation EngineerApex, North CarolinaThe nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice.
Post Silicon Validation Engineer II Cadence Design Systems IncPost Silicon Validation Engineer IICARY, NCOur customers are the world's most innovative companies, delivering extraordinary electronic products-from chips to boards to systems-for dynamic market applications including consumer, hyperscale computing, 5G communications, automotive, aerospace, industrial, and health. Collaborate with several groups such as analog designers, digital designers, system designers in devising experiments, drive data collection, and present results analysis.
Product Validation Engineer RFA EngineeringProduct Validation EngineerFuquay-Varina, North CarolinaOur work includes concept development, product design, documentation, problem-solving, simulation, optimization, and testing of components, systems and complete machines. RFA Engineering (www.rfamec.com) is an engineering service provider dedicated to delivering our clients with timely engineering support and expertise.
QC Validation Engineer Zp Group LlcQC Validation EngineerClayton, NC$90,000–$120,000 / yearSupport validation of a broad range of QC laboratory and facility equipment across production, warehouse, and QC areas, including analytical instrumentation, temperature‑controlled units, storage systems, and general lab equipment. We are seeking a highly skilled and detail‑oriented QC Equipment Validation Engineer to support laboratory validation and equipment qualification activities for a QC expansion project in Clayton, NC.
NewFacilities and Validation Engineer Carolina Components GroupFacilities and Validation EngineerDurham, NCFull timeSummary:The Facilities and Validation Engineer is responsible for the operation and maintenance (scheduled / emergent) of the mechanical systems / equipment in the warehouse and manufacturing areas at CCG’s facilities, the calibration of instruments and measurable tools, and the maintenance and validation of parts and components used in manufacturing. Additionally, they support new equipment installations, including protocol generation and field execution to bring onboard for manufacturing use, and work directly within the company’s ERP equipment module to manage equipment, maintenance, and calibration records.
Validation Engineer II Alcami CorporationValidation Engineer IIMorrisville, North CarolinaFull timeThis position will perform a wide range of validation activities focused on environmental chambers, including: cryo-freezers, cold rooms, refrigerators, incubators, depyrogenation ovens, stability chambers and warehouses, as well as sterilizers and CSV. You will occasionally be exposed to wet or humid conditions, work near moving mechanical parts, work in high places, near toxic or caustic chemicals, in outdoor weather conditions and exposure to vibration.
NewValidation Engineer III Novartis Group CompaniesValidation Engineer IIIDurham, NC$98,700–$183,300 / yearBusiness Continuity, Change Control, Cost Management, Data Analytics and Digital, Engineering Technical Expertise, GDP Knowledge, gmp knowledge, HSE Knowledge, Knowledge Of Relevant Tools And Systems, Manufacturing Process (Production), Operational Excellence, Quality Compliance, Resilience and Risk Management, Total Productive Maintenance As a Validation Engineer III, you will play a critical role in bringing manufacturing systems to life-leading validation efforts that ensure compliance, quality, and operational excellence in a cutting-edge GMP environment.
Sr. Validation Engineer (cGMP) - Project Farma PerkinElmer US LLCSr. Validation Engineer (cGMP) - Project FarmaRaleigh, NCProject Farma (PF) team members collaborate with cross-functional teams to build trusted client relationships, deliver an exceptional customer experience, and contribute to business growth by identifying opportunities and applying data-driven insights to support project planning, cost, schedule, and performance management. Bachelor's Degree in Life Science, Engineering, or related discipline (OR a combination of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable military experience.
Validation Engineer Validation & Engineering GroupValidation EngineerHolly Springs, NCValidation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. Description: The role demands deep technical expertise across the full validation lifecycle including URS development, FAT/SAT execution, and Computer System Validation (CSV) as well as hands-on experience with systems and controls integration.
Validation Engineer III NovartisValidation Engineer IIIDurham, North CarolinaBusiness Continuity, Change Control, Cost Management, Data Analytics and Digital, Engineering Technical Expertise, GDP Knowledge, gmp knowledge, HSE Knowledge, Knowledge Of Relevant Tools And Systems , Manufacturing Process (Production), Operational Excellence, Quality Compliance, Resilience and Risk Management, Total Productive Maintenance As a Validation Engineer III, you will play a critical role in bringing manufacturing systems to life—leading validation efforts that ensure compliance, quality, and operational excellence in a cutting-edge GMP environment.
Sr. Validation Engineer (cGMP) - Project Farma PerkinElmerSr. Validation Engineer (cGMP) - Project FarmaRaleigh, North CarolinaProject Farma (PF) team members collaborate with cross-functional teams to build trusted client relationships, deliver an exceptional customer experience, and contribute to business growth by identifying opportunities and applying data-driven insights to support project planning, cost, schedule, and performance management. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.
Engineer 3, Commissioning Qualification Validation FujifilmEngineer 3, Commissioning Qualification ValidationHolly Springs, North CarolinaAll resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. This role performs validation activities to include but not limited to equipment set up, building dashboards, creating work orders, managing protocols, and reading and reviewing documents.
Engineer 3, Commissioning Qualification Validation FUJIFILM Biotechnologies USA IncEngineer 3, Commissioning Qualification ValidationHolly Springs, NCAll resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (FDBN_PNC@fujifilm.com).
Sr. Engineer 1, Commissioning Qualification and Validation FujifilmSr. Engineer 1, Commissioning Qualification and ValidationHolly Springs, North CarolinaAll resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity.
Sr Scientist-Engineer 1, Process Validation FujifilmSr Scientist-Engineer 1, Process ValidationHolly Springs, North CarolinaServes as subject matter expert (SME) to support TT stage gate reviews on incoming processes for manufacturing readiness (e.g., acceptable process characterization and validation, risk assessments, mitigation, and robust supporting data for proposed changes). All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place.
Software Engineer - PLMX Digital Thread Validation Siemens AGSoftware Engineer - PLMX Digital Thread ValidationCary, NCThis communication does not constitute a promise or guarantee of future employment opportunities beyond the current scope.#LI-PLM #SWSaaS#LI-Hybrid Job ID 506790 Posted since 16-Jun-2026 Organization Digital Industries Field of work Research & Development Company Siemens Industry Software (India) Private Limited Experience level Mid-level Professional Job type Full-time Work mode Office/Site only Employment type Permanent Any Siemens location in India Siemens Digital Industries Software is a leading provider of solutions for the design, simulation, and manufacture of products across many different industries. Software Engineer - PLMX Digital Thread Validation Job ID 506790 Posted since 16-Jun-2026 Organization Digital Industries Field of work Research & Development Company Siemens Industry Software (India) Private Limited Experience level Mid-level Professional Job type Full-time Work mode Office/Site only Employment type Permanent Any Siemens location in India Siemens Digital Industries Software is a leading provider of solutions for the design, simulation, and manufacture of products across many different industries.
Software Engineer Senior - PLMX Digital Thread Validation Siemens AGSoftware Engineer Senior - PLMX Digital Thread ValidationCary, NCSoftware Engineer Senior - PLMX Digital Thread Validation Job ID 506791 Posted since 16-Jun-2026 Organization Digital Industries Field of work Research & Development Company Siemens Industry Software (India) Private Limited Experience level Experienced Professional Job type Full-time Work mode Office/Site only Employment type Permanent Any Siemens location in India Siemens Digital Industries Software is a leading provider of solutions for the design, simulation, and manufacture of products across many different industries. Responsibilities: Design, develop, and maintain end‑to‑end cross‑product scenarios spanning Teamcenter and its integrations validating customer workflows across the Digital Threadworld customer usage patterns.product testing.product runs; identify root causes, drive defect resolution, and validate fixes across affected systems.product quality strategies, including environment setup, data management, dependency coordination, and execution pipelines.
Sr. Engineer 1, Commissioning Qualification and Validation FUJIFILM Biotechnologies USA IncSr. Engineer 1, Commissioning Qualification and ValidationHolly Springs, NCAll resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.
Sr Scientist Engineer 1, Process Validation FUJIFILM Biotechnologies USA IncSr Scientist Engineer 1, Process ValidationHolly Springs, NCServes as subject matter expert (SME) to support TT stage gate reviews on incoming processes for manufacturing readiness (e.g., acceptable process characterization and validation, risk assessments, mitigation, and robust supporting data for proposed changes). All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place.
Process Engineer II/III - Cleaning Validation Novo Nordisk ASProcess Engineer II/III - Cleaning ValidationClayton, NCMay consider an Associate's Degree in Engineering, Science, or relevant technical field of study from an accredited university with six (6) years of relevant experience operating in a GMP regulated environment required, preferably in a GMP regulated environment May consider High School Diploma or equivalent with eight (8) years of relevant experience operating in a GMP regulated environment required, preferably in a GMP regulated environment. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of state-of-the-art equipment, and houses the Fermentation, Recovery and Purification in the production of ingredients for Novo Nordisk's innovative oral products.
Product Validation Engineer Rogers Freels & Associates IncProduct Validation EngineerFuquay-Varina, NC$65,000–$80,000 / yearPart timeOur work includes concept development, product design, documentation, problem-solving, simulation, optimization, and testing of components, systems and complete machines. RFA Engineering (www.rfamec.com) is an engineering service provider dedicated to delivering our clients with timely engineering support and expertise.
Senior Engineer, Process Validation Danaher CorpSenior Engineer, Process ValidationRaleigh, NCRemote$100,000–$130,000 / yearLead the planning, execution, and lifecycle management of sterile fill-finish process validation strategies and qualification programs for aseptic manufacturing processes including sterile filtration, aseptic process simulation, sterile filling, visual inspection, container closure integrity testing, filter validation, labelling, packaging and shipping. In this role, you will have the opportunity to: Design, execute, and summarize deliverables across the three stages of process validation supporting process characterization and qualification spanning critical starting materials, drug substance, and drug product, product classifications aligned with FDA guidance, EU GMP Annex 15, and lifecycle approach.
Senior Commissioning/Validation Specialist Stantec IncSenior Commissioning/Validation SpecialistRaleigh, NCIn this role you will prepare and implements project commissioning/validation plans for existing or new buildings related to bio-pharmaceutical dosage forms, nutraceutical facilities and other regulated FDA or similar facilities where drug products are manufactured, stored in GMP conditions and distributed, including computerized and automated systems which require qualification and validation for compliance. The commissioning and validation of equipment, facilities, utility systems and computerized systems are intended to verify that they are designed, installed, qualified, and capable of being operated and maintained for performance in conformity with specifications, design intent and client/user and regulatory requirements.
Validation Team Manager (Raleigh, NC) EupryValidation Team Manager (Raleigh, NC)Raleigh, NCThis role offers the perfect blend of technical leadership, team development, and project oversight within a cutting-edge, fast-growing company revolutionizing temperature mapping and monitoring in the life sciences sector. Join us at Eupry and take the helm of a talented group of validation engineers who are delivering industry-leading CQV (Commissioning, Qualification, and Validation) services to global pharmaceutical and logistics clients.
R & D Manager - Verfication and Validation - Patient Systems AscomR & D Manager - Verfication and Validation - Patient SystemsMorrisville, North CarolinaThis hybrid position combines people leadership, verification strategy, and cross-functional influence—ideal for someone who wants to elevate engineering quality while helping deliver technology used in mission-critical healthcare environments. You will sit at the center of product quality and regulatory confidence: leading verification and validation strategy, driving continuous improvement in test engineering, and ensuring our medical device solutions meet both internal quality expectations and external compliance requirements.
Sr Computer Systems Validation Analyst Novo Nordisk ASSr Computer Systems Validation AnalystClayton, NCUtilize problem solving skills to handle deviations to ensure they are properly documented, investigated, and resolved in a timely manner, as well as ensuring subsequent changes are properly documented, assessed for impact, and implemented in a controlled manner. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of state-of-the-art equipment, and houses the Fermentation, Recovery and Purification in the production of ingredients for Novo Nordisk's innovative oral products.
R & D Manager - Verfication and Validation - Pa... Global Products & Solutions · US Raleigh Ascom Holding AGR & D Manager - Verfication and Validation - Pa... Global Products & Solutions · US RaleighRaleigh, NCThis hybrid position combines people leadership, verification strategy, and cross-functional influence-ideal for someone who wants to elevate engineering quality while helping deliver technology used in mission-critical healthcare environments. You will sit at the center of product quality and regulatory confidence: leading verification and validation strategy, driving continuous improvement in test engineering, and ensuring our medical device solutions meet both internal quality expectations and external compliance requirements.
Sr/Principal Computer Systems Validation Specialist KBI Biopharma IncSr/Principal Computer Systems Validation SpecialistDurham, NC$118,000–$162,800 / yearWorking closely with partners in Quality Validation, this individual provides strategic and technical expertise for all global software validation related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the KBI internal requirements. Individual will be responsible for the validation review and approval of enterprise software validation lifecycle deliverables and the validation technical oversite of change controls, CAPAs, and deviations associated with enterprise software.
Sr/Principle Computer Systems Validation Specialist KBI Biopharma IncSr/Principle Computer Systems Validation SpecialistNC$118,000–$162,800 / yearWorking closely with partners in Quality Validation, this individual provides strategic and technical expertise for all global software validation related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the KBI internal requirements. Individual will be responsible for the validation review and approval of enterprise software validation lifecycle deliverables and the validation technical oversite of change controls, CAPAs, and deviations associated with enterprise software.
Sr. Validations Specialist Alcami CorporationSr. Validations SpecialistMorrisville, North CarolinaFull timeSpecific responsibilities include reviewing SOP’s, composing/revising SOP’s and validation master plans; supporting facility, utility, manufacturing equipment, conducting reviews of validation documentation such as validation plans, system/functional requirements, protocols and summary reports; ensuring compliance with 21 CFR Part 11, Data Integrity, and functional requirements; developing documentations as required for projects; serve as the subject matter expert during audits and inspections and consulting on validation and cGMP questions and issues. At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
National Accounts Data Validation Specialist GFL Environmental, IncNational Accounts Data Validation SpecialistRaleigh, North CarolinaThe role will support the US National Accounts department by collaborating with other National Accounts users and database developers to resolve quality and integrity issues, performing data audits, identifying enhancements for data collection and storage procedures, and preparing reports. Reporting to the Manager, National Accounts Operations Support, the Data Validation Specialist is responsible for developing and implementing procedures to enhance the accuracy, quality, and integrity of US National Accounts data.
Sr/Principal Computer Systems Validation Specialist KBI BiopharmaSr/Principal Computer Systems Validation SpecialistDurham, North Carolina$118,000–$162,800 / yearWorking closely with partners in Quality Validation, this individual provides strategic and technical expertise for all global software validation related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the KBI internal requirements. Individual will be responsible for the validation review and approval of enterprise software validation lifecycle deliverables and the validation technical oversite of change controls, CAPAs, and deviations associated with enterprise software.
Cleaning Validation Specialist Cencora IncCleaning Validation SpecialistRaleigh, NCThis encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave. To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more.
Facility Automation Engineer Apperture SolutionsFacility Automation EngineerRaleigh, NCThe ideal candidate will have a strong background in building management systems and other facility automation systems (including access control systems, video surveillance systems, and other complimentary solutions), excellent problem-solving skills, project management experience, and the ability to work effectively as a lead in a team environment. Apperture Solutions is a 100% employee-owned company that offers a comprehensive, industry leading benefits package to all eligible Associates: Participation in the Employee Stock Ownership Program (ESOP).
NewSenior DeltaV Controls Engineer head\-huntress.comSenior DeltaV Controls EngineerRaleigh, North CarolinaOffice Work: Office desk/cubicle environment Frequent use of computers, engineering tools, and industrial control systems Our People Empowered Individuals â Employee-owned, we are able to hire the best and empower them to develop and deliver solutions Rewarded & Motivated â Investing in continuing education and world-class benefits keeps our staff motivated Positive Attitudes â Dedicated experts are committed in the long run and bring a positive, can-do attitude to your project Knowledgeable â Recognized industry experts reinforced with ongoing training remain knowledgeable on the latest industry trends and directions *Job Descriptions are not exhaustive lists of all skills, responsibilities, or efforts associated with a job. The ideal candidate will have a proven track record of managing complete project life cycles, ensuring compliance with industry regulations, and collaborating with cross-functional teams to optimize biopharmaceutical and medical device manufacturing processes.
Senior Analytics Engineer Avison Young (Canada) IncSenior Analytics EngineerNC$93,000–$120,000 / yearAnalytics Engineering & Data Modeling (Core Focus): Design, develop, and maintain scalable, business-aligned data models in Snowflake using dbt (staging, intermediate, marts layers). You will act as a player-coach, balancing hands-on development with leadership of other engineers, while partnering closely with business stakeholders to define metrics, data models, and semantic consistency across the company.
Data Engineer - Senior Associate PricewaterhouseCoopers LLPData Engineer - Senior AssociateNC$77,000–$202,000 / yearPreference for at least one of the following fields of study: Management Information Systems, Computer and Information Science, Systems Engineering, Electrical Engineering, Chemical Engineering, Industrial Engineering, Mathematics, Statistics, Mathematical Statistics. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy.
Lead Robotics Application Engineer Merck & Co IncLead Robotics Application EngineerDurham, NC$142,400–$224,100 / yearRequired Skills: Asset Management, Benefits Management, Emerging Technologies, Industrial Robotics, Intelligent Automation (IA), IT Operation, Laboratory Automation, Management System Development, Product Management, Project Leadership, Project Management, Project Planning, Requirements Management, Robotic Automation, Stakeholder Relationship Management, Strategic Planning, System Designs, System Integration, Technical Issues, Technical Leadership. The ideal candidate will combine deep technical knowledge of robotics platforms and application development with strong leadership, stakeholder management, and delivery capabilities.
Senior SoC Verification Engineer Microsoft CorpSenior SoC Verification EngineerRaleigh, NC$119,800–$234,700 / yearRequired Qualifications: Doctorate in Electrical Engineering, Computer Engineering, Computer Science, or related field AND 1+ year(s) technical engineering experience OR Master's Degree in Electrical Engineering, Computer Engineering, Computer Science, or related field AND 4+ years technical engineering experience OR Bachelor's Degree in Electrical Engineering, Computer Engineering, Computer Science, or related field AND 5+ years technical engineering experience OR equivalent experience. To achieve this goal, the Silicon IP & Custom Products (SCIPS) team is instrumental in defining and delivering operational measures of success for hardware manufacturing, improving the planning process, quality, delivery, scale and sustainability related to Microsoft cloud hardware.
Staff Engineer, Analog Design Engineering Analog Devices IncStaff Engineer, Analog Design EngineeringDurham, NCAnalog Circuits Design : Expert-level ability to design and analyze complex analog circuits, examples include PLL, amplifiers, or ADC/DAC with the skill to optimize designs for specific applications and lead architectural decisions • Circuit Architecture Development : Demonstrated ability to develop innovative circuit architectures that balance performance requirements with practical implementation constraints and business objectives • Simulation Modeling and Analysis : Advanced proficiency with simulation tools such as SPICE, MATLAB, and Cadence Design Suite to validate complex designs across various conditions and lead statistical validation efforts • Integrated Circuit Layout : Deep understanding of physical IC layout considerations and experience optimizing layouts for performance, including guiding layout engineers on critical aspects • CMOS Technology : Comprehensive knowledge of CMOS circuit design principles and implementation techniques for integrated circuits with the ability to make architectural tradeoffs. • Cross-Functional Collaboration : Collaborate with system/architecture team, layout team, product engineering, test engineers, applications and software team to ensure designs meet performance objectives and business goals • Mentorship and Knowledge Transfer : Provide technical guidance and mentorship to junior engineers, reviewing their work and contributing to their professional development • Innovation and Problem Solving : Contribute to the development of new theories, methods, and architectural approaches to solve complex design challenges.
Power System Modeling Principal Engineer Eaton Corporation PlcPower System Modeling Principal EngineerRaleigh, NC$154,000–$225,000 / yearPower System Study Development • Develop and own models for power system studies such as protection coordination, load flow, short circuit behavior, harmonics and power quality analysis, converter interactions, transient stability, dynamic response, resilience/blast radius analysis, and greenfield/brownfield datacenter evaluations. • Lead multitool modeling workflows using electrical system tools (PSS®E, CYME, ETAP, DIgSILENT PowerFactory, etc.) and Modelica based or other specialized environments for thermal fluid, mechanical, and Multiphysics studies, ensuring cross tool alignment and fidelity across all study types.