NewSoftware Development Engineer JobotSoftware Development EngineerCarmel, IN$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.
Data Engineer IV BC ForwardData Engineer IVIndianapolis, INRemoteFull timeThe ideal candidate will have strong experience in building scalable data pipelines, data architectures, and self-service analytics with AI enablement and a proven ability to deliver actionable insights, automate workflows, and improve customer experience outcomes . With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.
NewManufacturing Engineer Gables Search GroupManufacturing EngineerIndianapolis, IN$80,000–$105,000These roles will provide hands-on engineering support for electrical, electronic, and mechanical assembly operations, including one urgent opening focused on assembly support and another supporting key medical device customers. • Partner with production, quality, engineering, supply chain, and vendors to resolve manufacturing issues.
Senior Healthcare Data Engineer JobotSenior Healthcare Data EngineerIndianapolis, IN$120,000–$150,000 / yearYou'll partner closely with software engineers, product leaders, and external integration partners to solve challenging data quality problems while helping build a scalable framework for future healthcare integrations. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
Sr. Equipment Validation Engineer StratAcuity Staffing Partners IncSr. Equipment Validation EngineerLebanon, IN$40–$55 / hourIn terms of professional development, Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts.
NewValidation Engineer II Barry-Wehmiller Companies IncValidation Engineer IICarmel, INBy blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.
Software Design Engineer in Test 3 Bucher & Christian Consulting, Inc. dba BCforward (BCF)Software Design Engineer in Test 3Indianapolis, INFull timeThe ideal candidate will have strong experience in designing and implementing automated test suites, CI/CD integration, and defect analysis and a proven ability to improve test coverage, ensure software quality, and support release readiness for prototype devices and builds. With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.
6321 - Validation Engineer / CQV Engineer - Change Control & Deviations Verista6321 - Validation Engineer / CQV Engineer - Change Control & DeviationsIndianapolis, IndianaThis role will play a critical part in maintaining compliance, supporting quality systems, and ensuring manufacturing changes are properly assessed, documented, and executed in a regulated cGMP environment. The 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.
Validation Engineer 1 Bristol-Myers Squibb CoValidation Engineer 1Indianapolis, IN$82,236–$99,650 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Working under the guidance of senior team members, the Validation Engineer I contributes to validation activities that support the transition from construction to clinical development and ongoing GMP commercial operations.
NewSenior Validation Engineer Bristol-Myers Squibb CoSenior Validation EngineerIndianapolis, IN$107,904–$130,754 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. The Senior Validation Engineer will be responsible for the drafting and executing commissioning, qualification, and validation (CQV) documents and protocols which support the use of highly specialized facility, utility, analytical, and process equipment.
New6459 - Senior CQV Engineer / Senior Validation Engineer Verista6459 - Senior CQV Engineer / Senior Validation EngineerIndianapolis, IndianaConducting and documenting impact and risk assessments with a full understanding of equipment/system/software operation and ability to assess direct, indirect, and no impact systems and functions within complex processes. The 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.
CQV Engineer - Commissioning, Qualification & Validation PACIVCQV Engineer - Commissioning, Qualification & ValidationIndianapolis, INFull timeResponsibilities Develop and drive completion of Commissioning & Qualification (C&Q) deliverables, including validation plans, risk assessments, project strategies, user requirements, functional specifications, design specifications, impact assessments, traceability matrices, test cases, engineering studies, and final summary reports. CQV Engineer, Commissioning Engineer, Qualification Engineer, Validation Engineer, C&Q Engineer, Commissioning & Qualification Engineer, Pharmaceutical Validation Engineer, GMP Validation Engineer, Capital Projects Validation Engineer.
NewLead Validation Engineer Bristol-Myers Squibb CoLead Validation EngineerIndianapolis, IN$124,449–$150,803 / yearThe position applies broad engineering and GMP knowledge to support the transition from construction to clinical development and commercial operations, while also providing leadership in process improvement, deviation investigation, CAPA management, new technology implementation, and future expansion initiatives. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Process Validation Engineer Karwell TechnologiesProcess Validation EngineerIndianapolis, INThe ideal candidate will have experience with process validation, equipment qualification, CSV, temperature mapping, and regulatory compliance. We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment.
Process Validation Engineer Katalyst Healthcares & Life SciencesProcess Validation EngineerIndianapolis, INThe ideal candidate will have experience with process validation, equipment qualification, CSV, temperature mapping, and regulatory compliance. We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment.
Senior Validation Engineer INCOG BioPharma Services IncSenior Validation EngineerFishers, INIf you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
Validation Engineer - Project Farma PerkinElmer US LLCValidation Engineer - Project FarmaIndianapolis, IN$68,000–$80,000 / yearProject 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. Experience Required: 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 III/Lead - Project Farma PerkinElmer US LLCValidation - Engineer III/Lead - Project FarmaIndianapolis, INContinually develop technical aptitude of Project Farma's core services within the life science space including but not limited to: Capital Project Management, Tech Transfers, Validation Life Cycles including CQV and Computer system Validation, Quality, Regulatory and Compliance, GxP Automated Systems, and Quality Control including clinical and commercial. Project 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.
Validation - Engineer III/Lead - Project Farma PerkinElmerValidation - Engineer III/Lead - Project FarmaIndianaContinually develop technical aptitude of Project Farma’s core services within the life science space including but not limited to: Capital Project Management, Tech Transfers, Validation Life Cycles including CQV and Computer system Validation, Quality, Regulatory and Compliance, GxP Automated Systems, and Quality Control including clinical and commercial. Project 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.
Validation Engineer (Contract) GenoviceValidation Engineer (Contract)Indianapolis, IndianaOur client, an innovative and fast-growing pharmaceutical manufacturing company, is seeking an experienced Equipment Validation Engineer to support validation efforts across its cGMP manufacturing and laboratory operations. Local candidates are preferred , but hybrid arrangements may be considered for candidates willing to travel on-site to Indianapolis 2–3 days per week.
Validation Engineer - Project Farma PerkinElmerValidation Engineer - Project FarmaIndianaProject 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.
Validation - Engineer I/II - Project Farma PerkinElmerValidation - Engineer I/II - Project FarmaIndianaProject 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.
New6454 - Deviation Investigator / Validation Engineer Verista6454 - Deviation Investigator / Validation EngineerIndianapolis, IndianaThe 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.
NewCQV Validation Engineer: Change Control & Deviation Lead VeristaCQV Validation Engineer: Change Control & Deviation LeadIndianapolis, INVerista, Inc. is looking for a CQV Engineer in Indianapolis, IN, to support change control and deviation management in a regulated cGMP environment. Candidates should possess a Bachelor's degree and have over 3 years of experience in CQV or Quality Engineering.
Validation Engineer Actalent IncValidation EngineerNoblesville, IN$48.08–$55.29 / hourThis role combines hands-on work on the manufacturing floor with extensive documentation, protocol development, and collaboration across Quality, Manufacturing, and Engineering teams to support innovative, life-saving medical devices. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
Sr. Validation & Compliance Engineer Katalyst Healthcares & Life SciencesSr. Validation & Compliance EngineerIndianapolis, INThe role involves developing and executing IQ/OQ/PQ protocols, supporting process validation and technology transfer activities, ensuring compliance with FDA/EMA regulations, and collaborating cross-functionally to deliver compliant and inspection-ready systems. Validation & Compliance Engineer to support commissioning, qualification, and validation (CQV) activities for equipment, utilities, and facilities within a regulated pharmaceutical/biotech manufacturing environment.
Validation - Lead Engineer - Project Farma PerkinElmer US LLCValidation - Lead Engineer - Project FarmaIndianapolis, INContinually develop technical aptitude of Project Farma's core services within the life science space including but not limited to: Capital Project Management, Tech Transfers, Validation Life Cycles including CQV and Computer system Validation, Quality, Regulatory and Compliance, GxP Automated Systems, and Quality Control including clinical and commercial. Project 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.
Validation - Lead Engineer - Project Farma PerkinElmerValidation - Lead Engineer - Project FarmaIndianaContinually develop technical aptitude of Project Farma’s core services within the life science space including but not limited to: Capital Project Management, Tech Transfers, Validation Life Cycles including CQV and Computer system Validation, Quality, Regulatory and Compliance, GxP Automated Systems, and Quality Control including clinical and commercial. Project 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.
Validation - Engineer I/II - Project Farma PerkinElmer US LLCValidation - Engineer I/II - Project FarmaIndianapolis, IN$65,000–$80,000 / yearProject 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.
Senior Engineer, Process Validation Danaher CorpSenior Engineer, Process ValidationIndianapolis, INRemote$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.
Validation Engineering Roles Barry-Wehmiller Companies IncValidation Engineering RolesIndianapolis, INTechnical Skills & Qualifications: • Bachelor's degree in Engineering (Bioengineering, Biomedical, Chemical, Electrical, Mechanical, or equivalent technical degree) • Validation experience in automation, packaging, general drug substance and/or drug product systems/equipment, computer systems, utilities, and/or facilities • Strong technical writing and oral communication skills • Proficiency with project documentation and computer skills (Microsoft Office, Microsoft Project, AutoCAD) • Experience with entire project lifecycle from concept development through startup (preferred). Project Management & Leadership: • Lead all aspects of client relationship development and project execution • Develop project plans, strategies, and manage project resources, budgets, and schedules • Oversee complete project lifecycle from concept through design, implementation, installation, commissioning, and startup • Manage multiple project responsibilities simultaneously with excellent organizational skills • Focus on project success related to scope, schedule, budget, and client satisfaction.
Senior CSV Validation Specialist EXOS (formerly Sondhi Solutions)Senior CSV Validation SpecialistIndianapolis, INProven ability to author and execute validation deliverables, including Validation Plans, User Requirement Specifications, Functional Specifications, Design Specifications, Installation Qualification, Operational Qualification, Performance Qualification, Requirements Traceability Matrices, and Validation Summary Reports. The role supports the Site Automation Engineering organization and works closely with automation engineers, IT, system integrators, and site leadership to ensure systems are validated and maintained in a compliant state.
NewPackaging Engineering Lead - Validation, Compliance & Innovation HarbaPackaging Engineering Lead - Validation, Compliance & InnovationIndianapolis, INYou will own validation activities (IQ/OQ/PQ), drive tech transfers, support FDA/regulatory inspections, and partner with Manufacturing, QA, Regulatory, and Supply Chain to ensure compliant, efficient packaging operations.#J-18808-Ljbffr. Harba in Indianapolis is seeking a Packaging Engineer to lead design, qualification, and troubleshooting of pharmaceutical packaging lines, including blister, cartoning, labeling, serialization, and filling/capping processes.
Senior QA Validation Specialist INCOG BioPharma Services IncSenior QA Validation SpecialistFishers, INThe Senior Quality Validation Specialist provides Quality Assurance oversight of validation activities across the site, with a focus on new equipment commissioning and qualification, equipment change controls, and equipment life cycle documentation. This role is responsible for ensuring that User Requirements Specifications (URS), risk assessments, qualification protocols, and cleaning validation activities are compliant with applicable regulatory expectations, industry guidance documents, and internal procedures.
Senior Quality Process Validation Specialist INCOG BioPharma Services IncSenior Quality Process Validation SpecialistFishers, INSupport deviation investigations and CAPA activities related to process validation, PPQ, and continued process verification; review and approve deviations associated with process validation • Maintain current knowledge of regulatory trends, guidance documents, and industry best practices related to process validation, including FDA's 2011 Process Validation Guidance, EU Annex 15, and ICH Q8-Q12. This role is responsible for ensuring validation protocols, risk assessments, PPQ studies, and CPV programs meet applicable regulatory expectations and internal procedures, while taking direct, hands-on ownership of protocol design, execution, lifecycle documentation, and ongoing process monitoring.
Engineer - Automation Engineering - Historian Admin and Data Architect - Lilly Medicine Foundry Eli Lilly and CoEngineer - Automation Engineering - Historian Admin and Data Architect - Lilly Medicine FoundryLebanon, IN$64,500–$167,200 / yearIn the project delivery phase and startup phase of the project (startup expected 2025 to 2028), automation engineering roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Engineer - Plant Engineering Automation Eli Lilly and CoEngineer - Plant Engineering AutomationIndianapolis, IN$66,000–$171,600 / yearOur current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Position Brand Description: Plant Engineering Automation in Indianapolis Parenteral Manufacturing is responsible for maintaining the site's facility infrastructure including buildings, HVAC, UAF Hoods, GMP utilities, steam, water, sewer, and other utility systems to a state of compliance.
Senior Engineer, Control Systems Simulation Allison Transmission Holdings IncSenior Engineer, Control Systems SimulationIndianapolis, INSolicit inputs & requirements from cross-functional engineering teams of Systems, Algorithm, Calibration and Validation engineers to develop existing and new tools designed to enable & optimize engineering workflows. The successful candidate will be responsible for designing, implementing, and testing software tools that support and enhance the functionality of our products, thus providing the most reliable and valued propulsion solutions in the world to enable our customers to work more efficiently.
Senior Control Systems Engineer Allison TransmissionSenior Control Systems EngineerIndianapolis, IndianaYou will be responsible for designing, implementing, and testing embedded controls software to provide the most reliable and valued propulsion solutions in the world enabling our customers to work more efficiently. From the first person hired by James Allison in 1915 to the thousands across the globe who work for Allison today, we're driving progress everywhere because we employ top talent worldwide.
Microsoft Fabric Data Engineer The AES GroupMicrosoft Fabric Data EngineerIndianapolis, INExperience designing and implementing document ingestion and AI search solutions, including OCR, chunking, embeddings, vector databases, and retrieval-augmented generation (RAG) using Azure OpenAI, OpenAI, Claude, or similar technologies. Proven expertise delivering production workloads on Microsoft Azure, including Azure Fabric (Lakehouse, Data Factory, Pipelines, Delta Lake), Azure Functions, Storage, and AI Services.
Senior Engineer, Control Systems Simulation Allison TransmissionSenior Engineer, Control Systems SimulationIndianapolis, IndianaSolicit inputs & requirements from cross-functional engineering teams of Systems, Algorithm, Calibration and Validation engineers to develop existing and new tools designed to enable & optimize engineering workflows. The successful candidate will be responsible for designing, implementing, and testing software tools that support and enhance the functionality of our products, thus providing the most reliable and valued propulsion solutions in the world to enable our customers to work more efficiently.
[497] - Technology Operations Senior Engineer inSync Staffing[497] - Technology Operations Senior EngineerIndianapolis, INThis role will contribute to engineering initiatives focused on workflow orchestration, business rules management, automation, and scalable platform solutions. Collaborate closely with Product Owners, Architects, Developers, Operations, and other cross-functional stakeholders to ensure alignment with business objectives and technical strategy.
Data Engineer (SMTS/LMTS) - Knowledge Graph & AI Salesforce IncData Engineer (SMTS/LMTS) - Knowledge Graph & AIIndianapolis, IN$148,500–$260,100 / yearSemantic Routing Mastery: Demonstrated hands-on experience designing, optimizing, and productionizing custom semantic routers using Python (leveraging native embeddings, LangChain, semantic-router, or specialized mathematical logic like cosine similarity) to decouple intent handling from expensive LLM calls. Semantic Routing & AI: Hands-on experience developing and deploying custom semantic routers using Python (leveraging native embeddings, LangChain, or mathematical logic like cosine similarity) alongside RAG architectures, vector search platforms, and AI workflows.
Electrical Engineer Top Gun Staffing IncElectrical EngineerShelbyville, INThis role is responsible for troubleshooting control systems, programming PLCs and HMIs, supporting equipment installations, and improving the reliability and performance of automated manufacturing processes. Bachelor's Degree in Electrical Engineering, Electrical Engineering Technology, Controls Engineering, Automation Engineering, Mechatronics, or a related technical discipline preferred.
Digital Automation Engineer -DeltaV Central Solutions and Transformation Eli Lilly and CoDigital Automation Engineer -DeltaV Central Solutions and TransformationIndianapolis, IN$66,000–$171,600 / yearOur current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). This role will be part of a team that develops central automation solutions to streamline and reduce cost of delivery for large scale capital projects in the Drug Substance (API) manufacturing network.
Automation Engineer (R3) Eli Lilly and CoAutomation Engineer (R3)Indianapolis, IN$97,718–$137,921 / yearExperience must include a minimum of: 2 years of experience performing hands-on testing on production equipment; 2 years of experience identifying and resolving manufacturing non-conformances and performing root cause analysis; 2 years of experience preparing, reviewing, and revising SOPs, performing failure mode analysis assessments, deviations, protocols, risk assessments, and creating training documentation; 2 years of experience writing change controls involving technical and process scope updates; 1 year of experience connecting computer systems per the S95 architecture; 1 year of experience managing projects and interacting with equipment vendors to design machines and computer systems per requirements; and 1 year of experience establishing and maintaining the reliable operation and qualified state of manufacturing equipment. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Intermediate Systems Engineer Cybermedia Technologies LLCIntermediate Systems EngineerIndianapolis, INHeadquartered in McLean, VA, CTEC has over 300 team members working on mission-critical systems and projects for agencies such as the Department of Homeland Security, Internal Revenue Service, and the Office of Personnel Management. The Systems Engineer participates in all phases of the system development lifecycle (SDLC), with emphasis on planning, analysis, evaluation, integration, testing, verification, validation, and acceptance activities, including Independent Verification & Validation (IV&V) and Developmental Test & Evaluation (DT&E).
NewSystems Engineer Science Applications International CorpSystems EngineerINRemote$80,001–$120,000 / yearDevelop and deliver required SETR documentation and artifacts, including Systems Engineering Management Plan (SEMP), Test and Evaluation Master Plan (TEMP), Integrated Master Plan (IMP), Block Definition Diagrams (BDD), and Requirements Traceability Verification Matrix (RTVM). This position will play a critical role in utilizing Model-Based Systems Engineering (MBSE) principles and tools to develop comprehensive Systems Requirements Models and ensure adherence to rigorous Systems Engineering Technical Review (SETR) processes.
NewPrincipal DeltaV Automation Engineer Matrix TechnologiesPrincipal DeltaV Automation EngineerIndianapolis, INRemote$150,000–$180,000Unlike many traditional engineering roles, this position provides the opportunity to influence technical strategy, build a growing DeltaV practice, and develop the next generation of automation engineers while remaining actively involved in challenging client projects. While performing the duties of this job, the employee is occasionally required to stand; walk; sit; stoop, kneel, crouch; use hands to finger, handle, or feel objects, tools, or controls; reach with hands and arms; talk, and hear.
Principal Systems Engineer, Weapon System Integration V2X IncPrincipal Systems Engineer, Weapon System IntegrationIndianapolis, INOur Indianapolis facility supports a variety of product lines serving multiple DoD customers providing the opportunity to work on a diverse set of programs and roles supporting the continued advancement of your career. The Principal Systems provides technical and programmatic leadership throughout the development life cycle, from concept development, requirements definition, functional analysis, design review support, system implementation, integration, verification, and validation.