Software Development Engineer JobotSoftware Development EngineerAvalon, NJ$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.
NewSr. Specialist Project Engineer L3Harris TechnologiesSr. Specialist Project EngineerCamden, NJ$110,000–$200,000 / yearBachelor's degree in related Engineering/Science field and a minimum of 6 years of prior related experience, Or, master’s degree in progress in related Engineering/Science field and a minimum of 4 years of prior related experience, Or, in lieu of a degree, a minimum of 10 years of prior related technical and project management experience. Manage day-to-day technical aspects of the project, including cross-functional decision making, task/schedule management, issue resolution/escalation, communication, requirements management, and risk management activities.
NewImplementation Engineer Vaco LLCImplementation EngineerDenville Township, NJ$80,000–$85,000 / yearDetermining compensation for this role (and others) at Vaco by Highspring depends upon a wide array of factors including but not limited to: the individual’s skill sets, experience and training; licensure and certification requirements; office location and other geographic considerations; other business and organizational needs. Determining compensation for this role (and others) at Vaco/Highspring depends upon a wide array of factors including but not limited to the individual’s skill sets, experience and training, licensure and certifications, office location and other geographic considerations, as well as other business and organizational needs.
NewSupplier Quality Engineer GCR Professional ServicesSupplier Quality EngineerDover, New Jersey$100,000–$110,000 / yearThe Quality Engineer is a key individual contributor responsible for monitoring quality performance against business objectives and driving continuous improvement initiatives that enhance product quality, process capability, and operational excellence. This role partners closely with Engineering and Operations to prevent defects, improve manufacturing processes, and ensure compliance with customer and regulatory requirements throughout the product lifecycle.
Aerospace Electrical Engineer (Entry-Level to Experienced) STS Technical ServicesAerospace Electrical Engineer (Entry-Level to Experienced)Lakehurst, NJIf you’re ready to advance your aerospace engineering career while supporting military aircraft integration and national defense programs, apply today to join STS Technical Services in Lakehurst, New Jersey. STS Technical Services is a Top 100 Staffing Firm that partners with leading aerospace, defense, manufacturing, and industrial organizations throughout the United States.
NewQuality Assurance Engineer JouléQuality Assurance EngineerMahwah, NJ$32–$37 / hourCollaborate with Manufacturing Engineering, Sterility Assurance, and Design Teams to ensure quality and compliance success through risk-based process controls and equipment maintenance measures. Advance your quality engineering career with a global medical technology leader known for its collaborative culture, innovation, and commitment to improving patient care.
NewSr. Specialist, Systems Engineering (System/Software) L3Harris TechnologiesSr. Specialist, Systems Engineering (System/Software)Camden, NJ$106,500–$197,500 / yearIRAD Development may include hardware and software prototypes for proof-of-concept efforts involving the design and test of new embedded software with built in test features for integration with hardware and support for final qualification testing. The systems portion of this role involves working closely with electrical, mechanical, software and test engineers to capture system requirements and develop traceable contract SDRL documentation, customer specifications and operators’ manuals when required.
NewTest Engineer Kforce Inc.Test EngineerJersey City, NJ$53–$60Employee pay is based on factors like relevant education, qualifications, certifications, experience, skills, seniority, location, performance, union contract and business needs. By clicking “Apply Today” you agree to receive calls, AI-generated calls, text messages or emails from Kforce and its affiliates, and service providers.
Cloud Engineer GlobantCloud EngineerJersey City, NJ$100,000–$150,000 / yearParental leave for both birthing (up to 14 weeks of paid leave) and non-birthing parents (up to 4 weeks paid leave), as well as adoption leave (up to 8 weeks of paid leave), subject to qualifications. This role will be involved in building and running the internal platform capabilities (automation, golden paths, guardrails) that enable secure, scalable application onboarding on GCP.
Senior Quality Engineer- Medical Device- Mount Laurel, NJ Michael Page USASenior Quality Engineer- Medical Device- Mount Laurel, NJMount Laurel, NJ$110,000–$150,000 / yearFull timeThe Senior Quality Engineer will be responsible for supporting new product development in a regulated environment, with responsibility for design controls, risk management, quality systems, and regulatory compliance. With a growing market presence and ongoing investment in research, product development, and commercialization efforts, the company offers a dynamic environment for professionals seeking to make a meaningful impact in healthcare.
NewPackaging and Product Device Engineer AtriumPackaging and Product Device EngineerSomerset, NJThe business continues to scale rapidly, supported by a growing, distributed global team united by a shared passion for innovation, creativity, and elevating how consumers discover and enjoy fragrance. Preferred Experience/Skills for the Packaging and Product Device Engineer: Strong problem-solving, decision-making, and project management skills; ability to manage multiple projects simultaneously.
NewManufacturing Engineer- Aerospace- Mount Laurel, NJ Michael Page USAManufacturing Engineer- Aerospace- Mount Laurel, NJMount Laurel, NJ$70,000–$75,000 / yearFull timeThis company is a specialized manufacturer serving highly regulated industries, providing engineered connectivity, electronic assembly, and custom production solutions for mission-critical applications. Manufacturing Engineer responsible for developing production processes, work instructions, and tooling for complex electrical and cable assembly products.
NewJunior Radio Frequency (RF) Electrical Engineer LeidosJunior Radio Frequency (RF) Electrical EngineerEgg Harbor Township, NJ$57,850–$104,575Knowledge of and experience with various frequency policy organizations, including National Telecommunications and Information Administration (NTIA), Interdepartmental Radio Advisory Committee (IRAC), and associated sub-committees, and the Federal Communications Commission (FCC). The Spectrum Engineering Group is responsible for securing, managing, and protecting all civil aviation spectrum resources to ensure interference-free operation of FAA communications, navigation, and surveillance (CNS) systems across the National Airspace System (NAS).
Process Engineer â Pharmaceutical Synerfac Technical StaffingProcess Engineer â PharmaceuticalWhippany, NJ$40–$42 / hourTemporaryContractorBy applying for this job, you agree to receive calls, Al-generated calls, text messages, or emails from Synerfac Technical Staffing and our contracted partners. A contract development and manufacturing organization that specializes in producing topical, semi-solid, and liquid pharmaceutical products for both prescription and over-the-counter markets.
Electrical Validation Engineer ZT SystemsElectrical Validation EngineerSecaucus, NJWhat You will Do Interface with architecture, design, platform, firmware, and system engineering process Aid in test specifications, requirements, strategies, and methodologies Efficiently execute test plans to meet time-to-market requirements Understand how systems work and be able to identify defects and issues Confidently describe test procedures and issues to internal and external stakeholders Track and aid in documenting and summarizing test results and collaborating in automation efforts for validation What You Bring A bachelor's degree in Electrical Engineering, Computer Engineering, System Engineering, Computer Science, or equivalent 0-2+ years of working knowledge in systems in a electrical/system test or validation setting Ability to aid in scripting for testing and debugging purposes Ability to provide clear report findings #LI-PW #LI-Onsite About ZT Systems At ZT Systems, a Sanmina Company, you'll get to do work you are proud of alongside smart, passionate people. The Electrical Validation Engineer will be working with cross functional teams to aid in developing as well as executing test plans which will verify product hardware functionality, adherence to electrical specifications and production requirements including SW stack and use case testing.
NewThermal Design & Validation Engineer Advanced Micro Devices, IncThermal Design & Validation EngineerSecaucus, New JerseySpanning cold plate design, liquid cooling architecture, thermal-mechanical analysis, CFD simulation, and lab validation, you'll partner with thermal architects, package and board designers, system engineers, manufacturing, and external suppliers to deliver high-performance, reliable, and manufacturable cooling solutions from concept through production. As a Thermal Design & Validation Engineer in the Data Center Platform Engineering (DPEG) Thermal Mechanical Engineering team, you will design, simulate, validate, and qualify liquid cooling solutions for AMD's next-generation AI and Data Center GPU products.
Validation Engineer Barry-Wehmiller Companies IncValidation EngineerEast Brunswick, NJBy 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.
6421 - CSV Engineer (Laboratory) / Validation Engineer 2 Verista6421 - CSV Engineer (Laboratory) / Validation Engineer 2Summit, New JerseyThe 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 ideal candidate should have hands-on experience supporting GxP laboratory instrument implementations and be comfortable managing validation activities for both technologies in parallel.
Validation Engineer Inteletech GlobalValidation EngineerJersey City, New JerseyOur onsite teams work directly with our clients to understand and analyze the current-state of problems and design specifically tailored conceptual solutions. With a mix optimized to the specific goals of each client and the character of their target customer demographics, we provide true integration across media platforms and channels.
Validation - Engineer III / Lead Engineer - Project Farma PerkinElmer US LLCValidation - Engineer III / Lead Engineer - Project FarmaNJContinually 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 Zp Group LlcValidation EngineerRaritan, NJPiper Companies is currently looking for an experienced (CQV) Validation Engineer in Raritan, NJ to work for an innovative and growing pharmaceutical organization. Responsibilities for the (CQV) Validation Engineer include: Assist with the development of equipment validation protocols (IQ/OQ/PQ) for new instruments and ensure compliance with applicable regulations and guidelines.
NewValidation Engineer (CQV - LCMS) Zp Group LlcValidation Engineer (CQV - LCMS)Titusville, NJ$60–$65 / hourPiper Companies is seeking a Validation Engineer (CQV - LCMS) in Titusville, NJ to support an industry-leading pharmaceutical organization. Qualifications for the Validation Engineer (CQV - LCMS): Bachelor's degree in chemistry, Engineering, or related field.
Commissioning Qualification Validation Engineer Zp Group LlcCommissioning Qualification Validation EngineerRaritan, NJPiper Companies is currently looking for an experienced (CQV) Commission Qualification Validation Engineer in Raritan, NJ to work for an innovative and growing pharmaceutical organization. Responsibilities for the (CQV) Commission Qualification Validation Engineer include: Assist with the development of equipment validation protocols (IQ/OQ/PQ) for new instruments and ensure compliance with applicable regulations and guidelines.
Associate Validation Engineer WuXi Biologics Cayman IncAssociate Validation EngineerCranbury, NJ$54,700–$87,500 / yearThe Associate Validation Engineer supports the successful operation of facility, laboratory, cGMP Manufacturing and business functions at the Cranbury NJ site through interaction with internal customers and external service providers. This individual will participate in the work group on multi-disciplinary and cross-functional teams and uses established relationships to contribute to teams and stakeholders with fact-based, business value knowledge.
Validation Engineer Amneal Pharmaceuticals IncValidation EngineerPiscataway, NJ$80,000–$90,000 / yearEssential Functions: Design, review and execute validation document activities such as Factory acceptance test (FAT), Installation qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) for equipment /utilities/facilities and generate reports which summarize results, specification and its acceptance criteria. Description: The Validation Engineer II is responsible for performing validation and Engineering activities, conducting development studies, analyzation and assist in improving pharmaceutical systems and processes.
Validation Engineer III ForDoz Pharma CorpValidation Engineer IIIEast Windsor, NJ$80,000–$120,000 / yearInstallation Qualification, Operational Qualification and Performance Qualification), · Supports 3rd party/vendor qualification activities, if applicable · Work closely with various departments in the design and development of validation protocols · Manages validation projects and prepares status reports · Assist with commissioning, FATs and SATs · Perform periodic review of equipment /systems · Responsible for planning and oversight of onsite cleaning validation programs compliant with FDA requirements · Collaborate with cross functional groups: QC, Operations, Product Development, Facilities, QA. · Computer system validation experience is a plus · Experience and knowledge of HVAC systems, clean rooms, sanitary processing, sterilization equipment, and WFI systems, computer control systems, cleaning processes and aseptic manufacturing · Extensive knowledge in cGMPs, ICH, 21CFR Part 11, and other pharmaceutical regulations · Experience in Quality Systems including deviation management and change control process.
0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 Consultant Two River Consulting Partners0065V6421 CSV Engineer (Laboratory)/Validation Engineer 2 ConsultantSummit, NJDevelop, review, and/or execute validation deliverables including validation plans, risk assessments, test protocols, traceability matrices, summary reports, and related documentation. The ideal candidate should have hands-on experience supporting GxP laboratory instrument implementations and be comfortable managing validation activities for both technologies in parallel.
Associate Validation Engineer Amneal Pharmaceuticals IncAssociate Validation EngineerPiscataway, NJSupports process validation and cleaning validation by providing product contact surface area, equipment qualification parameter ranges and challenge tests criteria to technical service. Description: The Validation Engineer I provides support in performing equipment, facility and utility qualification activity and re-qualification activity to ensure compliance to cGMP and Amneal''s quality requirements.
R&D Test and Design Validation Electrical Engineer Keysight Technologies IncR&D Test and Design Validation Electrical EngineerNJThis role owns the full lifecycle of test set development: defining test concepts, architecting the measurement approach, selecting and integrating instruments/fixtures, writing and maintaining test code, and generating the documentation required to support production and quality systems. Overview Keysight Technologies, the worlds largest test and measurement equipment manufacturer, has an outstanding research and development full-time position available for an electrical engineer or computer engineer to work in Keysights Budd Lake, NJ facility.
(Sr.) Validation Engineer GenScript/ProBio(Sr.) Validation EngineerHopewell, NJ$80,000–$120,000 / yearProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.
(Sr.) Validation Engineer GenScript ProBio(Sr.) Validation EngineerNew JerseyProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.
Lead Validation Engineer Karwell TechnologiesLead Validation EngineerJersey, NJLead CQV activities for facility and utility upgrade projects, including AHU replacements, boiler replacements, generator improvements, clean steam generator replacements, RODI (reverse osmosis deionized) water skid upgrades, parts washer upgrades, and installation and qualification of autoclaves. Preferred experience supporting facility and utility upgrade projects, including AHU replacements, boiler replacements, generator improvements, clean steam generator replacements, RODI water skid upgrades, parts washer upgrades, and installation/qualification of autoclaves.
NewValidation Engineer TTECValidation EngineerJersey City, NJJob Title: Validation Engineer (Contractor)Location: Summit – West, New JerseyType: ContractJob Description:We are seeking a Validation Engineer with 4–7 years of relevant experience to support validation activities in a pharmaceutical/biotech environment. Must-Have Qualifications:Bachelor's degree in Engineering, Computer Science, or equivalent (or Associate's degree with 4+ years of experience).4–7 years of experience in pharmaceutical or biotech industry.
Validation - Engineer I / II - Project Farma PerkinElmer US LLCValidation - Engineer I / II - Project FarmaNJProject 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.
Sr. Validation Engineer Genscript Biotech CorpSr. Validation EngineerPennington, NJ$90,000–$120,000 / yearProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.
Lead Validation Engineer Katalyst Healthcares & Life SciencesLead Validation EngineerJersey, NJLead CQV activities for facility and utility upgrade projects, including AHU replacements, boiler replacements, generator improvements, clean steam generator replacements, RODI (reverse osmosis deionized) water skid upgrades, parts washer upgrades, and installation and qualification of autoclaves. Preferred experience supporting facility and utility upgrade projects, including AHU replacements, boiler replacements, generator improvements, clean steam generator replacements, RODI water skid upgrades, parts washer upgrades, and installation/qualification of autoclaves.
Validation Engineer II Medvacon Life Sciences, LLCValidation Engineer IIEast Windsor, NJFull timeESSENTIAL JOB FUNCTIONS: Manages the full lifecycle of Computer System Validation, qualifying facilities, equipment, and processes, and developing key validation documentation, including Factory Acceptance Testing, Site Acceptance Testing, Installation Qualification, Operational Qualification, Performance Qualification, and Process Qualification for sterile and non-sterile manufacturing. It oversees multiple projects, develops documentation, and collaborates with teams to enhance efficiency, support product development, and drive continuous improvement aligned with our mission to provide high-quality, accessible medications.
Product Line Integratioin Verification & Validation Lead Engineer BAE Systems PlcProduct Line Integratioin Verification & Validation Lead EngineerTotowa, NJfor description visit the url https://jobs.baesystems.com/global/en/job/BAE1US124728BREXTERNAL/Product-Line-Integratioin-Verification-&-Validation-Lead-Engineer .
NewVerification and Validation Test Engineer Advanced Sciences and Technologies (AS&T)Verification and Validation Test EngineerPomona, NJPrevious Experience Required: Review Baseline Change Request (BCR) documentation, Use Case, related Automated Information Management System (AIMS), TFMS Deployment Team TFMDT provided documents, mockups, and any other related document to understand the change/enhancement. Support the Developmental Test & Evaluation (DT&E) and Operational Test & Evolution (OT&E) of the FAA Traffic Flow Management System; Follow Test Processes/Best Practices; Develop/Review Test Procedures, System Docs; Assist in identifying, analyzing, coordinating, resolving & reporting the resolution of system improvements and defect resolution.
Senior Validation Engineer (I, II, III) Cellares CorpSenior Validation Engineer (I, II, III)Bridgewater, NJ$90,000–$210,000 / yearGenerate and develop qualification and validation lifecycle documents, templates, protocols, reports including but not limited to the following: SOPs related to the commissioning, qualification and validation programs, Risk Assessments, System Impact Assessments, Validation Master Plans, URS, project plans, Validation Master Lists. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
Validation - Validation Specialist TechDigital CorporationValidation - Validation SpecialistWarren, NJThe Senior Validation Specialist, Computerized Systems, is responsible for performing initial and routine validation activities for GxP computerized systems. • Working understanding of site quality GxP systems supporting document management, change controls, deviations, CAPAs.
Validation Specialist Legend Biotech CorpValidation SpecialistRaritan, NJHeadquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
Project Manager, Validation Barry-Wehmiller Companies IncProject Manager, ValidationEast Brunswick, NJBy 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.
Validation Lab Manager ZT SystemsValidation Lab ManagerSecaucus, NJ$124,125–$182,000 / yearPlease be aware that certain positions may require the applicant to either 1) be a (i) U.S. citizen or national, (ii) U.S. lawful, permanent resident (aka green card holder), (iii) Refugee under 8 U.S.C. § 1157, or (iv) Asylee under 8 U.S.C. § 1158, or 2) be eligible to obtain an export control license or license exception from the Bureau of Industry and Science & U.S. Department of Commerce. Work with management to manage lab's current needs, anticipate growth, and utilize feedback from engineers and program managers to plan for the future.
Software Test Method Validation (TMV) Katalyst Healthcares & Life SciencesSoftware Test Method Validation (TMV)South Plainfield, NJExpertise in Software Verification & Validation (V&V), automated testing, embedded firmware validation, and risk-based testing aligned with IEC 62304, ISO 13485, ISO 14971, IEC 62366, IEC 60601/61010, and FDA 21 CFR Part 11/820 regulations. Proven success in validating infusion pumps, hemodialysis systems, and PCR-based diagnostic platforms while supporting FDA 510(k) submissions, CAPA, and audit readiness.
Validation Specialist Karwell TechnologiesValidation SpecialistLawrenceville, NJJob Description: This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area. Experience developing, executing, and reviewing: Validation protocols and reports, Risk assessments (FMEA, impact assessments), SOPs, deviation investigations, and CAPAs.
Senior Quality Validation Specialist Cellares CorpSenior Quality Validation SpecialistBridgewater, NJ$90,000–$210,000 / yearThe Quality Validation team at our IDMO Bridgewater facility will be responsible for providing Quality Assurance oversight of environmental, equipment (analytical and production), facility & utility, site automation, process validation & engineering documents, test protocols, CAPAs, deviations, change control records, and additional site based technical documentation and activities. Provide oversight of cleanroom lifecycle programs including aseptic process simulations, environmental monitoring performance qualification, cleanroom certification & recertification, cleaning & sanitization, and facility controls.
Validation Specialist Artech LLCValidation SpecialistLawrence Township, NJ$81–$81.06 / hourExperience with electronic document management systems (e.g., Qumas, SharePoint, etc.); application development and lifecycle management (e.g., ALM, JIRA, etc.); and IT service management systems (e.g., ServiceNow). This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area.
Validation Specialist Katalyst Healthcares & Life SciencesValidation SpecialistLawrenceville, NJJob Summary: This role will focus on the Computer System Validation (CSV) activities for enterprise GxP systems, specifically for a critical set of projects in the Cell Therapy functional area. Experience developing, executing, and reviewing: Validation protocols and reports, Risk assessments (FMEA, impact assessments), SOPs, deviation investigations, and CAPAs.
Sr. Specialist Project Engineer L3Harris Technologies IncSr. Specialist Project EngineerCamden, NJ$110,000–$200,000 / yearQualifications: Bachelor's degree in related Engineering/Science field and a minimum of 6 years of prior related experience, Or, master's degree in progress in related Engineering/Science field and a minimum of 4 years of prior related experience, Or, in lieu of a degree, a minimum of 10 years of prior related technical and project management experience. To help spot these scams, remember that during our formal recruitment process, L3Harris will NOT (1) ask you for money; (2) offer to send you a check before doing any work; (3) require you to provide sensitive personal information early in the process or sensitive information about your previous employer; (4) send you emails from free commercial services (e.g.