NewHybrid Medical Writer Inizio EngageHybrid Medical WriterTrenton, NJ$88,000–$163,000As needed, provide medical review for scientific accuracy and provide input on the development/use of scientific and promotional materials consistent with approved client processes and policies (Product Review Committee [PRC], Reprint Dissemination Committee[RDC]) and in close partnership with client Medical Content Strategy Leads and MI leadership team to identify and address training needs of Medical Information and Communications staff, internal partners, or external vendors. Our passionate, global workforce augments local expertise and diverse mix of skills with data, science, and technology to deliver bespoke engagement solutions that help clients reimagine how they engage with their patients, payers, people, and providers to improve treatment outcomes.
Technical Writer Nexagen Networks, Inc.Technical WriterMonroe, NJWith more than 20 years of industry expertise, we deliver exceptional lifecycle professional services spanning Research and Development, Cloud Engineering, Digital Modernization, Systems and Software Engineering, DevSecOps, ITSM, Cybersecurity, Satellite Communication (SATCOM), RMF-FedRAMP, Logistics, Training, Exercises, COMSEC, and IT/Networking. Nexagen Networks considers various factors when determining base salary offers, including the scope and responsibilities of the position, as well as the candidate’s experience, education, skills, and current market conditions.).
NewTechnical Writer Macpower Digital Assets Edge Private LimitedTechnical WriterJersey City, NJ$70–$85 / hourKey Skills: Software development role, legacy financial institutions technology and API Integration architecture, Technical Writer, with a focus on API and ABI Documentation, Blockchain and Web3 technologies. JOB SUMMARY The ideal candidate will be responsible creating, editing and maintain high-quality documentation that communicates complex technical information clearly and concisely to a variety of audiences.
Quality - Technical writer MindlanceQuality - Technical writerNew Brunswick, NJo Primary Responsibilities: o Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports. o Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy.
NewTechnical Writer JSR Tech ConsultingTechnical WriterNewark, NJThey should be able to quickly understand technical concepts, work effectively with subject matter experts, and produce practical documentation for both technical and operational audiences. This role will work with subject matter experts to document procedures, update technical and engineering specifications, and improve the quality and usability of existing documentation.
Senior Technical Writer Aditi ConsultingSenior Technical WriterHoboken, NJRemote$56–$57 / hourConsent to Communication and Use of AI Technology: By submitting your application for this position and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated (including auto telephone dialing systems or automatic text messaging systems), pre-recorded, AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates at the phone number and/or email address you have provided. The User Assistance team for Higher Ed creates user-focused, data-informed, accessible, web- and mobile-based content to help students and educators use our products to accomplish their goals.
Technical Writer Advanced Technology Innovation Corp.Technical WriterFarmingdale, NJ$40–$50 / hourCoordinate the creation of all applicable technical publications in ATA iSpec2200, S1000D, and/or OEM's authoring specifications for the entry into service of new programs or systems in portfolio. Coordinate the update of existing technical publications in the portfolio such as Component Service Bulletins, Maintenance Manuals, and Service Information Letters.
Technical writer Sunrise Systems IncTechnical writerNew Brunswick, NJ$40–$42 / hourPrimary Responsibilities: Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports. Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy.
Regulatory CMC Technical Writer SOKOL GxP ServicesRegulatory CMC Technical WriterNew Brunswick, NJ$68,702–$87,256This includes supporting Module 2.3 and Module 3 content, coordinating source documentation, managing submission timelines, reviewing and adjudicating comments, facilitating data verification, and helping ensure consistency and clarity across the dossier. This position requires close collaboration with Process Development, Analytical Development, Cell Therapy Technical Operations, Quality, Regulatory Sciences, CMC matrix team leaders, project management, document management, and external suppliers as needed.
Senior Technical Writer Fiserv IncSenior Technical WriterBerkeley Heights, NJ$71,250–$114,000 / yearIn this role, you will also provide guidance to junior writers, support training and knowledge sharing, and lead documentation efforts across assigned workstreams to improve content quality, usability, and consistency across modern delivery platforms. You will work with product, support, and artificial intelligence teams, along with subject matter experts, to create modular documentation that supports intelligent search, automation, and chatbot experiences.
On Site Technical Writer - Union, NJ AdaptationOn Site Technical Writer - Union, NJUnion, NJ$45–$50Experience authoring a variety of document types, including system design documents, project management-related plans, user guides/manuals, and training materials. Advanced skills using Microsoft Word (including creating, editing, deleting styles; track changes; and maintaining proper version control), Excel, and PowerPoint.
Technical Writer HireTalentTechnical WriterNewark, NJWe are seeking an experienced Technical Writer / Documentation Governance Specialist to support enterprise-wide documentation initiatives. Proven ability to work directly with Product Owners, SMEs, and cross-functional teams.
NewTechnical Writer Macpower Digital Assets EdgeTechnical WriterJersey City, NJKey Skills: Software development role, legacy financial institutions technology and API Integration architecture, Technical Writer, with a focus on API and ABI Documentation, Blockchain and Web3 technologies. The ideal candidate will be responsible creating, editing and maintain high-quality documentation that communicates complex technical information clearly and concisely to a variety of audiences.
Technical Writer PlaybookTechnical WriterHoboken, New JerseyPlaybook is seeking a talented and experienced technical writer to work alongside our development team to create, maintain, and publish articles in our knowledge base for our SAAS serving small sports, fitness, and activity organizations. Through our best in class technology and integrated platform services we are revolutionizing the way that sports, education, and activity entrepreneurs launch and manage programs for students and communities across the world.
Quality - Technical writer ECLAROQuality - Technical writerNew Brunswick, NJ$42.85–$45.45 / hourResponsibilities: Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports. Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy.
Technical Writer Marotta Controls, Inc.Technical WriterParsippany, NJ$75,000–$100,000 / yearThe team designs and develops valves and fluid control products for launch vehicles, spacecraft, satellites, and space station applications. The Technical Writer will create and maintain technical documentation to support new product development, training initiatives, and legacy programs.
Technical Writer Syntricate Technologies IncTechnical WriterMt Laurel, NJIf you do not want to receive any further emails or updates, please reply and request to %20unsubscribe@syntricatetechnologies.com?subject=Unsubscribe%20Me. You have received this email as we have your email address shared by you or from one of our data sources or from our member(s) or subscriber(s) list.
Senior Technical writer Pyramid, IncSenior Technical writerBasking Ridge, NJFull timeWorked as a technical writer for complex software, telecommunications, and/or network technologies. Job ID: 20-28070 Key Requirements and Technology Experience: Bachelor's degree or four or more years of work experience.
Technical Writer Axient LLCTechnical WriterNJ2 years of experience using QuickSilver software in processing and preparing technical documentation • 2 years of experience with Adobe Communique (CQ5) Software • Must be able to write in a wide variety of formats, styles, and "voices." • Proficient in the use of the MS Office Suite (Word professional documentation styles, features and production, Excel, PowerPoint) • Must have strong oral communication, interpersonal, and problem-solving skills.
Technical Writer - Operations Experic LLCTechnical Writer - OperationsCranbury, NJ$80,000–$110,000 / yearThis role will partner closely with Manufacturing, Packaging, Warehouse, Facilities, and Quality Assurance teams to draft, revise, route, and maintain controlled documentation in support of compliant GMP operations. Drafts, revises, formats, and coordinates controlled GMP documentation including: Coordinates document review, approval, and implementation activities between Operations and QA.
Maintenance Technical Writer Interaction 24Maintenance Technical WriterSeabrook, New JerseyRequired qualifications • 2+ years of experience in technical writing within a manufacturing, industrial, or maintenance environment • Demonstrated ability to write SOPs, work instructions, and maintenance procedures from OEM documentation and subject matter expert input • Strong understanding of manufacturing maintenance operations and equipment terminology • Experience writing or reviewing LOTO procedures in compliance with OSHA • Excellent written communication skills — ability to translate complex technical content into clear, concise language for technician-level readers • Proficient in Microsoft Office (Word, Excel) and document management systems. From expertly managed resource services to strategic consulting, we provide end-to-end solutions that align with your goals—delivering the right talent, expertise, and execution to power your most critical initiatives.
NewTechnical Writer Hire TalentTechnical WriterNewark, NJWe are seeking an experienced Technical Writer / Documentation Governance Specialist to support enterprise-wide documentation initiatives. Required Qualifications: 5+ years of Technical Writing, Process Documentation, or Documentation Governance experience.
Technical Writer AstrionTechnical WriterEgg Harbor Township, New JerseyMust have the ability to establish and maintain professional, positive relationships with a wide variety of customers, including senior executives, engineers, technicians, managers, and administrative staff. Meet with and receive guidance/technical direction from Subject Matter Experts, and produce an original written draft based on those discussions, to be reviewed, refined and finalized.
Technical Writer Actalent IncTechnical WriterSomerset, NJ$30–$40 / hourWe 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. This role focuses on creating clear, accurate, and user-friendly technical documentation that supports complex capital and semiconductor equipment used worldwide.
Senior Technical Writer CQ Medical CareersSenior Technical WriterVirtual, New JerseyDevelop and Write Labeling Content: Create, write, and edit high-quality, clear, concise, and accurate labeling materials for medical devices, including product labels, user manuals, instruction guides, and packaging inserts. Collaborate with Design and Engineering Teams: Work with product development, engineering, and design teams to understand product specifications, functionality, and key messages that should be included in the labeling.
Senior Technical Writer MedTec LLCSenior Technical WriterNJDevelop and Write Labeling Content: Create, write, and edit high-quality, clear, concise, and accurate labeling materials for medical devices, including product labels, user manuals, instruction guides, and packaging inserts. Collaborate with Design and Engineering Teams: Work with product development, engineering, and design teams to understand product specifications, functionality, and key messages that should be included in the labeling.
NewPharmaceutical CMC Writer Macpower Digital Assets Edge Private LimitedPharmaceutical CMC WriterParamus, NJ$45–$49 / hourThis role bridges drug development, manufacturing, and quality control to deliver high-quality eCTD submissions. Compliance & Risk Management: Identify/escalate CMC regulatory risks and propose mitigation strategies.
Grant Writer & Grant Compliance Administrator Vets HiredGrant Writer & Grant Compliance AdministratorNewark, New JerseyThis role collaborates with internal and external stakeholders to develop funding proposals, monitor regulatory compliance, prepare reports, assist with audits, and support grant management throughout the funding lifecycle. The Grant Writer & Grant Compliance Administrator is responsible for preparing competitive grant applications, ensuring compliance with federal and state funding requirements, and supporting grant administration activities.
Grant Writer & Grant Compliance Administrator NjtransitGrant Writer & Grant Compliance AdministratorNewark, NJSUMMARY: Candidate will be responsible for drafting high-quality, comprehensive competitive grant applications for submission to federal and state funding agencies and ensuring that statutory and administrative requirements are met prior to application submission. EDUCATION, EXPERIENCE AND QUALIFICATIONS: Bachelor's degree in Business or Public administration and three (3) years of grant administration/management, technical/business writing experience or any combination of the beforementioned.
Nonclinical Regulatory Document and Scientific Writer Artech LLCNonclinical Regulatory Document and Scientific WriterGiralda Farms, NJ$64–$68.45 / hourReporting to the Program Management Lead, the incumbent will be part of the late development translational group based in Giralda Farms NJ and will be responsible for writing scientific documents including biomarker reports, regulatory documents (eg, non-clinical summaries, translational portions of clinical/pharmacology summaries, briefing books, CSRs, investigator brochures) in conjunction with Translational scientists. " Strong verbal and written communication skills with experience in developing written documents such as primary manuscripts/publications/reviews, disease strategies, mechanism slides, regulatory submissions, strategic communications, literature/market/pt segment analyses.
Medical Writer Knowesis, Inc.Medical WriterEast Orange, NJ$85,000–$89,000 / yearDevelop, write, and edit a wide range of clinical, scientific, and research-based documents, including study protocols, leadership reports, manuscripts for publication, regulatory submissions, grant proposals, and other technical materials essential to research and clinical operations. Maintain up-to-date VHA-required training for all personnel involved in patient care and/or research studies, including but not limited to: VA Privacy and Information Security Awareness and Rules of Behavior; VHA Privacy Policy Web Training; and Collaborative Institutional Training Initiative (CITI) Program Training.
Science Writer II Thorlabs IncScience Writer IINJThis role builds upon the Science Writer I role by demonstrating a firm understanding of Thorlabs extensive product portfolio; using existing technical experience and photonics knowledge to engage in meaningful conversations with engineering teams to gain an understanding of new product additions and how they fit into our existing portfolio; proposing and planning changes to Thorlabs website to enhance the buying experience for customers; and successfully executing plans to produce high-quality content requiring minimal feedback. The Science Writer II role is responsible for strengthening Thorlabs position as a leading manufacturer of Photonics products through the creation of effective technical presentations, application images, and other marketing collateral that inform and educate the photonics community about Thorlabs products/capabilities and their applications.
Grant Writer – Workforce & Career Training Programs American Medical and Trade InstituteGrant Writer – Workforce & Career Training ProgramsPassaic, NJRemoteThe role requires close coordination with AMTI leadership to ensure grant proposals align with existing certification programs such as Certified Medical Assistant (CMA), Phlebotomy Technician, EKG, and criminal justice pathways, as well as managing submission timelines and post-award requirements when applicable. This includes researching federal, state, county, workforce, and education-adjacent funding sources; preparing competitive grant narratives and budgets; and positioning AMTI appropriately as a program provider, fiscal agent, or contracted partner.
NewSecurity Operations Center (SOC) SOP Writer - Physical Security Macpower Digital Assets Edge Private LimitedSecurity Operations Center (SOC) SOP Writer - Physical SecurityFolsom, NJ$60–$65 / hourThe ideal candidate will have previous experience in physical security management and, ideally, experience in a SOC environment. This role will involve drafting, refining, and finalizing SOPs for a variety of physical security processes and systems.
Associate Report Writer GeneDX LLCAssociate Report WriterCranbury, NJRemote$90,000–$118,000 / yearWith a focus on accuracy, scientific rigor, and cross-functional communication, the Associate Report Writer supports team objectives, maintains current knowledge of best practices, and helps facilitate timely and reliable reporting. The role contributes to the curation of internal variant databases, collaborates with clinical and laboratory teams, and may serve as a subject matter expert for specific genes, disorders, or workflows.
Medical Writer Oxford Global Resources, LLCMedical WriterRaritan, NJCompensation $55.00 - $55.00 / Hourly ### Hours Per Week 40 ### Number Of Positions 1 ### Job Description Summary: The purpose of this role is to write, or coordinate the preparation of, all clinical, regulatory and scientific documents intended to support clinical and regulatory deliverables for drug development project teams. The scope of the role includes authoring, review, and quality assurance check of documents, and management of external medical writers.
RFP Grant Writer Neuropath Healthcare SolutionsRFP Grant WriterUnion, New JerseyMaturity, strong interpersonal skills, and discretion; Excellent oral and written communication skills; Strong critical thinking and problem-solving skills; Proficiency in MS Office Suite and donor management software. Neuropath Behavioral Healthcare is seeking an experienced RFP Grant Writer to manage all aspects of the RFP/RFI/ RFQ response process to improve the accuracy and efficiency, of the process.
Medical Writer Tata Consultancy Services LtdMedical WriterWestfield, NJ$130,000–$140,000 / yearPerform exhaustive Medical and Regulatory review of content respect to ensure Medical and Regulatory accuracy, consistency with references, sequencing and accuracy of bibliography references and ensure the scientific information in branded or promotional content is current, valid and adheres to the respective countrys pharma regulations. • To Check the Scientific accuracy and correctness of content to ensure whether content is adequately supported by evidence, depicted tables/graphs and artwork accurately represent the data and there are no contradictory messages in the body of the content.
Service Writer/Sales Midas Tire & Auto ExpertsService Writer/SalesTRENTON, NJWe’re looking for a driven, customer-focused Service Advisor who thrives in a fast-paced automotive environment and understands that customer service and a great service starts at the counter. This role is perfect for someone who can build trust with customers, communicate repairs clearly, and drive strong sales while maintaining integrity.
Strategy & Communications Lead - Lead Technical Program Manager JPMorgan Chase & CoStrategy & Communications Lead - Lead Technical Program ManagerJersey City, NJAs a Lead Technical Program Manager in Asset Management Technology, you will drive the successful delivery of complex technology projects and programs that will help reaching business goals across the firm. Identifying and implementing ways to constantly improve communications across Asset Management Technology, making them fresh, creative, and engaging by suggesting new ideas and engaging channel strategies.
Aircraft Electrical Engineer III Yulista SolutionsAircraft Electrical Engineer IIILakehurst, New JerseyInterface and communicate with other Electrical, Mechanical and EMI/EMC Engineers, Program Managers, Quality Assurance Manager, Configuration Manager, Engineering Manager and others as required for the design and integration on all assigned project requirements. Report writing and test plans including air worthiness documentation reports that includes but not limited to: Electrical Load and Power Source Capacity and Analysis, System Safety Assessment, and others as required.
Senior Specialist - Architecture LTM LtdSenior Specialist - ArchitectureJersey City, NJ$99,815–$148,400 / yearPowered by nearly 90,000 talented and entrepreneurial professionals across more than 30 countries, LTIMindtree - a Larsen & Toubro Group company - combines the industry-acclaimed strengths of erstwhile Larsen and Toubro Infotech and Mindtree in solving the most complex business challenges and delivering transformation at scale. As a digital transformation partner to more than 700+ clients, LTIMindtree brings extensive domain and technology expertise to help drive superior competitive differentiation, customer experiences, and business outcomes in a converging world.
Chemist II Hikma Pharmaceuticals PlcChemist IICherry Hill, NJ$56,600–$95,000 / hourIn the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma. Recruiters: Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions.
NewCommissioning Associate Project Manager Jones Lang LaSalle IncCommissioning Associate Project ManagerTrenton, NJRemoteWhat your day-to-day will look like: Project coordination: Oversee commissioning project development and execution, including budget management, schedule adherence, quality control, and coordination of commissioning activities across HVAC, electrical, plumbing, and other building systems. Project documentation: Maintain accurate project documentation, including commissioning plans, test procedures, status reports, meeting minutes, and technical reports using tools such as Microsoft Office, Adobe Acrobat, Bluebeam, Smartsheet, and commissioning software platforms.
NewDirector of Quality Engineering - Growth and Corporate Functions Segment Humana IncDirector of Quality Engineering - Growth and Corporate Functions SegmentNJRemote$156,600–$215,400 / yearWork at Home Requirements: To ensure Home or Hybrid Home/Office employees' ability to work effectively, the self-provided internet service of Home or Hybrid Home/Office employees must meet the following criteria: At minimum, a download speed of 25 Mbps and an upload speed of 10 Mbps is required; wireless, wired cable or DSL connection is suggested. Decisions are typically related to the implementation of new/updated programs or large-scale projects for the function and supporting technical/operational procedures and processes, and implements strategic plans, drives goals and objectives, and improves performance.
Specialist, Configuration Management L3Harris Technologies IncSpecialist, Configuration ManagementClifton, NJ$76,500–$141,500 / yearRequires strong technical knowledge of configuration management and practical knowledge of project management, typically obtained through advanced education combined with prior experience in an engineering support role such as configuration manager (CM), quality assurance technician (QA/QE/QC), design drafter, technical writer, program operations analyst, systems support engineer, integration and test engineer, specialty engineer, or similar. This role provides additional on-demand support to various engineering and program management teams as a subject matter expert for analyses, consultations, special topic discussions, tools support, DevOps support, and other tasking as required.
Power Generator Technician GenServe Inc. (Inactive)Power Generator TechnicianPennsauken, NJEstablished in 1990, GenServe has the largest team of EGSA-certified technicians in the Northeast and a growing presence across the U.S. Through a combination of organic growth and strategic acquisitions, GenServe is rapidly expanding its national footprint as a one-stop shop for generator solutions. This position requires advanced expertise in diagnosing, repairing, and maintaining a wide range of generator systems, including diesel, natural gas, and propane-powered units, as well as complex automatic transfer switches (ATS) and control systems.
Associate Director, Medical Writing Taiho OncologyAssociate Director, Medical WritingPrinceton, NJRemote$194,650–$229,000 / yearFull timeFDA and EMA) including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and clinical summary sections of Common Technical Documents (CTDs) in support of worldwide (outside of Asia) regulatory submissions. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Adjunct Faculty - First-Year Writing, Department of Writing Arts Rowan UniversityAdjunct Faculty - First-Year Writing, Department of Writing ArtsGlassboro, NJIn compliance with The State of New Jersey''''s Pay Transparency Act, and in accordance with the current MOA, Rowan University adjuncts are provided with a minimum of $2,225 per credit for all courses taught, with a maximum teaching load of 8 credits per semester and 12 credits in an academic year. A master's degree is required in the field of Composition/Rhetoric or a related field, such as English, Creative Writing, Literacy Studies, or Urban Education.
Sr. Manager, Medical Writing Terumo Medical CorpSr. Manager, Medical WritingSomerset, NJ$150,000–$198,000 / yearD, MA/MS or MPH) in a medical/biomedical/scientific discipline with a minimum of 5 years of experience in medical writing of regulatory documentation (clinical research documentation is optional) OR Bachelor's Degree, preferably in life sciences with 10 years of relevant work experience; OR equivalent combination of education, training and relevant experience. TMC places a premium on providing customers with world-class products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients.