eTeam Inc.Senior Technical Writer Life Sciences (GxP/SDLC) eTeam Inc.Senior Technical Writer Life Sciences (GxP/SDLC)Parsippany, NJDetailed Job Description: Previous experience with SDLC and GLPGCP validation is preferred Technical writing or documentation experience in a regulated industry is preferred and Bachelors Degree in Computer Science or related field 8 to 10 of technical writing or documentation experience, preferably in a regulated industry Experience with MS Office, specifically Word, Visio, and Excel, is required Experience in life sciences or pharmaceuticals RD is preferred. Job Title* Technology Lead | Life Sciences | Regulatory Systems.
Macpower Digital Assets Edge Private LimitedTechnical 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 SUMMARYThe 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.
AdaptationOn 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 .
Macpower Digital Assets EdgeNewTechnical 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.
CEDENTTechnical Writer CEDENTTechnical WriterSpringfield, NJThis role will work closely with internal and client cross-functional teams, including quality assurance, regulatory, production, and project management, to ensure timely delivery, accuracy, and clarity of all technical documents essential for the manufacturing and regulatory processes in a pharmaceutical industry. Document Management: Assist in the management of controlled documents in document control systems (e.g., electronic document management systems), ensuring traceability, version control, and appropriate distribution of approved documents.
Seven Seven SoftwaresNewTechnical Writer Seven Seven SoftwaresTechnical WriterNewark, NJThe successful candidate must be able to:Partner with SMEs, technical developers, 3rd party vendors, support teams and other stakeholders to create and maintain high-quality documentation. Bachelor's or Master's degree in Technical Communication, Information Systems, English, Computer Science, Communications or related field/experience a plus.
Compass ConsultingTechnical Writer - Molecular Diagnostics (IFU Specialist) Compass ConsultingTechnical Writer - Molecular Diagnostics (IFU Specialist)Branchburg, NJPerforming meticulous proofreading to ensure accuracy in scientific terminology, unit conversions, and symbol usage; adhering to ISO 13485, FDA 21 CFR Part 820, and IVDR. Utilizing advanced Microsoft Word skills for complex document structures (nested numbering, cross-references, tables, multi-language layouts).
StaffingagencyrecruitmentMedical Writer StaffingagencyrecruitmentMedical WriterParamus, 07652The ideal candidate will collaborate with cross-functional teams, including Clinical, Regulatory, Biostatistics, and Medical Affairs, to create well-structured, scientifically accurate, and regulatory-compliant documents. Regulatory Document Writing:Prepare and author clinical and regulatory documents, including but not limited to:Clinical Study Protocols (CSPs) and Protocol Amendments.
Artech LLCNonclinical 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.
Integrated Resources, IncNonclinical Regulatory Document and Scientific Writer Integrated Resources, IncNonclinical Regulatory Document and Scientific WriterMadison, NJContractorTechnical Skills In-depth understanding of hematological malignancies or solid tumors or Neuroscience disorders especially the clinical landscape, evolving therapy, competitive scenarios Strong understanding of clinical, translational and mechanistic data with Client assets and Client agents Strong background in writing and in communication strategy development, disease and or brand planning, regulatory documents preparation for in-line and late-stage development compounds in disease areas, preferably in hematology Familiarity and working knowledge of CARA or other documentation systems Understanding of late-stage drug and translational development processes Proven ability to work with global disease teams to develop strategies to support life cycle management efforts tailored to regional markets (i.e, US, EU, CAN) 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 Ability to synthesize complex scientific and business problems into strategy and tactics Basic understanding of IP, contracting terms and provisions Responsibilities Ensure timely delivery for the TD writing book of work such as pre-clinical reports, and Translational biomarker reports across areas of focus (eg, multiple myeloma, lymphoma, myeloid, erythroid disorders) In conjunction with TD scientists, establish annual publication goals, publication plan with priority rankings, and estimated timelines for submission, with focus to ensure all deadlines for regulatory submissions/requests are met. Routinely interact with TD Program Manager(s) on status of Heme publications Supports regulatory submissions, regulatory interactions, writes translational sections for regulatory response and answers to regulatory queries for the TD group in conjunction with biomarker lead(s) Collaborate with TD scientists and representatives of other functions (eg, Clinical, Non-Clinical Development, Pharmacology, Drug Metabolism & Pharmacokinetics) as needed to execute publications/reports/regulatory documents Collaborate with TD Scientists and review data to determine the appropriate tabular and textual formats to ensure clarity, logic and order of presentation.
Sunrise Systems IncNonclinical Regulatory Document and Scientific Writer Sunrise Systems IncNonclinical Regulatory Document and Scientific WriterMadison, NJ$65–$68 / hourSummary Reporting 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.
Macpower Digital Assets Edge Private LimitedPharmaceutical 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.
Katalyst Healthcares & Life SciencesMedical Writer Katalyst Healthcares & Life SciencesMedical WriterParamus, NJThe ideal candidate will collaborate with cross-functional teams, including Clinical, Regulatory, Biostatistics, and Medical Affairs, to create well-structured, scientifically accurate, and regulatory-compliant documents. Collaboration & Review: Work closely with cross-functional teams, including medical, clinical, regulatory, statistical, and quality assurance teams.
American Medical and Trade InstituteGrant 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.
AECOMWater Treatment Technical Leader AECOMWater Treatment Technical LeaderNew Jersey, NJAECOM's Water Business Line is seeking a talented and experienced Water Technical Leader to support water treatment and distribution related planning, design, and construction projects throughout the Northeast US Region (Chelmsford, MA, Boston, MA, Manchester, NH, Philadelphia, PA, Rocky Hill, CT, Pittsburgh, PA, New Jersey, NJ). We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world.
Seven Seven SoftwaresNewDevOps Techwriter Seven Seven SoftwaresDevOps TechwriterNewark, NJSome of the duties and responsibilities of a Technical Writer include: Work with DevOps and different CTO team to understand technical solution and write up internal and external content. A successful candidate will have experience with building documentation to support devops, pipelines or software delivery and will understand devops concepts and terminology.
IMCS Group IncTechnology Lead | Life Sciences | Regulatory Systems IMCS Group IncTechnology Lead | Life Sciences | Regulatory SystemsParsippany, NJDetailed Job Description: Previous experience with SDLC and GLPGCP validation is preferred Technical writing or documentation experience in a regulated industry is preferred and Bachelors Degree in Computer Science or related field 8 to 10 of technical writing or documentation experience, preferably in a regulated industry Experience with MS Office, specifically Word, Visio, and Excel, is required Experience in life sciences or pharmaceuticals RD is preferred. Company Description: IMCS Group is one of the fastest growing MWBE (Minority Woman Owned Enterprise) staffing firms in the U.S. We focus on bringing a Diversity Recruitment approach to Fortune 500 companies within North America and EMEA region contingent labor programs.
Artech LLCTechnology Lead | Life Sciences | Regulatory Systems Artech LLCTechnology Lead | Life Sciences | Regulatory SystemsParsippany, NJA Bachelor's Degree in Computer Science or a related field is required, along with 8 to 10 years of technical writing or documentation experience, preferably in a regulated industry. We are seeking a highly skilled Technology Lead with expertise in Life Sciences and Regulatory Systems for a 6-month contract position in Parsippany, NJ.
MaximusBusiness Systems Analyst MaximusBusiness Systems AnalystNewark, NJFull timeMaximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment. - Bachelor's degree in Business Management, Information Systems, Computer Science/Engineering, Telecommunications, Technical Communications or related field, or equivalent work experience.
Integrated Resources, IncDocumentation Specialist I Integrated Resources, IncDocumentation Specialist IPearl River, NY$30–$35 / hourManager Notes: High School diploma 5 years AA Degree, 3 + years of experience Bachelor's degree, final batch review 1+ year of experience . Must Have: Experience; CAPA, Batch review, technical writing, knowing how use documentation systems, locate errors and change action requirements.
Pyramid Consulting, IncDocumentation Specialist I Pyramid Consulting, IncDocumentation Specialist IPearl River, NY$30–$33 / hourPossibility of extension High School diploma 5 years AA Degree, 3 + years of experience bachelor’s degree, final batch review 1+ year of experience. By applying to our jobs, you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners.
BerkleySr. Production Underwriter BerkleySr. Production UnderwriterParsippany, New Jersey$82,000–$152,000 / yearThe company offers a competitive compensation plan and robust benefits package for full time regular employees which for this role includes: Base Salary Range: $82,000 - $152,000 The actual salary for this position will be determined by a number of factors, including the scope, complexity and location of the role; the skills, education, training, credentials and experience of the candidate; and other conditions of employment. Responsible for new and renewal underwriting execution, including selecting risks in line with BLG’s strategy and underwriting guidelines, operating within authority and documentation guidelines, following up on accounts and closing new business.
Services For The Underserved, Inc.Public Fundraising Specialist Services For The Underserved, Inc.Public Fundraising SpecialistNew York, New YorkWe help make this possible by providing access to permanent housing, the cornerstone of stability, along with essential support services such as food access, counseling, job training, and mental health care to help people remain housed, healthy, and connected to their communities. Manager of Government and Institutional Partnerships, research, develops, and submits competitive city, state, and federal grant proposals to secure public funding aligned with organizational priorities.
Via Transportation IncStrategy Associate Principal, Proposals Via Transportation IncStrategy Associate Principal, Proposalsnew york city, NY$85,000–$115,000 / yearOur teams of world-class engineers, data-scientists, product managers, operations specialists, marketers, transit experts and more bring cutting-edge AI-powered software and innovative technology-enabled operations to our partners across the globe. Founded in 2012, Via builds solutions to digitize, automate, and enable data-driven decision making for entire transportation networks; fixed-route buses, microtransit, paratransit, school buses, autonomous vehicles, and more.