Writing & Editing jobs in New JerseyPart-time

A career at Whole Foods Market is more than just the work you do- it's about your personal growth and creating meaningful change.Our purpose is to nourish people and the planet.That means improving how people eat, funding grants for school gardens, providing access to fresh and healthy food to peopl

Pride Health is seeking a Technical Writer (IFU & Labeling) for one of the world’s largest biotech companies. Job Title: Technical Writer (IFU & Labeling) Location: Branchburg, NJ - Hybrid (3 days on site, 2 days remote) Job Type: Contract Length: 6-Months Hours: Mon-Fri, 8am-4:30pm Pay Rate: $23.00 - $26.60 per hour Overview: Lead the end-to-end development, writing, and rigorous editing of Instructions for Use (IFU) and technical labeling for complex molecular diagnostic assays. Translate complex scientific data into clear, compliant, and user-friendly documentation for laboratory professionals and clinicians. Responsibilities: • Creating and revising IFUs and Quick Reference Guides (QRGs) for molecular diagnostic products., • Utilizing advanced Microsoft Word skills for complex document structures (nested numbering, cross-references, tables, multi-language layouts)., • Performing meticulous proofreading to ensure accuracy in scientific terminology, unit conversions, and symbol usage; adhering to ISO 13485, FDA 21 CFR Part 820, and IVDR., • Managing full document lifecycle within an Electronic Document Management System (EDMS)., • Partnering with cross-functional stakeholders to gather content and ensure alignment., • Managing translations of IFUs and labeling as needed. Who You Are • Associates Degree or equivalent level of education in a scientific discipline, technical writing, or other related technical field, • Proficient in MS Office, • Strong proofing and editing skills, • Comfortable working independently through the IFU lifecycle, • High attention to detail and strong organizational skills, • 2–4 years of industry experience in Medical Device or In Vitro Diagnostics (IVD) technical writing of IFUs, • Familiarity with regulatory requirements (IVDR, FDA), • Experienced in collaborating with cross-functional teams to meet project deadlines, • Ability to spot minor discrepancies in large, complex datasets Preferences: • Previous IFU knowledge Benefits that Pride Health offers: Pride Health offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors. Apply Today! If you are interested in the position, please email your resume to rob.vanriet@pride-health.com for immediate consideration.

Job Description: • Stefanini is seeking an Executive Editor, Insights with advanced data fluency and a strong background in data journalism and AI to lead the creation of high-impact editorial products that translate quantitative findings into meaningful insights for healthcare professionals., • This editor will oversee flagship Reports franchise including physician compensation, lifestyle, and sentiment surveys as well as emerging AI-driven, data-focused features that help readers understand trends in medicine, practice management, and clinician well-being., • The ideal candidate is a data-literate, AI-savvy editor who is as comfortable interpreting complex analyses and algorithmic models as they are shaping compelling, evidence-based stories. This person will collaborate closely with analytics, research, and AI innovation teams to identify significant patterns, ensure statistical and methodological integrity, and surface insights that guide editorial strategy and deepen audience engagement. Key Responsibilities • Lead the development and execution of Reports and data-driven editorial series, from concept through publication., • Partner with research, analytics, and AI teams to design, refine, and interpret physician surveys, audience studies, and predictive analyses., • Analyze quantitative findings and AI-generated insights to identify trends, correlations, and signals that can be transformed into clear, credible stories., • Use AI to create and edit data visualizations, infographics, dashboards, and interactive tools in collaboration with designers and data visualization specialists., • Think creatively about new multimedia formats and AI-enhanced storytelling methods including visuals, audio, and video that make data and insights more accessible and engaging., • Ensure that survey methods, AI models, and data analyses meet the highest standards of accuracy, transparency, and reproducibility., • Develop editorial frameworks for tracking metrics across specialties, audience segments, and timeframes to inform ongoing coverage., • Write and edit features that contextualize quantitative and AI-driven findings within broader clinical, social, or economic narratives., • Mentor editors and writers on interpreting, validating, and applying data and AI insights in their reporting and editing., • Serve as the editorial liaison to data science, AI, and business intelligence teams to ensure alignment across content, analytics, and product strategies. Qualifications • Minimum of 8 years of experience in health, science, or business journalism, with at least 4 years focused on data journalism or data-driven storytelling. At least 1 year of experience using AI applications to assist in the creation of content., • Strong proficiency in Excel, Google Sheets, and data visualization tools such as Tableau, Data wrapper, Flourish, or Power BI, • Proficiency in databases and software like MySQL, • Proven ability to interpret survey data, statistical models, and AI-generated analyses to extract meaningful editorial insights., • Familiarity with quantitative and computational analysis concepts, including sampling, weighting, regression, machine learning, and confidence intervals., • Demonstrated success in producing or editing reports or stories grounded in quantitative and algorithmic evidence., • Excellent ability to translate complex findings into clear, engaging narratives that resonate with medical professionals., • Strong project-management and communication skills; able to coordinate across analytics, design, AI, and editorial teams., • 5+ years of experience in multimedia formats (interactive graphics, video explainers, podcasts, or data dashboards)., • Bachelors degree required; advanced degree in journalism, data science, statistics, AI, or public health preferred. Ideal Candidate • You have a journalists curiosity, a data scientists precision, and an AI researchers analytical mindset. You know how to turn spreadsheets and models into stories, and you see patterns where others see noise. You are driven by accuracy, fascinated by emerging technologies, and motivated by helping healthcare professionals understand the data shaping their work.

Responsibilities: • Serve as the primary liaison between customers and technicians, • Accurately document repair needs, generate estimates, coordinate efficient workflow, and ensure timely completion of services., • Prepare detailed repair orders , explain repair recommendations, timelines, and cost estimates, • Obtain approvals for services and maintain consistent communication throughout the repair process, • Recommend necessary and preventive maintenance services based on manufacturer guidelines, • Upsell additional services ethically and transparently, • Review completed repair orders with customers and explain final invoices, • Coordinate closely with towing dispatch to ensure smooth vehicle intake and monitor job progress to ensure efficiency and on-time delivery, • Order parts and communicate with vendors when necessary, • Maintain organized digital and physical repair records, • Process payments and handle billing documentation, • Ensure compliance with company procedures and safety standards, • Assist management with reporting and KPI tracking Requirements: • Minimum 3–5 years of experience as an Automotive Service Writer or Service Advisor, • Strong knowledge of automotive systems, diagnostics, and repair terminology, • Experience in high-volume automotive repair environments, • Proficiency with shop management software and estimating systems, • Excellent written, verbal communication skills and multitasking skills, • Sales-oriented mindset with a customer-first approach, • Bilingual (English/Spanish) is a plus, • Valid driver’s license What We Offer: • Competitive base salary pay plus performance-based bonuses, • Health, dental, and vision benefits, • Paid time off and holidays, • Ongoing training and advancement opportunities

Design Space InPharmatics, a leading international pharmaceutical consulting organization, is seeking an experienced Regulatory Medical Writer to support NDA submission programs for our growing portfolio of drug development clients. We are looking for a consultant with demonstrated expertise authoring and compiling FDA New Drug Application (NDA) submissions, specifically NDA Module 2 and Module 5 content in CTD/eCTD format. The ideal candidate will bring strong experience in clinical regulatory writing, integrated summaries, clinical study report development, and NDA submission strategy across small molecule and/or biologic drug products. This is a high-impact consulting engagement offering flexibility, and meaningful work at the forefront of regulatory drug development. Role and Responsibilities In this high-impact consulting role, the Regulatory Medical Writer will provide expert-level authoring and regulatory documentation support across a range of FDA NDA submission programs. Working remotely within a collaborative consulting team, the successful candidate will: • Author, edit, and compile NDA Module 2 clinical summaries and overviews, including Clinical Overview (Section 2.5), Clinical Summary (Section 2.7), Benefit-risk assessments and Integrated summaries of safety and efficacy., • Prepare and/or manage NDA Module 5 clinical documentation, including Clinical study reports (CSRs), Protocols and protocol amendments, Statistical analysis plans (SAPs), Case report tabulations, and listings coordination., • Ensure all documents comply with FDA guidance requirements, ICH CTD/eCTD standards, Good Clinical Practice (GCP), and internal quality and style standards., • Participate in submission planning, document gap assessments, and submission readiness reviews., • Support the preparation of responses to FDA information requests and review comments., • Coordinate timelines and deliverables to support NDA submission milestones., • Collaborate cross-functionally with clinical development teams, biostatistics, data management, pharmacovigilance, regulatory affairs, and medical affairs., • Function as a trusted regulatory writing subject matter expert within client project teams and CMO relationships., • Proactively flag gaps or risks relative to FDA expectations or industry best practices. Qualifications and Education Requirements • Advanced degree preferred (PharmD, PhD, MD, MS, or equivalent scientific discipline), Minimum 8–10 years of pharmaceutical or biotechnology regulatory writing experience., • Direct, hands-on experience authoring FDA NDA Module 2 and Module 5 content., • Strong knowledge of FDA NDA submission requirements, ICH E3 and CTD/eCTD structure, clinical trial documentation standards, and drug development processes. Preferred Skills • Experience with small molecule drug development programs., • Demonstrated expertise preparing integrated summaries of safety (ISS) and integrated summaries of efficacy (ISE)., • Familiarity with publishing systems and eCTD submission platforms., • Prior interaction with FDA review teams or support during regulatory agency meetings., • Consulting experience supporting multiple sponsors or parallel drug development programs., • Excellent scientific writing, editing, and data interpretation skills., • Ability to work independently and manage multiple deliverables in a fast-paced consulting environment. Additional Notes • Candidates who bring experience across both small molecule and biologic programs, or who have supported multiple NDA submissions across different therapeutic areas, will be especially well regarded. The responsibilities outlined in this position represent a general summary of the consulting role and are not intended to be all-inclusive. DSI reserves the right to amend this description as client program needs to evolve., • This is an excellent opportunity for a seasoned regulatory writing professional seeking to apply their expertise within a dynamic, market-leading consulting organization at the forefront of pharmaceutical regulatory strategy and drug development services., • This is a fully remote, independent consultant role. Consultants are engaged on a project basis and may be assigned to one or multiple concurrent engagements. Hours are not fixed and will fluctuate based on project requirements, milestones, and client needs., • All applications are reviewed by our human hiring team. No automated screening or AI-based filtering is used to evaluate or eliminate candidates. Every candidate receives personal consideration.

Medical Writer – Clinical Content & Health Economics and Outcomes Research (HEOR), Clinical Content Creation Group Location: Remote Duration: 6 month contract with the potential for extension, based on performance Culture and Values Our people are our strength—combining collaboration, speed, and quality while fostering a positive team culture and strong standardization to enable confident, compliant decision‑making. Purpose / Role Summary The Medical Writer – Clinical & HEOR is responsible for developing high‑quality, scientifically rigorous, compliant, and engaging content across clinical, medical, and HEOR domains. This role plays a critical role in shaping scientific and value‑based narratives that support engagement with diverse stakeholders, including HCPs, payers, IDNs, and health systems. The position requires strong scientific and HEOR literacy, excellent writing skills, and the ability to translate complex clinical, economic, and outcomes data into clear, audience‑appropriate materials aligned with therapeutic area and brand objectives. Key Responsibilities Scientific & Medical Content Development • Author and support complex scientific deliverables including abstracts, posters, manuscripts, oral presentations, publication extenders, response documents, and white papers across therapeutic areas., • Develop Medical Information content such as standard response letters, FAQs, and customer‑facing materials., • Draft, edit, and review HEOR‑related outputs including value dossiers, slide decks, economic evidence materials, and submissions. HEOR & Data Interpretation • Conduct comprehensive literature searches and systematic or targeted reviews to support clinical and HEOR narratives., • Partner with health economists, TA researchers, analysts, and statisticians to accurately interpret and translate data from clinical studies, real‑world evidence, cost‑effectiveness analyses, and budget impact models. Publications & Congress Support • Support preparation and submission of content for peer‑reviewed journals and scientific congresses., • Ensure adherence to publication standards and best practices (e.g., GPP, ICMJE, ISMPP) throughout the content lifecycle. Compliance, Quality & Standards • Ensure all materials comply with client policies and external regulatory and ethical guidelines (e.g., FDA/EMA, AMA style)., • Maintain high standards for accuracy, consistency, and scientific integrity across all deliverables. Collaboration & Project Management • Collaborate cross‑functionally with internal creative, editorial, medical, and strategic partners., • Manage multiple concurrent projects while meeting timelines, quality expectations, and stakeholder needs., • Provide flexible writing support across group initiatives as priorities evolve. Qualifications Required • PharmD or advanced scientific degree OR Bachelor’s degree in life sciences, pharmacy, public health, health economics, or related field with relevant experience., • 1–3+ years of experience in medical writing, medical communications, pharma, consultancy, or related environment; HEOR experience preferred., • Strong scientific literacy with the ability to interpret and synthesize clinical, medical, and economic data., • Excellent writing and editing skills tailored to both scientific and non‑scientific audiences., • Knowledge of clinical research processes, publication practices, and regulatory standards., • Strong attention to detail, organization, and ability to work independently within cross‑functional teams., • Proficiency with standard authoring and reference tools (e.g., Microsoft Office, EndNote, Adobe Acrobat). Preferred / Nice to Have • Experience with HEOR methodologies (e.g., real‑world evidence, cost‑effectiveness analyses, budget impact models)., • Familiarity with publication and approval platforms (e.g., Veeva Vault, Pubstrat, iEnvision/Datavision, Nubela)., • Knowledge of AMA style and global publication guidelines., • Professional certification (e.g., CMPP)., • Background working within a pharmaceutical company or healthcare consultancy.

A career at Whole Foods Market is more than just the work you do- it's about your personal growth and creating meaningful change.Our purpose is to nourish people and the planet.That means improving how people eat, funding grants for school gardens, providing access to fresh and healthy food to peopl

Job Description Job Title: On-Call Foreign Language Role Player / Interpreter Job Type: Contractor (1099) Company: GrowToPro Staffing Location: Joint Base McGuire-Dix-Lakehurst, New Jersey Schedule: Weekdays, 7:00 AM – 1:00 PM (paid for 8 hours per day) Position Overview: GrowToPro Staffing is seeking reliable and professional foreign language speakers to support Air Force training exercises. This is a part-time, on-call opportunity for individuals who enjoy interactive environments and want to contribute to meaningful military preparedness training. Selected candidates will participate in structured role-play scenarios as either a foreign commander or interpreter. These exercises help Air Force students prepare for real-world deployment situations by exposing them to different cultural, communication, and operational scenarios they may encounter overseas. This is a fun, engaging, and educational role in a safe and supervised training environment. Schedule & Commitment: On-call position: 2 to 3 days per month Possible increase in frequency in the future based on training needs Weekdays only (Monday–Friday) Schedule provided 2 to 3 weeks in advance Hours: 7:00 AM – 1:00 PM (paid for 8 hours per day) Compensation $20 – $25 per hour (1099 contractor) Rate depends on experience and language proficiency Languages Needed: We are actively seeking speakers of the following languages: Arabic Afghan languages (Dari / Pashto) Turkish Russian Chinese (Mandarin preferred) French German All other languages are welcome except Spanish and Portuguese. Responsibilities: Participate in structured role-play training scenarios Act as a foreign commander or interpreter during exercises Follow scenario instructions provided by training staff Communicate clearly and professionally during simulations Support a realistic training environment for Air Force students Requirements: Must be a U.S. citizen or Green Card holder Must be fluent in at least one non-English language (excluding Spanish and Portuguese) Must be reliable and able to commit to scheduled training days Must pass required background checks Professional demeanor and ability to follow structured instructions Additional Details Background checks required for all candidates Independent contractor (1099) position Safe, structured, and supervised training environment Opportunity for increased assignments over time Equal Opportunity Employer We are an equal opportunity employer and value diversity in our company. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or any other characteristic protected by law. Company DescriptionAt GrowToPro, we're not just about filling roles or finding jobs – we're about transforming lives and businesses. Whether you're a dynamic professional ready to take the next step in your career journey or a company eager to elevate your team with top talent, you're in the right place. Our dedicated team is here to support you every step of the way, with personalized service, innovative solutions, and a genuine passion for helping you succeed. So, dive in, explore all that we have to offer, and get ready to embark on an exciting new chapter of growth and opportunity. Welcome To The GrowToPro Family!At GrowToPro, we're not just about filling roles or finding jobs – we're about transforming lives and businesses. Whether you're a dynamic professional ready to take the next step in your career journey or a company eager to elevate your team with top talent, you're in the right place.\r\n\r\nOur dedicated team is here to support you every step of the way, with personalized service, innovative solutions, and a genuine passion for helping you succeed. So, dive in, explore all that we have to offer, and get ready to embark on an exciting new chapter of growth and opportunity.\r\n\r\nWelcome To The GrowToPro Family!

Job Description We are seeking a reliable and professional Wolof Interpreter for community-based assignments in and around the Lawrence Township, NJ area. This is a freelance (independent contractor) opportunity ideal for individuals who are fluent in Wolof and English and enjoy supporting diverse communities. Key Responsibilities: Provide accurate, in-person Wolof interpretation in community settings (e.g., social services, or local appointments) Facilitate clear communication between Wolof-speaking clients and English-speaking providers Maintain confidentiality and adhere to professional ethics standards Arrive on time and be prepared for scheduled assignments Qualifications: Fluency in Wolof and English (spoken and comprehension required) Prior interpretation experience preferred (community, medical, or social services settings a plus) Strong interpersonal and communication skills Reliable transportation and willingness to travel locally Professional demeanor and dependability Work Arrangement: Freelance / independent contractor Flexible, assignment-based scheduling Competitive per-assignment or hourly rates Powered by JazzHR oPuV7FtK0V

Writer/Journalist Internship: The role is focused on content creation for BORGEN Magazine or The Borgen Project Blog.

Entry Level translators capable of interpreting and translating from English to target language and vice versa. Entry Level Translator needed Asap.

APM Terminals in Mexico, Michoacán is seeking an Operations Lean Associate to support the Sensei Program by translating between Japanese and English for Lean experts.The role involves driving Lean practices, providing specialized knowledge for process optimization, and assisting with audits.Candida

High-volume, family-owned Toyota dealership in Wood-Ridge, NJ seeking experienced Service Advisors who can present value-driven recommendations in a fully digital service environment.Commission-based pay with strong earning potential.We are a family-owned Toyota dealership with a busy, well-run serv

Experience with Regulatory CMC Technical Writing. IT staffing and consulting firm operating since 1967, specializing in providing technical talent, project management, and specialized services across various industries, including energy, financial services, and life sciences. TSR Consulting is curre

Breaking Data is a boutique healthcare agency serving a broad portfolio of global pharmaceutical and biotech companies.Our team partners closely with clients to develop medically accurate, strategically aligned, and highly actionable content across sales training, marketing, payer access, and medica

A global financial institution is hiring a senior professional to join its capital analytics and regulatory reporting function, focused on enterprise-level risk-weighted asset (RWA) frameworks across credit and market risk.This role sits at the intersection of capital regulation, regulatory analytic

Be a Part of the Fastest Growing Sports Channel Worldwide. With a global footprint and a deep passion for combat sports, we connect fans and athletes through compelling storytelling, live action, and dynamic digital engagement. The candidate must have experience producing and editing short and longf

Design, develop, and maintain high-quality reports and dashboards using.Sigma Data Models and semantic layers.Data Modeling & Performance.Troubleshoot performance and data issues across.Snowflake and Sigma environments.Own Sigma architecture decisions including:.Define and promote reporting stan

The technical writer develops and authors chemistry, manufacturing, and controls (CMC) common technical documents (CTD) for development and post-approval regulatory dossiers within pre-established timelines. Additionally, the technical writer authors and evaluates change controls for global regulato

The Medical Writer – Clinical & HEOR is responsible for developing high‑quality, scientifically rigorous, compliant, and engaging content across clinical, medical, and HEOR domains. Medical Writer – Clinical Content & Health Economics and Outcomes Research (HEOR), Clinical Content Creation Gro

At EY, we're all in to shape your future with confidence.We'll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.Join EY and help to build a better working world.Tax Services Manager - Financial Services Office - Customer Tax Operati

Regulatory Reporting Associate | Broker-Dealer | $44/hr | Jersey City, NJ (Hybrid) | Temp-to-Perm Looking for a Regulatory Reporting Associate with strong broker-dealer experience to support SEC & CFTC reporting in a fast-paced financial services environment. This is a 12-month contract with clear temp-to-perm potential — ideal for someone who can step in and contribute immediately across core regulatory reporting functions. What you'll be doing: • Preparing and reviewing SEC & CFTC regulatory reports, • Ensuring accurate, timely submission of required filings, • Partnering cross-functionally to gather, validate, and analyze financial data, • Supporting Net Capital (15c3-1) and Customer Reserve (15c3-3) reporting, • Assisting with CFTC / FCM filings, • Monitoring and adapting to evolving regulatory requirements, • Supporting audits and regulatory examinations, • Maintaining and enhancing internal controls, • Identifying opportunities to improve reporting processes and efficiency What we're looking for: • 5+ years of broker-dealer regulatory reporting experience, • Hands-on experience with: – SEC Rule 15c3-1 (Net Capital) – SEC Rule 15c3-3 (Customer Reserve) CFTC / FCM reporting • Strong understanding of accounting and financial reporting principles, • High attention to detail with strong analytical skills, • Experience with financial reporting tools/systems, • Ability to operate effectively in a dynamic regulatory environment, • Strong communication and collaboration skills ?? Jersey City, NJ (Hybrid) ?? $44/hour ?? 12-month contract ? strong temp-to-perm potential ?? Full-time Why this role stands out: You'll be working on core regulatory reporting tied directly to compliance and business operations, with exposure to key SEC and CFTC frameworks in a hands-on environment. ?? Message me directly or apply below Must be authorized to work in the United States Russell Tobin offers eligible employees comprehensive medical, dental, and vision coverage, a 401(k) retirement savings plan, life and disability insurance options, pet insurance, employee discounts, and access to an employee assistance program, identity theft protection, and legal support.

Bachelor’s degree in Graphic Design, Fine Arts, or related field (or equivalent experience). Research and share visual inspiration to inform design direction. Execute design projects from brief through final production.

A leading insurance company is seeking an Associate Underwriter for their Transportation division.

Assistant Division Director - Office of Data Management and Reporting (Posting #188-26) SALARY: $140,000.00-$159,000.00 (Commensurate with education and experience) The Department of Children and Families (DCF), Office of Data Management and Reporting, is seeking a qualified individual to fill the Assistant Division Director position located in Trenton. This position may be eligible to work remotely for up to two days in a calendar week. DEFINITION: Under the direction of a Division Director, Deputy Director, or other senior official in a state department or agency, directs the staff and activities of an operational unit responsible for providing general administrative and/or fiscal management, program policy and planning services, or delivering a variety of social, medical, assistance, health care, and other services to a specific client population; does other related duties as required. ROLE SUMMARY: Under the leadership of the Director of Data Management & Reporting, the incumbent will lead NJ DCF's enterprise data platform, governance, and analytics enablement so DCF staff, providers, and partners can rely on well-governed, secure, and timely data to improve outcomes for children and families. The Assistant Director implements the cloud data strategy (Azure and/or AWS), supports pragmatic data governance, and manages a multidisciplinary technical team while partnering closely with program leadership to deliver high-value data products, reporting, and research support. This leader is expected to be hands-on when needed—capable of prototyping, reviewing code, troubleshooting pipelines, and guiding engineers through complex incidents while maintaining high standards for security, privacy, and compliance. KEY RESPONSIBILTIES: Strategic & Roadmap Leadership · Play an active role in implementing NJ DCF's Information Management Strategy Roadmap. · Translate business needs into technical roadmaps and manage intake and prioritization. · Advise leadership on the impact of federal/state statutory changes. · Develop and implement business-first processes for program management and data management capabilities. Platform Architecture, Operations & Reliability · Own the architecture, delivery, and optimization of DCF's cloud data lake/warehouse, including orchestration, CI/CD, monitoring, security, and cost management. · Champion observability, documentation, and change management across the data ecosystem. · Oversee data integration processes to facilitate seamless data flow between systems and applications. · Establish data privacy policies and implement disaster recovery and business continuity strategies to ensure organizational data protection. Governance, Quality, Compliance & Security · Participate in governance committees, support implementation of data policies, steward roles, and compliance standards. · Implement and maintain an enterprise data catalog and a data quality program with clear SLA. · Facilitate implementation of data governance policies and procedures to ensure the accuracy, reliability, and security of data across the organization. · Ensure compliance with federal/state mandates and internal policies. · Leverage reporting tools to track data quality, usage trends, and KPIs for data products, ensuring actionable insights for stakeholders. Data Products, Analytics & AI Enablement · Design reusable data products for reporting, dashboards, statutory submissions, and research partnerships. · Guide responsible use of AI and automation with applicable safeguards. Leadership, Team Management & Stakeholder Engagement · Lead, develop, and mentor a technical team of engineers, data modelers, and stewards. · Manage performance evaluations and operational functions for assigned staff. · Build and maintain a positive, inclusive work environment. · Support vendor selection, contract oversight, and delivery standards. · Represent DMR and DCF in meetings, conferences, and stakeholder engagements. General Responsibilities · Perform additional duties as assigned. Minimum Qualifications: Bachelor's degree in information systems, computer science, engineering, or related field (Master's preferred). 10+ years in data engineering/analytics/platform roles, including 5+ years managing technical teams. Hands-on experience with Azure/AWS cloud data platforms; strong SQL and Python skills. Experience with CI/CD and Infrastructure-as-Code. Knowledge of AI/ML concepts and responsible AI practices. Strong communication and stakeholder management skills. Experience in data management, business intelligence and analytics environments is required. Experience across product life cycles (emerging, launch, in-line, mature) is preferred. Preferred Qualifications: Familiarity with regulatory reporting processes and prior experience working in a highly regulated environment. Demonstrated experience in governance including catalog/lineage and data quality. Knowledge of open data programs and API-based data exchange. Experience with modern data stack components such as Databricks, Spark, dbt, Terraform, and containerization/orchestration frameworks (e.g., Docker/Kubernetes). Experience in software development, including an understanding of programming concepts and the logic flow of applications, is preferred. REQUIREMENTS: Applicants must meet one of the following or a combination of both experience and education. Thirty (30) semester hour credits are equal to one (1) year of relevant experience. Ten (10) years of professional experience in a public or private organization involved in programs providing either social/community, medical/health, rehabilitation/education, or vocational/occupational services to a specific client population (physical, intellectual, or developmental disability, juvenile offenders, socially/economically disadvantaged, etc.), three (3) years of which shall have been in a supervisory capacity. OR Ten (10) years of professional experience as an administrator responsible for planning, budgets, and administration of programs in a large public or private agency, three (3) years of which shall have been in a supervisory capacity. OR Possession of a bachelor's degree from an accredited college or university; and six (6) years of the above-mentioned professional experience, three (3) years of which shall have been in a supervisory capacity. OR Possession of a master's degree from an accredited college or university in a field relevant to the position; and five (5) years of the above-mentioned professional experience, three (3) years of which shall have been in a supervisory capacity. "Professional experience" refers to work that is creative, analytical, evaluative, and interpretive; requires a range and depth of specialized knowledge of the profession's principles, concepts, theories, and practices; and is performed with the authority to act according to one's own judgment and make accurate and informed decisions. RESUME NOTE: Eligibility determinations will be based upon information presented on the resume only. Applicants who possess a degree from a college or university outside the United States must provide an evaluation of one's transcripts from a recognized evaluation service at the time of submission by the above closing date. Failure to do so may result in your ineligibility. LICENSE: Appointees will be required to possess a driver's license valid in New Jersey only if the operation of a vehicle, rather than employee mobility, is necessary to perform the essential duties of the position. IMPORTANT NOTICES EMPLOYEE BENEFITS: The Department of Children and Families provides many employee benefits, including but not limited to: • Alternative Workweek Program*, • Deferred Compensation, • Health, Dental and Life Insurance, • Flexible and Health Spending Accounts, • Pension, • Telework*, • Public Service Loan Forgiveness, • Benefit Leave (Vacation, Sick, Administrative Leave), • 13 Paid Holidays *Pursuant to Department policy, procedures and/or guidelines PUBLIC SERVICE LOAN FORGIVENESS: As a prospective employee of the State of New Jersey, you may be eligible for federal loan forgiveness programs and state repayment assistance programs. For more information, please visit the U.S. Department of Education's website at _ SAME APPLICANTS: If you are applying under the NJ "SAME" program, you must submit any of the supporting documentation specified in N.J.S.A. 11A:7-13.3 along with your resume by the closing date indicated above. RESIDENCY LAW Please refer to the New Jersey Department of Children and Families' website at _ TO APPLY: You must submit a cover letter, resume, and completed Application for Employment as a single PDF document, saving the file by your Last Name, First Name. Please indicate in your cover letter where you found this job opportunity and send the file to: mail: Job.Posting@dcf.nj.gov NOTE: Applicants are required to submit a completed _ with their resume at the time of application. Failure to do so will result in disqualification for this position. The Department of Children and Families is an Equal Employment Opportunity Employer and is committed to fostering a respectful and inclusive work environment which reflects the diversity of the state we serve.

Medical interpretation certification if performing interpreter duties - Arabic (Required).

Pride Health is seeking a Technical Writer (IFU & Labeling) for one of the world’s largest biotech companies. Job Title: Technical Writer (IFU & Labeling) Location: Branchburg, NJ - Hybrid (3 days on site, 2 days remote) Job Type: Contract Length: 6-Months Hours: Mon-Fri, 8am-4:30pm Pay Rate: $23.00 - $26.60 per hour Overview: Lead the end-to-end development, writing, and rigorous editing of Instructions for Use (IFU) and technical labeling for complex molecular diagnostic assays. Translate complex scientific data into clear, compliant, and user-friendly documentation for laboratory professionals and clinicians. Responsibilities: • Creating and revising IFUs and Quick Reference Guides (QRGs) for molecular diagnostic products., • Utilizing advanced Microsoft Word skills for complex document structures (nested numbering, cross-references, tables, multi-language layouts)., • Performing meticulous proofreading to ensure accuracy in scientific terminology, unit conversions, and symbol usage; adhering to ISO 13485, FDA 21 CFR Part 820, and IVDR., • Managing full document lifecycle within an Electronic Document Management System (EDMS)., • Partnering with cross-functional stakeholders to gather content and ensure alignment., • Managing translations of IFUs and labeling as needed. Who You Are • Associates Degree or equivalent level of education in a scientific discipline, technical writing, or other related technical field, • Proficient in MS Office, • Strong proofing and editing skills, • Comfortable working independently through the IFU lifecycle, • High attention to detail and strong organizational skills, • 2–4 years of industry experience in Medical Device or In Vitro Diagnostics (IVD) technical writing of IFUs, • Familiarity with regulatory requirements (IVDR, FDA), • Experienced in collaborating with cross-functional teams to meet project deadlines, • Ability to spot minor discrepancies in large, complex datasets Preferences: • Previous IFU knowledge Benefits that Pride Health offers: Pride Health offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors. Apply Today! If you are interested in the position, please email your resume to rob.vanriet@pride-health.com for immediate consideration.

Technical Writer and Document Specialist.Work Schedule: Mon-Friday(normal business hours).Duration:12 months( possibility of extension).Location: New Brunswick NJ/ PPK NJ.The Technical Writer and Document Specialist (TW/DS) will sit within the Cell Therapy Development (CTD) Project and Portfolio Man

Audit And Risk Operations Coordinator, Commercialization Analytics.

A public sector solutions firm is seeking a Senior Manager of Data Analytics & Reporting to oversee EDPlan reporting. Candidates should have over 10 years' experience in data analytics, particularly in education, and possess strong analytical and communication skills.

As the Associate Acquisitions Editor, you will be joining a leading global trade book publishing team and will have the opportunity to contribute to one of our largest and most dynamic programs related to business, success and self-improvement topics. As the Associate Acquisitions Editor, you will b

Compensation is based on several factors including, but not limited to education, relevant work experience, relevant certifications, and location.

We consider all qualified applicants for employment without regard to race, color, religion, creed, national origin, sex, pregnancy, age, sexual orientation, transgender status, gender identity, disability, alienage or citizenship status, marital status or partnership status, genetic information, ve

Exceptional writing and editing skills across formats:. This role is primarily focused on content writing and content strategy, ensuring a consistent, compelling brand voice across channels and audiences.

Ability to obtain a Public Trust: US Citizenship required.Astrion has an exciting opportunity for a.REQUIRED QUALIFICATIONS / SKILLS.Ability to complete and pass a Public Trust Security Investigation (US Citizenship required for all applicants).DESIRED QUALIFICATIONS / SKILLS.Must have the ability t

We seek a dogged reporter who loves developing deep sourcing in and around all levels of government, breaking news and exposing wrongdoing that others cannot crack. We also want an independent reporter who can work collaboratively with a team when necessary. Coverage will include longform investigat

This job requires reliable transportation to meet with sources and/or cover events in New Jersey during occasional traditional breaking news shifts. Experience in breaking news and headline optimization. An interest and enthusiasm to forge new AI-driven workflows to improve newsroom-wide efficiency

Medical Writer / Copywriter application”. As a Medical Writer / Copywriter at Breaking Data, you’ll sit at the intersection of high-science medical writing and promotional copy. We are not considering freelance, contract, or part-time applicants for this role.

Medical Editor (Regulatory Documents + QC) - US Home based. Serves as a member of the medical writing team for projects with medical writing deliverables. Advises medical writers, medical editors, and study teams on quality review, compilation, and editorial standards.

As a Technical Writer, you will work with the Federal NOTAM System (FNS) team to provide first level documentation, recommendations, and new documentation to FNS first level support; documentation includes technical instruction books, handbook, and other technical directives.

About the job Russian Interpreter Us based WE ARE HIRING INTERPRETERS!!! LANGUAGE: RUSSIAN Requirements: Steady wired internet connection USB Wired headset Windows 10 or MacOS WHAT WE OFFER YOU: Fully remote position with a clear schedule Full-time or part-time position Immediate availability to sta

A global financial institution is hiring a senior professional to join its capital analytics and regulatory reporting function, focused on enterprise-level risk-weighted asset (RWA) frameworks across credit and market risk. This role sits at the intersection of capital regulation, regulatory analyti

Job Title: Regulatory Reporting Business Analyst.We are seeking a Regulatory Reporting Business Analyst with strong experience in CCAR FR Y-14Q and FR Y-14A reporting within large banking institutions.The candidate will work across regulatory data and functional requirements, including data discover

Minimum 3–5 years of experience as an Automotive Service Writer or Service Advisor.

Candidates should possess a PhD, MD, or equivalent doctoral degree and show capacity for leading federally funded research in a variety of neuroscience areas.

Stefanini is seeking an Executive Editor, Insights with advanced data fluency and a strong background in data journalism and AI to lead the creation of high-impact editorial products that translate quantitative findings into meaningful insights for healthcare professionals. Develop editorial framewo

The technical writer assures regulatory dossier compliance and independently authors high quality CMC content by:.

TSR Consulting is currently seeking a highly motivated Technical Writer / Document Specialist for a hybrid opportunity in New Brunswick, NJ.Role: Technical Writer / Document Specialist.We are looking for a Technical Writer / Document Specialist with strong Regulatory CMC documentation experience in