Trabajos Writing & Editing en New Jersey

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

Maintains, or ensures maintenance of, a clean and sanitary working and shopping environment; maintains equipment in accordance with WFM cleanliness and safety standards.

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants. Company: One of Our Clients Job Description: Job Title: Scientific Writer – Translational Development Location: Onsite/Hybrid: 50% at Giralda Farms, Madison, NJ 07940 Duration: 12+ Months (Extendable) Pay Rate: $60.00 - 67.97/hr on W2 Top Requirements: • 8-10 years of scientific or regulatory writing experience, • 5+ years of experience in drug development/pharmaceutical industry, • Experience utilizing CARA, VERITY, and other writing tools, • Experience with publishing regulatory documents; interacting with Health Authority related submissions, • Masters or PhD in molecular biology or oncology or other scientific discipline Summary 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. This individual will also contribute to abstracts, posters, manuscript and other scientific communications arising from the group. Technical 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 novel 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. Provide suggestions to improve flow and clarity of narrative and presentation of data, • Engage with Writers and other functions (eg, SciCom, Regulatory, Medical Affairs, Clinical, NCD) outside of TM as needed to stay current on writing SOPs, platforms, resources, and company guidelines, • Communicates regularly and prepares and makes presentations within the department and externally as required, • Participate in recruitment and hiring of new writers as needed Qualifications • Masters or PhD in Hematology/Oncology/Neuroscience or related field with 6-8 years in industry or an academic setting, • Ability to manage scientific collaborations and projects, • Proven written and oral communication skills, • Ability to interpret data and craft key communication points from tables, listings, graphs, • Ability to clearly organize presentations of data into a clear narrative, • Experience with regulatory submissions (eg, IND, NDA/sNDA) required, • Effective team building and teamwork skills with multiple functions, • Detail-oriented with the ability to identify and implement creative solutions, • Ability to prioritize and manage time efficiently Other Attributes • Highly detail-oriented with excellent record keeping and organizational skills, • Must be a highly flexible, results oriented, independent self-starter who enjoys working in a fast-paced dynamic environment, • Able to anticipate problems at project level, • Proven track record of scientific approach to complex problem solving, • Demonstrate in-depth, scientific-directed, innovative thinking, • Recognizes interrelationships of facts/factors, processes, and systems, • Recognize risk and propose contingency plans, • Independently (or using collaborations) develop scientific direction for assignments, • Recognize cross-functional issues, • Communicates within the larger organization, • Develops constructive relationships across organization to achieve the goals of the function and the business through leadership roles on cross-functional/divisional teams, • Communicates within the larger organization and external community, • Provides expert guidance to multi-disciplinary teams and senior management Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Awards and Accolades: America's Most Honored Businesses (Top 10%) Awarded by USPAAC for the Fastest Growing Business in the US 12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020) Fastest 50 by NJ Biz (2020, 2019, 2020) INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list) Top 100 by Dallas Business Journal (2020 and 2019) Proven Supplier of the Year by Workforce Logiq (2020 and 2019) 2019 Spirit of Alliance Award by Agile1 2018 Best of the Best Platinum Award by Agile1 2018 TechServe Alliance Excellence Awards Winner 2017 Best of the Best Gold Award by Agile1(Act1 Group)

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

Dear Applicant, Please let me know if you are interested. Title: Technical Writer Location: Alpharetta, GA or Berkeley Heights, NJ (5 Days Onsite) Hire Type: Long Term Contract Job Description: Ensure accurate, concise, and successful delivery of process technical documentation. The Senior Infrastructure Technical Writer is required for production of internal support documentation of Enterprise-class infrastructure and cloud platforms. PRIMARY RESPONSIBLITIES: • Research and analyze requirements for new infrastructure environment builds. Independent study of proposed data center and cloud solutions for all associated systems and hardware components., • Create and maintain complex Visio flow diagrams that illustrate transaction traffic patterns, network connectivity, and all configurable system components., • Work with project managers to map out documentation strategies and schedules., • Collaborate with distributed engineers (Windows, Unix, and Cloud engineers, Network, Security, SQL DB, and Monitoring) to gather technical build information for documentation deliverables., • Author and publish the documentation suite for each infrastructure project for two core audiences (online HTML knowledge articles for global Operations Support teams authored in ServicePoint Knowledge Management System, and infrastructure reference guides for Platform Engineering authored in MS Word)., • Host virtual documentation turnover sessions to Operations Support teams using Microsoft Teams. QUALIFICATIONS: • Four-year college degree, preferably in Computer Science or English., • Ten years minimum experience producing technical documentation, preferably in the systems/hardware and data center infrastructure IT areas., • Working knowledge of infrastructure server farms, network communications protocols, firewall security, system/application monitoring, WAN/LAN configurations., • Strong Visio diagramming skills/experience., • Excellent written and verbal skills. Must be able to build a rapport with infrastructure engineers, working closely with them to produce comprehensive documentation that describes sophisticated distributed platforms for internal support staff consumers., • Excellent organizational and time management skills. Must be able to juggle multiple projects under tight deadlines while being flexible to accommodate shifting schedules., • Self-starter. Must be able to take projects and run with them with very little supervision. Must be analytical with a thirst for new technological knowledge. Proven track record of performing research and independent self-study as part of production of documentation deliverables., • Experience with running/hosting Teams meetings. Position requires hosting both large Teams meeting presentation-type sessions and smaller collaborative Teams meetings., • Knowledge/experience of documentation standards and processes with ability and willingness to collaborate with peers in the documentation team to develop and refine them., • MS Visio, • Microsoft Word, • HTML or XML online authoring application, • Adobe Acrobat, • SharePoint, • MS Excel, • MS PowerPoint

Job Title: Nonclinical Regulatory Document and Scientific Writer Duration: 12 Months Contract Location: Madison, NJ 07940 (Hybrid – 50% onsite) Schedule: Monday–Friday | 8:00 AM – 5:00 PM Pay Rate: $67.98/hr (W2) Role Summary Reporting to the Program Management Lead, this role supports the Late Development Translational team by developing high-quality scientific and regulatory documents. The Scientific Writer will partner closely with Translational scientists to produce biomarker reports, regulatory submission content, and scientific communications supporting late-stage drug development programs. Key Responsibilities • Author and deliver scientific and regulatory documents including biomarker reports, non-clinical summaries, translational sections of clinical/pharmacology summaries, briefing books, CSRs, and investigator brochures., • Contribute to abstracts, posters, manuscripts, and scientific communications., • Support regulatory submissions and responses, including IND/NDA documentation and regulatory queries., • Develop and manage publication strategies, timelines, and annual publication plans in collaboration with Translational Development teams., • Partner cross-functionally with Clinical, Non-Clinical Development, Pharmacology, DMPK, Regulatory, Medical Affairs, and Scientific Communications teams., • Analyze and synthesize complex scientific data into clear narratives, tables, and visual presentations., • Ensure compliance with writing SOPs, documentation systems (e.g., CARA, VERITY), and company standards., • Strong knowledge of hematological malignancies, solid tumors, or neuroscience disorders, including clinical landscape and emerging therapies., • Deep understanding of clinical, translational, and mechanistic data for late-stage development programs., • Experience preparing regulatory documents and scientific communications., • Familiarity with documentation systems such as CARA, VERITY., • Understanding of global development processes and lifecycle management across US, EU, and Canada., • Ability to translate complex scientific data into clear, strategic messaging., • Master’s or PhD in Hematology, Oncology, Neuroscience, or related field., • 6–8 years of industry or academic experience in scientific/medical writing., • Experience supporting regulatory submissions (IND, NDA/sNDA)., • Strong communication, project management, and collaboration skills., • Highly organized, detail-oriented, and proactive problem solver., • Strong cross-functional collaboration and leadership skills., • Ability to anticipate risks and propose solutions., • Passion for advancing therapies that improve patient outcomes.

Title: Scientific Writer – Translational Development Location: Madison, NJ (Onsite/Hybrid: 50%) Duration: 12+ months Hours: Mon-Fri 8am-5pm Overview: • A background as a scientist is considered a strong advantage, given the complexity of the reports., • Author and contribute to nonclinical regulatory documents, including Biomarker documentation, Summary reports, Manager scripts and Scientific abstracts., • Support disease and brand planning through strategic scientific content development., • Collaborate closely with the Medical Communications group to ensure alignment and consistency., • Produce highly technical reports that meet regulatory standards and internal expectations., • Work within and across documentation systems, including those used by teams such as Cara and Verity Influence cross-functional partners. Top Requirements: • 8-10 years of scientific or regulatory writing experience., • 5+ years of experience in the drug development/pharmaceutical industry., • Experience utilizing CARA, VERITY, and other writing tools., • Experience with publishing regulatory documents; interacting with Health Authority related submissions., • Masters or PhD in molecular biology or oncology or other scientific disciplines. Job Summary: • 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., • This individual will also contribute to abstracts, posters, manuscripts, and other scientific communications arising from the group., • In-depth understanding of hematological malignancies or solid tumors or Neuroscience disorders especially the clinical landscape, evolving therapy, and 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 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., • 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 plans 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. Provide suggestions to improve flow and clarity of narrative and presentation of data., • Engage with Writers and other functions (eg, SciCom, Regulatory, Medical Affairs, Clinical, NCD) outside of TM as needed to stay current on writing SOPs, platforms, resources, and company guidelines., • Communicates regularly and prepares and makes presentations within the department and externally as required., • Participate in recruitment and hiring new writers as needed. Qualifications • Masters or PhD in Hematology/Oncology/Neuroscience or related field with 6-8 years in industry or an academic setting., • Ability to manage scientific collaborations and projects., • Ability to interpret data and craft key communication points from tables, listings, and graphs., • Ability to clearly organize presentations of data into a clear narrative., • Experience with regulatory submissions (eg, IND, NDA/sNDA) required.

Customs Entry Writer Iselin, NJ We are seeking a detail-oriented and experienced Customs Entry Writer to join our team. The ideal candidate will be responsible for preparing and processing import documentation, ensuring compliance with U.S. Customs regulations, and coordinating with clients, carriers, and government agencies to facilitate the timely clearance of shipments. This role requires strong organizational skills, accuracy, and the ability to thrive in a fast-paced logistics environment. Key Responsibilities: • Prepare and submit accurate import documentation to U.S. Customs and other government agencies., • Classify goods using the Harmonized Tariff Schedule (HTSUS) and determine duty rates., • Review commercial invoices, packing lists, and other shipping documents for accuracy., • Communicate with clients, carriers, and customs officials to resolve issues and ensure smooth cargo clearance., • Maintain up-to-date knowledge of U.S. Customs regulations, trade compliance requirements, and industry best practices., • Track and monitor shipments to ensure timely delivery and proper documentation flow., • Maintain organized records of all entries and compliance-related documents., • Minimum 2 years of experience in customs brokerage or entry writing., • In-depth knowledge of U.S. Customs regulations, HTS classification, and import processes., • Familiarity with ABI (Automated Broker Interface) software and other industry platforms., • Strong attention to detail and excellent organizational skills., • Effective communication skills, both written and verbal., • Ability to multitask and work under pressure in a deadline-driven environment., • Competitive salary and benefits package., • Opportunities for professional growth and career development., • Collaborative and supportive work environment.

Are you detail-oriented, organized, and ready to take the next step in your logistics career? Our client is looking for someone to join their team as a Customs Entry Writer, where you’ll play a key role in ensuring smooth import operations, compliance with regulations, and outstanding service to future and existing clients. Responsibilities: • Review and organize import files to ensure all information and documentation is accurate and complete., • Communicate with Customer Service when additional documents or information are needed from clients., • Classify documentation based on operations system data and follow client-specific SOPs., • Support the Import Manager with classification and compliance needs., • Research and provide HTS or product codes when missing, ensuring accuracy for future use., • Input entry data and handle FDA (PGA) requirements, including “may proceed” releases., • Immediately notify clients when FDA exams are required (document or merchandise)., • Prepare and annotate delivery orders with FDA release status., • Issue written instructions to carriers/steamship lines when shipments must be held for release., • Ensure shipments are properly released once clearance is completed., • Pass completed files to Post-Entry team for final assembly., • Monitor releases by Customs, FDA, and other authorities, and resolve census or entry errors., • Correct bill of lading and related errors promptly. Qualifications: • High School Diploma or GED required., • 3+ years of entry writing and/or brokerage operations experience (data entry & PGA focus)., • Experience with CargoWise One preferred; QuestaWeb a plus., • Strong knowledge of U.S. and international geography (countries, cities, ocean ports)., • Proficiency in Microsoft Outlook, Word, and Excel., • Ability to work independently while delivering top-quality customer service., • Excellent attention to detail, organization, and multitasking skills., • Strong written and verbal communication abilities. Why You’ll Love Working Here We know our success depends on our people. That’s why we offer a competitive benefits package designed to support your health, well-being, and future: • Medical, Dental, and Vision Insurance, • Health Savings Account (HSA) – 100% employer-paid, plus $1,000 annual employer contribution, • Short-Term Disability Insurance – 85% of base pay, • Long-Term Disability Insurance – 60% of base pay, • Life Insurance & AD&D Coverage – $25,000 each, • 401(k) with Profit Sharing (annual contribution if eligible), • Paid Time Off (PTO) for work-life balance

We're looking for native Indonesian speakers with a strong STEM background to evaluate AI-generated translations of science, technology, engineering, and math content.What you'll do:** - Review translated responses to STEM questions and rate which translation is higher quality - Write reference (gol

We're looking for native Arabic (Modern Standard Arabic) speakers with a strong STEM background to evaluate AI-generated translations of science, technology, engineering, and math content.What you'll do:** - Review translated responses to STEM questions and rate which translation is higher quality -

We're looking for native Hindi speakers with a strong STEM background to evaluate AI-generated translations of science, technology, engineering, and math content.What you'll do:** - Review translated responses to STEM questions and rate which translation is higher quality - Write reference (golden)

The ideal candidate will have prior experience facilitating bilingual communication in corporate or professional settings, particularly where business discussions, negotiations, or client presentations are involved. Responsibilities** - Provide simultaneous or consecutive translation during virtual

Research and share visual inspiration to inform design direction.

Provide over the phone language support to All Hallows Catholic Church families contacting the ESOL office. Provide over the phone language support to district staff communicating with All Hallows Catholic Church families. Conduct ESOL Program All Hallows Catholic Church meeting in the target langua

Auto Care Center Service Writer. These Auto Care Center roles focus on the needs of our customers who entrust us with the care of their vehicles as they shop for merchandise and services offered at Walmart. The Auto Care Center is a rewarding place to work with opportunities for advanced associate t

Familiarity with Karmak, ADP, Reynold, RO Writer or similar programs. Strong computer and Windows office suite skillset, and the ability to learn new platforms (such as DFS IT Systems, including Web Wrench, MobileFrame, RO Writer).

Cox Fleet is currently hiring a Shop Service Writer to support future growth of the Company at this location. Familiarity with Karmak, ADP, Reynold, RO Writer or similar programs. Strong computer and Windows office suite skillset, and the ability to learn new platforms (such as DFS IT Systems, inclu

Report unsafe conditions to the Crew Leader as appropriate.

Internal Reporting is a key finance organization with an opportunity to build and provide critical support to the finance and leadership teams. Coordinate and communicate with various levels of accounting and finance management across the global organization. Bachelor's degree in Finance or Accounti

CHB Delivery Associate/Customs Entry Writer They are looking for someone who writes customes reports for shipping So specifically someone who has Customs writing for imports/exports High-Level Position PurposeThe CHB Delivery Associate is responsible for coordinating and executing shipments to ensur

Experienced Service Advisors looking for a modern, high-volume Toyota service department with real earning potential are encouraged to apply. We are seeking experienced Service Advisors who take a consultative, professional approach to service. High-volume, family-owned Toyota dealership in Wood-Rid

This Senior Property Underwriter will manage a property renewal book while also producing new business. The position will primarily be focused on underwriting mono-line property opportunities; however, the underwriter will be charged with cross selling and uncovering other lines of business for othe

This is a part-time 12-hours per week, 12 week, unpaid remote internship.

Associate Director, Financial Control & FRB/OCC Regulatory Reporting.Lead the Federal Reserve Bank Regulatory Reporting & Financial Control function for the capital markets and wealth management branches, ensuring timely and accurate reporting while maintaining a robust control framework.Support gov

San Bruno, CA / Hoboken, NJ / Bentonville, AR.W2, Benefits and 401k matching.Hybrid position and you must reside in the following areas:.Hoboken, NJ / San Bruno, CA / Bentonville, AR.Our retail client's Seller Education team is seeking a skilled.In this role, you will not only edit and produce writt

Job description: The Financial Reporting Manager will play a key role in helping to enhance our oversight of the local operations and perform a variety of accounting, finance, and analytic.

Discuss and coordinate information requested from business representatives pertaining to the state of Enterprise's subsidiary businesses to determine necessary inclusion in SEC disclosure. Review other company documents, presentations and external communications to maintain consistency with SEC fili

The Team At Deloitte Tax LLP, our Global Information Reporting team provides expertise to clients to gain a competitive advantage by properly managing tax transparency regimes, enhancing their customer's experience and deploying effective technology to facilitate compliance with FATCA, CRS and other

In addition to reporting the group supports the client portfolio review meeting process, client ad-hoc requests related to portfolio information, and client questionnaires. Complete client reports, as well as data for client due diligence questionnaires and fund or portfolio level presentations, whi

Working with guidance from senior underwriters and leadership, this person will help evaluate risks, participate in portfolio management activities, and contribute to delivering strong service to brokers and clients. Partner with senior underwriters and leadership to support profitable growth of the

Automotive Customer Service Representative/Service Writer.At Midas we are dedicated to providing quality services to customer vehicles in the areas of inspection, diagnosis and repair utilizing the expertise attained through ASE Certifications and/or years of automotive repair experience.We are look

Compose compelling copy that speaks to business leaders and partners across LinkedIn, B2B site assets, industry-focused emails, whitepapers, and digital trade ads. Independently manage multiple projects—from rapid-response scripts to long-term content strategies—on varying timelines.

Remote applicants will be considered.

SAP Revenue Accounting And Reporting Consultant. SAP Revenue Accounting and Reporting (RAR) as well as Functional consultant. Deep understanding of RAR (Revenue Accounting & Reporting) module in SAP S/4 Understanding of peripheric integrations (CRM, Document management, Sales & Distribution, Logisti

As you develop, you will benefit from being led and mentored by nationally recognized tax professionals who include some of the firm's most senior tax talent. Financial Services - Customer Tax Operations and Reporting - Tax Senior. A minimum of 2 years of relevant tax consulting or tax operational e

Are you detail-oriented, organized, and ready to take the next step in your logistics career? Our client is looking for someone to join their team as a.Review and organize import files to ensure all information and documentation is accurate and complete.Communicate with Customer Service when additio

Underwriters are responsible for underwriting a complex book of business, employing the methods necessary to meet projected profitability, gross written premium, and expense goals, management and growth of the overall portfolio of business, implementing proper underwriting discipline/guidelines, mar

The Financial Analyst plays a key role in supporting financial operations, compliance, and strategic planning across the Americas division. Coordinate activities with the external financial Shared Service Center in Manila. This role requires the ability to deliver high-quality business insights whil

Helping the customers and businesses we serve to make better and smarter financial decisions and enabling the communities we support to grow and succeed. Reviews the accounting and financial statement information provided for audit and tax reviews, documentation and set-up of the accounting principl

The successful candidate combines strong quantitative capabilities with accounting and external-reporting proficiency, and thrives in a controls-driven, deadline-oriented environment.

Providing our US and Japanese Inbound clients with domestic federal tax advice and guidance tailored to their unique needs. Japanese Business Services (JBS) -Federal Tax Senior -Global Compliance and Reporting - NYC, Open.

The Accounting Implementation-Financial Reporting Specialist will partner with project leads to support the assessment, design, and implementation accounting for new business initiatives, ensuring Prudential's financial reporting remains best-in-class. Prudential welcomes all applicants, even if you

Are you a strategic and creative tax professional who would like to work on international tax regimes contributing to global tax transparency? Would you like to understand financial services and products across an array of industries (banking, asset management, hedge funds, insurance) and how comple

Entry Writer Customs Brokerage. We're seeking a highly experienced Entry Writer to join our import operations team.

Genesis10 is seeking a Regulatory Reporting Analyst for our financial services client in Jersey City, NJ. Summary: We are seeking a detail-oriented finance professional to support daily regulatory reporting and compliance activities.

Customs Entry Writer On-site | Springfield, NJ. Minimum of 2 years' experience in Customs Brokerage/Entry Writing. Manage the full lifecycle of Customs filings, including Release Applications and Entry Summaries.

Bachelor's degree in English or the Humanities with a minimum of five years of successful grant writing experience. Comprehensive mastery of best practices in grant writing. Neuropath Behavioral Healthcare is seeking an experienced RFP Grant Writer to manage all aspects of the RFP/RFI/RFQ response p