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Technical Writer 3
Govcio
Technical writer job in Trenton, NJ
Govcio are seeking a detail-oriented TechnicalWriter to join our team. The primary responsibility of this position is to create, maintain, and continuously improve our internal and external document libraries. This role serves as the bridge between complex technical concepts and clear, accurate, and user-friendly documentation. The ideal candidate has expert-level proficiency in Microsoft Office Products, including, but no limited to Word, Excel, PowerPoint and Visio, exceptional writing skills, and a strong understanding of software development methodologies and documentation standards.
**Responsibilities**
Responsibilities
+ Create, update, and maintain a comprehensive library of software documentation, including system design and requirements, user guides, internal process documents, API references, release notes, and technical specifications.
+ Collaborate closely with software engineers, product managers, architects, and QA teams to gather, understand, and accurately document technical requirements, designs, and implementation details.
+ Write clear, concise, and well-structured technical documents tailored to different audiences (developers, testers, stakeholders, end-users).
+ Ensure consistency, version control, and traceability across all documentation artifacts.
+ Apply best practices in technical writing, including the use of templates, style guides, and structured authoring techniques.
+ Format, edit, proofread, and finalize documents using advanced features of Microsoft Word (styles, templates, tables, headers/footers, track changes, references, TOC automation, etc.).
+ Manage document repositories, implement version control processes, and ensure documentation remains current throughout the software development lifecycle.
+ Participate in peer reviews, gather feedback, and continuously improve documentation quality and usability.
+ Assist in creating visual aids (diagrams, tables, flowcharts) to enhance understanding when appropriate.
**Qualifications**
Required Skills and Experience:
Clearance Required: Secret with eligibility to Acquire a Top-Secret clearance
+ Bachelor's with 5-8 years of experience
+ Proven experience (3+ years preferred) as a TechnicalWriter in a software development environment.
+ Expert-level proficiency in Microsoft Word, including advanced formatting, styles, templates, fields, macros, and document automation.
+ Strong working knowledge of other Microsoft Office tools (Excel, PowerPoint, Visio for diagrams).
+ Demonstrated ability to understand and document complex technical concepts and translate them into clear, audience-appropriate language.
+ Familiarity with software development lifecycle (SDLC) methodologies (Agile, Waterfall, Scrum, etc.).
+ Strong attention to detail, organizational skills, and ability to manage multiple documentation projects simultaneously.
+ Self-motivatedwith the ability to work independently and collaboratively in a fast-paced environment.
Preferred Skills and Experience:
Experience supporting **DCSA, DoD, or federal security agencies** .
+ Familiarity with **RPA tools and automation initiatives** .
+ Knowledge of federal and DoD documentation and compliance standards.
+ Experience with documentation tools such as Confluence and SharePoint- Knowledge of diagramming tools and screenshot/markup tools.- Understanding of version control systems (Git) and content management practices.- Previous experience writing for regulated industries or enterprise software.- Bachelor's degree in Technical Writing, Communications, Computer Science, Engineering, or related field.
\#NSS
\#DL
**Company Overview**
GovCIO is a team of transformers--people who are passionate about transforming government IT. Every day, we make a positive impact by delivering innovative IT services and solutions that improve how government agencies operate and serve our citizens.
But we can't do it alone. We need great people to help us do great things - for our customers, our culture, and our ability to attract other great people. We are changing the face of government IT and building a workforce that fuels this mission. Are you ready to be a transformer?
**What You Can Expect**
**Interview & Hiring Process**
If you are selected to move forward through the process, here's what you can expect:
+ During the Interview Process
+ Virtual video interview conducted via video with the hiring manager and/or team
+ Camera must be on
+ A valid photo ID must be presented during each interview
+ During the Hiring Process
+ Enhanced Biometrics ID verification screening
+ Background check, to include:
+ Criminal history (past 7 years)
+ Verification of your highest level of education
+ Verification of your employment history (past 7 years), based on information provided in your application
**Employee Perks**
At GovCIO, we consistently hear that meaningful work and a collaborative team environment are two of the top reasons our employees enjoy working here. In addition, our employees have access to a range of perks and benefits to support their personal and professional well-being, beyond the standard company offered health benefits, including:
+ Employee Assistance Program (EAP)
+ Corporate Discounts
+ Learning & Development platform, to include certification preparation content
+ Training, Education and Certification Assistance*
+ Referral Bonus Program
+ Internal Mobility Program
+ Pet Insurance
+ Flexible Work Environment
*Available to full-time employees
Our employees' unique talents and contributions are the driving force behind our success in supporting our customers, which ultimately fuels the success of our company. Join us and be a part of a culture that invests in its people and prioritizes continuous enhancement of the employee experience.
**We are an Equal Opportunity Employer.** All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, disability, or status as a protected veteran. EOE, including disability/vets.
**Posted Pay Range**
The posted pay range, if referenced, reflects the range expected for this position at the commencement of employment, however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, education, experience, and internal equity. The total compensation package for this position may also include other compensation elements, to be discussed during the hiring process. If hired, employee will be in an "at-will position" and the GovCIO reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, GovCIO or individual department/team performance, and market factors.
**Posted Salary Range**
USD $92,500.00 - USD $113,850.00 /Yr.
Submit a referral to this job (***********************************************************************************************************************
**Location** _US-Remote_
**ID** _2026-7387_
**Category** _Cyber Security & Intelligence_
**Position Type** _Full-Time_
$92.5k-113.9k yearly 9d ago
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Technical Writer III
Integrated Resources 4.5
Technical writer job in Raritan, NJ
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Qualifications:
Background: • BS or MS degree in arts or sciences
• 4+ years of technical writing experience
• Experience in change management
• Experience in medical, pharmaceutical, or other FDA regulated environment
• Understanding of CAPA and Quality process
• Strong knowledge of the English Language -- Knowledge of the structure and content of the English language including the meaning and spelling of words, rules of composition, and grammar.
• Knowledge of computer hardware and software, including Microsoft Office, Visio, Adobe Acrobat applications.
• Communicating effectively in writing as appropriate to the audience.
• Strong prioritization and multitasking skills. Managing one's own time and the time of others.
Responsibilities:
• Manage the documentation, change order, and change control processes
• Experience with computer based change management software. Write change plans, document change orders
• Maintain records and files of work and revisions
• Develop SOPs and associated technical documentation as required
• Interview and build relationships with SMEs in cross functional groups, including walking down a process to insure completeness and verify correctness
• Edit, standardize, or make changes to material prepared by SMEs or other Company personnel
• Manage new documentation and revised documentation through lifecycle and document management system
• Help with investigations, non-conformances and CAPA process
• Confer with customer representatives, vendors, regulatory personnel, or others to establish technical specifications
• Review established documentation and recommend revisions or changes in scope, format, and content
• Spend time with SMEs observing production, developmental, and experimental activities to determine operating procedure and detail.
• Develop specific goals and plans to prioritize, organize, and accomplish your work.
Additional Information
Regards,
Sweta Verma
IT Recruiter
Integrated Resources, Inc.
Inc. 5000 - 2007-2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
(Direct) 732 549 5907 | (W) 732 -549 - 2030 x 210| (F) (732) 549 5549
$55k-76k yearly est. 60d+ ago
Technical Writer
Mindlance 4.6
Technical writer job in Raritan, NJ
Mindlance is a national recruiting company which partners with many of the leading employers in the Life Sciences, IT, and Financial Services sectors, feel free to check us out at *************************
Job Description
JOB TITLE:- TechnicalWriter
LOCATION:- Raritan, NJ
DURATION:- 06+ MONTHS (with possible extension)
JOB OVERVIEW
As part of the Portfolio Management Office within the AS Operations and Continuous Process Improvement organization, the Content Manager will curate and write content and communications to support key AS PMO programs and initiatives. This includes but not limited to the AS Portfolio Playbook and AS Service Catalog. Additional content to author includes reference guides and knowledge articles for AS PMO processes and tools. This role will function as a member of AS Portfolio Management Office and will be based in Raritan, New Jersey.
Specific responsibilities include:
Lead the development of the AS Portfolio Playbook, which will educate AS employees regarding key AS Portfolio Processes. The AS Portfolio Playbook content will be developed and continually improved throughout 2016, and the candidate will lead development and refinement of content. This includes partnering with various Portfolio Managers and stakeholders to create the content.
Lead the development of content within the AS Service Catalog content, which enables AS customers to review examples of successful AS service engagements and read service descriptions. This includes partnering with various service owners to create customer-friendly content, and managing the drafting, review, and publication of the content in the catalog application.
In addition to writing content, partnering with Service Owners to create customer-friendly service descriptions may provide opportunities to influence the strategy and design of services.
The candidate will organize additional content and communications for the AS PMO. This includes the PMO Newsletter, Best Practice Documentation, and Process Reference Guides. The candidate will need to collaborate with team members and stakeholders to collect, organize, curate, and publish content.
Qualifications / Skill Requirements:
College degree in journalism, communications, or related discipline, or equivalent combination of education and experience required
Strong verbal communication and writing skills required
Ability to conduct independent research required
Excellent attention to detail and proofreading skills to ensure accurate, error-free work
High level of computer literacy and knowledge, including Microsoft Office products
Ability to work under pressure, meet deadlines, and take critiques as needed
Ability to understand the IT operational model and PMO processes of demand, financial, resource, benefit and service management.
Excellent oral communications and interpersonal skills
Prior experience with Pharmaceutical and Application Services preferred
Additional Information
Thanks & Regards,
Shipra Chauhan | Team Recruitment | *************
$56k-74k yearly est. 60d+ ago
Technical Writer-29088
OLSA Resources
Technical writer job in Princeton, NJ
This position is NonExempt. Hours over 40 will be paid at Time and a Half. Writes a variety of technical articles, reports, brochures, and/or manuals for documentation for a wide range of uses. May be responsible for coordinating the display of graphics and the production of the document. Familiar with variety of the field's concepts, practices and procedures. Relies on experience and judgment to plan and accomplish goals. May lead and direct the work of others. A wide degree of creativity and latitude is expected. May require a bachelor's degree or 4-6 years experience.
NOTES FROM MANAGER:
Technicalwriter to reformat our Risk Management Plan (RMP) documentation. Existing RMP documents are a critical part of the company's product definition. These documents need to be reformatted to include updated definitions and references. The senior technicalwriter should preferably have experience working with FDA - or other regulated industry - practices and ISO systems.
Qualifications
Required:
• Proficient in Microsoft Word: advanced editing, commenting, routing, formatting
• Proficient in Microsoft Excel: editing, formatting
Prior experience Technical Writing in the medical device industry needed with particular emphasis in writing SOPs and document changes.
Additional Information
America Networks is a leading sensor and networking solutions partner for companies in any Industrial, Manufacturing, and Waste management space. We design and manufacture sensors for storage tanks, water metering, energy metering, gas monitoring, and asset management.
Our founders are hardcore telecommunications engineers with combined 200 + years of experience in designing, optimizing and performance engineering; for several mid - large wireless carriers internationally - that saw a need to provide low power, cost efficient sensors to collect data, create alerts, and predict needed actions. We have combined these sensors with low power, wide area (LPWA) networking technologies to provide clients various options to decrease re-occurring costs associated with operating an IoT network of sensors and connected devices.
We specialize in design, deployment, optimization, and support of these Networks. Whether an off-the-shelf or custom solution is needed, we'll create a solution and push the data on the best cloud platform to fit your needs, including your own.
Job Description
Basking Ridge-NJ-USA
Client is seeking an experienced Web Content Creator/Copywriter to help create a best-in-class online identity for our corporate website. This position creates, coordinates and repurposes multimedia brand content (text, photography and video) across a variety of corporate sections. Working closely with the Web Content Strategist and Web Designer, this person will also help manage and execute a content projects
The Content Creator/copywriter must have experience in writing for websites, have knowledge of content management, possess strong organizational skills and demonstrate excellent verbal and written communications. A successful candidate will have strong qualities of diplomacy, problem solving and decisiveness, and be comfortable managing multiple duties in a high-visibility production environment.
Responsibilities:
• Write, edit and proofread corporate web content, including headlines, page titles, keywords and meta descriptions
• Ensure that all web content is timely, accurate and adheres to Client's voice and tone guidelines
• Working with our content agency, develop innovative approaches to corporate messaging and be a source of imaginative content ideas
• Help develop, document and maintain content management standards and procedures
• Participate in all meetings with business stakeholders to review content calendar and prioritize new projects
Qualifications:
• Minimum of 6 years of digital content creation; web writing experience is required. Experience with Corporate websites or a Journalism background is preferred but not required.
• Ability to write professional, relevant and engaging content
• Ability to proofread and edit copy, correcting grammatical, typographical or composition errors
• Familiarity with search engine optimization (SEO)
• Familiarity with content management systems (CMS) and how to prepare content for production.
• Ability to collaborate with a Web Designer and work with limited supervision
• Must have excellent verbal and written communications skills
• Solid understanding of web industry standards, best practices and trends
• Bachelor's degree in English, Marketing, journalism or related field
Additional Information
Vivek Salvatore
vivek.salvatore(@)americanetworks.com
(
*************
$56k-76k yearly est. 1d ago
Technical Writer
Wescorp 3.8
Technical writer job in Newtown, PA
Company Culture & Values
At WESCORP, we value people who show up ready to work hard and do things right. As a family-owned company since 1962, we take pride in building things that last - starting with our team. Our culture is built on trust, accountability, and mutual respect. We believe in putting in an honest day's work, supporting one another, and holding ourselves to high standards of quality and performance.
Whether you're working on the shop floor, in engineering, or supporting operations, you'll be part of a team that values reliability, craftsmanship, and a hands-on mindset. We're not looking for shortcuts - we're looking for people who take ownership, stay focused, and care about the work they do. If that sounds like you, you'll find a long-term home here.
Job Summary
The TechnicalWriter is responsible for preparing, maintaining, and organizing the documentation that supports our engineering and production processes. This includes maintaining travelers, work orders, and other paperwork associated with manufacturing orders. The TechnicalWriter will work closely with Engineering, Quality, and Production to translate complex technical content.
Key Responsibilities
Review technical specifications and flow down requirements into the work order traveler
Conduct research, including reading source material and meeting with subject matter experts
Organize and maintain documentation in accordance with the QMS
Work with engineering, quality, and production teams to gather needed information
Track revisions and ensure the most current versions of documents are available
Support audits and reviews by providing documentation as requested
Help standardize templates and formatting for consistency across documents
$46k-65k yearly est. 44d ago
IT Business Analyst
Zydus Pharmaceuticals USA 4.3
Technical writer job in Pennington, NJ
We are seeking an innovative and technically skilled IT Business Analyst with 5+ years of experience, preferably in pharmaceutical sales and distribution. The ideal candidate will possess expertise in SAP S/4HANA (SD, FI, MM, PP, QM modules) and Vistex Revenue Management in a business facing role, with a strong understanding of core business processes such as finance, supply chain, sales, and revenue management. This role requires a blend of business acumen and technical capability to analyze requirements, design solutions, and drive process improvements. The candidate will work closely with different teams to understand business needs, support data-driven decisions, and apply modern technologies such as AI, automation tools, and machine learning to improve processes and drive innovation.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Collaborate with business users to elicit, analyze, and document functional and non-functional requirements.
Identify and drive process improvement initiatives to optimize operational efficiency and ensure compliance with industry standards and best practices.
Perform data analysis to uncover actionable insights, identify root causes of issues, and detect trends that inform strategic decisions and continuous improvement.
Create and maintain key artifacts including process flows, data flows, system architecture diagrams, business cases, functional specifications, and other documentation to support solution design, implementation and stakeholder understanding.
Collaborate with technical teams to ensure proper configuration, integration, and optimization of solution.
Lead and support testing activities, including system validation and facilitation of User Acceptance Testing (UAT), ensuring solutions meet defined requirements and quality standards.
Assist in change control, deployment planning, and execution to ensure smooth transitions and minimal disruption to business operations.
Develop and manage project plans, timelines, and deliverables, ensuring successful execution of initiatives within scope, budget, and schedule.
Develop, maintain, and enhance dashboards and reports using tools such as Microsoft Fabric BI to support real-time business intelligence and performance monitoring.
Conduct user training sessions and create documentation to support the adoption and effective use of new technologies, systems, and processes.
KNOWLEDGE / SKILLS /COMPETENCY
Excellent verbal and written communication skills, with the ability to convey complex concepts clearly to both technical and non-technical audiences.
Exceptional organizational, prioritization, and time management skills, with the ability to manage competing priorities and adapt to changing business needs.
Analytical mindset with the ability to define and solve complex problems, even when faced with incomplete or ambiguous information.
Self-driven and proactive, with the ability to work independently and take ownership of tasks with minimal supervision.
High level of initiative and accountability, consistently driving tasks to completion and delivering results.
Requirements
EDUCATION/EXPERIENCE
Bachelor's degree in business administration, Information Systems, Data Analytics, or a related field.
5+ years of experience as a business analyst, preferably within the pharmaceutical sales and distribution industry. Industry-specific knowledge of the generic pharmaceutical sector is desirable.
Hands-on experience with SAP S/4HANA modules (SD, FI, MM, PP, QM) and Vistex Revenue Management is strongly preferred.
Experience working with pharmaceutical-specific processes such as Government Pricing, Medicaid, Chargebacks, Fees and Incentives or Gross-to-Net (GTN) calculations is desirable.
Knowledge of regulatory and compliance requirements in the pharmaceutical industry.
Other Preferred Skills and Experience:
Microsoft Fabric or similar platforms for data analytics, reporting, and business intelligence.
Salesforce Service Cloud for customer support operations.
Tracelink Serialization or similar for pharmaceutical product tracking and compliance.
Cloud platforms such as Microsoft Azure or Amazon Web Services (AWS).
Project management expertise, including certifications such as PMP or Agile, and hands-on experience with tools like Planview, JIRA, ALM, Microsoft Project, and Azure DevOps.
Cloud-based AI/ML platforms such as Azure AI, Google AI, or AWS ML.
Python, R, and SQL for data analysis, automation, and predictive modeling.
RPA platforms (e.g., UiPath, Automation Anywhere) and implementing automation solutions.
WORK ENVIRONMENT
The physical demands described here are representative of those that must be met by an individual to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job the individual is:
Frequently required to sit and/or stand, walk, talk and hear.
Constantly required to use hands and fingers to operate office machines and equipment.
Frequently required to reach with hands and arms.
Occasionally required to stoop, kneel and crouch.
Required to occasionally lift, carry, push, pull, or otherwise move objects.
Occasional travel required between various locations in US and some international travel.
The work environment characteristics described here are representative of those that an individual encounters while performing the essential functions of this job.
Zydus Pharmaceuticals (USA) provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Zydus is committed to providing reasonable accommodation to, among others, individuals with disabilities and disabled veterans. If you need an accommodation because of a disability to search and apply for a career opportunity with Zydus, please contact us and let us know the nature of your request.
Salary Description $140,000-$160,000
$140k-160k yearly 60d+ ago
Pharmaceutical Technical Writer
Prostaff Solutions 3.9
Technical writer job in New Brunswick, NJ
Are you looking to be a part of a growing pharmaceutical company? One of our largest clients is currently seeking a Pharmaceutical TechnicalWriter to join their New Brunswick, New Jersey 08901 team. Our client is one of the leading pharmaceutical companies specializing in developing and manufacturing solid dosage products. If you believe you are qualified, we would be excited to connect and discuss this opportunity in more detail.
Full-time Onsite
Direct Hire
Pay Rate: DoE
Job summary:
Perform investigation's and assist manufacturing and packaging operations on investigations, Product quality complaints. Assist in cross functional investigations for out of specification (OOS), out of trend (OOT), Laboratory Events, CAPAs, and change controls.
Areas of responsibility:
Ensure timely closure of all manufacturing/packaging and Quality Management System records.
Organize and participate in and reviews of cross functional investigation's
Represents Operations at cross-functional meetings.
Work with process owners and SMEs to implement agreed upon procedural documentation and to develop cross-functional process models
Collect input from stakeholders and consolidate comments for conflict resolution
Drive the improvement in established KPI's / metrics for manufacturing and packaging departments
Assist operations in responses to any internal audit, corporate audit, or regulatory audit observations involving manufacturing or packaging Control.
Travel Estimate: Up to 5%
Required Qualifications:
Associate degree in Life Sciences, Pharmacy, or equivalent required.
Minimum of three (3) years working in a pharmaceutical environment with at least two (2) years of experience within manufacturing area.
Demonstrated excellent communication: verbal, written and presentation skills.
A self-starter with a hands-on approach and a can-do attitude.
A team building champion driving innovative cross functional synergies.
Excellent project management and problem solving skills.
Excellent computer skills; MS Office (Word, Excel, PowerPoint), Track wise, EDMS, Outlook.
Knowledge of GDP, GMP, QA Documentation, QA Batch records, Quality Systems, Archiving, Retrieval, EDMS workflow, Document Life Cycle and Audit Compliance.
The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR).
Our client offers a competitive compensation package as well as an excellent benefits package for eligible candidates.
About ProStaff Workforce Solutions
We are a fast growing and successful agency that treats all its clients and candidates with a personal touch. ProStaff Workforce Solutions is a group of industry experts-many hailing from larger agencies-who know their business well and enjoy working in a more hands-on and flexible environment, with attention to detail. Our mission is to match quality people with quality jobs and quality companies to maximize productivity and profitability. We develop long-term relationships and provide a level of customer service and expertise that instill confidence and trust in our client companies and candidates.
Our Values
• Integrity
• Commitment
• Quality
• Diversity
Please visit us at https://www.prostaffworkforce.com/ to explore all opportunities.
#IND1
$49k-73k yearly est. 60d+ ago
Group Underwriting Senior Technical Writer
Guardian Life 4.4
Technical writer job in Holmdel, NJ
Take the next step in your career path and join a team that facilitates the efficient operation of our Group Underwriting organization. As the Group Underwriting Senior TechnicalWriter in Group Benefits Underwriting, you will collaborate with colleagues in Underwriting, Underwriting Operations, and other functional areas to ensure that our colleagues have all the information needed to perform. This requires being systematic in analyzing, developing, validating, and publishing information about processes, policies, and our systems. This role also requires an ongoing evaluation of the information management and communication approach and continuous improvement of our processes, based on input from our colleagues and industry best practices.
**You are:**
+ A team member who can manage multiple priorities, and who is passionate about logically organized and comprehensive information for our Group Underwriting colleagues.
+ Work together with teammates, content contributors, SMEs, leaders, and other interested parties on projects and to consistently improve our information management approach.
+ Skilled in documentation tools like Microsoft Word, SharePoint, and other web based knowledge management or online help systems; familiarity with policy administration systems is a plus.
+ Ability to interpret and document sophisticated underwriting processes, risk assessment criteria, and decision-making frameworks.
+ Comfortable working with underwriting teams, product managers, legal, and IT to gather source material and validate content.
+ Familiarity with regulatory standards and documentation practices in insurance.
**You have:**
+ Proficiency in writing and editing technical content related to complex business processes, preferably in regulated industries such as insurance or healthcare.
+ A 4-year college degree in English, Communications, Technical Writing, or a related field, or equivalent work experience.
+ Knowledge of Group insurance products and services (a plus).
+ Project management experience (a plus).
+ Familiarity with process improvement and process design (Lean Six Sigma).
+ Experience completing tasks in a disciplined manner and meeting deadlines.
+ Optional: Ability to develop training materials using instructional design principles.
**You will:**
+ Independently lead the development of reference information for complex projects to support the effectiveness and efficiency of our Group Underwriting organization. This information is commonly related to new products, policies, systems, tools, and processes.
+ Create Underwriting-specific content for our Information Management System (IMS).
+ Occasionally lead the weekly publication of the newsletter for all of Group Underwriting.
+ Lead the review process of existing Group Underwriting policies with team members.
+ Collaborate with the Information Management and Learning team to coordinate and work together on projects, and at times manage communications.
+ Collaborate with various areas including compliance, legal, and IT.
**Location:**
+ Preferred location is Guardian's Office in Bethlehem, PA. 3 days onsite Hybrid
**Salary Range:**
$67,450.00 - $110,815.00
The salary range reflected above is a good faith estimate of base pay for the primary location of the position. The salary for this position ultimately will be determined based on the education, experience, knowledge, and abilities of the successful candidate. In addition to salary, this role may also be eligible for annual, sales, or other incentive compensation.
**Our Promise**
At Guardian, you'll have the support and flexibility to achieve your professional and personal goals. Through skill-building, leadership development and philanthropic opportunities, we provide opportunities to build communities and grow your career, surrounded by diverse colleagues with high ethical standards.
**Inspire Well-Being**
As part of Guardian's Purpose - to inspire well-being - we are committed to offering contemporary, supportive, flexible, and inclusive benefits and resources to our colleagues. Explore our company benefits at *********************************************** . _Benefits apply to full-time eligible employees. Interns are not eligible for most Company benefits._
**Equal Employment Opportunity**
Guardian is an equal opportunity employer. All qualified applicants will be considered for employment without regard to age, race, color, creed, religion, sex, affectional or sexual orientation, national origin, ancestry, marital status, disability, military or veteran status, or any other classification protected by applicable law.
**Accommodations**
Guardian is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. Guardian also provides reasonable accommodations to qualified job applicants (and employees) to accommodate the individual's known limitations related to pregnancy, childbirth, or related medical conditions, unless doing so would create an undue hardship. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact applicant_accommodation@glic.com .
**Current Guardian Colleagues: Please apply through the internal Jobs Hub in Workday.**
Every day, Guardian helps our 29 million customers realize their dreams through a range of insurance and financial products and services. Our Purpose, to inspire well-being, guides our dedication to the colleagues, consumers, and communities we serve. We know that people count, and we go above and beyond to prepare them for the life they want to live, focusing on their overall well-being - mind, body, and wallet. As one of the largest mutual insurance companies, we put our customers first. Behind every bright future is a GuardianTM. Learn more about Guardian at guardianlife.com .
Visa Sponsorship:
Guardian Life is not currently or in the foreseeable future sponsoring employment visas. In order to be a successful applicant, you must be legally authorized to work in the United States, without the need for employer sponsorship.
$67.5k-110.8k yearly 60d+ ago
Technical Writer
Ventures Unlimited
Technical writer job in Hopewell, NJ
Ventures Unlimited is a service centric organization. Our success begins with our ability to apply our relationships, leverage technologies, and identify talent - often in combination - to an endless array of real-world customer needs
Job DescriptionTitle: TechnicalWriter
Location: Hopewell, NJ
Type: Fulltime// permanent
Interview Process: Phone and Skype Hire
Compensation: Base Salary + Benefits + Relocation expenses (if required)
Start Date: ASAP
Domain: Financial & banking
Description:
• The TechnicalWriter/Presentation Specialist will be a member of architecture team, helping to deliver technical solutions and strategies.
• Bachelor's degree, or equivalent work experience
• 5+ experience in creating presentation materials
• 5+ years technical writing experience
• Advanced PowerPoint skills
• Analytical Thinking
• Strong aptitude towards IT
• “Eye” for design and creativity
• Passion for learning new technology ideas/concepts
• Strong ability to lead and collaborate
• Advanced Excel skills
• Basic Visio skills
Responsibilities:
• Produce high quality PowerPoint presentations
• Translate ideas into easily digestible language/diagrams
• Able to grasp high level technical concepts, then translate to laymen
• Technical writing experience
• Collaboration with technical teams to gather ideas
• Creates many different types of documentation (IT strategies, Whitepapers, Technical diagrams)
• Work directly with Senior Execs.
• Sense of urgency, Well organized and routine updates.
Qualifications• Bachelor's degree, or equivalent work experience
• 5+ experience in creating presentation materials
• 5+ years technical writing experience
• Advanced PowerPoint skills
• Analytical Thinking
• Strong aptitude towards IT
Additional Information
Contact "Mohit Maurya" for more details at ************ Ext:141
$56k-76k yearly est. 60d+ ago
Senior Technical Writer
Buzzclan
Technical writer job in Franklin, NJ
Buzz Clan is a business consulting company collaborating to provide Oracle and other software advisory services & implementation Services specialists by our Public & Private sector clients. We have been catering to wide-ranging technologies and platforms and have consistently been delivering the best available talent to Fortune 500 clients across different industry verticals and public sector clients of North America.
I would like to discuss the opportunity with you. Please go through the job description and let me know if you are interested in applying for this position.
Additional Information
All your information will be kept confidential according to EEO guidelines.
$60k-80k yearly est. 60d+ ago
EHS Technology Business Analyst
DPR Construction 4.8
Technical writer job in Edison, NJ
The Business Analyst (BA) for EHS Technology acts as a critical link between DPR's EHS business function and technology and innovation (T&I). This role works closely with EHS, Data Engineering, Data Analytics, and other integrated workgroups to understand business processes, identify opportunities for improvement, and translate those needs into actionable system requirements.
The BA ensures that technology solutions implemented by DPR's Construction Technology team are grounded in real-world business and operational needs to deliver measurable value in efficiency, visibility, and integration across the enterprise.
Key Responsibilities
Discovery & Analysis
* Partner with teams to document current-state workflows, system touchpoints, and pain points across Environment, Health, and Safety processes.
* Conduct interviews, workshops, and process reviews to understand workflows, integrations, and reporting requirements.
* Identify and prioritize business requirements, translating them into clear functional and non-functional specifications.
* Quantify process gaps and potential impacts using data-driven analysis and benchmarking.
Solution Definition
* Co-develop future-state process maps, data models, and system designs with internal team.
* Translate business needs into user stories, use cases, or requirement documents for internal or external development teams.
* Support "build vs. buy" analysis and vendor evaluations by defining functional fit and value alignment.
* Participate in design sessions to ensure requirements are understood, feasible, and traceable through delivery.
Implementation Support
* Partner with Solution Architects and/or System Administrators to validate solution configurations against business requirements.
* Support user acceptance testing (UAT) by developing test cases, coordinating participants, and documenting results.
* Capture feedback from pilot implementations and contribute to iteration and improvement before full rollout.
* Assist in the development of training materials and user documentation for end users and super users.
Data & Insights
* Help define data structures and reporting needs that enable visibility into enterprise EHS data.
* Support the development of dashboards and KPIs in collaboration with System Administrators and BI teams.
* Ensure data integrity and alignment across systems during transitions or integrations.
Continuous Improvement
* Monitor performance and adoption of implemented solutions, identifying opportunities for refinement.
* Document lessons learned, process improvements, and reusable templates for future initiatives.
* Participate in DPR's Project Controls & Assurance Integrated Work Group (IWG) to share learnings and align priorities across initiatives.
Qualifications
* 5+ years of experience in similar roles, ideally with exposure to construction and Environmental, Health and Safety.
* Strong process analysis and documentation skills, including the ability to create process maps, swimlane diagrams, and data flow diagrams.
* Experience gathering and translating requirements for EHS, RMIS, ERP, CRM or similar systems.
* Familiarity with systems such as Power BI, Hammertech, Riskonnect, Autodesk Construction Cloud, CMiC, Workday, or comparable platforms.
* Excellent communication, facilitation, and analytical skills with the ability to translate between technical and operational audiences.
* Bachelor's degree in Business Administration, Information Systems, Data Analytics, Computer Science, or Communications preferred.
Success Criteria
* Clearly defined and prioritized business requirements that result in effective, scalable technology solutions.
* Accurate and up-to-date process documentation supporting continuous improvement.
* Strong alignment between business workflows and system functionality.
* Positive feedback from users on clarity, usability, and impact of deployed systems.
* Demonstrated contribution to measurable improvements in productivity, visibility, or data quality.
In compliance with local law, we are disclosing the compensation, or a range thereof, for roles in locations where legally required. Actual salaries will vary based on several factors, including but not limited to external market data, internal equity, location, skill set, experience, and/or performance. Salary is just one component of DPR's total compensation package. Pay Range: $75,000 to $125,000.
DPR Construction is a forward-thinking, self-performing general contractor specializing in technically complex and sustainable projects for the advanced technology, life sciences, healthcare, higher education and commercial markets. Founded in 1990, DPR is a great story of entrepreneurial success as a private, employee-owned company that has grown into a multi-billion-dollar family of companies with offices around the world.
Working at DPR, you'll have the chance to try new things, explore unique paths and shape your future. Here, we build opportunity together-by harnessing our talents, enabling curiosity and pursuing our collective ambition to make the best ideas happen. We are proud to be recognized as a great place to work by our talented teammates and leading news organizations like U.S. News and World Report, Forbes, Fast Company and Newsweek.
Explore our open opportunities at ********************
$75k-125k yearly Auto-Apply 21d ago
Medical Writer
Artech Information System 4.8
Technical writer job in Pennington, NJ
Artech Information System , a global staffing and IT consulting company. We are constantly on the lookout for professionals to fulfill the staffing needs of our clients and we currently have a job opening that may interest you.
Position: Medical Writer
Location: Pennington, New Jersey-08534
Duration: 6 Months
Job Description:
Scientific Writer for Aggregate Reports:
Coordinate and author documents needed for regulatory submissions (eg, CSRs, CTD summary documents, aggregate safety reports, risk management plans), ensuring the coordination and integration of the scientific, medical, and regulatory input from cross-functional team members.
Participate in relevant document sub team(s) and ensure effective planning and management of timelines for all components of assigned documents.
Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects.
Comply with internal and external processes and guidelines while managing the review process and, on an ongoing basis, resolve issues, errors, or inconsistencies with pertinent team members to ensure timely completion and high quality of assigned documents.
Review and edit documents as required.
Considerable experience in Assignment on Cross Functional Teams would be an advantage.
Qualifications:
PhD/MD/PharmD in a relevant scientific discipline or MS / BS with a minimum of 3 years (MS) to 5 years (BS) in pharmaceutical regulatory documentation, or equivalent, and good understanding of requirements for regulatory submission documents. In addition, (i) demonstrated strong writing skills as evidenced by good quality writing in pharmaceutical regulatory documentation and/or publications in peer-reviewed journals, (ii) good understanding of global pharmaceutical drug development and requirements for submission of regulatory dossiers to global health authorities, (iii) demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation and interpersonal skills in a cross-functional team, (iv) working knowledge of a document management system and basic knowledge of document publishing process, (v) analyzed and interpreted complex data from a broad range of scientific disciplines.Coordinate and author regulatory documents (e.g. phase I/II clinical study reports, Investigator's Brochure) ensuring the coordination and integration of the scientific, medical and regulatory input from development team members.2. When assigned as Lead Writer, ability to lead other writers, including developing strategies/ plans and managing projects, in order to complete multiple documents for regulatory submissions.3. Demonstrate mastery of complex writing assignments (e.g., Phase III CSRs, CSS, CSE, Background Packages, etc.) across therapeutic areas or multiple projects.4. Participate in relevant filing subteam(s) and ensure effective planning and management of timelines for all components of assigned documents.5. Lead or co-lead (with Doc Lead) teams to define content and data displays for CSR prototypes and shells. 6. Able to collaborate with project team to respond to health authority questions, requests, etc.7. Provide departmental management with adequate information to help assess resource needs.
Additional Information
All your information will be kept confidential according to EEO guidelines.
$79k-111k yearly est. 1d ago
Proposal Writer/Manager
Plurilock
Technical writer job in Branchburg, NJ
Proposal Writer / Manager
We are seeking an experienced Proposal Writer to lead and manage the development of high-quality responses to both federal government solicitations and commercial RFPs. The ideal candidate will combine strong writing skills with proven proposal management capabilities to help us win new business opportunities.
Key Responsibilities:
Overall Proposal Response Coordination
· Manage the end-to-end proposal development process for US federal procurements and commercial RFPs
· Develop proposal schedules and coordinate with contributors to meet strict submission deadlines, including draft reviews, leadership reviews, and final white-glove reviews
· Coordinate production of final deliverables and ensure timely proposal submission
Proposal Writing
· Lead proposal strategy sessions and develop win themes tailored to each opportunity
· Write, edit, and coordinate compelling proposal narratives that address the evaluation criteria client will use to review our proposals
· Ensure compliance with solicitation requirements, as specified in the RFP/RFQ documents
· Support oral presentation preparation and other proposal-related activities as needed
· Develop and maintain proposal templates, content libraries, and lessons learned documentation
Required Qualifications
· Bachelor's degree
· Excellent writing, editing, and communication skills
· Prior experience as a Proposal Manager responding to US federal government procurements and/or commercial RFPs
· Strong understanding of federal procurement processes and proposal evaluation criteria
· Strong organizational skills and attention to detail, with ability to manage multiple proposals simultaneously under tight deadlines
· Proficiency with Microsoft Office Suite, specifically Word and PowerPoint
Preferred Qualifications
· Experience working at a consulting firm
· Experience with proposal automation tools
$59k-90k yearly est. 60d+ ago
Grant Writer
Easterseals New Jersey 4.4
Technical writer job in Jamesburg, NJ
Grant Writer - Jamesburg, NJ (Hybrid) Shift: Full-Time, Monday - Friday, 8:30 AM - 4:30 PM About Us: Operating in 21 counties throughout the state, Easterseals New Jersey offers various disability and mental health services to help people with various needs address life's challenges. Annually, Easterseals New Jersey serves over 4,000 individuals at our over 100 sites with direct services, advocacy, and education. We believe everyone, no matter their circumstance or level of ability, deserves the opportunity to increase their independence and achieve their goals. Focusing on ability over disability, our family of over 1,000 well-trained and passionate staff members works in partnership with individuals and families to bring equality, dignity, and opportunity.
What You'll Do:
The Grant Writer will focus on grant writing, revenue growth, and strategic collaboration by securing funding, managing grants, and identifying new revenue streams. They will work with internal teams to align funding priorities, develop proposals, and drive innovative partnerships.
Key responsibilities include:
Research and identify potential public and private grant opportunities aligned with Easterseals NJ's mission and program needs.
Write, prepare, and submit compelling grant proposals, ensuring accuracy, completeness, and alignment with funder guidelines.
Manage the full grant lifecycle, including proposal development, submission, follow-up, and reporting.
Assist in identifying alternative revenue streams to expand Easterseals NJ's programs and services, including partnerships with corporate sponsors, community organizations, and other stakeholders.
Research market trends, community needs, and competitor activities to identify opportunities for expansion and innovation.
Assist in drafting business plans, program proposals, and financial projections for new initiatives.
Work closely with program directors, finance, and marketing teams to ensure alignment of funding priorities with Easterseals NJ's overall mission and strategic goals.
Who You Are:
Education: Bachelor's degree in business, communications, nonprofit management, or related field (Master's preferred).
Experience: 3-5 years of experience in grant writing, fundraising, or business development, with expertise in proposal development for social services, health, or disability sectors, and proficiency in data analysis tools to evaluate program outcomes and grant effectiveness.
Requirements: Proven track record in securing grants and building successful business partnerships, along with expertise in government regulations and compliance for disability services and nonprofit funding.
Skills: Exceptional written and verbal communication skills for crafting persuasive grant proposals and presentations, along with strong project management and organizational abilities to handle multiple projects and deadlines efficiently.
What We Offer:
Competitive Pay & Benefits - Including Medical, Dental, Vision, and Flexible Spending Accounts
Employer-Paid Coverage - Life, AD&D, and Long-Term Disability Insurance
Retirement Savings - 403(b) Plan with Employer Match
Generous Time Off - Paid Time Off, Holidays, Medical Leave, and PTO Buy-Back options
Convenience & Support - Direct Deposit, Payroll Cards, Mileage Reimbursement, and Employee Assistance Program
Wellness & Recognition - Wellness Program, Referral Bonuses, and a Recognition Program
Training & Development - Paid Orientation and Ongoing Training
Easterseals NJ provides a comprehensive benefits package. For full details, visit ********************
Easterseals Is An Equal Opportunity Employer
As one of our core values, we strive to provide equal opportunity to all of our employees without regard to their age, gender, religion, race, color, national origin, marital status, sexual orientation, or disability which is unrelated to the ability to perform essential job functions, unfavorable military discharge (except dishonorable), veteran status, marital status, parental status, genetic information, source of income or other legally protected categories in accordance with applicable law with regard to receipt of services, appointment or election to voluntary office or hiring for, assignment to, or promotion in staff positions.
$37k-44k yearly est. 13d ago
Medical Writer I
Lancesoft 4.5
Technical writer job in Raritan, NJ
The applicant will write Product Risk Assessment documents for Pharmaceutical Products and require specific experience in Risk assessments of combination products and/or medical devices. The applicant should have experience using risk management methodologies, tools, incorporate appropriate data and information, and conduct risk calculations. The applicant must understand pharmaceutical and/or device manufacturing processes, design controls, and be able to lead and conduct FMEAs. Specific experience with user/design/process FMEAs for medical devices is desirable. A minimum of Five (5) years experience is required. The applicant should be proficient in Microsoft Word, Excel, Visio, Microsoft Project and have experience with documentation systems. The applicant must have experience in leading and facilitating teams to finalize reports with approvals per standard operating procedures.
The incumbent will work with medical, technical, manufacturing, and quality groups to develop Product Risk Assessments by conducting risk analysis for pharmaceutical products. Job Responsibilities include:
• Collate appropriate and pre-populating the document based on product information, patient/user information, and other supporting documents.
(the incumbent should have the ability to search these documents, understand the process and extract required information)
• Ensure proper formatting, proof read, and route for approval in documentation system.
• Maintain and update project status in Microsoft Project, excel.
Key Decisions:
• Participates in decisions and provides input and prepares product risk management reports regarding the adequacy, accuracy, interpretation, and clarity, and final decisions made by the project team.
• Consults with appropriate groups (as required) regarding the acceptability of documentation
Key Competencies:
Project Management
Organization and Time Management
Communication (Verbal, Written, and Interpersonal)
Qualifications
Education/Experience Requirements:
• Bachelor's degree in Chemistry, Pharmacy or a related science field plus 4-6 years of relevant experience industrial experience in the healthcare industry
• OR MS/PhD/Pharm.D. plus 3-4 years of pharmaceutical industrial experience
• Minimum of 1-2 years of technical writing experience for manufacturing related activities is mandatory
• Experience working in the Pharmaceutical manufacturing industry (preferably in Technical Services, Operations, manufacturing plant or Research & Development or QA, knowledge of pharmaceutical development processes, cGMPs and regulatory requirements are required.
• Excellent English, writing and oral presentation skills is mandatory
• Prior experience with Pharmaceutical Industry is mandatory
• Prior experience managing projects is preferred
Additional Information
Job Description:
Write technical materials, such as SOP's, appendices
Duties and Responsibilities:
• Organize material and complete writing assignment according to set standards regarding order, clarity, conciseness, style, and terminology.
• Maintain records and files of work and revisions
• Edit, standardize, or make changes to material prepared by other writers or establishment personnel
• 2+ years experience as a TechnicalWriter
• 2+ years primary role writing user documentation for a variety of products, prepared as part of an integrated team
• Proofing/preparation of documentation
$82k-112k yearly est. 1d ago
Technical Writer
Integrated Resources 4.5
Technical writer job in Somerville, NJ
Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.
Job Description
The TechnicalWriter/Analyst Medical Affairs, Business Process & Operations will support the file standardization for a new controlled document management system.
S/He gathers documents, compiles information, and maintains records for creation of Medical Affairs internal documents. Reviews documents for accuracy and elevates issues to supervisor.
This person will participate in change management activities relating to harmonizing Medical Operations processes across the Medical Device (MD) operating companies.
This person will collaborate with Medical Affairs associates to help ensure that Medical Affairs' documents align with the global cross-functional strategy.
The candidate will be an experienced professional with a focus on creating forms, templates, data entry and organizing files in structured folders and SharePoint sites.
This candidate shall also have experience creating training guides and Work Instructions.
This person shall possess strong editorial skills including a good understanding of medical terminology and scientific publication bibliographic material.
The successful candidate will contribute to dictionary of terms for understanding the hierarchy of products, disease states and specialties to build the smart search tools.
This requires an understanding of medical terminology and evaluating synonymous keywords. This person shall support the Medical Affairs SharePoint team site creation and maintenance.
This includes creating and assigning User Groups and Permissions, SharePoint Lists and Libraries. S/He will support medical operations cross-functionally within a matrix organization of medical device companies
Qualifications
A Bachelor's Degree with 6+ years of related medical/ healthcare industry experience is required.
Experience with MS Office applications (Word, SharePoint Online/2013, Outlook, Excel) is required.
Ability to synthesize and understand search terms to create dictionary lists.
Demonstrated knowledge and experience with medical terminology and medical device products in regulatory compliance or healthcare compliance is preferred.
Strong typing and MS Office365 and SharePoint skills are required. Previous experience managing short deadlines, working with colleagues in different time zones and countries is required.
The ability to work with people in a matrixed organization is highly preferred. This position will be located in Somerville, NJ and will require 0% travel.
Additional Information
Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.
Thank you.
Kind Regards,
Harris Kaushik
Clinical Recruiter
Integrated Resources
, Inc.
IT Life Sciences Allied Healthcare CRO
DIRECT # - (650)-399-0891
Gold Seal JCAHO Certified ™
for Health Care Staffing
“INC
5
0
0
0
's
FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)
$55k-76k yearly est. 1d ago
Technical Writer - II
Amnet Services
Technical writer job in Bernards, NJ
America Networks is a leading sensor and networking solutions partner for companies in any Industrial, Manufacturing, and Waste management space. We design and manufacture sensors for storage tanks, water metering, energy metering, gas monitoring, and asset management.
Our founders are hardcore telecommunications engineers with combined 200 + years of experience in designing, optimizing and performance engineering; for several mid - large wireless carriers internationally - that saw a need to provide low power, cost efficient sensors to collect data, create alerts, and predict needed actions. We have combined these sensors with low power, wide area (LPWA) networking technologies to provide clients various options to decrease re-occurring costs associated with operating an IoT network of sensors and connected devices.
We specialize in design, deployment, optimization, and support of these Networks. Whether an off-the-shelf or custom solution is needed, we'll create a solution and push the data on the best cloud platform to fit your needs, including your own.
Job Description
Basking Ridge-NJ-USA
Client seeks textual content specialist to help improve customer-facing wording on mobile devices, instructional materials, apps, marketing websites etc. The job involves: understanding users and tasks; generating and reviewing compelling, precise and high quality textual content; working with developers and project teams as they write text for applications and devices.
We are looking for a full-time contractor for this position on-site in Basking Ridge, NJ.
Responsibilities:
Write clear, concise, consistent and compelling UI content for interactive products and services
Collaborate with other writers, UX designers and product managers
Analyze and develop a deep understanding of product flows and logic in order to create accurate and pleasing textual content.
Review and edit content created by others to interpret, clarify and improve it to create better experiences for our customers.
Solicit and integrate team feedback.
Desired Skills & Experience:
· Thorough command of written English and familiarity with common style guides (AP, Chicago, etc.)
· Experience writing user interface text (instructions, error messages, etc.) for applications aimed at a general, non-technical audience
· Experience writing compelling, customer-focused content for websites and other marketing materials
· Ability to identify techie, confusing language and translate it into clear, user-friendly English
· Excellent written and spoken communication skills
· Experience designing and writing text for mobile devices including smartphones and tablets a plus
· Experience working with corporate language and branding guidelines a plus
· Usability experience a plus
Additional Information
Vivek Salvatore
vivek.salvatore(@)americanetworks.com
(
*************
$56k-76k yearly est. 1d ago
Medical Writer
Artech Information System 4.8
Technical writer job in Peapack and Gladstone, NJ
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
• Create documents pertaining to clinical data to support product development, license application, and post-marketing maintenance, on behalf of and in conjunction with corresponding project teams. Some examples of such documents include briefing documents to support meetings with regulatory agencies, clinical documents for marketing authorization (new drug) applications (Clinical Overviews and ICH module 2.7 clinical summaries), and responses to clinical and safety questions from regulatory authorities.
• Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission. Provide project teams with expertise and strategic guidance on analysis and presentation of clinical and safety data and on benefit-risk assessment in documents.
• Assess document requirements, gauge document complexity, and identify information gaps or other potential issues. In collaboration with the relevant project team, the author proposes or contributes to strategies to resolve any identified issues.
• Lead a team of internal or external (contractor) authors if multiple or complex documents are required for a particular project.
• Support clinical teams by providing analyses of clinical data, reviews of the medical literature, and similar related activities.
Responsibilities
• Communicate clinical's position on resource and timeline needs for assigned documents to project team members, negotiating as needed with the team on these matters and keeping line management informed.
• Ensure assigned documents are produced in accordance with relevant internal SOPs and external regulatory guidance, alerting project teams and line management in a timely manner of any definite or potential deviations.
• Drive the document strategies and messages in a collaborative way with relevant project team subject matter experts. Ensure clear, factual, effective, and appropriately concise presentation of analyses and associated discussions in assigned documents.
• Deliver assigned documents on or before deadline, alerting project teams and line management in a timely manner of any anticipated delays, information gaps or potential shortcomings in quality.
• If leading a team of other authors (internal or external), be accountable for timely delivery of high-quality, fit-for-purpose documents to the project team.
• Produce documents in conjunction with external vendors. Review documents produced by vendors and help evaluate vendor performance.
•Collaborate with quality lines and relevant project team subject matter experts, ensuring the accuracy and quality of information presented in assigned documents.
• Develop and sustain constructive relationships within other Pharmaceutical lines including country organizations.
• If assigned by manager, serve as the clinical 'point of contact' for all document issues for a given product or set of products.
• Identify potential areas for process improvements and possible solutions, and communicate these to line management or appropriate functional line.
Position Comments visible to MSP and Supplier:
Additional Skills:Technical Skills:
• Writing skills. Excellent scientific writing skills, including an ability to summarize and interpret complicated data effectively, concisely and persuasively.
• Analytic skills. Ability to examine data, formulate reasonable hypotheses, and design and execute analyses to test them.
• Oral presentation skills. Strong oral presentation skills, including ability to present, explain and defend data analyses before internal and external (including Regulatory Authority) audiences
• Language skills. High fluency in written English and strong functional fluency in spoken English. Knowledge of additional languages is an asset.
• Personal skills. Strong organizational skills and ability to prioritize multiple projects and meet deadlines.
• Interpersonal skills. Effective influencing and negotiating skills, including when appropriate an ability to guide decision-making for document content strategy. Ability to work well with all levels and roles in cross-functional, global teams. Ability to mentor more junior colleagues and external vendors.
• Regulatory knowledge. Familiarity with global regulatory guidance (especially ICH, FDA and EMA) relevant to clinical and safety data.
• Software. Previous experience with software commonly used to present and analyze data (Word, PowerPoint, Excel) is preferred.
• Statistics. Proficiency with statistical concepts
Additional Information
Regards,
Anuj Mehta
************
$79k-111k yearly est. 60d+ ago
Technical Writers
Integrated Resources 4.5
Technical writer job in Somerville, NJ
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
TechnicalWriters is the frequent open position in Johnson & Johnson. Please share below the details and your updated resume with us so that I would be able to submit you first compare to other candidates in order to get the in -personal interview request from the company.
I would like to mention that Johnson & Johnson has fastest interview process, as per our multiple year of experience, they moves very fast with the in - personal and offer. We have placed so many candidates, those we have submitted in an hours when the position comes in.
Take some smart step and get the job in one of the leading healthcare company - Johnson & Johnson.
Please provide the below details
Total Experience -
Expected Rate -
Current Rate -
Visa Status -
DOB( Just Date and month is require for submission purpose ) -
Available for in person -
Available to Join -
Location -
Work Status -
Qualification-
In considering candidates, time is of essence so please respond ASAP.
Additional Information
Contact- Tel: (732) 549 2030 x 210
Sweta Verma
How much does a technical writer earn in West Windsor, NJ?
The average technical writer in West Windsor, NJ earns between $49,000 and $88,000 annually. This compares to the national average technical writer range of $48,000 to $87,000.
Average technical writer salary in West Windsor, NJ
$65,000
What are the biggest employers of Technical Writers in West Windsor, NJ?
The biggest employers of Technical Writers in West Windsor, NJ are: