This Technical Writer role focuses on reviewing and developing technical documentation and supporting engineering, purchasing, and sales teams throughout the quotation and order process. You will compare customer specifications, bills of materials, and engineering designs for accuracy, perform technical evaluations of supplier quotations, and help prepare cost estimates. The position requires strong technical writing skills, the ability to interpret blueprints and specifications, and close coll…

Catalent's Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs.…

Albuquerque, NM Full time 8865 Worker Type Regular Job Description Summary AV's Directed Energy division is seeking a Technical Writer/Editor to develop clear, accurate, and compliant documentation for technical and non-technical audiences. This role translates complex technical information into well-structured deliverables, including test plans, technical manuals, assessment reports, and other customer documentation. The successful candidate will work independently and collaboratively with eng…

Date Posted: 2026-10-15 Country: United States of America Location: US-NC-WILSON-4200 ~ 4200 Airport Dr ~ BLDG 4200 Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance Type: None/Not Required Security Clearance Status: Not Required RTX, the world's largest aerospace and defense company, 185,000 great minds are united by pu…

$30-$33 per hour Fairport, NY Contract Duration: 06 months with possible extension Responsibilities: Documentation Creation: Develop and improve work instructions, standard operating procedures, troubleshooting guides, and job aids. Collaboration: Work closely with subject matter experts, engineers, and operations gather information and ensure accuracy in documentation. Research: Investigate and analyze technical information from various sources to create comprehensive documentation that mee…

Description Draft, edit, review, and maintain IT Procurement Documents that will support the acquisition of professional services, products purchased, infrastructure, and system implementations. Requirements for documents will be provided by IT Leadership, project managers, and subject-matter experts. Preparation of clear accurate, and compliant Statements of Work (SOWs), Scopes of Work, Request for Proposals (RFPs), Request for Information (RFIs), Request for Quotation (RFQs), Service -Level A…

Quality Control Investigation Writer Category: Quality Assurance / Quality Control (QA/QC) Industry: Pharmaceutical / Biotechnology Location: High Point, NC Pay Rate: $34- $36 Hourly Position Summary We are seeking an experienced Quality Control (QC) Investigation Writer to lead, author, and coordinate laboratory investigations in a GMP-regulated pharmaceutical manufacturing environment. This role is responsible for developing scientifically sound, thorough, and compliant investigation reports …

It all started when engineer Fred Luddy wrote code that automated a tedious task for his coworker, Phyllis. She cried tears of joy. That moment inspired Fred to build a company that could do that for everyone-freeing people from busywork so they could focus on meaningful work. Today, ServiceNow is the AI control tower for business reinvention. Our ServiceNow AI platform brings together any AI, any data, and any workflow- helping 85% of the Fortune 500® work smarter, faster, and better. We're bu…

Job Description Skills and Requirements We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, natio…

Job Title: Engineering – Technical Writer Location: North Haven, CT | Lafayette, CO | Mounds View, MN Duration: 12 months Job Summary We are seeking an experienced Technical Writer to develop, update, and manage medical device labeling and Instructions for Use (IFUs). The ideal candidate will have strong technical writing skills, experience with authoring tools, and knowledge of regulated medical device environments and quality processes. Key Responsibilities Develop, review, and update medical…

Job Title: Senior Technical Writer Location: Hoboken, NJ, 07030 Duration: 5 Months Job Type: Temporary Assignment Work Type: Remote Pay Rate: $61.37-$61.37/HR Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Job Description: ROLE SUMMARY The User Assistance team for Higher Ed creates user-focused, data-informed, accessible, web- and mobile-based content to help students and educat…

Position Summary The Technical Writer serves as a bridge between customers, product management, and software engineering. This position is responsible for documenting product requirements, creating customer-facing documentation, and supporting product delivery from concept through implementation. This role works closely with stakeholders, development, QA, support, and product teams to translate product and technical information into documentation and requirements materials that help internal an…

SUMMARY/OBJECTIVE: The Technical Writer is responsible for leading Quality Management System (QMS) documentation activities within Operations. This role will partner closely with Manufacturing, Packaging, Warehouse, Facilities, and Quality Assurance teams to draft, revise, route, and maintain controlled documentation in support of compliant GMP operations. This position serves as a key liaison between Operations and Quality Assurance. The role requires strong technical writing skills, attention…

SUMMARY/OBJECTIVE: The Technical Writer, Analytical is responsible for supporting and coordinating Quality Management System (QMS) documentation activities for the laboratory and Analytical functions. This role will partner closely with laboratory personnel and Quality Assurance to draft, revise, route, and maintain compliant GMP laboratory documentation supporting analytical testing and development activities. This individual will serve as a key liaison between Analytical R&D and Quality Assur…

The ideal candidate will be responsible for creating and writing various types of user documentation, including how-to guides, manuals, references, or instructions. This candidate should have strong communication skills which enable them to explain complicated concepts in a simple manner. This individual will also meet with customer representatives frequently in order to understand required content. ⚠️ Direct applicants only. No C2C, agencies, or third-party vendor submissions. Must Have: Activ…

Job Title: Quality Control Investigation Writer Location: High Point, NC 27265 Duration: 12 Months - Contract Pay Rate: $20.00 - $36.00/hr w2 Position Summary: The Quality Control (QC) Investigation Writer is responsible for leading, authoring, and coordinating laboratory investigations within the Quality Control department in support of GMP-regulated pharmaceutical manufacturing operations. This role serves as a subject matter expert in the investigation process and is responsible for ensuring…

Onsite in New haven, CT (4 days onsite weekly) 1 year contract Responsibilities may include the following and other duties may be assigned. • Plan, research, develop, and write medical device labeling, and manage labeling deliverables as part of cross-functional project teams under general supervision. • Simultaneously manage up to two labeling updates and one small, new-product-introduction project that involves multiple labeling pieces. • Understand and adhere to all quality management system…

Job Description Job Description Onsite: Travel: 0% Join the Maverick Power Team! At Maverick Power, we don’t just build power distribution solutions—we redefine industry standards. Recognized on the 2025 Inc. 5000 list as 16 in the U.S., 2 in Manufacturing, and 1 in Texas, we are committed to driving innovation, quality, and speed. With multiple manufacturing facilities across North Texas and Phoenix, we are expanding rapidly and looking for top talent to grow with us If you are ready to be par…

Overview Working across the globe, V2X builds smart solutions designed to integrate physical and digital infrastructure from base to battlefield. We bring 120 years of successful mission support to improve security, streamline logistics, and enhance readiness. Aligned around a shared purpose, our $3.9B company and 16,000 people work alongside our clients, here and abroad, to tackle their most complex challenges with integrity, respect, responsibility, and professionalism. V2X is seeking a Techn…

Adecco Healthcare and Life Science is hiring for a Technical Writer in Plainville, MA. Apply today if you meet the qualifications listed below! Location: Plainville, MA Duration: 12 month contract Schedule: 7:30am - 4:00pm Pay rate: $45-50/hour Job Summary: The RSO, Technical Writer II is an associate with a minimal level of expertise and experience with general biopharmaceutical manufacturing equipment, principles and processes and has a good understanding of current GMP and safety standards t…