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Job Description Job Summary: We are seeking a highly skilled Principal Regulatory Medical Writer to lead and contribute to key regulatory documentation efforts. The ideal candidate will have 4-8 years of experience in regulatory medical writing and a strong background in drafting essential regulatory documents, including Investigator’s Brochures (IBs), briefing books, responses to regulatory inquiries, and clinical study reports (CSRs). Additionally, this role will be responsible for leading contract medical writers, ensuring consistency, quality, and alignment with AMA and regulatory requirements. Responsibilities: • Author and edit high-quality regulatory documents, including IBs, briefing books, CSRs, and responses to regulatory authorities., • Lead and mentor contract medical writers, providing guidance, oversight, and quality assurance in regulatory document development., • Ensure regulatory compliance by following industry standards, guidelines, and best practices., • Collaborate cross-functionally with clinical, regulatory, and scientific teams to ensure clarity and accuracy in submissions., • Manage timelines and oversee document preparation schedules to meet regulatory submission deadlines., • Implement strategic input provided by the regulatory team to ensure alignment with strategy within and across content of documents., • Review and QC documents for consistency, scientific accuracy, and regulatory alignment. Qualifications: • Bachelor’s degree in life sciences (a higher degree such as Master’s, Ph.D., or PharmD is preferred)., • 4-8 years of experience in regulatory and/or clinical medical writing within the pharmaceutical or biotech industry., • Strong leadership skills with prior experience leading medical writers., • Deep knowledge of AMA style guide requirements., • Excellent writing and editing skills with the ability to convey complex scientific information clearly and concisely., • Detail-oriented with strong organizational skills to manage multiple projects simultaneously., • Proficiency in Microsoft Word and other document management tools (StartingPoint templates, Veeva RIM, etc)., • Expertise in writing and managing complex regulatory submission documents for clinical development programs., • Strong understanding of medical terminology and clinical trial methodology. This role is ideal for an experienced regulatory medical writer looking to take on leadership responsibilities while driving key regulatory submissions. The above statements are intended to describe the general nature and level of the work being performed by colleagues assigned to this position. This is not intended to be an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary. As part of Aquestive’s employment process, final candidate will be required to complete a drug test and background check prior to employment commencing. Please Note: Aquestive is a drug-free workplace and has a drug free workplace policy in place. Aquestive provides equal employment opportunities to all colleagues 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. The Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education. Expected Base salary range: $96,000 to $150,000 USD

83415 **Please only local candidates to New Brunswick NJ **MUST have Cell Therapy or Biologics experience TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading pharmaceutical company is hiring a Technical Writer for a 12+ months contracting assignment. Must have skills: • Bachelor’s degree in Biology or related discipline with a minimum of 2 years’ experience, • Minimum of 2 year of experience in Technical Writing specifically for Regulatory CMC documentation within the pharmaceutical or biotechnology industry, • Familiarity with eCTD structure for regulatory submissions, • Proficiency in commonly used Microsoft Office applications (Word, Excel, SharePoint, PPT) is required Pay: $43-44/hour W2 Location: New Brunswick NJ Responsibilities: • Will be responsible for delivering CMC documentation (dossier and supporting documents) to support the regulatory strategy from early stage through registrational application, • This role requires effective collaboration across technical functions to deliver on timelines for submissions, • The position interfaces with experts in Process Development, Analytical Development, Cell Therapy Technical Ops, Quality and Regulatory Sciences, • Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports, • Plan and facilitate submission kick-off for clinical regulatory submissions across CTD pipeline assets, • Manage the logistical process and detailed timeline for regulatory submissions, • Partner with SMEs to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy

Job Description The Business Development Associate Director is responsible for leading the growth of revenues of IEEE's IP and non-IP related products and services. This will include identifying, capturing and maintaining >$20mil in revenues from licensing, governmental capacity building, training, conformity assessment, registries, grants and other opportunities worldwide. The incumbent will use strategic perspectives and possess a demonstrated track record of monetization across North America, EMEA, Latin America, and Asia Pacific. This role will be responsible for building a team of regional sales staff, contractors, and distributors to meet the financial goals. They will also be a change agent that can work across the organization to institute best practices and be mission-oriented. The incumbent will represent IEEE and grow IEEE revenues of the aforementioned products to both existing customers and new prospects globally, and have a strong personal brand with a deep understanding of both customers and industry peers for a global standards developing organization. The Business Development Associate Director will be highly attuned to cultural differences and be an effective communicator who can interact with all levels of customer leadership, global regulatory agencies, competitors, and internal company executives. This role reports to the Senior Director, Product, Business Development and Marketing and will perform with minimal supervision. This position will have no direct reports at this time. Key Responsibilities • Lead business development activities within IEEE standards Association with a keen focus on diversified monetization opportunities, • Identify new contacts at global regulatory authorities that span across North America, Latin America, Europe, Asia Pacific, and Middle East, • Manage new business prospecting by working to expand the reach of IEEE’s non-legacy products via an annual pre-defined list of new business targets, leads generated by IEEE’s lead generation programs, or own prospecting efforts., • Build a team of sales staff that can adequately support and take potential customers through a seamless buying experience, • Devise a sales and marketing strategy to increase sales to prospect regions and organizations., • Develop and maintain a business development plan that may be strategic to regions across a collective of all of IEEE SA’s product offerings, • Manage and oversee all opportunities utilizing Salesforce and other CRM. Periodically provide reports to senior management., • Engage customers to identify and shape their critical needs and deliver proposals that address them. This will require clear communications and actionable intelligence being shared back to the line of business and functional staff., • Manage key business relationships: Work with Fortune 500 companies, strategic mid-size companies, and small organizations to promote use of IEEE non-IP related products., • Foster relationships with engineering and R&D management at client and prospect organizations to raise the awareness and profile of the IEEE. Understand each account’s problems, needs and people., • Collaborate with the product Managers and partner organizations to address their needs to ensure a high level of customer satisfaction., • Travel for customer visits, to attend industry tradeshows and conferences, and to provide onboarding or training to new clients. Frequent overnight travel will be required due to territory size., • Manage front line customer service issues, and route advanced service problems and complaints from customers to the appropriate department within IEEE in a timely fashion and stay involved with ongoing issue resolution., • Assist in Marketing Efforts:, • Identify and develop new product and service opportunities with product marketing and product management organizations, • Test potential product offerings with customer base for feasibility, • Design marketing campaigns for target markets, • Training/Knowledge Advancement:, • Establish and maintain product knowledge - stay on top of product enhancements/changes and incorporate these features/benefits into sales presentations., • Administrative:, • Manage weekly reporting by submitting descriptive and actionable sales reports and updating CRM system daily., • Forecasting – Submit accurate sales pipeline forecast via SFDC monthly and keep total expenses up to date. Responsible for personal Travel Expense budget - Reconcile business expenses on a monthly basis at minimum. Travel Information • 50-75% Domestic and International Education • Bachelor's degree or equivalent experience Business, Finance, Engineering or related field Req, • 4-7 years Business experience Req, • 4-7 years Direct sales experience selling high ticket items to global regulatory bodies, Engineering, IT, Intellectual Property or R&D groups. Req, • 4-7 years Experience in the Engineering or training, testing, inspection and certification industry Pref, • 4-7 years Experience managing accounts, working with high level procurement groups and managing complex negotiations for Enterprise-wide contracts vs. transactional selling. Req, • 2-4 years Comfortable working with C-level executives, regulators and policy makers. Req, • Strong skills in communication, project management and time management required, • Must be technologically savvy knowledge worker who seeks out technology solutions to business challenges, • Specific technology knowledge and experience needed to produce desired outcomes include: PC skills particularly with Microsoft Word, PowerPoint, Excel, CRM software, • Excellent presentation skills to audiences of up to 100 people. Territory reviews (in person) at least once per year to the Sales and Marketing department and managers is required., • Must possess strong written communication skills in order to prepare reports, sales quotations, recommendations and requests for action that may be addressed to the IEEE Board, Senior Volunteers and Staff Leadership. Excellent writer able to convey key messages concisely, able to draw recipient / reader into action., • Business fluency in other languages will be looked upon favorably since some of the new business leads are international is preferred., • Must understand the standards and intellectual property market-places and competitive landscape and any opportunities or threats facing our organization. Must be able to effectively convey our value proposition and know how our products differ from others in its class. PLEASE NOTE: This position is not budgeted for employer-sponsored immigration support, this includes all persons in F (both CPT and OPT), J, H, L, or O status. For information on work demands and conditions required for this position, please consult the reference document, ADA Requirements. This position is classified under Category II – Mobile Positions. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Disclaimer: This job description is proprietary to IEEE. It outlines the general nature and key features performed by various positions that share the same job classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties and qualifications required of all employees assigned to the job. Nothing in this job description restricts management’s right to assign or re-assign duties to this job at any time due to reasonable accommodations or other business reasons. Company DescriptionAdvancing Technology for Humanity IEEE and its members inspire a global community through highly-cited publications, conferences, technology standards, and professional and educational activities.Advancing Technology for Humanity\r\nIEEE and its members inspire a global community through highly-cited publications, conferences, technology standards, and professional and educational activities.

Job Description Technical Order Writer Reports to: Client Engineering Manager FLSA Status: Exempt About CompoSecure Founded in 2000, CompoSecure (Nasdaq: CMPO) is a technology partner to market leaders, fintechs and consumers enabling trust for millions of people around the globe. The company combines elegance, simplicity, and security to deliver exceptional experiences and peace of mind in the physical and digital world. CompoSecure's innovative payment card technology and metal cards with Arculus security and authentication capabilities deliver unique, premium branded experiences, enable people to access and use their financial and digital assets, and ensure trust at the point of a transaction. For more information, please visit and . Position Overview: The Technical Order Writer I is an entry-level responsible for assisting in the creation and release of Engineering Masters and Work Orders. These documents guide the planning and processing of orders for the Supply Chain and Prototype Team. The role involves documenting operation steps, instructions, and material needs, while working closely with various departments to ensure accuracy and consistency. Key Responsibilities: Documentation • Help create and distribute Finished Goods Parts documentation., • Attend team meetings to understand special processing or material needs., • Use Visual software to assist in creating and reviewing Engineering Masters and Work Orders., • Support the release of documentation to Supply Chain, Prototype Team, Engineering Teams, and Quality Control., • Record and implement standard practices and updates., • Understand and support Part ID creation., • Assist in reviewing and applying changes to Engineering Masters and Work Orders based on Engineering Change Notices (ECNs) or email instructions., • Help distribute updated documents to relevant teams., • Develop/Follow documentation process to make updates., • Follow company policies and safety procedures., • Manage basic email communications related to documentation., • Conform to department best practices., • Create/Attend Meetings as necessary., • Associate's degree (bachelor's degree preferred)., • 0–2 years of experience in a technical writing or manufacturing support role., • Familiarity with Visual Database systems is a plus., • Experience in a manufacturing environment is a plus., • Basic proficiency in Microsoft Office Suite., • Familiarity with Workflow software is a plus., • Strong written and verbal communication skills., • Detail-oriented with a willingness to learn and self-review work., • Ability to manage time and prioritize tasks effectively., • Enthusiastic attitude, cooperative team player, adaptable to a highly dynamic environment, professional demeanor, sensitive to client needs, self-motivated, creative and innovative., • Capable of working in an office setting for extended periods., • Frequent use of computer, phone, and office equipment., • Must be able to lift 20 lbs;, • Must be able to sustain office work for 8+ hours per day including:, • Sitting in an office chair or walking through the shop, • Typing, and sight for computer use., • Reaching for the telephone, hearing for phone use, • Office environment is of moderate noise level. CompoSecure is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, or national origin. We are also an equal opportunity employer of individuals with disabilities and protected veterans.

Job Description Automotive service writer with experience in ordering parts, customer service and scheduling. Competitive wages, medical, 401K and vacation

Job Description SOKOL GxP Services is hiring a Technical Writer – CMC Regulatory Submissions to support our client’s team in New Brunswick, NJ. This hybrid role will be part of the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). As a key contributor, you will be responsible for preparing CMC documentation, including dossiers and supporting materials, that shape the regulatory strategy for the Cell Therapy clinical portfolio — spanning from early-stage development through registrational filings. This role offers the opportunity to collaborate closely with subject matter experts across Process Development, Analytical Development, Technical Operations, Quality, and Regulatory Sciences, ensuring high-quality, timely submissions that advance transformative therapies to patients. Key responsibilities include: • Author and co-author CMC content for CTD Quality sections, ensuring alignment with regulatory strategy and scientific accuracy., • Plan and lead submission kick-offs, managing detailed timelines, deliverables, and cross-functional collaboration., • Coordinate and track submissions, including responses to Health Authority questions, data verification, and final dossier preparation., • Partner with subject matter experts (SMEs) across CTDO to identify source documents, align on timelines, and deliver approved technical content., • Ensure consistency, clarity, and accuracy of messaging across all CMC documentation., • Review and reconcile comments with SMEs, manage revisions, and facilitate efficient comment resolution., • Provide oversight for eCTD Modules 2.3 and 3, ensuring compliance with formatting, structure, and regulatory requirements., • Collaborate with external partners as needed to review and finalize CTD content., • Drive process improvements and contribute to best practices in regulatory writing and document management. Bachelor’s degree in Biology or a related discipline; advanced degree preferred. Minimum 2 years of experience in biotech or pharma, with a focus on end-to-end product development. Strong knowledge of regulatory requirements and guidance for CMC documentation; cell therapy CMC experience required. Familiarity with eCTD structure and BLA submissions strongly preferred. Exceptional scientific writing and editing skills with strong attention to detail. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, SharePoint); experience with document preparation tools and compliance-ready standards. Excellent planning, organizational, and communication skills, with the ability to manage multiple priorities in a fast-paced environment. Proven ability to work independently while thriving in cross-functional team settings. Benefits Competitive hourly rate: $34 – $44/hr (W-2 only, no C2C) Hybrid schedule (50% onsite Tu – Thu; full onsite during the first month) 12-month contract with possible extension Health benefits, holiday pay, and 401(k) program Paid time off (PTO) and professional development support Employee referral bonus program Opportunity to contribute to high-impact projects with a leading biopharma company

Job Description Job Description: * The Technical Writer will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). * This individual will be responsible for delivering CMC documentation (dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application. * This role requires effective collaboration across technical functions to deliver on timelines for submissions. * The position interfaces with experts in Process Development, Analytical Development, Cell Therapy Technical Ops, Quality and Regulatory Sciences across CTDO. * Will work effectively in cross-functional project teams to accomplish company goals. * Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and responses to health authority questions based on high quality technical reports. * Plan and facilitate submission kick-off for clinical regulatory submissions across CTD pipeline assets. * Manage the logistical process and detailed timeline for regulatory submissions. * Partner with SMEs across CTDO to identify source documents and align delivery of approved technical documents in accordance to project timelines and aligned with CTD requirements and regulatory strategy. * Provide input and scientific oversight for content generation for Module 2.3 and 3. * Must possess a thorough understanding of the source documentation requirements needed for regulatory submissions and the correlation to the authoring process. * Review and adjudicate comments in collaboration with technical SMEs, facilitate comment resolution, revise draft sections. * Ensures content clarity/ consistency in messaging across dossier. * Facilitate and manage the data verification process. * Assist with dossier creation and system compliance for regulatory submissions * Coordinate response authoring, review and data verification to queries from HA for submissions. * Track upcoming submissions and ongoing submission progress * Maintain submission content tracker for regulatory submissions and work with doc specialist/PM/ Reg CMC to update tracker. * Represent Tech Writing and Document management in cross-functional CMC teams as required. * Collaborate and coordinate with CMC matrix team leaders to ensure timely submissions. * Collaborate with external suppliers as needed for CTD content and review. * Support and implement continuous process improvement ideas and initiatives. * Train others on procedures, systems access and best practices as appropriate. * Mentor and train employees on the document management process * Work independently under supervision and collaborate with other teams. Qualifications: * Required Bachelor's degree in Biology or related discipline with a minimum of 2 years' experience * PhD accepted * Familiarity and understanding of regulatory requirements and guidance pertaining to CMC documentation is preferred; Cell therapy CMC experience required. * Familiarity with eCTD structure for regulatory submissions is required; BLA experience is strongly preferred. * Outstanding verbal and writing communication skills, strong attention to detail, planning, organizational and negotiating skills, demonstrated ability for timely delivery. * Proficiency in commonly used Microsoft Office applications (Word, Excel, SharePoint, PPT) is required. * Experience with computer-assisted document preparation tools is preferred along with proficiency in compliance ready standards for final publication. * Experience in bio tech/pharma e2e product development required. * Must be capable of working in a fast-paced changing team environment, prioritizing multiple tasks to meet filing deadlines. * Take ownership of the section - formatting, language check, connections to other sections / tables. * Works independently under supervision and collaborates with other team members from scientific functions, project management, document management in cell therapy. * Minimum of 2 year of experience in Technical Writing specifically for Regulatory CMC documentation within the pharmaceutical or biotechnology industry Benefits: Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st. Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification. Synectics is an equal opportunity employer.

High standards for writing, detail, editing, and information design that lead to accurate, concise, usable, highly-polished content. BA/BS in English, Technical Writing, or related field; or equivalent work experience. Minimum 3 to 5 years of Technical Writing, content management, process improvemen

As a Midas Service Writer, you will manage and direct all automotive and general service technicians in the operation of the shop, including:. The Midas Service Writer is responsible for operations and performance (safety, efficiencies, etc. In addition, the Service Writer owns overall operations in

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

Order product (via iPad Tablet) for shelf and display to ensure in stock conditions. Full Time Nabisco Merchandiser/Order Writer. Join our team of Full Time Nabisco Merchandiser/Order Writers and fulfill the merchandising needs of our customers through communication & relationship building, stocking

The successful candidate will work effectively in cross-functional project teams to accomplish company goals. Experience with computer-assisted document preparation tools is preferred along with proficiency in compliance ready standards for final publication. Must be capable of working in a fast-pac

Regulatory Affairs Specialist – Technical Writing. Represent Tech Writing and Document management in cross‑functional CMC teams as required. Outstanding verbal and writing communication skills, strong attention to detail, planning, organizational and negotiating skills, demonstrated ability for

Excellent technical writing skills and proficiency with Microsoft Word formatting functions; ability to efficiently create technically accurate documents for system lifecycle deliverables in alignment with the site validation program; highly attentive to spelling, grammar, punctuation, and overall d

Collaborates with internal and external teams for content ideas; and assists content creation team members or freelance writers with outlines, suggestions, copy editing, and other general support. Exceptional writing, editing, and proofreading skills with an eye for detail.

Job Title: Pharma Technical Writer Location: New Brunswick, NJ Hours/Schedule: Mon-Friday (normal business hours) Compensation: $34.Type: Contract Overview Leading pharmaceutical company looking for an experienced Technical Writer.Ideal candidates should have at least 2 years of experience specifica

Minimum 5 years of experience in technical writing, with 3 years of technical writing experience in the pharmaceutical industry. The Technical Writing Specialist supports the successful implementation of laboratory equipment and systems at multi-use sites through interaction with internal customers

Work Schedule: Mon-Friday (normal business hours) Duration: 12 months (high possibility of extension for the right candidate depending on performance or budget) The Technical Writer will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Po

Location: New Brunswick, NJ - 50% Remote role.Duration: 12 Months+ (Possibility of Extension).The Technical Writer will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO).This individual will be responsible

The Technical Writer will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). Sunrise offers ACA-compliant medical coverage/dental insurance/vision insurance to all employees.

Excellent technical writing skills and proficiency with Microsoft Word formatting functions; ability to efficiently create technically accurate documents for system lifecycle deliverables in alignment with the site validation program; highly attentive to spelling, grammar, punctuation, and overall d

Required Qualifications*** Degree or degree level (Translation, writing, studies in English and French), or a combination of relevant experience in fields of interest;* Bilingualism in English and French;* Strong analytical skills;* Ability to negotiate on timelines;* Effective at building relations

Innova Solutions has a client that is immediately hiring for a Regulatory- Technical writer. As a Regulatory- Technical writer you will:. Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy for clinical and life-cycle CMC regulatory submissions and respon

Implement strategic input provided by the regulatory team to ensure alignment with strategy within and across content of documents.

Our client, a leading pharmaceutical company is hiring a Technical Writer for a 12+ months contracting assignment.

Our client, a leading pharmaceutical company is hiring a Technical Writer for a 12+ months contracting assignment.

Our client, a leading pharmaceutical company is hiring a Technical Writer for a 12+ months contracting assignment.

Service Advisor / Dispatcher – $18–$24/hr + Full Benefits Location: Mine Hill, NJ Company: Nationwide Truck Repair Center, Inc.Job Type: Full-Time | In-Person Nationwide Truck Repair Center, Inc.We’re currently seeking a Service Advisor / Dispatcher to join our dedicated team.If you thrive in

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

Location: Dallas, TX or Jersey City, NJ or Tampa, FL (NO REMOTE 2 days per week in the office).The candidate should have a technical background and be able to write documentation for the development community.Develops and maintains user and technical documentation and project process documentation.U

About The Role: As a UX Writer, you will be a key contributor within the Client Experience Design group of the Experience & Design team, responsible for crafting clear, intuitive, and engaging copy that guides KeyBank's consumers through our digital banking experiences.

Technical Writer/ Process Engineer. Technical Writer/ Process Engineer.

Technical Content Writer - Buffalo, NY. As a Technical Content Writer at Odoo, you'll create accurate, engaging technical content across User Documentation, Product Tours, eLearning Tutorials, Microcontent, and Whitepapers. You'll become a product expert, manage documentation through GitHub, write s

Research, write, edit and proofread complex technical data.Create, maintain and update manuals, procedures, specifications and other documents.Create, maintain and update installation instructions, training material and other technical documents.Design and establish style guidelines and standards fo

Staff UX Writer and Content Designer, Trust, Core. Senior Copy Writer/ Associate Creative Director. We are seeking a senior level Technical Writer that will be responsible for planning, writing, editing, and verifying high-quality technical documents.

Associate Director, Writer (Branded Content). Technical Writer [Must Have ISO 13485] - REMOTE. Technical Writer (Instructional Designer & SAAS)-US.

You are an experienced technical writer with at least 5 years of relevant experience developing documentation with a developer or SRE audience, including SDK documentation.

Our client, a top-tier management consulting firm, has partnered with a leading Financial Services provider to hire a Financial Technical Writer.

CGS Federal (Contact Government Services) is seeking an experienced Senior Technical Writer to provide consultative, analytical, and documentation support for a large Federal agency initiative.

Baseten powers inference for the worlds most dynamic AI companies, like OpenEvidence, Clay, Mirage, Gamma, Sourcegraph, Writer, Abridge, Bland, and Zed. Were looking for a Documentation Engineer / Technical Writer who will own our documentation strategy and execution, and treat it like a true pr

We are seeking a Solicitation/Specifications Writer to collaborate with programs to develop solicitations, facilitate the Request for Proposal process, and subsequent scope development for awarded contracts. Solicitation/Specifications Writer.

An exceptional writer and communicator with an instinctive appreciation for tone and structure; your colleagues have told you that they enjoy reading your work (and maybe you've even won awards).

We are actively recruiting an experienced Senior Specification Writer to join our Technical Design Services team in our Dallas office location.

I can succeed as a Senior Writer - Investments & Analytics at Capital Group. As a Senior Writer, you will join our broader Marketing team as part of the Investments and Analytics organization to produce creative, customized content for key audiences. You are a highly experienced financial/investment

At Ripple, we're building a world where value moves like information does today.It's big, it's bold, and we're already doing it.Through our crypto solutions for financial institutions, businesses, governments and developers, we are improving the global financial system and creating greater economic

E/E & Semiconductor Engineer - Technical writer. E/E & Semiconductor Engineer - Technical writer.

We are seeking a skilled Technical Writer to join our IT department. Technical Writer, preferably within an IT department or creating content for internal audiences.

We are seeking a Grant Writer who will be responsible for expanding the portfolio and revenue generation of both foundation donor partners for Autism Speaks (private, public, corporate foundations) and U.