Technical writer jobs in Milford, NH - 186 jobs

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team. Bristol Myers Squibb Cell Therapy Manufacturing is seeking a Specialist, Technical Documentation, Cell Therapy Manufacturing who can bring enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be goal-oriented, flexible, and able to work collaboratively with safety and quality in mind. We are searching for passionate and innovative individuals with a strong understanding of current good manufacturing practices to support the creation, revision, and approval of all procedures and related documentation for Cell Therapy operations. BMS Values Our values move us toward our mission to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. Candidates must exemplify the BMS values of Passion, Integrity, Inclusion, Accountability, Innovation, and Urgency: Passion Demonstrate dedication to quality and accuracy in documentation, understanding the critical role these play in advancing patient care Engage with team members and SMEs to support shared goals with enthusiasm and commitment Urgency Performs functions following all SOPs and compliance standards. Supports manufacturing in meeting deadlines for documentation updates. Innovation Support process improvement initiatives, identifying opportunities to improve GMP documentation and close compliance gaps Able to propose new ideas or methods to streamline document creation and compliance. Accountability Take responsibility for assigned tasks from initiation to completion, consistently meeting deadlines and quality standards. Own documentation workflows and associated quality actions and drive to completion. Integrity Exhibit attention to detail by ensuring documentation is accurate and adheres to regulatory guidelines, internal policies, and ethical standards. Maintain compliance through diligent adherence to established procedures, escalating concerns when necessary. Inclusion Collaborates cross-functionally and contributes to a culture of inclusion and diversity. Shifts Available: Monday - Friday, 8am - 4pm Responsibilities: Author and revise Standard Operating Procedures (SOP), and associated documentation for cell therapy manufacturing in accordance with Current Good Manufacturing Practices (cGMP's). Work closely with department SME's to align on procedural updates, tech transfers, and ensure proper reviewers/approvers on all documentation Accountable for ensuring quality and regulatory compliance of Manufacturing GMP documentation. Work as a liaison between manufacturing, Quality Operations and relevant Management systems. Assist with Tech Transfer activities. Communicate to all functional area managers and supervisors Quality-related initiatives and actions. Must have the ability to challenge and make recommendations. Escalate compliance concerns to management in a timely manner. Review and approve change controls as the manufacturing representative. Communicate with team, support resources, and management regarding issue identification and resolution. Develop solid understanding of quality and documentation systems (BMSDocs and Infinity) Identify, manage, and own quality actions as required. Develop solid understanding of Cell Therapy Manufacturing processes. Tracks deliverables and manages timelines effectively. Supports internal/external audits, taking urgent action to support requests. Assist with team metrics, identifying improvements & ensuring prompt action is taken. Obtain access to and develop solid understanding of various electronic systems utilized by Manufacturing (MES, SAP, ValGenesis, DeltaV, Maximo etc.). Minimum Requirements: Education: A Bachelor's Degree in a related field is preferred. A combination of education and relevant experience may be considered in lieu of degree. Experience: 3+ years in a Biotechnology/Pharmaceutical Manufacturing Operations or Support role. Knowledge of cGMP and manufacturing production is preferred. Experience authoring cGMP documentation and Cell Therapy manufacturing experience is preferred. BMSCART #LI-ONSITE GPS_2025 If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: Devens - MA - US: $35.50 - $43.02per hour The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit ************************************* Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: Health Coverage: Medical, pharmacy, dental, and vision care. Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. *Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to **************************. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: ********************************************* Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at ***************************************** Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at ********************. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley. R1597692 : Specialist, Technical Documentation, Cell Therapy Manufacturing in Devens, MA

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Qualifications Software Skills MS Excel Intermediate Yes 2 - 4 Years Software Skills MS Word Intermediate Yes 2-4 YEARS Requirements: Intermediate MS Excel and MS Word. GMP data verification experience; experience working with documentatum system for controlled document workflow management; working experience with Laboratory Information Management System (LIMS) desired. Technical Writer/Data Verifier ?Author technical report summarizing production, laboratory, validation activities and associated data ?Collate and compile data report, data sheet, and/or database from paper-based and electronic sources ?Provide independent verification of data accuracy on report and database ?Execute and coordinate necessary documentum workflow activities for the authoring, review, and approval of documents Additional Information $45/hr 3 months

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 BRD organization within the Pharm Sci BTx organization needs to hire a technical writer. This colleague will perform the following activities: (1) Assist with verification of data within regulatory documents or reports. (2) Support the bioprocess R&D (BRD) teams in tracking document completion, data verification strategies and completion of edits. (3) Create drafts of new technical or regulatory documents using existing examples, templates or reports (4) Assist Bioprocess team authors in assembling, formatting, and proofreading figures, tables and content. (5) Prepare documents using Regulatory templates in Microsoft Word and Predict and work within GDMS document management system. Skills 1) Excellent oral and written communications with experience in technical writing of reports and/or regulatory documents 2) Regulatory, GMP or Pharmaceutical experience, preferably in bioprocess or cell line development areas is desirable detail oriented 3) Additional soft skills include - able to work independently, strong interpersonal skills, able to multi-task, team player 4) Advanced use of MS Office Background/Experience 1) Scientific Background; BS or higher Biology, Chemistry, Biochemistry, Molecular Biology, Engineering, or similar 2) 3 - 5 years' experience 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)

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity. To find out more about Real Staffing Group please visit http://www.RealStaffingGroup.com Job Description • Author technical report summarizing production, laboratory, validation activities and associated data • Collate and compile data report, data sheet, and/or database from paper-based and electronic sources • Provide independent verification of data accuracy on report and database • Execute and coordinate necessary documentum workflow activities for the authoring, review, and approval of documents Qualifications - Intermediate MS Excel and MS Word - GMP data verification experience - Experience working with documentatum system for controlled document workflow management - Working experience with Laboratory Information Management System (LIMS) desire Additional Information All your information will be kept confidential according to EEO guidelines.

Job Description: · Job Title: Technical Writer\- Marketing Communication Specialist · Location: Can sit in Boston MA or Andover MA · Contract Terms: 6 month contract with possible extension · Schedule: M\-F 8\-5 PM EST hybrid 2 days onsite · Top 3 Skills Needed: · 1.) Copy Editing\- this professional will be managing 1000's of Marketing Brochures\/ Marketing Collateral Material, they will need to provide grammar, spelling checks, and ensure materials are synchronized with Branding. · 2.) Template Implementation: They will be creating guidelines to ensure documents and future marketing material is consistent and aligned with a central branding\/ look\/feel , and will need to manipulate PPT's , Word docs etc. · 3.) Organization Skills\- this professional will be responsible for updating the SharePoint site with said brochures, documents, and PPT material, responsible for clear messaging across the company, they will need to organize the content and upload accordingly for Client accessibility for Sales Reps to access. · Technical Writer \/ Marketing Communications Specialist · Client's Cybersecurity Solutions Team is seeking a versatile Technical Writer or Marketing Communications Specialist to work with Product Management in the creation, publication, and maintenance of marketing collateral. Key Responsibilities · Content editing · Review, correct, and update product and promotional materials to ensure clarity, proper construction, and appropriate language. · Document formatting · Implementation of company branding rules, application of corporate templates when required, organization of how content is displayed, and graphic treatments to improve appeal. · Document consistency · Governance to ensure consistency across documents that support multiple different products. · Publication management · Maintenance of SharePoint site used to publish contents internally, administration of internal social media account to disseminate information within client. · Content management · Maintain an ordered repository of content to be reused. Qualifications The ideal candidate must have experience or show proficiency in the following aspects: · Copy editing of marketing collateral such as brochures, data sheets, and presentations. · Editing of technical documentation such as product briefs, white papers, SOPs, user guides. · Creation and maintenance of SharePoint Communication sites, or similar. · Interaction with technical teams and SMEs distributed in multiple countries. · Organizing of work request from multiple sources, and proper maintenance of document library. Other skills that would be valuable, but not required, include: · Web publishing. · Animation and video generation. Familiarity with technical topics related to Cybersecurity, Operational Technology (OT) and Information Technology (IT), industrial automation, product development. Requirements · Top 3 Skills Needed: · 1.) Copy Editing\- this professional will be managing 1000's of Marketing Brochures\/ Marketing Collateral Material, they will need to provide grammar, spelling checks, and ensure materials are synchronized with Branding. · 2.) Template Implementation: They will be creating guidelines to ensure documents and future marketing material is consistent and aligned with a central branding\/ look\/feel , and will need to manipulate PPT's , Word docs etc. · 3.) Organization Skills\- this professional will be responsible for updating the SharePoint site with said brochures, documents, and PPT material, responsible for clear messaging across the company, they will need to organize the content and upload accordingly for Client accessibility for Sales Reps to access. · Technical Writer \/ Marketing Communications Specialist Client's Cybersecurity Solutions Team is seeking a versatile Technical Writer or Marketing Communications Specialist to work with Product Management in the creation, publication, and maintenance of marketing collateral. "}}],"is Mobile":false,"iframe":"true","job Type":"Contract","apply Name":"Apply Now","zsoid":"650037088","FontFamily":"Verdana, Geneva, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"IT Services"},{"field Label":"Work Experience","uitype":2,"value":"5+ years"},{"field Label":"City","uitype":1,"value":"Andover"},{"field Label":"State\/Province","uitype":1,"value":"Massachusetts"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"01810"}],"header Name":"Technical Writer","widget Id":"**********00072311","is JobBoard":"false","user Id":"**********00176003","attach Arr":[],"custom Template":"3","is CandidateLoginEnabled":true,"job Id":"**********10467015","FontSize":"12","google IndexUrl":"https:\/\/performixbiz.zohorecruit.com\/recruit\/ViewJob.na?digest=XOy61irGcubSAdEVKNPghM5nFKo@UUGlwQOWk3MajO0\-&embedsource=Google","location":"Andover","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"76zgi95be612420ed4dc9a71d04ccf008a9c2"}

About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities, equipment, and processes meet regulatory standards, enabling the safe and efficient production of pharmaceuticals. cGMP Consulting is based in Lake Forest, IL. This position will be located in Worcester, MA. Position Summary cGMP Consulting, Inc. is seeking technical writers who would support engineers of all experience levels to provide technical support/ documentation to Engineering and Validation teams with a focus on change management and SOP updates for a variety of on-going projects in the pharmaceutical industry. Knowledge and application of the CFR's and cGMP's is preferred. The ideal candidate for this job is resourceful, independent, organized, and capable of working in a fast-paced environment. Assuring a steady and accurate completion of the workload on time is key to success in this position. Responsibilities Author and revise SOPs, Work Instructions, and controlled documents to ensure clarity, compliance, and alignment with current Good Manufacturing Practices (cGMP), regulatory requirements (e.g., 21 CFR Part 11, EU Annex 11), and internal quality standards. Translate change control records into clear procedural updates by collaborating with QA, Validation, Manufacturing, and Engineering to interpret change requests and accurately reflect them in controlled documentation. Manage document lifecycle in electronic document management systems (EDMS) such as Veeva Vault, MasterControl, or Documentum, ensuring version control and audit readiness. Participate in cross-functional change control meetings, including Change Control Board (CCB) or Quality Review Board (QRB) sessions, to gather context, clarify scope, and align on documentation impacts. Conduct impact assessments for procedural changes, evaluating how proposed changes affect existing SOPs, training materials, and regulatory filings, and identifying required updates. Ensure traceability and compliance in documentation updates by maintaining clear linkage between change control records, risk assessments (e.g., PFMEA), and revised documents. Support training deployment for revised procedures by collaborating with Learning & Development to ensure timely training assignment and completion tracking for impacted personnel. Standardize documentation practices across departments, promoting consistency in formatting, terminology, and structure in line with internal style guides and regulatory expectations. Prepare documentation for internal audits and regulatory inspections, and respond to document-related queries and CAPAs to support audit readiness. Drive continuous improvement in documentation processes by identifying inefficiencies in SOP workflows and proposing enhancements to improve clarity, usability, and compliance. Requirements Bachelors' degree in Engineering, Science, or a related field of study. 0-2 years' experience in a GMP manufacturing environment. Experience in technical writing including drafting standard operating procedures, protocols, and/or reports is preferred. Familiar with regulatory (FDA) requirements. Business minor or coursework is strongly encouraged. Advanced critical thinking and technical writing skills. Strong organizational, communication, and interpersonal skills. Compensation and Benefits Expected pay range per year: $65,000-$85,000 USD Expected benefits include: Medical, Dental, Vision, PTO, 401K Disclaimer The duties and responsibilities described are not a comprehensive list and additional tasks may be assigned to the employee from time to time; or the scope of the job may change as necessitated by business demands. All duties and responsibilities are subject to possible modification to reasonably accommodate individuals with disabilities. The requirements listed are the minimum levels of knowledge, skills, or abilities necessary to perform this job successfully. The company is an Equal Opportunity Employer, drug-free workplace, and complies with ADA regulations as applicable.

We are seeking a highly experienced Lead, Technical Writer to support the development and automation of technical documentation for our software products. This role will focus on creating clear, accurate, and user-friendly content. It involves using automation and intelligent technology solutions to improve documentation workflows, including release notes and product guides. Key Responsibilities * Define and maintain documentation standards, style guides, and best practices. * Compose and edit high-quality technical content, including product documentation, release notes, and API guides. * Design and implement automated workflows for generating release notes and product documentation using AI tools. * Collaborate with engineering and product teams to integrate documentation automation into CI/CD pipelines. * Partner with product managers, developers, and UX teams to ensure documentation aligns with product functionality and user needs. * Contribute to the evolution of documentation processes across the organization. * Continuously improve documentation quality through user feedback and analytics. Required Qualifications * Experience: * 8+ years in technical writing for software products, with at least 3 years in a senior role. * Proven experience in automating documentation workflows, including release notes and product guides. * Hands-on experience with AI-driven documentation tools and CI/CD pipelines and automation frameworks. * Education: * Bachelor's degree in Technical Communication, Computer Science, or related field (or equivalent experience). Preferred Qualifications * Experience with scripting languages (Python, JavaScript) for automation. * Familiarity with AI/ML concepts and their application in content generation. * Knowledge of cloud platforms and SaaS environments. Click here to view how Epsilon transforms marketing with 1 View, 1 Vision, 1 Voice. Base Salary: $87,100 - $173,700 Actual compensation within the range will be dependent upon, but not limited to the individual's skills, experience, qualifications, location and application employment laws. The salary pay range is subject to change and may be modified at any time. The application deadline for this job posting is 2/11/2026. Additional Information When You Join Us, We'll Create Something EPIC Together Epsilon is a global data, technology and services company that powers the marketing and advertising ecosystem. For decades, we've provided marketers from the world's leading brands the data, technology and services they need to engage consumers with 1 View, 1 Vision and 1 Voice. 1 View of their universe of potential buyers. 1 Vision for engaging each individual. And 1 Voice to harmonize engagement across paid, owned and earned channels. Epsilon's comprehensive portfolio of capabilities across our suite of digital media, messaging and loyalty solutions bridge the divide between marketing and advertising technology. We process 400+ billion consumer actions each day using advanced AI and hold many patents of proprietary technology, including real-time modeling languages and consumer privacy advancements. Thanks to the work of every employee, Epsilon has been consistently recognized as industry-leading by Forrester, Adweek and the MRC. Epsilon is a global company with more than 9,000 employees around the world. Our pillars aren't just words. They're how we show up every day. * People centricity: We focus on employee well-being in an environment where colleagues truly care about each other. * Collaboration: We work together, support one another, and collectively achieve goals. * Growth: There are endless opportunities for growth through learning, development and career advancement. * Innovation: We drive progress through cutting-edge solutions and forward-thinking approaches. * Flexibility: We've created a balance between work and personal life, and we encourage adaptability to solve problems creatively. Our values guide us to create value for our clients, our people and consumers. * Act with integrity * Work together to win together * Innovate with purpose * Respect all voices * Empower with accountability These pillars and values are our foundation-shaping our culture, guiding our decisions, and uniting us in common purpose. Because You Matter As an Epsilon employee, you deserve perks and benefits that put you, your family and your finances first. Our benefits encompass a wide range of offerings, including but not limited to the following: * Time to Recharge: Flexible time off (FTO), 15 paid holidays * Time to Recover: Paid sick time * Family Well-Being: Parental/new child leave, childcare & elder care assistance, adoption assistance * Extra Perks: Comprehensive health coverage, 401(k), tuition assistance, commuter benefits, professional development, employee recognition, charitable donation matching, health coaching and counseling Epsilon benefits are subject to eligibility requirements and other terms. Epsilon is an Equal Opportunity Employer. Epsilon's policy is not to discriminate against any applicant or employee based on actual or perceived race, age, sex or gender (including pregnancy), marital status, national origin, ancestry, citizenship status, mental or physical disability, religion, creed, color, sexual orientation, gender identity or expression (including transgender status), veteran status, genetic information, or any other characteristic protected by applicable federal, state or local law. Epsilon also prohibits harassment of applicants and employees based on any of these protected categories. Epsilon will provide accommodations to applicants needing accommodations to complete the application process. Please reach out to ************************** to request an accommodation. For San Francisco Bay and Los Angeles Areas: Epsilon will consider for employment qualified applicants with criminal histories in a manner consistent with the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance and San Francisco Police Code Sections 4901-4919, commonly referred to as the San Francisco Fair Chance Ordinance. Applicants with criminal histories are welcome to apply. #LI-NK1

Qualifications: * 4+ years in a writing or lead writing role * Proven ability to work with developers and write for a developer audience * Experience working with a programming language such as Java, C#, or C++ is essential * Proven experience designing documentation for software APIs * Strong interpersonal, written, and verbal communications skills * Passion to thrive in a fast-paced, ever-changing environment * Experience with XML-based publishing systems * Some experience with web services and related technologies a plus Compensation: $40-45 hourly DOE We look forward to reviewing your application. We encourage everyone to apply - even if every box isn't checked for what you are looking for or what is required. PDSINC, LLC is an Equal Opportunity Employer.

Small software company developing, marketing, installing, and supporting solutions for healthcare enterprises (primarily hospitals). In business for 20 years, we have customers in 49 states (plus DC and Puerto Rico), several Canadian provinces, and the UK. Job Description Provides writing and/or technical editing of materials and manuals for Interbit Data, Inc. Writes and/or edits technical materials such as user manuals, specifications or scripts with technical content. Prepares written documents, including reports, articles, formal proposals, memoranda, and formal correspondence. Edits portions of reports and assists in or directs the development and presentation of the information. Analyzes changes to various products and prepares reports of changes for review. Creates technically accurate and comprehensive documentation and website support. Performs other related duties as assigned. Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Must be confident utilizing Microsoft Office (including Excel, Word, Power Point, Outlook), Adobe tools including Framemaker, P.C. and electronic communication equipment such as facsimile, scanner, digital camera, multi-line phone and printer. This position requires Background Check. LANGUAGE SKILLS Communicates effectively in both oral and written communication. Builds a partnership with customers by regularly demonstrating a high level of expertise and professionalism. Works as part of a team by contributing to Company goals, offering input and pursuing new ideas. REASONING ABILITY Ability to define problems. Excellent organizational skills, including time management and follow-up. Ability to handle several tasks and juggle multiple priorities. Flexible and possess ability to change focus at a moment's notice. Take ownership and accountability of assigned tasks Ability to produce results given tight deadlines. Additional Information All your information will be kept confidential according to EEO guidelines.

Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion dollar IT company, Collabera's client-centric business model, commitment to service excellence and Global Delivery Model enables its global 2000 and leading mid-market clients to deliver successfully in an increasingly competitive marketplace. With over 8200 IT professionals globally, Collabera provides value-added onsite, offsite and offshore technology services and solutions to premier corporations. Over the past few years, Collabera has been awarded numerous accolades and Industry recognitions including. Collabera awarded Best Staffing Company to work for in 2012 by SIA. (hyperlink here) Collabera listed in GS 100 - recognized for excellence and maturity Collabera named among the Top 500 Diversity Owned Businesses Collabera listed in GS 100 & ranked among top 10 service providers Collabera was ranked: 32 in the Top 100 Large Businesses in the U.S 18 in Top 500 Diversity Owned Businesses in the U.S 3 in the Top 100 Diversity Owned Businesses in New Jersey 3 in the Top 100 Privately-held Businesses in New Jersey 66th on FinTech 100 35th among top private companies in New Jersey *********************************************** Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance. Job Description Position Details: Industry Telecom Work Location Waltham - MA - 02451 Job Title Technical Writer Duration 6+ months (High possibility of extension) Job Id 78_36470_Technical Writer Skills and Qualifications: • Goal is to convert so please be aware of your candidates right to work status when submitting. • Technical writer with experience writing and delivering documentation for network hardware end users rather than API. API is nice to have but not a requirement. • Experience and knowledge of mobile services/apps and cloud platforms (mobile advertising a plus). • Experience writing technical content for end users and developers, including reference manuals, user guides, and design specifications. • Familiarity with scripting and programming concepts/languages preferred. Work closely with product management, engineering project teams, and other stakeholders to write and deliver customer-focused technical documentation for product releases. • Address content gaps, act on internal and direct customer feedback, and promote continuous improvement on the documentation experience. If you are not interested in the role or if now isn't a great time for a move, just let me know if I can help in the future or if you need assistance in making a connection. To know more about Collabera, please visit us on ***************** Should you have any questions, please feel free to call me on ************. I look forward to working with you. Additional Information If you are interested, you may reach me at: Deeksha Mathur ************ *******************************

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 Ensure timely and efficient creation/review of QCRM documents (material specifications, standard operating procedures, test methods, technical protocols and reports, etc.) Contribute scientific knowledge, analytical skills, and interpretation of the information to be captured on the document Ensure a consistent style of presentation of QCRM documents to maintain quality and ease of review Execute activities, associated with optimization, validation, transfer, and life cycle management of test methods used for release testing of raw materials Coordinate and conduct tasks for laboratory equipment calibration, qualification, preventative maintenance and re-qualification program Act as subject matter expert (SME) for method validation, laboratory equipment management and supplier certification testing, and provide input in cross-functional teams, including during Consent Decree remediation activities. Provide training and ensure adequate proficiency of QCRM staff with respect to analytical method principle and critical parameters; ensure understanding and interpretation of test results Support readiness for regulatory inspections and compliance audits. Assess routine compendial updates and ensure timely revision of test methods Review data generated by contract laboratories (internal and external labs) Support development of junior analysts through mentoring Execute and ensure timely closure of compliance events, including deviations, CAPA, change controls Revise standard operating procedures as needed Practice safe work habits and adhere to Genzyme s safety procedures and guidelines Maintain proficiency training per assigned curricula Qualifications Skills: Basic Qualifications: Bachelor s degree in a related discipline Minimum of 5 years of experience in cGMP laboratory environment Previous experience with management of lab equipment Previous experience with lab control operations and quality systems Education: Bachelor s degree in a related discipline Previous experience with lab control operations and quality systems . Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Creatio is a global vendor of an AI-native platform to automate workflows and CRM with no-code and a maximum degree of freedom. Our platform combines an AI-first architecture, composable no-code tools, and enterprise-grade governance to help organizations build and scale faster. We're proud to be recognised by top industry analysts as a Leader and Strong Performer in multiple Gartner and Forrester reports. In 2025, Creatio was named to Inc.'s Best Workplaces list, recognizing our commitment to employee wellbeing and a strong workplace culture. Who We're Looking For: The RFP/Proposal Technical Writer is a key member of the centralized Product Marketing & Strategic Advisory team responsible for creating high-quality, compelling proposal and RFP responses that support Creatio's global sales organization. This role operates in a high-volume, fast-turnaround environment serving sales teams across multiple industries, geographies, and languages. The successful candidate will leverage AI-powered tools, deep product knowledge, and exceptional writing skills to produce winning proposals that clearly articulate Creatio's value proposition as the leading agentic platform for CRM and workflow automation with no-code and AI at its core. The role is based in Poland (Remote / Hybrid). Team composition: Team of 4, consisting of the Head of Strategic CRM Advisory a RFP Team Leader, and two RFP / Proposal Technical Writers. Responsibilities: Proposal Development & RFP Response * Manage end-to-end RFP/RFI/RFQ response process from intake to submission, ensuring all deadlines are met; * Author clear, accurate, and persuasive responses to technical and functional requirements; * Tailor responses to specific industry verticals, buyer personas, and regional requirements; * Complete security questionnaires and compliance documentation accurately and efficiently; * Collaborate with solution engineers, product managers, and subject matter experts to gather technical information while minimizing their time commitment. Content Library & Knowledge Management * Develop and maintain centralized content library of reusable response components, boilerplate content, and industry-specific modules; * Create and update standardized templates for common RFP sections and question types; * Ensure content library remains current with product updates, new features, and messaging framework changes; * Document best practices and lessons learned from win/loss analysis to continuously improve response quality. Quality Assurance & Compliance * Ensure all responses are accurate, consistent, and aligned with Creatio's brand voice and messaging framework; * Conduct thorough quality reviews before submission, including compliance checks and proofreading; * Translate technical product capabilities into business value statements appropriate for different buyer personas (BDMs vs. TDMs); * Maintain version control and audit trails for all proposal content. Technology & Tools * Utilize AI-powered writing tools and prompt engineering techniques to accelerate content creation while maintaining quality; * Operate RFP tools (e.g., Responsive.io, Loopio, or similar) to streamline response workflows; * Leverage Microsoft 365 ecosystem (SharePoint, Teams, etc.) for collaboration and content management; * Identify opportunities for process automation and efficiency improvements. Stakeholder Management & Collaboration * Manage and prioritize multiple concurrent requests from global sales teams across different time zones; * Build strong working relationships with solution engineers, product managers, legal, security, and other cross-functional teams; * Communicate proactively with stakeholders on request status, timelines, and any blockers; * Coordinate with localization resources for multi-language submission requirements. Requirements: Experience * 5+ years of experience in proposal writing, RFP response management, or technical writing for enterprise software; * Demonstrated experience with CRM software proposals and understanding of CRM/sales/marketing/service automation concepts; * Proven track record of managing high-volume workloads with fast turnaround times; * Experience working in SLA-driven environments with defined quality and delivery targets. Skills * Exceptional English language skills (written and verbal); * Strong technical writing skills with ability to communicate complex concepts clearly and persuasively; * Excellent attention to detail with strong proofreading and editing capabilities; * Strong organizational and project management skills with ability to prioritize competing demands; * Proficiency with Microsoft 365 suite (Word, Excel, PowerPoint, SharePoint, Teams); * Experience using AI-assisted writing tools and willingness to adopt new technologies. Competencies * Self-motivated with ability to work independently in a remote/distributed team environment; * Strong interpersonal skills with ability to extract information efficiently from subject matter experts; * Adaptable and comfortable working across multiple industries, regions, and stakeholder groups; * Results-oriented with focus on continuous improvement and winning outcomes. Preferred Qualifications * Familiarity with workflow automation, no-code platforms, or enterprise software concepts beyond CRM; * Experience with RFP automation software (Responsive.io, Loopio, RFPIO, Qvidian, or similar); * APMP (Association of Proposal Management Professionals) certification or equivalent; * Understanding of B2B enterprise software buying processes and procurement requirements; * Experience with security questionnaires and compliance frameworks (SOC 2, GDPR, ISO 27001); * Additional language skills (Ukrainian, Polish, German, French, or other European languages); * Background in SaaS, cloud software, or technology industry. What you should expect from us: * Growth & Development: Clear career paths, mentorship opportunities, and access to continuous learning to help you reach your full potential; * Flexibility & Well-Being: We provide flexible work arrangements and initiatives that empower you to manage your schedule effectively, stay productive, and thrive both personally and professionally; * Recognition & Impact: A culture that celebrates achievements, values your ideas, and empowers you to make real contributions from day one; * Innovative Culture: Be part of a company that embraces new ideas, modern technologies, and bold thinking to stay ahead of the curve; * Benefits & Rewards Package: We provide competitive compensation and benefits designed to support you and your family. Our rewards approach goes beyond salary, recognizing your contributions and commitment. The exact package may vary depending on your country of residence and employment type.

The ideal candidate will be responsible creating, editing and maintain high-quality documentation that communicates complex technical information clearly and concisely to a variety of audiences. This role requires collaboration with subject matter experts, product managers, engineering team, and other stakeholders to ensure accurate and accessible content. Key Responsibilities: Provide expertise and guidance and best practices on product documentation set up for commercial purposes Review existing documentation related to product and applications and identify areas of improvement for our documentation strategy Work with UX team to optimize the setup of documentation on Resource Hub Work with Product, engineering and commercial teams to generate content and publish product requirements, operational flows, user and technical related material Establish standardized process and templates where possible for the efficient delivery of a consistent library of documentation for LedgerScan, CMP and Factory to include the following (not limited): Product architecture diagram User Guide Production functional features APIs and EndPoints (where applicable) ABIs and Scripts (where applicable) Workflow Diagrams Infrastructure Requirements Deployment Diagrams Assist with content generation and production of documents as necessary Assist in creating content strategies and documentation plans to support product development. Collaborate with cross-functional teams to understand end-user needs and incorporate feedback Skills and Experience Required - 5+ years of experience as a Technical Writer, with a focus on API and ABI documentation - 2+ years of experience in a software development role - Experience with legacy financial institutions technology and API integration architecture. - Experience with Blockchain and Web3 technologies. - Strong understanding of APIs, RESTful web services, and programming concepts - Proficiency with various authoring, CMS, and task management tools - Familiarity with API documentation tools, such as Swagger, Postman, or similar. - Proficiency with Confluence, JIRA, and JSON. - Basic diagramming skills using tools like draw.io, Miro or similar. - Experience using tech stacks like Python, MongoDB, CDC, and Kafka - Experience working in a fast-paced, dynamic environment. - Strong time management skills. - Ability to thrive in an environment that grants you a lot of autonomy to explore creative solutions.

Are you looking for an opportunity with plenty of growth potential? Do you enjoy working in an exciting, fast-paced, collaborative environment? Are you interested in working with the world's most innovative companies to create a more connected world? Connecting Continents. Impacting Communities. The backbone of the Internet is a series of high-tech subsea fiber optic cables deployed throughout the globe - SubCom has deployed over 50% of them. Our employees ensure data communications networks are engineered, manufactured, deployed to the highest standards, enabling faster and more reliable connectivity to communities worldwide. Every member of the SubCom team plays a role in an end-to-end process that is critical to enterprises, governments, big cities, and rural towns. We encourage, expect, and value creativity, thoughtful risk taking, openness to change, and diverse perspectives. Whether you're a seasoned applicant seeking a new and exciting challenge, or you're new to the workforce and looking for a flexible, rewarding, and fast-paced position with an innovative and stable organization (since 1953), SubCom has opportunities to advance your career. Position Overview The End User Documentation (EUD) Technical Writer is responsible for producing and maintaining SubCom's established set of technical equipment user manuals, system operations & maintenance descriptions, and product-specific training manuals. This work is conducted in direct support of existing supply contracts, new bids and proposals, and future hardware and software development. The production of these highly technical documents must satisfy contractually required customer deliverable requirements as well as ensure safe and sustaining use of SubCom provided equipment for our customers. Responsibilities * Gather and review source material from Subject Matter Experts (SMEs) from R&D and other functional groups. * Write, construct, assemble and edit manuals based upon SubCom's established styles, guidelines and processes. * Cross check all information against known sources, submit completed manuals to SMEs for review and sign-off. * Develop potential new EUD for new products via SME interviews, requirements documents, and actual use of said product under laboratory conditions. * Design, edit and manipulate graphics in multiple formats, for inclusion within documents. * Support the development and maintenance of on-line help for SubCom's software products. * Desktop publish completed documents for delivery to SubCom Purchasers. * Work to specific and changeable development and delivery schedules. * Attend weekly team status meetings to report on progress of assignments and share key information with other members of the writing staff.

Duration: 12+ month Top 3 critical skills: · Strong working knowledge of the validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures. · Working knowledge of data integrity regulations, guidance, and principles · Strong technical writing skills Minimum education experience required: BS in Scientific discipline Years of experience required: 3-5 years Job Description: This role will provide support to the QC Analytical and Microbiology departments for QC instrument data integrity assessments and remediation activities. This scope includes QC Instruments (both portable and computer-controlled), paper-based systems, and local instances of enterprise system data management. Systems and processes within scope will require assessment via company's pre-established criteria in order to identify gaps against company data integrity expectations. The candidate will be responsible for executing or facilitating execution of these gap assessments through collaboration with laboratory subject matter experts (SMEs) at company. Upon completion of gap assessments, the candidate will be responsible for leveraging the results as follows: • Facilitating, proposing, and/or assembling gap closure recommendations, through collaboration with SMEs • Summarizing results from their assessments into reports utilizing a supplied format • Authoring Corrective & Preventive Action plans (CAPAs) for systems with long-term remediation activities, and authoring final reports for systems with short term/completed remediations • Managing all gap assessment and remediation reports through company review and approval workflows • Performing supporting remediation work in the form of SOP revisions as well as authoring and executing change controls and validation test plans/protocols when required per remediation plans Additional Skills: Successful candidate requires: • Strong working knowledge of the validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures. • Working knowledge of data integrity regulations, guidance, and principles • Working knowledge of CAPA and change control processes • Strong technical writing skills • Strong interpersonal, oral and written communication skills as there is a high degree of collaboration required between members of QC, QA Validation, Instrument Validation, and IS/IT functions. • A detail-oriented approach to deliverables as the main job responsibility is generation, review, and approval of GMP documentation. • A BS degree in science, engineering, computer science, or related technical discipline with minimum 2-3 years pharmaceutical/biopharmaceutical experience in a relevant GMP role (validation, quality control, quality assurance, IS/IT compliance, etc.) Past experience working with QC instrumentation in the biopharmaceutical field is preferred but not required. Qualifications • Strong working knowledge of the validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures. • Working knowledge of data integrity regulations, guidance, and principles • Working knowledge of CAPA and change control processes • Strong technical writing skills •Strong interpersonal, oral and written communication skills as there isa high degree of collaboration required between members of QC, QA Validation, Instrument Validation, and IS/IT functions. •A detail-oriented approach to deliverables as the main job responsibility is generation, review, and approval of GMP documentation. •A BS degree in science, engineering, computer science, or related technical discipline with minimum 2-3 years pharmaceutical/biopharmaceutical experience in a relevant GMP role (validation, quality control, quality assurance, IS/IT compliance, etc.) Past experience working with QC instrumentation in the biopharmaceutical field is preferred but not required. Additional Information All your information will be kept confidential according to EEO guidelines.

+ We are looking for a Technical Writer to make our existing content more complete, organize it in a more friendly way and make implementation and optimization more independently actionable by partners. + The team mission is to be the trusted place where travelers go for the most useful information to make fast, effortless decisions. Our team helps scale the growing Travel ecosystem through high-value services and solutions that empower partners and travelers worldwide. + The contractor will work with program managers, engineers and subject matter experts to gather business requirements and product knowledge, identify gaps and areas for improvement and create required content. **Responsibilities:** + Write, review, publish, and maintain high-quality technical content while adhering to client's documentation standards. + Incorporate feedback from relevant stakeholders (e.g., engineers, product managers, program managers, customers) to align content with user needs and product/program goals + Address primary critical documentation needs as compiled in Documentation Needs Analysis and this component. + Identify and address gaps in help content and assist with content development prioritization. + Expand help content to make it actionable and partners more self-sufficient. + Ensure breadth of features/functionality has been documented with best practices and sample use cases. + Address backlog of outstanding bugs and feature requests filed against the Help Center by internal/external users. **Experience:** + Experience in technical writing, product documentation, or online publishing. + Experience working in collaboration with technical and sales stakeholders on a daily basis. + Must be a self-starter who is able to manage multiple tasks under tight deadlines and work independently. + Ability to quickly grasp and communicate technical concepts. **Desired Skills:** + Experience with travel industry a strong plus. **Education:** + Bachelor's degree or equivalent practical experience. **About US Tech Solutions:** US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit *********************** (********************************** . US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

To create revolutionary, story-driven RPGs which go straight to the hearts of gamers - this is our mission. Want to dive deeper into our company's culture? Explore our social media and check out our YouTube channel and Beyond the Game Blog where we share behind-the-scenes insights and stories direct from our team members! Job Description CD PROJEKT RED is seeking a highly skilled and visionary Lead Writer to join our team working on Project Sirius, a multiplayer game set within the world of The Witcher. In this role, you will be responsible for crafting captivating narratives, compelling dialogues and innovative quests for a brand new adventure set in The Witcher universe. This is a leadership role that combines hands-on creative writing alongside team management and cross-functional collaboration. The ideal candidate will have extensive experience in writing for games and a passion for leading teams to success. Responsibilities Collaborate closely with the Game Director, Narrative Director, Mission Director and Lead Narrative Designer. Drive development of the main story, side quests and character stories. Lead, guide and support a team of dedicated and experienced writers. Develop narrative elements and features of our game, including writing engaging dialogues, compelling scenarios and memorable characters. Build and maintain documentation for all owned features, script, story, and scenes Collaborate with other stakeholders to ensure that the story elements are delivered in consistency with gameplay mechanics and visuals. Manage task delegation and workflow across the writing team. Maintain the vision and tone of The Witcher IP. Qualifications At least 3 years of experience as a Lead Writer in AAA projects. Strong storytelling abilities and a deep understanding of interactive and player driven narratives. Excellent writing skills, including the ability to create compelling characters, immersive storylines, and engaging dialogue. Knowledge of game design principles and an understanding of how narrative elements integrate with gameplay mechanics. Ability to lead and manage a team, providing guidance, feedback, and support. Excellent communication and collaboration skills to work effectively with cross-functional teams. Nice to Have: (Please note that these skills are not required to apply for the position) Professional experience with Unreal Engine. Bachelor's degree in English, Creative Writing, or a related field. Experience with storytelling on a multiplayer title. Please provide 2-3 writing samples of no more than 10 pages total, with at least one featuring examples of dialogue. We are most interested in work that showcases the ability to capture the tone and voice of an existing IP. Please include your samples as an extension of your resume or ensure a link to your work is listed on your application. Additional Information The application window for this position will close by 04/30/2026. This job requires working in Boston, US. Working mode: in-office in a hybrid or full-time capacity. Remote roles in the US are only available to candidates that reside in the following states: California, Colorado, Connecticut, Florida, Illinois, Kentucky, Maryland, Massachusetts, Minnesota, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, Rhode Island, Tennessee, Texas, Washington, Wisconsin. Health & Well-Being Company-paid medical healthcare (dental, vision, and mental). Free mental health support, including access to counseling, psychiatric care, and a variety of well-being webinars. Paid leave - 20 days of holiday per year (26 days after two years). 401K with employer matching. Gym Membership Reimbursement. Menstrual leave - employees who menstruate can take one extra day off when experiencing period pain. RED Parents Network - support for working parents, including childcare benefits, and family-friendly events. Perks & Professional Growth Flexible working hours. Trainings, lectures, and courses - internal workshops, knowledge-sharing initiatives, online tutorials, and e-learning classes are all available. A welcome pack filled with goodies - to help you feel right at home once you join the team. Life in the Office Dog-friendly office - bring your pooch with you and look after them while working! There's always a furry friend or two to meet. Truly international working environment - a chance to meet and work with a diverse selection of people from all around the world. No dress-code - we like to keep it casual. This position is a new role. Estimated pay range for this position: $151,400 - $231,200 USD annually This role may also be eligible for discretionary stock options. At CD PROJEKT RED compensation for our roles in North America are determined based on competitive market data, geographic location, and individual factors tied to business needs. The base pay range is subject to change and may be modified in the future. Final offers are dependent on job-related factors like experience, qualifications, and location. If you've observed any irregularities (i.e. legal or ethical violations) in our recruitment process, please click here to report them anonymously. #LI-Hybrid #LI-ONSITE

To create revolutionary, story-driven RPGs which go straight to the hearts of gamers - this is our mission. Want to dive deeper into our company's culture? Explore our social media and check out our YouTube channel and Beyond the Game Blog where we share behind-the-scenes insights and stories direct from our team members! Job Description CD PROJEKT RED is seeking a highly skilled and visionary Lead Writer to join our team working on Project Sirius, a multiplayer game set within the world of The Witcher. In this role, you will be responsible for crafting captivating narratives, compelling dialogues and innovative quests for a brand new adventure set in The Witcher universe. This is a leadership role that combines hands-on creative writing alongside team management and cross-functional collaboration. The ideal candidate will have extensive experience in writing for games and a passion for leading teams to success. Responsibilities * Collaborate closely with the Game Director, Narrative Director, Mission Director and Lead Narrative Designer. * Drive development of the main story, side quests and character stories. * Lead, guide and support a team of dedicated and experienced writers. * Develop narrative elements and features of our game, including writing engaging dialogues, compelling scenarios and memorable characters. * Build and maintain documentation for all owned features, script, story, and scenes * Collaborate with other stakeholders to ensure that the story elements are delivered in consistency with gameplay mechanics and visuals. * Manage task delegation and workflow across the writing team. * Maintain the vision and tone of The Witcher IP. Qualifications * At least 3 years of experience as a Lead Writer in AAA projects. * Strong storytelling abilities and a deep understanding of interactive and player driven narratives. * Excellent writing skills, including the ability to create compelling characters, immersive storylines, and engaging dialogue. * Knowledge of game design principles and an understanding of how narrative elements integrate with gameplay mechanics. * Ability to lead and manage a team, providing guidance, feedback, and support. * Excellent communication and collaboration skills to work effectively with cross-functional teams. Nice to Have: (Please note that these skills are not required to apply for the position) * Professional experience with Unreal Engine. * Bachelor's degree in English, Creative Writing, or a related field. * Experience with storytelling on a multiplayer title. Please provide 2-3 writing samples of no more than 10 pages total, with at least one featuring examples of dialogue. We are most interested in work that showcases the ability to capture the tone and voice of an existing IP. Please include your samples as an extension of your resume or ensure a link to your work is listed on your application. Additional Information The application window for this position will close by 04/30/2026. This job requires working in Boston, US. Working mode: in-office in a hybrid or full-time capacity. Remote roles in the US are only available to candidates that reside in the following states: California, Colorado, Connecticut, Florida, Illinois, Kentucky, Maryland, Massachusetts, Minnesota, Nevada, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, Rhode Island, Tennessee, Texas, Washington, Wisconsin. Health & Well-Being * Company-paid medical healthcare (dental, vision, and mental). * Free mental health support, including access to counseling, psychiatric care, and a variety of well-being webinars. * Paid leave - 20 days of holiday per year (26 days after two years). * 401K with employer matching. * Gym Membership Reimbursement. * Menstrual leave - employees who menstruate can take one extra day off when experiencing period pain. * RED Parents Network - support for working parents, including childcare benefits, and family-friendly events. Perks & Professional Growth * Flexible working hours. * Trainings, lectures, and courses - internal workshops, knowledge-sharing initiatives, online tutorials, and e-learning classes are all available. * A welcome pack filled with goodies - to help you feel right at home once you join the team. Life in the Office * Dog-friendly office - bring your pooch with you and look after them while working! There's always a furry friend or two to meet. * Truly international working environment - a chance to meet and work with a diverse selection of people from all around the world. * No dress-code - we like to keep it casual. This position is a new role. Estimated pay range for this position: $151,400 - $231,200 USD annually This role may also be eligible for discretionary stock options. At CD PROJEKT RED compensation for our roles in North America are determined based on competitive market data, geographic location, and individual factors tied to business needs. The base pay range is subject to change and may be modified in the future. Final offers are dependent on job-related factors like experience, qualifications, and location. If you've observed any irregularities (i.e. legal or ethical violations) in our recruitment process, please click here to report them anonymously. #LI-Hybrid #LI-ONSITE

About the role: Advisor360°'s Product Adoption and Enablement team is looking for a Technical Writer to manage our product In-App help documentation and advise on other user-facing content. This writer will create and maintain help content in our CMS Paligo. We'd love to hear from you if you have strong documentation skills, consideration for your audience, and the ability to reflect the Advisor360° voice, tone, and style while still letting your own character shine through. Our ideal candidate is clever, collaborative, and driven by their curiosity to solve problems and celebrate solutions. We are very good at supporting each other and working across teams, and this role has a special place at the center of that network. We'll ask you for a couple of relevant writing samples with explanations of your content decisions. We'll also talk more about this during the interview. What You'll Do: Create and maintain clear, friendly, accessible help content, including screencaptures and videos. Create videos for user workflow simulations with Storylane. Strive to understand user needs and be an advocate for their success. Evaluate questions and responses using metrics to gauge success and identify gaps in our AI First Documentation. Contribute to the optimization of help content to increase accuracy and scope of AI chatbot's responses. Tracking In-App Help usage and engagement, with a goal to improve usefulness of chatbot Help responses. Consult website data and our customer-facing teams to inform content decisions. Work with our product management, development, and QA teams to understand and author content for new and existing features. Be an editorial resource for our developer documentation, UX copy, and other projects. Create reports and internal announcements for content updates and performance enhancements.. Who You Are: You have 5+ years of experience authoring documentation in fintech for enterprise level SaaS products with Paligo or similar XML or markdown based content management systems such as Oxygen and ReadMe. You have experience with tools like Jira, Confluence, Slack, Google Analytics, and Storylane. You've scripted, storyboarded, and produced videos with tools like Storylane, Camtasia, or the Adobe suite. You've explored site traffic data as an indicator for user behavior and content needs. A collaborative communicator with a willingness to learn and grow, as well as guide others. Your annoyed by mistakes in job postings and can't wait to provide editorial feedback in your cover letter. Extra points if you're familiar with Storylane, Figma, UserPilot, basic HTML and CSS, and technical concepts like, branching, APIs, SSO, and webhooks. Portfolio of work or website with writing samples must be provided. Why You'll Love Working Here: It's not just about work-it's about building a career and enjoying the ride! Here's what you can expect: We believe in recognizing and rewarding performance. Our compensation package includes competitive base salaries, annual performance-based bonuses, and the chance to share in the equity value you and your colleagues create during your time with the company. We offer comprehensive health benefits, including dental, life, and disability insurance. We also trust our employees to manage their time effectively, which is why we offer an unlimited paid time off program to help you perform at your best every day. Join us on this journey. Advisor360° is an equal opportunity employer committed to a diverse workforce. We believe diversity drives innovation and are therefore building a company where people of all backgrounds are truly welcome and included. Everyone is encouraged to bring their unique, authentic selves to work each and every day. The way we see it, we are here to learn from each other. The estimated base salary range for this position is $117,000 - $137,000 + bonus & equity. Advisor360° provides an estimate of the compensation for roles that may be hired as required by state regulations. Compensation may vary based on factors including, but not limited to, individual candidate experience, skills, and qualifications. Additionally, Advisor360° leverages current market data to determine compensation, therefore posted compensation figures are subject to change as new market data becomes available. The salary, other forms of compensation, and benefits information is accurate as of the date of this posting. Advisor360° reserves the right to modify this information at any time, subject to applicable law. While we are interested in qualified applicants who are permanently eligible to work for any employer in the United States, we are unable to sponsor or transfer sponsorship for employment visas at this time. To all recruitment agencies: We do not accept unsolicited agency resumes and are not responsible for any fees related to unsolicited resumes. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.