senior technical writer

LBM SOLUTIONS, Mohali

We are seeking an experienced and detail-oriented Senior Technical Content Writer to join our team. The ideal candidate should have strong expertise in creating high-quality, engaging, and well-researched technical content across various digital platforms.Key Responsibilities:<ul><li>Create clear, concise, and compelling technical content (blogs, website content, case studies, whitepapers, etc.)</li><li>Conduct in-depth research on IT, software, and technology-related topics</li><li>Collaborate with developers, designers, and marketing teams to ensure content accuracy</li><li>Optimize content as per SEO guidelines</li><li>Edit and proofread content to ensure quality and consistency</li><li>Manage content calendars and meet deadlines</li></ul>Required Skills:<ul><li>3&ndash;5 years of experience in technical content writing</li><li>Strong understanding of IT, software development, and emerging technologies</li><li>Excellent writing, editing, and proofreading skills</li><li>Knowledge of SEO best practices</li><li>Ability to simplify complex technical concepts</li><li>Experience with CMS platforms and content tools</li></ul>Preferred Qualifications:<ul><li>Background in Computer Science, IT, or related field</li><li>Experience working with SaaS or IT companies</li></ul>Job Type: Full-timePay: ₹15,246.00 - ₹44,520.99 per monthWork Location: In person

Senior Technical Content writer

COZMALABS

We are seeking a highly experienced Senior Technical Writer to develop, manage, and maintain high-quality technical documentation in both English and Arabic. The role requires deep expertise in translating complex technical concepts into clear, accurate, and user-focused documentation for diverse stakeholders.Key Responsibilities<ul><li>Develop, edit, and maintain technical documentation including:</li><li>User manuals, system manuals, SOPs, policies, and procedures</li><li>Technical specifications, design documents, and reports</li><li>Training materials and operational guides</li><li>Produce bilingual documentation (English &amp; Arabic) with linguistic and technical accuracy</li><li>Collaborate with engineers, developers, SMEs, and project managers to gather requirements and validate content</li><li>Ensure documentation complies with organizational standards, regulatory requirements, and industry best practices</li><li>Review, standardize, and improve existing documentation for clarity, consistency, and usability</li><li>Manage document version control, reviews, approvals, and publication cycles</li><li>Establish and maintain documentation templates, style guides, and terminology glossaries</li><li>Support audits, tenders, and client deliverables with high-quality technical documentation</li><li>Mentor junior writers and provide editorial oversight when required</li></ul>Required Qualifications<ul><li>Bachelor&rsquo;s degree in Technical Writing, Engineering, Computer Science, Communications, or a related field</li><li>15+ years of proven experience as a Technical Writer in complex technical environments</li><li>Proficiency in both English and Arabic is mandatory</li><li>Strong experience documenting technical systems, software, infrastructure, or engineering solutions</li><li>Excellent command of grammar, structure, and technical terminology in both languages</li><li>Advanced proficiency with documentation tools (e.g., MS Word, FrameMaker, MadCap Flare, Confluence, SharePoint, or similar)</li><li>Strong stakeholder management and communication skills</li></ul>Preferred Skills<ul><li>Experience in regulated industries (government, defense, oil &amp; gas, utilities, telecom, or IT)</li><li>Familiarity with international documentation standards (ISO, IEEE, ITIL, etc.)</li><li>Experience supporting bids, proposals, or compliance documentation</li><li>Ability to work independently and manage multiple documentation streams</li></ul>Job Type: Full-time

Technical Writer

Elevatech Solutions Pvt. Ltd.

We Are Hiring Senior SEO Technical Content Writer (Application Industry)Job Type: Full-time | OnsiteLocation: Karachi, PK.JOB OVERVIEW:We are looking for a Senior SEO Technical Content Writer who can create high-quality, research-driven, and SEO-optimized content for the application development industry.KEY RESPONSIBILITIES: <ul><li>Write and optimize long-form SEO blogs, web pages, and technical articles related to;</li><li>Mobile app development (iOS/Android)</li><li>Web applications, SaaS products, enterprise apps</li><li>UI/UX, performance optimization, security, APIs, cloud, DevOps, AI integration, etc.</li><li>Create content for service pages, landing pages, product pages, and pillar pages.</li><li>Perform keyword research and develop content plans using tools like Ahrefs, SEMrush, Google Keyword Planner, etc.</li><li>Ensure content follows on-page SEO best practices.</li><li>Meta titles/descriptions.</li><li>Headings structure (H1&ndash;H4)</li><li>Internal linking strategy</li><li>Image alt text</li><li>Schema-ready content structure (bonus)</li><li>Collaborate with SEO specialists, designers, and developers to produce content aligned with business goals.</li><li>Improve existing website content through content audits and optimization.</li><li>Maintain brand tone and consistency across all communication channels.</li><li>Track content performance using Google Analytics, Search Console, and SEO tools and propose improvements.</li><li>Work on content for email marketing, social media, and marketing campaigns when required.</li><li>Ensure writing is original, plagiarism-free, and technically accurate.</li></ul>REQUIREMENTS:<ul><li>3&ndash;6+ years of experience in SEO content writing, preferably in IT / software / app development industry.</li><li>Strong understanding of technical concepts in software development and ability to explain them clearly.</li><li>Strong knowledge of SEO writing and ranking factors.</li><li>Excellent English writing, editing, and proofreading skills.</li><li>Hands-on experience with Keyword research and SEO tools (Ahrefs / SEMrush / Moz), CMS platforms (WordPress, Webflow, etc.)</li><li>Content optimization and readability tools (Yoast, SurferSEO &ndash; bonus)</li><li>Ability to create both informational and high-conversion content.</li><li>Comfortable working with multiple deliverables and deadlines.</li></ul>PREFERRED / BONUS SKILLS:<ul><li>Experience in B2B SaaS or software service companies.</li><li>Understanding of technical SEO basics (crawlability, site structure, internal linking, schema).</li><li>Familiarity with content formats like Whitepapers</li><li>Case studiesProduct documentation (bonus)Experience in writing content for app development agencies or tech companies.Knowledge of AI tools (ChatGPT, Jasper, Grammarly) for ideation and editing&mdash;without compromising originality.</li></ul>TO APPLY:Please share your updated resume at: career@elevatechsol.comJob Type: Full-timePay: Rs70,000.00 - Rs100,000.00 per monthWork Location: In person

We Are Hiring Senior SEO Technical Content Writer (Application Industry)

FileCloud

<div>FileCloud is looking for an enthusiastic Associate Technical Writer to join our team in Riyadh, Kingdom of Saudi Arabia. In this role, you will help create, update, and maintain clear, accurate, and user-friendly technical documentation that supports our customers and internal users. This is an excellent opportunity for a recent graduate with a Communications or Media degree or an early-career technical writer. This role is fully office-based and will require working in our office in Riyadh and connecting with the wider, global FileCloud team.

About the Product &amp; Company:
FileCloud is a hyper-secure EFSS (enterprise file sync and share) platform that provides industry leading compliance, data governance, data leak protection, data retention and digital rights management capabilities. FileCloud is a leader in content governance and collaboration for unstructured data, trusted and used worldwide across Global 1000 enterprises, educational institutions, government organizations, and service providers. In addition to its enterprise file sharing solution, FileCloud&rsquo;s product portfolio also includes Signority (acquired in May 2024), a Canadian-based e-signature and document workflow platform. We are currently expanding our team as we grow and improve FileCloud.
Key Responsibilities
<ul><li>Assist in the creation and maintenance of technical documentation including:
<ul><li>Product guides
</li><li>End user and administrator documentation
</li><li>Release notes and feature updates
</li></ul></li><li>Update documentation to reflect new features, enhancements, and bug fixes
</li><li>Help internal users maintain their teams&rsquo; documents on the company wiki
</li><li>Maintain written procedures of documentation team processes
</li><li>Work closely with the lead Technical Writer as well as Product Managers and Engineers to learn about the FileCloud product and the product releases process
</li><li>Review existing content for clarity and accuracy
</li><li>Try new features and confirm that documentation accurately describes their functions and behavior
</li><li>Follow established documentation standards, templates, and style guidelines
</li></ul>Required Qualifications:
<ul>
<li>0&ndash;2 years of experience in technical writing, documentation, or a related role. (internships and academic experience welcome)
</li><li>Strong proficiency in written and spoken English, with the ability to communicate concepts clearly, accurately, and professionally to a global audience
</li><li>Ability to learn technical concepts
</li><li>Ability to work with cross-functional teams and incorporate feedback effectively
</li><li>Strong attention to detail and commitment to content accuracy</li>
</ul>
Preferred Qualifications:
<ul><li>Experience documenting software products.
</li><li>Some understandings of basic coding concepts.
</li><li>Understanding of:
<ul><li>Web applications
</li><li>System administration such as maintaining users and assigning permissions.</li>
</ul>
</li></ul>What We Offer &ndash; These Do not change
<ul><li>Be part of a team of passionate, committed individuals dedicated to building a world-class product
</li><li>Dedicated time for training and education opportunities
</li><li>A mentorship model wherein your mentor and team support your development
</li><li>A competitive salary with an annual bonus
</li><li>Onsite work with flexible hours that fall outside of 8am -12pm (US Eastern Standard Time) / 4pm &ndash; 8pm (Arabic Standard Time)
</li><li>20 days of paid time off, which increases by a further 2 days after 3 years of service and 3 days after 5 years of service (in addition to 10 public holidays in your country)
</li><li>Paid day off on your birthday or on an alternative day if your birthday falls outside a typical working day
</li><li>Paid day off to volunteer with the charity of your choice
</li><li>Paid monthly internet cost, as well as lunch and a wellbeing stipend provided
</li><li>Reimbursement of all hardware costs associated with the role</li>
</ul>
Please note that we conduct background security checks for everyone joining our team.</div>

Associate Technical Writer (Riyadh, KSA)

<div>
 FileCloud is looking for an enthusiastic
 
 Associate Technical Writer to join our team in Riyadh, Kingdom of Saudi Arabia.
 
 In this role, you will help create, update, and maintain clear, accurate, and user-friendly technical documentation that supports our customers and internal users. This is an excellent opportunity for an early-career technical writer to grow in a fast-paced software environment while working closely with the Documentation team as well as Product Management, Engineering and Customer Support. This role is fully office-based and will require working in our office in Riyadh and connecting with the wider, global FileCloud team.
 
 
 
 About the Product &amp; Company:
 
 
 
 FileCloud is a hyper-secure EFSS (enterprise file sync and share) platform that provides industry leading compliance, data governance, data leak protection, data retention and digital rights management capabilities. FileCloud is a leader in content governance and collaboration for unstructured data, trusted and used worldwide across Global 1000 enterprises, educational institutions, government organizations, and service providers. In addition to its enterprise file sharing solution, FileCloud&rsquo;s product portfolio also includes Signority (acquired in May 2024), a Canadian-based e-signature and document workflow platform. We are currently expanding our team as we grow and improve FileCloud.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Assist in the creation and maintenance of technical documentation including:
 </li>
 <ul>
 <li>
 Product guides
 </li>
 <li>
 End user and administrator documentation
 </li>
 <li>
 Release notes and feature updates
 </li>
 </ul>
 <li>
 Update documentation to reflect new features, enhancements, and bug fixes
 </li>
 <li>
 Help internal users maintain their teams&rsquo; documents on the company wiki
 </li>
 <li>
 Maintain written procedures of documentation team processes
 </li>
 <li>
 Work closely with the lead Technical Writer as well as Product Managers and Engineers to learn about the FileCloud product and the product releases process
 </li>
 <li>
 Review existing content for clarity and accuracy
 </li>
 <li>
 Try new features and confirm that documentation accurately describes their functions and behavior
 </li>
 <li>
 Follow established documentation standards, templates, and style guidelines
 
 </li>
 </ul>
 
 Required Qualifications:
 
 
 
 <ul>
 <li>
 0&ndash;2 years of experience in technical writing, documentation, or a related role. (internships and academic experience welcome)
 </li>
 <li>
 Strong proficiency in written and spoken English, with the ability to communicate technical concepts clearly, accurately, and professionally to a global audience
 </li>
 <li>
 Familiarity using documentation tools to create web-based documentation
 </li>
 <li>
 Proven ability to learn technical concepts
 </li>
 <li>
 Some understanding of basic coding concepts
 </li>
 <li>
 Ability to work with cross-functional teams and incorporate feedback effectively
 </li>
 <li>
 Strong attention to detail and commitment to content accuracy
 
 
 </li>
 </ul>
 
 Preferred Qualifications:
 
 
 
 <ul>
 <li>
 Experience documenting software products.
 </li>
 <li>
 Basic coding experience.
 </li>
 <li>
 Understanding of:
 </li>
 <ul>
 <li>
 Web applications
 </li>
 <li>
 System administration such as maintaining users and assigning permissions.
 </li>
 <li>
 Data/feature sharing between applications
 </li>
 </ul>
 <li>
 Familiarity with version control.
 </li>
 <li>
 Experience working in Agile or Scrum-based environments.
 
 </li>
 </ul>
 
 What We Offer &ndash; These Do Not Change
 
 
 
 <ul>
 <li>
 Be part of a team of passionate, committed individuals dedicated to building a world-class product
 </li>
 <li>
 Dedicated time for training and education opportunities
 </li>
 <li>
 A mentorship model wherein your mentor and team support your development
 </li>
 <li>
 A competitive salary with an annual bonus
 </li>
 <li>
 Onsite work with flexible hours that fall outside of 8am -12pm (US Eastern Standard Time) / 4pm &ndash; 8pm (Arabic Standard Time)
 </li>
 <li>
 20 days of paid time off, which increases by a further 2 days after 3 years of service and 3 days after 5 years of service (in addition to 10 public holidays in your country)
 </li>
 <li>
 Paid day off on your birthday or on an alternative day if your birthday falls outside a typical working day
 </li>
 <li>
 Paid day off to volunteer with the charity of your choice
 </li>
 <li>
 Paid monthly internet cost, as well as lunch and a wellbeing stipend provided
 </li>
 <li>
 Reimbursement of all hardware costs associated with the role
 
 
 </li>
 </ul>
 Please note that we conduct background security checks for everyone joining our team.
</div>

サイネオス・ヘルス

<div><div><div>Updated: Today 
Location: Pune, MH, India 
Job ID: 25104934
<div><div>Not ready to apply? 
Join our Talent Network
</div></div><div>Description
Senior Medical Writer (Medical Information Writing)
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health<ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities<ul><li>
Mentors and leads less experienced medical writers on complex projects, as necessary.</li><li>
Acts as lead for assigned med info writing projects.</li><li>
Manages and coordinates medical information activities within and across departments with minimal supervision<ul><li>
Responds to escalated queries from client internal and external teams (HCPs, patients, caregivers)
</li><li>Create or update an existent global standard scientific response communications (gSSRCs)/FAQs/global response documents/global guidance documents/local response documents based on client provided template or as per style guide</li><li>
Conducts literature search on PubMed, and/or other client-subscribed databases; and validate relevant inclusions
</li></ul></li><li>Experience in developing or supporting a variety of documents that include, but not limited to:</li><li>
Clinical journal manuscripts, clinical journal abstracts, posters, and oral presentations.</li><li>
Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.</li><li>
Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.</li><li>
Serves as peer reviewer on internal review team providing review comments on draft and final documents.</li><li>
Adheres to established regulatory standards, including but not limited to Journal/congress specific guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.</li><li>
Familiarity with figure-creation and data visualization software, including tools such as GraphPad Prism and Adobe Illustrator, for developing high-quality scientific figures and graphics.</li><li>
Familiarity with publication planning software e.g. Datavision and PubConnect (VeevaVault Promomats)</li><li>
Reviews deliverables for scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets.</li><li>
Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.</li><li>
Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.</li><li>
Completes required administrated tasks within the specified timeframes.</li><li>
Performs other work-related duties as assigned. Minimal travel may be required (less than 25%).</li></ul>
Get to know Syneos Health 
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information 
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Serves as a senior medical writer on clinical study or regulatory or publication project teams. Writes, edits, and coordinates content for clinical/regulatory/scientific while serving as primary technical contact with the internal team and the client.</div></div></div></div><div></div>

Senior Medical Writer (Medical Information Writing)

Syneos Health

<div>Description
Senior Medical Writer (Medical Information Writing)
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health<ul><li>
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>
We are committed to our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul>
Job Responsibilities<ul><li>
Mentors and leads less experienced medical writers on complex projects, as necessary.</li><li>
Acts as lead for assigned med info writing projects.</li><li>
Manages and coordinates medical information activities within and across departments with minimal supervision<ul><li>
Responds to escalated queries from client internal and external teams (HCPs, patients, caregivers)
</li><li>Create or update an existent global standard scientific response communications (gSSRCs)/FAQs/global response documents/global guidance documents/local response documents based on client provided template or as per style guide</li><li>
Conducts literature search on PubMed, and/or other client-subscribed databases; and validate relevant inclusions
</li></ul></li><li>Experience in developing or supporting a variety of documents that include, but not limited to:</li><li>
Clinical journal manuscripts, clinical journal abstracts, posters, and oral presentations.</li><li>
Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.</li><li>
Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.</li><li>
Serves as peer reviewer on internal review team providing review comments on draft and final documents.</li><li>
Adheres to established regulatory standards, including but not limited to Journal/congress specific guidelines, as well as Company Standard Operating Procedures, client standards, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.</li><li>
Familiarity with figure-creation and data visualization software, including tools such as GraphPad Prism and Adobe Illustrator, for developing high-quality scientific figures and graphics.</li><li>
Familiarity with publication planning software e.g. Datavision and PubConnect (VeevaVault Promomats)</li><li>
Reviews deliverables for scientific accuracy, data and referencing quality, appropriate style, and correct branding of scientific/medical assets.</li><li>
Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.</li><li>
Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.</li><li>
Completes required administrated tasks within the specified timeframes.</li><li>
Performs other work-related duties as assigned. Minimal travel may be required (less than 25%).</li></ul>
Get to know Syneos Health 
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information 
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Summary
Serves as a senior medical writer on clinical study or regulatory or publication project teams. Writes, edits, and coordinates content for clinical/regulatory/scientific while serving as primary technical contact with the internal team and the client.</div>

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