Communications Writer Salary in India - PayScale

SummaryAs a Technical/Process Writer at Gainwell, you will play a pivotal role in supporting our commitment to delivering better health and human services outcomes through innovative solutions. Working within our dynamic Customer Experience (CX) team, you will contribute to our Design, Develop, and Implement (DDI) and Maintain and Operate (M and O) projects by documenting processes, enhancing efficiency, and ensuring the highest quality standards.Your role in our missionEssential Job Functions:Collaborate with cross:functional teams to understand project requirements and objectives.:Develop comprehensive process documentation and mapping for DDI and M and O projects, ensuring alignment with organizational goal.:Develop policy/procedure templates and write policies/procedures with consistent format and language, only in cases where company templates are not established.:Interface with workstream leaders and relevant stakeholders to create and audit policies and procedures documentation.:Write new technical documents and revise detailed process procedures, office work instructions, process maps, forms, etc.:Create new and/or revise existing procedures to document policy:driven standards:Review existing procedures and revise to align with departmental standard.:Create/maintain applicable progress reporting.:Utilize QMS and CMMI requirements as basis to interview and collaborate with subject:matter experts to produce succinct and effective documentation.:Ensure final written documents clearly and effectively communicate processes and are developed in accordance with applicable requirements (e.g., Company templates, stylistic/grammatical standards).:Communicate document and project status to program management staff, delivers related presentations, and assists in the document security classification process.What were looking for:Bachelor's degree or associate degree in any field is required, preferably in a business, communication, English or healthcare field.:Proven experience in process documentation, mapping, and continuous improvement initiatives.:Excellent analytical skills with the ability to interpret data and identify trends.:Strong communication and interpersonal skills, with the ability to collaborate effectively across diverse teams.:Highly organized with exceptional attention to detail and the ability to manage multiple priorities.:Proficiency in Microsoft Office Suite and process mapping software (e.g., Visio, Lucidchart).

We help the world run betterOur company culture is focused on helping our employees enable innovation by building breakthroughs together. How? We focus every day on building the foundation for tomorrow and creating a workplace that embraces differences, values flexibility, and is aligned to our purpose:driven and future:focused work. We offer a highly collaborative, caring team environment with a strong focus on learning and development, recognition for your individual contributions, and a variety of benefit options for you to choose from. Apply nowWhat youll do:In SAP, Technical Writers are called User Assistance Developers, because that's what you do : you assist the users of our software.In a nutshell, your job as a Technical Writer (User Assistance Developer) will be to understand how SAP Logistics work, become familiar with different types of consumers of documentation, defined as SAP Logistics personas, and then formulate complex technical information into user:friendly documentation.The Role:Technical Writers in SAP Public Cloud Logistics team work with developers and product owners on defining what information needs to be passed on to users, to ensure that they can fully leverage the software for their business needs. Once you've gathered the information, you'll formulate it in English in different formats (as a release notes announcement or a detailed instruction). After the information has reached the users, your job will be to listen to their feedback and see what can be improved.Additionally, you will participate in shaping the UI and UX of SAP Public Cloud Logistics team by defining labels, informational messages, and other in:app text.EDUCATION AND QUALIFICATIONS/ SKILLS AND COMPETENCIES University degree in Technical Writing, IT, Business Studies or a related subject or, alternatively, a language:based university degree Excellent written and spoken skills in English Outstanding communication, writing, and grammar skills Ability to work to deadlines, deliver on time, and ensure high quality Interest in software development Self:motivated team player Willingness to acquire comprehensive product knowledge and learn new skills Knowledge of Content Management Systems (DITA) is a plusWhat you bring::Around 1.5:3 years of experience in technical writing, content writing, or journalism.:The ability to synthesize technical information into a user:friendly written text.:Excellent knowledge of English grammar and vocabulary (focus on software terminology).:Technical abilities::The ability to manually test software to understand the behavior to be documented.:Willingness to learn to use highly configurable software and understand its complexities.:The ability to differentiate backend from frontend processes.Additional skills required for the role: Familiarity with the agile methodology. Understanding software development processes. Experience with writing in:app text (labels, button names, tooltips, messages, etc.). The ability to formulate a text for different types of users.Meet your team:The Public Cloud Logistics team in Bangalore has end to end responsibility for Transportation Charge Management, Settlement, Contract Management areas and specific responsibilities in Master data, Freight order management and planning areas.We build breakthroughs togetherSAP innovations help more than 400,000 customers worldwide work together more efficiently and use business insight more effectively. Originally known for leadership in enterprise resource planning (ERP) software, SAP has evolved to become a market leader in end:to:end business application software and related services for database, analytics, intelligent technologies, and experience management. As a cloud company with 200 million users and more than 100,0

DESCRIPTIONAre you an extraordinary communicator who can translate complex business concepts into clear, concise and easy-to-consume content? Amazon's Consumer Content Team is looking for an experienced Content Editor with excellent writing and critical thinking skills, who can work independently in a fast paced, ambiguous environment. The Consumer Content team within Customer Service uses customer activity data, feedback and metrics to identify customer pain points, then advocates for and drives change through the organization to reduce defects and improve customer experience.The ideal candidate will have superb writing skills paired with the ability to create visually appealing communication solutions for today’s audience. S/he will have demonstrated project management experience and the organizational discipline to track and manage editorial work for several complex projects simultaneously. You will apply strong project and stakeholder's management, will gather requirements, analyze gaps and manage competing priorities. You need to be strong at setting expectations and timelines, and need to be able to operate independently while following our global processes, guidelines, and criteria. Proficiency in Content Management Systems (preferable SDL package – XMetal, Publication Manager, Web-client), DITA, knowledge of translation and localization processes and tools are highly advised. You should be able to build a roadmap and present it to leadership and other stakeholders across multiple teams and job levels. The candidate will also have demonstrated the ability to make quick decisions under pressure in ambiguous circumstances and have a record of extraordinary attention to detail and follow-through.Key job responsibilitiesAs a Content Editor on the team, you will be responsible for - • Partnering with technical and business teams, Public Relations and Legal to define company policy related to customer issues• Creating and maintaining the Amazon Help pages that empower Amazon customers to answer their own questions about our services• Creating and maintaining smart content in English in Content Management tools using DITA attributes, in a way that's scalable and easy to localize• Outsource content for translation using computer assisted tools• Responding to time-critical requests and advocate for the right content solutions; display an ability to prioritize and meet deadlines• Utilize web analytics and SEO best practices to improve content discoverability across website help pages• Use a combination of data analysis, user research, benchmarking, and content audits to make content decisions and orchestrate content development• Leading continuous improvement projects related to content accessibility, usability, completeness and branding• Strategizing and writing content for complex projects impacting customer experience • Strong stakeholders' management We are open to hiring candidates to work out of one of the following locations:Bengaluru, KA, INDBASIC QUALIFICATIONS• 3-5 years as an editor, technical writer, or content developer• Exceptional written and oral communication skills• DITA and CMS proficiency• Experience with XML content; familiar with content authoring tools • Experience with translation processes and tools• Familiar working in an Agile environment/sprints • Experience managing content projects, including coordinating with other teams• Experience driving complex large-scale projects independently • Experience developing or editing multimedia (images, videos)• Experience collaborating with design, UX, and product teams• A desire to dive deep into detail, problem solve, and execute• Bachelor degree in English, Communications, Content Strategy, or a related field• Proficiency with MS ExcelPREFERRED QUALIFICATIONS• Basic understanding of HTML• Basic understanding of UX design concepts• Experience analyzing data and deriving actionable inputs to be presented and reviewed in Business meetings• Master Degree in English, Communications, Content Strategy, or a related field• Experience in a multi-language authoring, translating/localization and publishing environment • A background in taxonomy desired • Reading/writing proficiency in any of the 6 Indian languages (Kannada, Tamil, Telugu, Malayalam, Bengali and Marathi) would be a definite plus.

Job Title: Technical Writer: Exp 4:6 yearsJob Summary : As a Techincal Writer you will help to create to create comprehensive documentation for our Applications which are Web and Desktop based applications. The ideal candidate will have a strong background in technical writing, excellent communication skills, and the ability to understand complex technical concepts and translate them into clear and concise documentation for various audiences.Key Responsibilities::Documentation Creation: stylelist:style:type:disc::Develop clear, concise, and comprehensive documentation for our web application, including user guides, technical specifications, API documentation, release notes, and other supporting materials.:Content Maintenance: stylelist:style:type:disc::Ensure documentation is up:to:date with the latest product features, enhancements, and changes.:Collaboration:stylelist:style:type:disc::Work closely with cross:functional teams including developers, product managers, designers, and customer support to gather information and ensure accuracy of documentation.:User Experience:stylelist:style:type:disc::Collaborate with UX/UI designers to ensure documentation is aligned with the overall user experience and interface design.:Accessibility: stylelist:style:type:disc::Ensure documentation complies with accessibility standards and is accessible to users with disabilities.:Quality Assurance: stylelist:style:type:disc::Review and edit documentation for accuracy, clarity, and consistency.:User Feedback: stylelist:style:type:disc::Gather feedback from users and stakeholders to continuously improve documentation quality and usability.:Training Support:stylelist:style:type:disc::Assist in the development of training materials and resources for internal teams and end:users.:Knowledge Management: stylelist:style:type:disc::Contribute to the organizations knowledge base by documenting best practices, troubleshooting tips, and common user questions.:Adherence to Style Guidelines: stylelist:style:type:disc::Maintain consistency and adherence to company style guidelines, branding, and tone of voice across all documentation.Qualifications:stylemargin:bottom:11.0px::Bachelor's degree in English, Technical Writing, Computer Science, or a related field.:Proven experience as a technical writer, preferably in the software industry.:Excellent writing, editing, and proofreading skills with keen attention to detail.:Strong understanding of web technologies, including HTML, CSS, JavaScript, and RESTful APIs.:Experience with documentation tools such as Oxygen,X:Metal:Familiarity with version control systems such as Git.:Ability to work independently, manage multiple projects, and meet tight deadlines.:Strong communication and interpersonal skills with the ability to collaborate effectively with cross:functional teams.:Experience with Agile development methodologies is a plus.About Bentley Systems:Bentley Systems (Nasdaq: BSY) is the infrastructure engineering software company. We provide innovative software to advance the world's infrastructure : sustaining both the global economy and environment. Our industry:leading software solutions are used by professionals, and organizations of every size, for the design, construction, and operations of roads and bridges, rail and transit, water and wastewater, public works and utilities, buildings and campuses, mining, and industrial facilities. Our offerings, powered by the iTwin Platform for infrastructure digital twins, include MicroStation and Bentley Open applications for modeling and simulation, Seequent's software for geoprofessionals, and Bentley Infrastructure Cloud encompassing ProjectWise for project delivery, SYNCHRO for construction management, and AssetWise for asset ope

Department: Global Medical Affairs : Regions and Operations.Are you a postgraduate in medicine/ life science/biomedical research willing to be a credible and valued scientific expert of the organization to interact with key stakeholders across their regions / products / therapy areas? Do you enjoy collaborating with peers in the medical field, interpreting and communicating scientific data? Does interacting with global medical leaders interest you? Then we have an opportunity for you within our Global Medical Affairs department. Apply now and join a growing team, working in an international environment.The PositionAs a Global Medical Advisor, will assist closely in providing strategic and medical guidance covering portfolio of products and functionally be a part of IO : SO (International Operations : Strategic Operations) Medical affairs team. Furthermore, you will be working on medical education and guidance materials across therapy areas. Additionally, will be responsible for Generation, Interpretation and Communication of scientific data to ensure proper usages of Novo Nordisk products. Execute clinical importance of new findings and impact in future and current treatment of diabetes and other serious chronic disorders. Deliver timely accurate and credible scientific medical guidance across medical affairs focus areas towards internal and external stakeholders. Entrusted to fulfil the following responsibilities:stylemargin:bottom:11.0px::Ensure effective collaboration between IO SO medical affairs team and acts as a liaison between Novo Nordisk and Key Opinion Leaders.:Transforming clinical trial data into scientific and commercial communication, used to scope/plan the support of our products and provide early market access.:Cross:functional collaboration : Regions and Affiliates, Global Research, Global Development, Strategy Access Marketing, Medical Affairs Regulatory Safety.:Develop and maintain strong relationships with Global Key Opinion Leaders and provide input, develop and execute on global Health Care Professional strategy.:Support the development and execution of publication plan in collaboration with the publication team (Publication managers from global and IO:SO).Qualificationsstylemargin:bottom:11.0px::Should possess MBBS/M.D. in Medicine (Pharmacology, Biochemistry, Genetics etc./Any Specialization).:1:5 years of clinical and/or pharmaceutical industry experience.:Fluency in both spoken and written English.:Demonstrated research experience and good medical/scientific writing skills (e.g. publications), i.e. ability to provide high quality literature review, abstracts, posters, and slide sets, and Manuscripts (complex) working from various data sources including clinical study reports, patient profiles, protocols etc.:Additional education and experience in project management/business administration / marketing is an added advantage.:Minimum one year of study or work in a country other than the native country is preferred.About the departmentGlobal Medical Affairs, GBS is an extension of the Global Medical Affairs, headquartered in Denmark (HQ), and is part of Global Business Services (GBS), Bangalore, India. The team consists of highly motivated global medical advisors, global scientific advisors (medical writers), project managers, graphic designers and publication managers working together with the Global Medical Affairs department in Søborg, Denmark, the regional CMR departments, and the Medical Affairs department in the US affiliate of the company. Our core competencies include communicating scientific and medical knowledge on our products to the external scientific community and across the organisation, in:house content development, project management and publication planning for external medical events.Working at Novo NordiskNovo Nordisk is a leading global healthcar

Department : Clinical Reporting UnitDoes your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can:do attitude with continuous improvement as one of your career objectives? Then we might have the right position for you. Apply now and join a growing team, working in an international environment.About the departmentThe Clinical Reporting unit in GBS has seen a tremendous growth curve and has become an integral part of the Global Clinical Reporting community in a short span of 6:7 years, since its inception in 2011. The team is a dynamic mix of enthusiastic and qualified skilled medical writers, Disclosure Medical Writers, Publishers, and Document Controllers with master/PhD in life sciences, pharmacology, medicine, etc. The team is full of commitment, passion, skills, and talent with broad knowledge of different therapeutic areas and regulatory requirements for submissions. The team has an average experience of 7:8 years in writing and reviewing regulatory documents and publications. We use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials. Apart from writing and publishing regulatory documents, the team is also responsible for the distribution of documents (CONNECT portal) and largely contributes to NN's regulatory commitments by being involved in Public disclosure activities.The PositionAs a Medical Writer, you will ensure timely, clear, and proactive communication and collaboration with the stakeholders and colleagues globally. Furthermore, you will communicate across the time zones and in different professional environments. This job requires good communication and analytical skills. To meet timelines, you must be good at planning your work be proactive when problems arise, and seek help and advice from relevant people within GBS as well as within Head Quarters (HQ). Additionally, you will challenge the expert contributors on the clinical documents where the quality of their written contribution could be improved. You are entrusted to fulfill the following responsibilities::Ensure timely, clear, and proactive communication and collaboration with the stakeholders and colleagues globally.:You will contribute to process improvements, knowledge sharing, and skill building, and mentor and train other medical writers as needed. You will have to maintain good relationships with the stakeholders and colleagues.:Responsible for meeting timelines, the medical writer must be good at planning their work be proactive when problems arise, and seek help and advice from relevant people within GBS as well as within HQ.:You will challenge the expert contributors on the clinical documents where the quality of their written contribution could be improved.:Frequent traveling abroad to attend meetings in HQ and CMRs, and conferences and courses worldwide, will be part of the job.QualificationYou are expected to have the following skills and knowledge::Graduate (PhD, MSc., M Pharm, or equivalent).:4+ years of experience as a medical writer or other relevant work experience.:Experience working within a global setting.:Experience in the pharmaceutical /CRO industry.:Strong understanding of external requirements related to regulatory documents.:Good communication skills.:Works independently on smaller tasks.:Strong analytical skills.:Committed, persistent, and accountable.:Able to plan and manage variable workload.Working at Novo NordiskNovo Nordisk is a leading global healthcare company with a 100:year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reachi

Department : Clinical Reporting GBS We are looking for a Senior Medical Writer in the Clinical Reporting unit based out of Global Business Service (GBS), Bangalore, India. Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can:do attitude with continuous improvement as one of your career objectives? Then we might have the right position for you. Apply now and join a growing team, working in an international environment. About the departmentThe Clinical Reporting unit in GBS has seen a tremendous growth curve and has become an integral part of the Global Clinical Reporting community in a short span of 6:7 years, since its inception in 2011. The team is a dynamic mix of enthusiastic and qualified skilled medical writers, Disclosure Medical Writers, Publishers, and Document Controllers with master/PhD in life sciences, pharmacology, medicine, etc. The team is full of commitment, passion, skills, and talent with broad knowledge of different therapeutic areas and regulatory requirements for submissions. The team has an average experience of 7:8 years in writing and reviewing regulatory documents and publications. We use our scientific expertise to drive clear and impactful communication on the conduct and outcome of clinical trials. Apart from writing and publishing regulatory documents, the team is also responsible for the distribution of documents (CONNECT portal) and largely contributes toNN's regulatory commitments by being involved in Public disclosure activities. The positionThe key responsibilities in this position will be to perform medical writing tasks for trial and/or non:trial activities within clinical reporting including but not limited to the preparation of Protocols, Clinical Trial Reports (CTRs), Non:interventional study reports (NSRs), Layperson Summary (LPS), Investigator Brochure (IB), Regulatory response documents (Q and A), Clinical summaries and Clinical overviews. The tasks, to a large extent, will have to be performed independently. You will have to communicate the clinical data clearly and concisely. :Ensure timely, clear, and proactive communication and collaboration with the stakeholders and colleagues globally.:You will contribute to process improvements, knowledge sharing, and skill building, and mentor and train other medical writers as needed. You will have to maintain good relationships with the stakeholders and colleagues.:Responsible for meeting timelines, the medical writer must be good at planning their work be proactive when problems arise, and seek help and advice from relevant people within GBS as well as within HQ.:You will challenge the expert contributors on the clinical documents where the quality of their written contribution could be improved. :Frequent traveling abroad to attend meetings in HQ and CMRs, and conferences and courses worldwide, will be part of the job. QualificationYou are expected to have the following skills and knowledge::Graduate (PhD, MSc., M Pharm, or equivalent).:5+ years of experience as a medical writer or other relevant work experience.:Experience in CSR, protocol, IB, informed consent, and clinical summaries and clinical overviews.:Experience working within a global setting.:Experience in the pharmaceutical /CRO industry.:Strong understanding of external requirements related to regulatory documents.:Strong analytical skills., committed, persistent, and accountable.:Able to manage variable workload and able to handle numerous tasks simultaneously.Working at Novo NordiskWe are a proud life:science company, and life is our reason to exist. We're inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employe

Technical Writer/Senior Technical WriterYour role will involve:- Working with subject matter experts to obtain an in:depth understanding of products- Producing easy:to:understand user documentation for user guides, tutorials, FAQs, online Help, and release notes- Working with content in multiple formats including graphics, animation, and videos- Reviewing and revising content to improve clarity and follow style guidelines- Maintain existing content, working with experts to revalidate or update content- Proactively identifying opportunities and methods for improving processes and toolsIn return you will bring:- Proven track record of producing concise, grammatically correct technical documentation and learning assets to aid product adoption and usage- Familiarity with the Software Development Life Cycle and general software development. Experience using Confluence + Jira or other project management tools a plus- Excellent interpersonal and relationship:building skills - A strong learning motivation and the ability to seek out and rapidly absorb complex technology domains- Passion to thrive in a fast:paced, ever:changing environment and the ability to manage multiple projects simultaneously- A proactive and open:minded attitude to resolving problems and delivering results.- Strong attention to detail. Preferred qualifications: - Degree in English, Technical Writing, or a related field highly desirable.- Strong English language skills demonstrating proficiency in technical communication- An understanding of cloud computing, including cloud storage technologies.- HTML and Photoshop or other image management skillsAs a technical writer, you will ultimately impact the organization by producing easy:to:follow guides, tutorials and documentation that accelerate product adoption and significantly improves customers' integration experience.