762 Technical Writing Jobs

Summary -Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within a multifunctional project team coordinated by a Project Leader. Manage technical lab/plant activities. -Management TrackLead a team for the development of pharmaceutical / biological / cell-gene therapies working in a small manufacturing plant environment. Execute the functional strategy and drive operational excellence in line with TRD vision and strategy. Ensure full portfolio support in line with GDD, Sandoz, NTO and NIBR plans. -SANDOZ: -Associate Scientist: Design, plan, perform, interpret and report results of scientific experiments for the development and timely delivery of drug products (DP), processes and procedures within a multifunctional project team coordinated by a Project Leader. Manage technical lab/plant activities. -Scientist: -Design, plan, perform, interpret and report results of scientific experiments for the development and timely delivery drug products (DP), processes and procedures. Lead and manage all project/local network activities, support/coach team members, participate in sub-teams and contribute to overall SZ strategies and goals -Senior Scientist: Design, plan, perform -document and interpret scientific/developmental experiments and GMP testing or pilot plant processes for the preparation and timely delivery of generic products, processes or procedures; maintain and qualify equipment/infrastructure and manage operational aspects in lab or plant as assigned. About the Role Major accountabilities: Meet quality, quantity and timelines in all assigned projects. Ensure all own activities are aligned with overall drug development process. Plan, organize, perform and document scientific experiments/plant activities in collaboration with project teams and under minimal guidance from more experienced team members (eg. contribute to interpretation and report results). Seeks proactively for support and coaching from Project Leader, Scientific Expert or other team members during the whole process if necessary. Provide efficient and robust processes for the manufacture and/or specialized facilities e. g. containment/sterile labs as an expert w/ adequate guidance. Provide raw data documentation, evaluation and results interpretation. Propose and provide input for the design of next experiments. Optimize existing methods, procedures, workflows (lab or plant) and develop more efficient ones. Generate lab procedures, reports and/or instructions and/or SOP s. Actively transfer procedures/instructions to pilot plant or production, including troubleshooting, process steering controls etc Communicate and address problems, perform safety and literature searches under moderate guidance from more experienced team member. Keep record of and manage chemicals, intermediates, excipients and solvents within own area of responsibility. Collaborate with other team members to facilitate deliveries of DS and/or DP. Utilize special tools/equipment and/or specialized facilities e. g. , containment/sterile labs. Evaluate new lab equipment. Contribute to maintenance of infrastructure/equipment. Ensure all own activities are aligned with overall drug development process. Support team s resource planning and effective resource utilization Support and foster strong quality/compliance mindset for own projects and overall portfolio/initiatives. Ensure internal processes as per SOPs/guidelines are followed and internal quality metrics are met. Fully support GxP and general deliverables. Ensure training is up-to-date and on time; no overdue training assignments without acceptable cause. Ensure strict adherence to HSE rules and guidelines. Key performance indicators: Successful execution of assigned tasks within given timelines at expected quality; right first time and right in time -Adherence to appropriate standards as defined in Quality Manual, SOPs, ethical, health, safety, environment (HSE), and information security (ISEC) guidelines -Adherence to costs, quality, quantity, and timelines for all assigned tasks. Feedback from other team members/leaders. Refer to annual individual and team objective setting. Measurable contributions to increasing efficiency and productivity in the work related to assigned projects. Feedback from other team members/leaders. Refer to annual individual and team objective setting. Measurable contributions to increasing efficiency and productivity in the work related to assigned projects. Minimum Requirements: B. Pharm /M. Pharm with relevant experience of around 3-8 years. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment. Demonstrated successful experience with working in interdisciplinary and cross-cultural teams. Thorough knowledge of relevant SOP, GMP regulations and policies if applicable. Adequate knowledge in scientific/technical areas of collaboration. Proficient with laboratory and/or technical tools. Adequate knowledge of software and computer tools. Basic presentation skills and scientific/technical writing skills. Good Communication skills Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients lives. Ready to create a brighter future togetherhttps://www. novartis. com / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for youSign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork. novartis. com/network Benefits and Rewards: Read our handbook to learn about all the ways we'll help you thrive personally and professionally:

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don t settle for the mediocre. Each of us is driven to help improve patients lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Job Summary Job Title - Technical Leader - Drug Products and Sciences Location - Whitefield, Bangalore Shift - General Job Responsibilities and Skills: As Technical Leader, define, organize, plan and lead the projects that are technically complex and cross functional in nature at a global front Lead multi-functional project team for effective collaboration and deliverables Prior experience of managing diverse and cross functional teams at a global front Understanding of regulatory, process development, quality management systems, QbD tools, drug modelling and design of experiments in the field of drugs and medical devices Good knowledge of product development stages, Bio design process and life cycle management in the area of drugs and medical devices Prior experience with the new product and process development in the area of drugs, medical devices and combination drug/device systems Prior track record of translating new ideas to workable and commercially feasible products in the area of drugs and medical devices Being able to anticipate risks/challenges and willingness to deal with ambiguity Sound understanding of invention disclosures and patent filing processes Coordinate and ensure follow-up of technical activities in collaboration with key stakeholders, with respect of project commitment, quality procedures and business needs Propose options and develop action plans for problem-solving, product and process inventions and improvements Establish, maintain and update technical Design documentation according to Good Documentation Practices Fluent with Technical Writing, Documentation and reports generation Influential leadership and ability to flex as the role demands while interacting with internal and external stakeholders Out of the box and critical thinking ability Qualifications Ph.D/Masters in Pharmaceutics, Chemical Engineering, Biology, Biosciences and Biomedical engineering Minimum of 10 years of diverse industrial experience post Ph.D and about 15 years post Masters in the given technical domains of interest Desired if the incumbent had more than one jobs/roles and has interacted with many different global stakeholders in a given role Clear and effective communication (written, oral) and presentation skills. Good stakeholder management (local and global) A proven track record of effectiveness in a fast-paced environment. Proven ability to create results within budget, timeline, and product/project deliverables Skills Demonstrate strong project management and people leadership skills Ability to work independently Can effectively communicate with internal and external customers Demonstrates flexibility and the ability to shift gears between projects comfortably Fluency in English Good knowledge of Design Control documentation and medical writing Sound knowledge of international/regional/national regulations and standards for drugs and medical devices Acquire business acumen with time Experience with Statistics and Six Sigma tools Solid computer skills: email, documentation and collaboration tools: eg WebEx, Teams, Microsoft Office products, etc Reasonable Accommodation

The Technical Communications Manager (TC) is responsible for gathering inputs on the product requirements, identifying the requirements, and documenting them into the respective manuals of intended use. The TC should conceptualize the delivery of content and identify the tool to be used to deliver the conceptualized content. The TC should ensure that the deliverables are made on time in accordance to the project plan timelines (complete and/or interim releases) and by following the Siemens Style Guide, Technical Writing rules, and the Document Development Life Cycle. The TC is also responsible for conducting the review of the documents as per the process requirements and archiving them in the designated repositories as per the quality requirements. In addition to this, the TC is responsible for managing the localization and translation of the deliverables to the respective languages. Internal Interactions: Product Manager, Project Manager, Quality Manager, Development Team (eg Scrum Master, System Analyst, Architect, Developers, Testers), Usability Engineer, other stakeholders (eg Business Units) What are my tasks? Develop and deliver assigned content based on requirements of products and processes. Plan, control and support tracking of documentation, training and learning activities according to project schedule. Adhere to product/organizational processes and quality guidelines for content creation and tooling. Participate in team planning discussions and execute review activities. Work in close coordination with technical teams, product and project management for planning and delivery. Regular reporting to Team Lead as we'll as stakeholders/partners on status, risks and issues. Identify and resolve gaps and inconsistencies in the existing documentation. What do I need to know to qualify for this job? Minimum Qualification: Any non-technical graduate (B.A., B.Sc, B.Com) or B.E/B.Tech/ - Electrical \ Electronics \ Computer Science Experience: We are looking for someone with 2-4 years of experience in professional technical writing. Knowledge/Competencies: Expertise in technical documentation (analysis, concept, design). Knowledge of content management systems, authoring tools, graphic tools, documentation standards and rules. Good understanding of database concepts and terminology. Awareness of the agile method of software development. Familiarity with understanding of XML files and the use of XSD files. Excellent verbal and written communication skills and presentation skills. Ability to balance high quality work standards against time constraints. Sound analytical and problem-solving skills. Ability to work as an individual contributor and take ownership. Should be willing to travel for project requirements. The following competencies are desirable: Healthcare IT knowhow Clinical Workflow Knowledge Regulatory Requirements for medical devices (ie FDA 21CFR820QSR, ISO 13485) Presentation, Elicitation, Negotiation, Communication Product Standards (DICOM, IHE, etc) Leadership What experience do I need to have? Professional: Experience in conceptualizing, creating, and delivering documents as per technical documentation standards. Expertise in performing user analysis to determine the scope of update in a document. Expertise in working in a team environment. Project / Process: Experience in working in a SW development. Experience in agile development projects. Intercultural: Experience with international/ intercultural teams (desired, but not necessary). What else do I need to be strong at? Self-starter and quick learner Self-driven and Initiative Creative and strategic thinking Decision making skills Result orientation Self-motivated and provides motivation and inspiration to the team Strong analytical and problem-solving Skills. Strong team player and networking skills Strong written and oral communication skills. Strong interpersonal skills Strong customer focus

Lead the planning, coordination, preparation and review of EIA reports (Form 1, ToR, EIA, EMP, Public Hearing, etc) for various sectors (eg, Building Construction, Mining, Township). Manage all stages of EIA process including baseline survey planning, stakeholder engagement, impact assessment, and formulation of mitigation and monitoring plans. Ensure compliance with EIA Notification 2006, its amendments, and sector-specific guidelines. Coordinate with multidisciplinary teams (air, water, noise, ecology, land use, socio-economy) and integrate inputs for comprehensive reporting. Liaise with clients, regulatory agencies (MoEF&CC, SEIAA, SPCBs) other statutory bodies for compliance, submission, and presentation during appraisal meetings. Supervise baseline data collection, impact prediction, and mitigation planning using appropriate tools and modeling software. Ensure timely compliance to NABET Quality Management System (QMS) and maintain all project documentation for auditing and recordkeeping. Lead communication with clients and stakeholders; conduct public consultations and grievance redressal processes wherever applicable. Stay updated on regulatory updates, circulars, and best practices in EIA and environmental management. Contribute to training and capacity building of junior team members and interns and support business development efforts. Identify and pursue opportunities for new business development, RFPs, and sectoral expansion. Eligibility: Minimum 5-7 years of relevant experience in EIA with a NABET approved environment consultancy or organisation. Should have worked on at least 5 Category A and 20 Category B projects in various sectors. EIA Coordinator in atleast one or more sectors ,Approved Functional Area Expert (FAE) or Team Member (TM) under NABET Scheme in at least one or more areas (eg, AP, AQ, SC, WP, EB). Strong command over EIA Notification, 2006 and its amendments, CRZ Regulations, Environmental Clearance process, and environmental legislations (Water Act, Air Act, EPA, etc) Demonstrated experience in interacting with regulatory authorities, making presentations before SEAC, SEIAA, and MoEF&CC Expert Appraisal Committees. Project management, leadership, and client-handling capabilities. Excellent technical writing and communication skills in both Marathi and English mandatory. Advanced proficiency in Microsoft Word, Excel, PowerPoint, including formatting, data analysis, charting, and automated reporting. Experience in environmental modeling tools (eg, AERMOD, and QGIS/ArcGIS) Proven ability to manage multiple complex projects independently, handle client communications, and ensure quality delivery under deadlines. Strong analytical, documentation, and stakeholder engagement skills. Ability to interpret and analyze monitoring data, third-party lab reports, satellite imagery, and GIS maps Qualifications : M.Sc./M.Tech.in Environmental Science /Engineering or postgraduation in any related discipline

We are seeking a Technical Writer with Trainer capabilities who can create high-quality documentation while also delivering training sessions on IT products and technologies. This hybrid role requires strong technical writing skills to develop user manuals, API documentation, and training materials, as we'll as the ability to conduct live training sessions for employees and clients. Roles and Responsibilities: Develop, edit, and maintain technical documentation such as user guides, API documentation, FAQs, and product knowledge bases. Work closely with developers, product managers, and QA teams to understand technical concepts and translate them into clear, user-friendly documentation. Create step-by-step tutorials, system architecture diagrams, and other visual aids to enhance learning. Maintain document version control and ensure documentation is updated in line with product releases. Use documentation tools such as Confluence, MadCap Flare, RoboHelp, or Markdown to manage content effectively. Design and deliver technical training programs for internal teams, customers, and partners. Conduct live and virtual training sessions on software applications, IT tools, and best practices. Develop training materials, presentations, video tutorials, and e-learning modules. Assess trainees understanding and adjust training methods for better engagement. Stay updated on industry trends and incorporate new training techniques to improve learning outcomes. Skills and Qualifications: Bachelors degree in Computer Science, IT, Technical Communication, or a related field. 5+ years of experience in technical writing and IT training. Strong knowledge of software development, APIs, cloud computing, DevOps, or gitbook Proficiency in documentation tools such as MS Word, Confluence, MadCap Flare, RoboHelp, Git, and Markdown. Experience with Learning Management Systems (LMS) and training tools such as Articulate, Captivate, or Camtasia. Excellent writing, communication, and presentation skills. Ability to simplify complex technical concepts for different audiences. Relevant certifications in Technical Writing, Instructional Design, or IT Training are a plus.

The Technical Documentation team at Zuora is pivotal in ensuring the success of our customers. Our team of experienced technical writers owns the end-to-end documentation lifecycle for our cloud-based software solution, and we're looking for an excellent writer to join us as we expand the team within India into Chennai. you're a great fit if you love figuring out how things work, have a passion for technology, and are able to turn complex ideas into simple instructions and conceptual content. What you'll do Research, write, and maintain high-quality online documentation Become an expert on our products from both a technical and business standpoint Work independently and manage your own projects while building relationships across Zuora Collaborate closely with product managers, software engineers, customer support agents, and other technical writers Articulate the documentation needs of our customers, strategic partners, and internal users Lead initiatives to enhance the effectiveness and influence of the Technical Documentation team Your experience 6+ years of technical writing experience. We will also consider related experience Excellent spoken and written English. All of our documentation is written in English Great project management skills and knowledge of technical writing best practices Experience authoring in structured XML (DITA) Experience leading or mentoring other technical writers The ability to manage competing priorities in a fast-paced environment A passion for technology and a desire to learn. You will learn something new every day! It would be a bonus if you have: A strong technical background, such as a degree in Computer Science or a related subject Knowledge of accounting, finance, billing, payments, or another business function Experience using and documenting REST APIs Experience using web authoring tools and content management systems Experience of UX writing, content strategy, or information architecture Experience with the Agile software development process ZEOLife at Zuora As an industry pioneer, our work is constantly evolving and challenging us in new ways that require us to think differently, iterate often and learn constantly it s exciting. Our people, whom we'refer to as ZEOs are empowe'red to take on a mindset of ownership and make a bigger impact here. Our teams collaborate deeply, exchange different ideas openly and together we're making what s next possible for our customers, community and the world. As part of our commitment to building an inclusive, high-performance culture where ZEOs feel inspired, connected and valued, we support ZEOs with: Competitive compensation, variable bonus and performance reward opportunities, and retirement programs Medical insurance Generous, flexible time off Paid holidays, we'llness days and company wide end of year break 6 months fully paid parental leave Learning & Development stipend Opportunities to volunteer and give back, including charitable donation match Free resources and support for your mental we'llbeing

Must be able to document user manuals, release notes, installation documents, compliance documents, and so on from scratch and contribute to existing documents as we'll. Must be an avid learner of new technologies. Must be able to work extensively on internal engineering documents that will be used by developers and implementation specialists. Must have experience in documenting web-based technology like Dockers and API and Payment Gateways. Must be an individual contributor (take ownership and work with limited direction) and also coexist within a team of writers. Must be able to switch between multiple products (Cloud-based, iSeries-based, and OnPrem applications). Must have experience in standard technical writing tools; experience in ScreenSteps and AppCues is a value-add. Requirements Graduate in any discipline. Must possess at least 2 of the following skill sets Demo Environment Preparation. Design (Photoshop/Illustrator; Preferably Vector). HTML5/CSS. eLearning Content and training. Other Desired Experience Exposure to Hospitality Industry is greatest plus. Technical Writing,Technical Documentation,illustrator,api

Career Category Safety Job Description Join Amgen s Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it s because you are. Our shared mission to serve patients living with serious illnesses drives all that we'do. Since 1980, we've helped pioneer the world of biotech in our fight against the world s toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we'reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we'research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Pharmacovigilance Operations Senior Mgr What you will do This role supports the end-to-end writing and documentation process and ensures timelines are met. Provide audit external inspection support as required. Key Responsibilities: Periodic Report Process: Supervision of a team of Periodic Report Managers in Amgen India with Periodic Report responsibilities Organise the end-to-end process of report production and ensure the required quality standards and key timelines are met. Provide oversight to co-authors as applicable and be accountable for the quality of their work. Act as main point of contact for Director of PASR on all Periodic Aggregate Safety Report work Act as a writing coach, provide regular quality feedback, and share standard processes with team for promoting the use of clear and concise writing and alignment to style guides and templates as applicable. Support project management activities, including estimation of resource requirement. Implement and promote use of consistent, efficient and quality processes to meet timelines and work according to requirements and SOPs and assume accountability for the work Ensure compliance of operations with governing regulatory requirements. Analysis and communication of PASR quality with Director of PASR team Customer concern of issues around quality and KPIs to Director of PASR Provide metrics for audit/inspection support for PASR related activities Literature Management Process Supervision of a team of Literature review scientists Responsible for the business process of and oversight of the global literature review process Responsible for engagement and oversight of system vendors supporting the global literature review process Responsible for training and onboarding of literature review team Responsible for the proposal, generation, and maintenance of metrics and/or KPI/KCIs related to global literature review Stay ahead of technology and innovation to improve the efficiency and quality of scientific literature search and review Collaborate with TA Safety and Case Management on process and system improvement opportunities What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is someone with these qualifications. Basic Qualifications: Doctorate degree / Masters degree / Bachelors degree and 12 to 17 years of relevant experience Preferred Qualifications: Handling direct reports on a day-to-day basis and raising topics as needed to Director of PASR team Work within the Quality Management System framework including all applicable training and controlled documentation governing Pharmacovigilance processes Responsible for the growth and development of direct reports Ensure monthly review of performance metrics for the PASR process. Build and maintain good functional and multi-functional relationships globally Inspection Readiness: Undertake activities delegated by the QPPV as detailed in the PV System Master File and maintain a state of inspection readiness Support audit and inspection work, including but not limited to information requests and response QC. Extensive knowledge of global regulatory requirements for Pharmacovigilance Extensive knowledge of global PASR requirements Extensive knowledge of authoring PASRs Extensive people management experience Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment Understands and interprets data/information and its practical application Knowledge of scientific/technical writing and editing Excellent English written/oral communication, and strong time and project management skills strategic mentality, attention to detail, and the ability to work multi-functionally across multiple teams to ensure compliance, operational efficiency, and continuous improvement within Pharmacovigilance Operations. Demonstrate knowledge of global aspects of pharmacovigilance Strong knowledge of processes and global regulations for pharmacovigilance and periodic / aggregate reporting Ability to effectively handle challenging priorities and timelines Strong leadership skills, independence, networking and influencing skills Computer literate: knowledge of MS work, PowerPoint, Adobe Acrobat, MS Excel, SharePoint and Document Management Systems e. g. Veeva Vault Experience in use of AI and prompts would be useful What you can expect of us As we work to develop treatments that look after others, we also work to care for your professional and personal growth and we'll-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers. amgen. com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. .

The Supply Operation Quality (SOQ) Senior Associate will be responsible for supporting, maintaining, and implementing the Quality Management System (QMS) at the Pfizer Country Offices (PCOs) to ensure compliance with both Pfizer and Regulatory Authority expectations. The SOQ Senior Associate will work closely with relevant local stakeholders, such as Global Regulatory Sciences (GRS), Global Supply Chain (GSC), Medical, and PGS sites or ESOQ to ensure that the appropriate quality standards and systems are implemented and maintained for the product supply operation of the Pfizer India and neighboring market (Sri Lanka, Bangladesh, Nepal) business. Quality Assurance Inspections and Internal Audit Assists with the timely implementation of applicable quality management systems (SOPs) within the PCO. Assists with ensuring initial and continuous training programs are implemented and maintained for all relevant PCO colleagues. Ensures planned, permanent temporary changes of GMP/GDP related activities systems are managed documented appropriately. Ensures change actions are completed as per agreed timelines. Collects key quality performance indicators, evaluates and highlights any significant trends and identifies actions. Monitor Key Performance Indicators (KPIs) of the QMS, evaluate and highlight significant trends, and identify actions. Leads and/or participates in Quality Review Meetings as required. Provides support in the preparation and coordination of any Health Authority (HA) inspection and/or internal Pfizer audits of GMP/GDP activities in the PCO. Work with local cross functional team to define appropriate action plans to address the inspection/audit observation and tracks action implementation within the agreed timelines. Participates in the self-inspection program as an auditor and/or auditee, as required. Leads and/or participates in the Quality Risk Management program for the consistent application, documentation and communication of risks to product quality/patient safety in support of GxP activities under the remit of SOQ. Local Product Disposition Resolution of Product Quality Perform the local release process of Products under the PCOs distribution license, as required. Supports the coordination of all Product repackaging and/or relabelling activities in the PCO and at the third-party packaging site. Review and approve documentation related to the repackaging and/or relabelling of Pfizer Product, as required. Actions Quarantine Alert Notifications promptly, as needed. Ensures quarantine shipments are managed compliantly according to procedures, as required. Provides support for any market action operation in the PCO, as required. Complaint Handling - Perform Intake and Triage, issue correspondence letter as required. Acts as a contact point for Regulatory Agency/reporter in the PCO, as required. Lead and/or participate in deviation investigations using appropriate tools and works with cross-functional teams to implement CAPAs. Notify Management of significant concerns or deviations within the QMS which have the potential to impact product, regardless of release status. Where issues originate in the PCO, assist with the preparation of QRT meetings, where required. Assist with the implementation of local actions identified during QRT. Management of relevant corrective and preventative actions (CAPA) Supplier Quality Management Execute tasks associated with the management of GxP Suppliers including qualification, quality oversight in accordance with internal and regulatory requirements for GxP activities. Assists with ensuring appropriate customer screening processes are in place to align with Pfizer and local regulations, as required. Assist with the coordination of RQA audits at the Supplier. Leadership Skills Facilitate development and execution of objectives / projects consistent with SOQ Purpose Blueprint. Development and Maintenance of Quality culture, within the team and organisation. Qualifications A minimum Tertiary Education in Science, Pharmacy or related discipline A minimum of 5 years in the pharmaceutical industry in a quality role Fluent in English (written and verbal) Experience in Quality administered systems. Excellent computer system skills - Word and Excel essential. Experience with electronic documentation control systems advantageous. Demonstrated ability to influence, when necessary, particularly with stakeholders and external parties. Experience in GMP, GDP and QMS. Technical writing and reporting Previoususe of Trackwise , eQMS beneficial. Competencies Scientific knowledge and strong analytical skills to make sound quality assessments of project strategy. GMP/GDP Knowledge. Trained and experienced in the total application of GMP/GDP. Auditing. Knowledge of Auditing procedures. Technical writing. Ability to lead a technical investigation and report to all levels of oganisation. Ability to write we'll-structured technical reports. Problem solving. Ability to use problem solving skills and tools to identify and eliminate problems as they arise. Takes initiative and ownership to deliver on time without compromising on quality. Ability to communicate effectively verbally and in writing, good negotiation and influencing skills. Acts Decisively. Makes decisions in a timely manner, makes good decisions based upon a mixture of analysis, experience, and judgment. Able to demonstrate good planning and organisation. Dealing with Ambiguity. Can effectively cope with change and handle risk and uncertainty. Emotional Intelligence. Identify, assess and control the emotions of oneself and awareness of others. Takes Responsibility. Takes personal ownership of responsibilities and outcomes while following through on commitments Work Location Assignment: Hybrid Quality Assurance and Control #LI-PFE

So, what’ s the role all about? We are seeking a seasoned Senior Technical Writer to lead documentation initiatives across multiple product lines within NICE Actimize R&D. This is an advanced individual contributor role with strategic influence—requiring leading a small group of writers, content planning, cross-functional collaboration, and process improvement. How will you make an impact? Own end-to-end documentation for complex enterprise software products. Partner with SMEs, developers, and product managers to deliver high-quality, user-focused content. Create and maintain structured content: user guides, developer/API docs, and contextual help. Simplify complex concepts for diverse audiences including customers, support, and developers. Create and integrate visual aids and videos to enhance comprehension. Align deliverables with Agile sprints and release timelines. Provide editorial and mentoring support to other writers and content contributors Champion best practices in technical communication and drive process efficiencies within the team Have you got what it takes? 4+ years of experience as a technical writer in an enterprise software development environment. Experience working with large-scale enterprise products and understanding the nuances of multi-tenant, cloud-native platforms. Ability to translate functional specifications and test scenarios into user-friendly documentation, ensuring alignment with product behavior. Exposure to functional testing tools or frameworks, enabling collaboration with QA teams and validation of documented features. Skilled at documenting user workflows, product configurations, and system integrations within enterprise ecosystems. Deep experience in Agile environments and topic-based authoring. Strong grasp of APIs and developer-centric documentation. Ability to learn complex technology and tools. Experience creating clear and structured guides for different audiences, including developers (API documentation). Experience with Madcap Flare, Git, and Atlassian tools (JIRA and Confluence) Experience creating videos for technical documentation. Experience with Mimic or Camtasia is an advantage. Passionate about quality, great communication skills, and excellent teamwork capabilities. Excellent problem-solving and decision-making skills. What’ s in it for you? Join an ever-growing, market disrupting, global company where the teams – comprised of the best of the best – work in a fast-paced, collaborative, and creative environment! As the market leader, every day at NiCE is a chance to learn and grow, and there are endless internal career opportunities across multiple roles, disciplines, domains, and locations. If you are passionate, innovative, and excited to constantly raise the bar, you may just be our next NiCEr! Enjoy NICE-FLEX! At NiCE, we work according to the NiCE-FLEX hybrid model, which enables maximum flexibility: 2 days working from the office and 3 days of remote work, each week. Naturally, office days focus on face-to-face meetings, where teamwork and collaborative thinking generate innovation, new ideas, and a vibrant, interactive atmosphere. Requisition ID:7683 Reporting into: Tech Manager, Technical Writing, Actimize Role Type: Individual Contributor

Job Title: Consultant - Automation Anywhere Career Level : C2 Introduction to role Are you ready to leverage technology to make a real impact on patients lives? At AstraZeneca, we are looking for passionate individuals with expertise in information technology to join our team. If you have a knack for turning ideas into life-changing medicines through IT strategy, this might be the perfect opportunity for you! Accountabilities As a Bot Configurator, you will play a crucial role in designing, developing, coding, customizing, configuring, testing, deploying, and providing end-to-end support for automation-based solutions or Bots (Robots). You will build Robots using Automation Anywhere and other Microsoft Technologies such as .Net and client scripting languages. Your responsibilities will include handling automation support issues, gathering business requirements, and developing automation solutions. You will also perform unit/functional testing, support UAT, conduct compatibility testing, and provide Hypercare training and knowledge transfer. Additionally, you will implement best practices, identify bottlenecks/bugs, and motivate the team to meet tight deadlines while working collaboratively. Essential Skills/Experience Technical Degree Overall 3-5 years of IT Experience (Preferably .NET) Hands-on working experience in Automation Anywhere and Certified in the same. Create Technical specifications, Test plans and support documentations Sound knowledge on ITIL principles, Incident/Organizational change and AZ Access provisioning Strong Interpersonal, Technical writing, communication and presentation skills with Senior Partners Passionate to know the latest trends or developments in automation and adapt to the same Desirable Skills/Experience Knowledge of any one Technology Stack such as .Net/C#/ASP.net or Java/J2EE or Python Basic knowledge on Macros (VBA), vb script, java script Familiarity in SDLC methodologies (Classic, Agile methodologies etc), UI Path and Blue Prism (Or any other RPA tools) ITIL Certified or Trained Application knowledge related to Service Now, Jira Responsible for completing the Application Life Cycle plans for individual applications Has primary responsibility for maintaining and updating all documentation associated with Robotic Solution Delivery Ability to organize and prioritize work, meet deadlines and work independently Stays abreast of the development in area of professional competence AGILE / Scrum Certified At AstraZeneca, youll be part of a team that is at the forefront of digital healthcare innovation. We empower our employees to explore new technologies and tackle challenges that have never been addressed before. With a focus on data, analytics, AI, machine learning, and more, we are committed to transforming our ability to develop life-changing medicines. Our dynamic environment offers countless opportunities for learning and growth. Join us as we disrupt the industry and make a meaningful impact. Ready to take the next step in your career? Apply now and become part of our journey! 27-Jun-2025 03-Jul-2025

Global Scientific Communications Intern, Eli Lilly - Bangalore Hiring " Intern " for our Bangalore office. Experience: Fresher from Academics Global Scientific Communications (GSC) GSC - Intern Purpose: Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly The purpose of an Intern role is to learn and support teams across GSC Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position. Learn and support data integrity, scientific editing, encoring, clinical trial registry, Document Preparation, Development and Finalization/Document Management Learn the process of coordinating planning (including organizing/preparing outlines), writing (including first-draft authoring), editing, reviewing and completing disclosures in GSC documents. Learn coordinate quality checks for accuracy, Learn processes across sub-functions and learn effective project management skills to support team members on disclosures across GSC Learn to build/communicate credible writing project timelines. Learn ways of effective communication on project status to stakeholders. Learn therapeutic area knowledge including disease state and compound(s) for assigned project(s). learn to enhance scientific communication skills to align with audience needs and technology/digital evolution. Exhibit flexibility in moving across document types, therapeutic areas, and compounds, depending on project assignment. Learn and enhance knowledge of guidelines applicable across GSC Gain technical expertise in specific document development. Network with others (including other functions and regions) to identify and share best practices. Contribute to process improvements, suggesting opportunities where appropriate. learn applicable database and other tool (e.g., document management systems) across GSC. Minimum Qualification Requirements: Master s degree in a scientific, health, communications, health outcomes, health economics, public health related field Strong communication and interpersonal skills. Successful completion of DI exercise (a writing exercise is required as part of the candidate evaluation process) Other Information/Additional Preferences: Advanced degree (PhD, MD, PharmD, MA, MBBS) in science, health related field or other appropriate disciplines (economics, epidemiology, health administration, health services, Pharmacoeconomics, statistics other relevant sciences) Demonstrated mastery of verbal and written English skills in the medical, scientific, health outcomes, or technical writing fields. Previous training and experience in disseminating results in clinical, health economics, health outcomes, health literacy, disease management, and/or population health. Understanding in clinical development, clinical trial process, health-outcomes research, or regulatory activities. Clinical pharmacology, therapeutic area, health outcomes, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise). Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates). Ability to communicate clearly and succinctly with all audiences and forums through exemplary oral and written communication skills. . .

In this position this person will work within the IP Operations Tier 2 team o perating and maintaining a wide array of network elements both virtual and non-virtual. Those elements consist of Juniper MX960 s, F5 BigIP LTM/GTM, Cisco IOS/NXOS, HP6125/Flex10 and Nokia VMTR s. This person will in a BAU role take SMOPs provided by engineering teams, analyze them for accuracy and implement within the network ensuring no adverse impact to existing services. This person works in a break fix role and will run point on any trouble reported either via a ticketing system or otherwise. They will analyze the trouble and formulate a course of actions to resolve the trouble mitigating or preventing the impact. This person will work with ATS Tier 3 support, Tech Arch, and the vendors to implement patching and security tooling, new implementations and design changes to existing network designs on platforms such as Juniper MX960 and F5 LTM in the EPC Core Network within AT&T Mobility Service Operations. The role is in a 24x7 environment supporting all owned elements within the NTC comprising the EPC. The successful candidate for this position should have 3+ years experience operating and maintaining JUNOS, Cisco IOS/NXOS, F5 BigIP. Deep understanding of layer 1-7 technologies. Example: STP, RSTP, OSPF, BGP (emphasis placed on understanding community values and tagging), MPLS, IPSEC, layer 4-7 load-balancing. 2+ years of experience implementing and/or managing FirstNet requirements, or other US Government security requirements. 2+ years experience as an admin on Linux operating systems. Strong ability to troubleshoot complex technical and compliance issues Ability to work in a fast-paced environment while maintaining focus on goals Additional useful experience includes: 2+ years of experience implementing ASPR requirements Experience in a Cloud environment (AT&T AIC or Network Cloud, Azure, etc.) Experience using the following tools is desired: Ansible AOTS-Mobility Terminal Emulator with multiple machine implementation Ped-WO (IWOS) AOTS-Change Mgmt AT&T CSO Tools used for ASPR compliance (SACT, Sensage, MUAM, allmid, etc.) Required Qualifications - 3+ years experience Linux/Unix Skills (RedHat and Ubuntu) Strong troubleshooting skills Knowledge of mobility architectures Desired Qualifications - Bachelors degree in Math, Science, Engineering or equivilent related network experience Knowledge of Network Planning, Engineering, Construction and Mobility architectures Knowledge of cloud applications/networks, including Openstack, VMWare, Azure and Kubernetes Scripting knowledge such as Ansible and Python Certifications desired but not necessary (CCNA, CCNP, JCNIA, JCNIP) Excellent working knowledege of Cisco IOS, NX0S, Junos, F5 BIGIP(LTM/GTM) and F5VvE BIGIP. A foundational understanding of SDN networks understanding concepts of Virtual vnfs, Juniper Contrail, and spine/leaf architectures. Technical writing skills Job ID R-72584 Date posted 06/27/2025

OPENTEXT - THE INFORMATION COMPANY OpenText is a global leader in information management, where innovation, creativity, and collaboration are the key components of our corporate culture. As a member of our team, you will have the opportunity to partner with the most highly regarded companies in the world, tackle complex issues, and contribute to projects that shape the future of digital transformation. AI-First. Future-Driven. Human-Centered. At OpenText, AI is at the heart of everything we do powering innovation, transforming work, and empowering digital knowledge workers. Were hiring talent that AI cant replace to help us shape the future of information management. Join us. Opentext Working in the Product Information team, as part of the Engineering department, you are an integral part of a software development team that strives for perfection and is committed to success. Technical writers contribute to products across the Enterprise, Process, Customer Experience, Analytics, and Business Networks suites. The Opportunity OpenText is seeking a talented, personable technical writer who contributes to the Product Information team by creating sophisticated technical documentation for a variety of software products. As a technical writer at OpenText, you plan the documentation strategy, create content, contribute to department innovations, and produce professional online help and guides. As a customer advocate, you participate in the planning process and help define the product documentation requirements. You should be able to work independently and productively with minimal supervision as part of a geographically distributed team. Team members work individually as well as part of a larger group. Your ability to organize your time and see projects through to completion is extremely important. You Are Great At Producing high-quality, clear, accurate, and complete documentation with no errors, within established deadlines. Organizing and prioritizing tasks and have exceptional analytical skills. Managing multiple projects and deliverables. Working in an agile development environment and having the ability to gather information for a writing assignment from a variety of sources, including development, QA, UXD, and product management. Researching and learning new technologies in Technical Communications. What It Takes University degree or college diploma (BA or MA), preferably in English, Computer Science, Technical Writing, or Instructional Design, with 2 to 5 years of technical writing experience. Exceptional English and communication skills. Experience writing using a corporate style guide and following documentation processes. Excellent knowledge of content/help authoring tools, such as Arbortext Epic Editor, Adobe FrameMaker, MadCap Flare, and WebWorks ePublisher. Sound knowledge of XML and HTML and various help formats. Excellent knowledge of Configuration Management tools, such as Perforce, and bug tracking tools, such as JIRA. Experience writing in a structured authoring environment and creating single-source and minimalist content. Familiarity with DITA/DocBook and topic-based writing methodologies. Knowledge of documentation localization processes as well as software usability principles. Ability to create high quality graphics using tools, such as Microsoft Visio. Knowledge of video production techniques and experience with tools such as Camtasia. Excellent knowledge of computer development environments, operating systems, programming languages, and mobile devices. Ability to create customer-focused content using user personas and customer research. Experience defining and following documentation standards and best practices. Experience leading and managing documentation projects. Ability to meet target deadlines and project commitments. Ability to communicate clearly with all project stakeholders in distributed locations. Knowledge of Enterprise Information Management (EIM) products. OpenTexts efforts to build an inclusive work environment go beyond simply complying with applicable laws. Our Employment Equity and Diversity Policy provides direction on maintaining a working environment that is inclusive of everyone, regardless of culture, national origin, race, color, gender, gender identification, sexual orientation, family status, age, veteran status, disability, religion, or other basis protected by applicable laws. . Our proactive approach fosters collaboration, innovation, and personal growth, enriching OpenTexts vibrant workplace.

• Familiar with the use of graphic tools such as SNAGIT • Good working knowledge of Microsoft Word, Excel, and PowerPoint • Experience in using documentation tools like RoboHelp • Experience in developing HTML-based context-sensitive help Required Candidate profile • Write and update content for technical documents such as: Installation Guide User Guide Administrator Guide Release Notes Online Help Tutorials • Experience in MS Style Guide

Job Title: Technical Document Writer Location: Hosur Department: Product Engineering Division (PED) Employment Type: On Contract Salary: Up to 6 LPA Experience: 2 to 3 Years Team Size: 5 Reports To: Project Owner Job Description We are looking for a detail-oriented Technical Document Writer to create high-quality, user-friendly documentation for engineering projects and manufacturing processes. You will be responsible for developing standardized manuals that help communicate complex technical concepts in a clear and concise manner. This role is essential in supporting process standardization and internal knowledge sharing. Key Responsibilities Documentation Creation : Develop installation guides, FAQs, technical manuals, and white papers. Cross-functional Collaboration : Work with engineers, product managers, and SMEs to collect technical details; attend design/review meetings and conduct site visits. Content Management : Maintain organized document repositories and ensure version control. Editing & Proofreading : Ensure accuracy, clarity, and consistency in content across all formats. User-Centered Design : Create diagrams, flowcharts, and visuals to simplify complex information. Benchmarking : Write knowledge articles on industry trends and best practices. Education & Qualifications Diploma in Modern Office Practices / MA in English / Diploma in Mechanical Engineering. Excellent command of English (written and verbal). Preferred: Adobe Technical Communication Suite certification. Required Skills Strong writing, editing, and proofreading abilities. Understanding of engineering and manufacturing concepts. Familiarity with tools such as MS Word, Adobe Express, Adobe FrameMaker, Microsoft Visio, MadCap Flare, Google Docs, and ChatGPT. Bonus: Knowledge of Simplified Technical English (STE) High attention to detail and excellent organizational skills. Performance Metrics Number of Process Design Documents created and approved monthly. Timely delivery and version control compliance. Internal & External Interactions Internal: Cross-functional collaboration with PED, R&D, and QA teams. External: Occasional site visits and vendor coordination for technical accuracy. Apply Now If you are passionate about documentation and want to work in a fast-paced, innovation-driven environment, send your updated CV to naliniaarika.m@xpheno.com

About the Role The Technical Writer will be responsible for creating and managing technical documentation for various projects within the organization. This role requires strong communication skills and the ability to work independently in a fast-paced environment. Responsibilities Independently work on technical communication projects. Plan, author, review, validate, and test documents. Ensure project results meet requirements and ensure technical accuracy, quality, reliability, and schedule. Qualifications Graduate with an Engineering or Science degree preferred. 1 to 3 years of experience in Technical Writing. Semiconductor experience preferred. Candidate must join Applied Materials within 4 weeks of accepting the offer. Required Skills Excellent English language verbal, written, and interpersonal communication skills. Proficient in technical publishing software: Adobe Suite Acrobat Pro GraphicalMS Paint MS Office SuiteWord, PowerPoint, Excel, and Outlook Ability to work in a cross-functional organization and multitask on multiple projects. Must be a quick learner, and self-starter, with strong attention to detail, and can work with minimal supervision in a fast-paced, high-tech environment. May require 10% international travel. Preferred Skills Experience in the semiconductor industry. Familiarity with additional technical writing tools. Pay range and compensation package Compensation details will be discussed during the interview process.

Thorough understanding of technical writing with an enterprise product is mandatory. Experience in producing user documentation including Online Helps, User Guides, API Guides, Installation guides, and Release Notes including complex technical and functional material with limited, or no supervision. 8+ Years industry experience is a must. Excellent written and verbal communication skills, is mandatory. Strong working knowledge and application of style guides and industry practices. Well-versed with Agile and Waterfall methods of product documentation. A self-starter possessing excellent research skills and enjoys working hands on with the product. Ability to learn new product, technology, and tools quickly. Clear & Crisp phone & interpersonal communication skills. Attention to detail and result oriented.

Job Description Responsibilities of the Remote Support Engineer : - Possess a good understanding of Electrical distribution with the ability to Perform predictive / condition-based analyses of data generated by EAA Predictive into meaningful insights and actions. - Extracts and analyzes data, runs analytics (software/expert-based) - Observes health of assets, including condition-based analytics, and adjusts maintenance plans accordingly. - Develops recommendations based on the data, creates reports and shares reports with customers and provides direction to the customer as to actions required. - Interacts with customers and provides remote troubleshooting (e.g. phone, chat, email, etc) as needed - Acts based on customer requests to create cases, initiates work order creation to dispatch Field Services and/or engages Sales for service or product quotations - Interacts with Network of experts for advanced support of data analysis and recommendations to the customer Responsibilities of the Remote Support Engineer : - Possess a good understanding of Electrical distribution with the ability to Perform predictive / condition-based analyses of data generated by EAA Predictive into meaningful insights and actions. - Extracts and analyzes data, runs analytics (software/expert-based) - Observes health of assets, including condition-based analytics, and adjusts maintenance plans accordingly. - Develops recommendations based on the data, creates reports and shares reports with customers and provides direction to the customer as to actions required. - Interacts with customers and provides remote troubleshooting (e.g. phone, chat, email, etc) as needed - Acts based on customer requests to create cases, initiates work order creation to dispatch Field Services and/or engages Sales for service or product quotations - Interacts with Network of experts for advanced support of data analysis and recommendations to the customer Qualifications The Remote Support Engineer must have a proven track record of Providing excellent customer service and must possess a customer focused mindset Effective communication (written / oral / reading / listening) , with a command of the English language Ability to keep relevant stakeholders informed and build network of relationships that would aid in business development Candidate must have the ability to influence and convince Ability to effectively manage time and remain organized across multiple activities along with an attention to detail Curiosity and interest in new knowledge in various domains Minimum Knowledge Skill Expectations Service experience with power/power monitoring equipment and industrial applications Knowledge of electrical distribution systems and proficiency with one line diagrams Strong Technical writing and computer knowledge, fluency with Microsoft Office tools. Superior analytical abilities and high degree of proficiency in working with data Schedule: Full-time Req: 0099T3

Responsibilities of the Technical Publications Engineer are varied and may include but not are limited to: Creation / Revision of CMM, AMM, WDM. Write procedures, functional descriptions by interpreting Engineering Drawings, Schematics and Circuit Diagram. Experience/Tools requirement: Experience in Adobe Frame maker, Epic Editor, Adobe Professional. Familiarity with illustration tools (Iso Draw). Good knowledge on ATA 100, ATA iSpec 2200, S1000D, Simplified Technical English. Good verbal and technical writing skills

Organize material and complete authoring assignment according to set standards, clarity, style and/or terminology Write procedures, functional descriptions by interpreting schematics and circuit diagram Adobe Frame maker, Eagle Publishing System (EPS) or any S1000D Tools, Adobe Professional Familiarity with illustration tools (IsoDraw), UG, Solid works and Catia V5. Good knowledge on ATA 100, ATA iSpec 2200, S1000D, Simplified Technical English Ability to read and interpret Engineering Drawings, Electronic Circuit Schematics, Functional Diagrams, Printed Circuit Boards etc Ability to author Functional / Circuit description, Repair procedures based on source documents Ability to create Assembly / repair procedures for electro-mechanical LRUs independently Good verbal and technical writing skills

Job Description: Responsible for framing Solutions for EISBG Design and develop EISBG solution prepositions Developing new Applications and Solution pitch for Business Team Provide up to date technical information , Sales collaterals and Product information to Solution Sales team Responsible for all technical aspects of infrastructure Sales cycle from pre sales discussion , solution design ,pricing and proposals to handover to support & Projects implementation department Resolve Level 3 infrastructure support issues related to design Focusing on meeting the customer s needs Provide the design and cost structure to Business Liaison with industry consultants to understand the technology trends Interact with Product teams to understand Road map and guide in requirement of the region in consultation with Business team Interact with Supply chain to provide specs for cost structure for outsource products Skill Sets & Expertise: Go getter and early opportunity spotter Innovation and creativity Strong Business analysis skills Strong interpersonal skills Team player and good leadership, communication qualities Experience: Around 12~15 Years of total experience in framing Solutions , Min 8 years experience Energy Sector Strong knowledge of Power electronics Hardware and software s Education: Bachelor Degree in Electrical or Electronics Engineering

Strong written communication skills with a keen eye for detail and grammar. Ability to research and understand technical concepts and explain them in a clear and concise manner. Familiarity with SEO principles and content management systems (CMS) is a plus. Enthusiasm for learning and a proactive approach to tasks. Ability to meet deadlines and work effectively both independently and as part of a team. Responsibilities & Skills Content Creation: Write clear, concise, and engaging content for various platforms including blogs, articles, whitepapers, and website content. Research: Conduct thorough research on industry-related topics and generate ideas for new content to meet the needs of our target audience. Editing and Proofreading: Collaborate with team members to ensure content is accurate, error-free, and meets company standards. SEO Optimization: Implement basic SEO principles to enhance content visibility and drive organic traffic to our digital assets. Content Promotion: Assist in promoting content on social media platforms and other channels to increase reach and engagement. Learning and Growth: Actively seek feedback to improve writing skills and gain a deeper understanding of technical writing best practices. Benefits Hands-on experience in technical content writing and digital marketing. Mentorship and guidance from experienced professionals in the field. Education Pursuing a degree in English, Journalism, Communications, or a related field (or recent graduate). Experience 3 - 6 months Hiring For Technical Content Writer - Intern

POSITION: (IT Content Writer) LOCATION: GURUGRAM (Work from Office ) Exp: Min 2+years Responsibilities:- Content Writing Technical Creative Writing Non-Technical Skills:- v Must have excellent oral and written communication skills. v Must be dedicated to delivering high-quality work and adhering to timelines. v Must be a good team player, a good learner, and a self-starter. v Must have the ability to work independently.

Experience: 3+ Years Location: Hyderabad/Bangalore/Pune (Hybrid) Company: Derisk360 Are you a seasoned RPG Engineer ready to modernize core systems for the insurance industryJoin Derisk360?where we merge deep legacy expertise with cutting-edge AI and data analytics to deliver high-impact transformation projects What Youll Do: Create and maintain technical documentation for RPG LE applications, including system architecture, module designs, and integration points Develop comprehensive user manuals, release notes, support guides, and process documentation Keep documentation in sync with codebase changes and Agile sprint cycles Collaborate with developers, QA, and product teams to accurately represent application What You Bring: 3+ years of experience in technical writing or software documentation Strong ability to structure and communicate technical information clearly and concisely Familiarity with IBM iSeries environments and RPG LE terminology is a plus Proficient with tools like Confluence, MadCap Flare, or DITA-based documentation systems Comfortable operating in Agile environments with iterative deliverables What Youll Get: Competitive compensation + annual performance bonuses Lead strategic modernization projects for global insurance clients Work in a high-performing team with deep technical expertise Exposure to complex technical platforms and risk-tech systems Culture of engineering excellence and continuous learning