550 Publications jobs in India

1. This role will support the Publications Leads in the execution of publications plans in compliance with Global Pharma Company policies as well as with all related good publication practices and guidelines. The team s mission is to ensure high quality and timely delivery of scientific publications according to set plans.

2. This role is responsible for working on specific publication deliverables and ensure timely delivery of high-quality publications, in compliance with Global Pharma Company policies as well as with all related good publication practices and guidelines through the scrupulous respect of an established, auditable process, and transparency of process to involved stakeholders. The role works on the delivery of the plan by working with in house functions and service providers according to the sourcing strategy identified.

3. In partnership with the Publications Leads, assure successful management of Global Pharma Companys publication delivery.

4. Ensure the use of good publications practices and principles among authors and internal stakeholders to guarantee that all publications are being authored, written and reviewed according to good publication practice standards (GPP/ICMJE guidelines) and are consistent with all relevant company policies.

5. Coordinate the delivery of specific publications (manuscripts, abstracts, presentations, publication enhancements, etc.) with the authors and cross-functional teams of experts within TAs

Ensuring high scientific integrity of data interpretation

Following publication from submission through publication (including active input in consolidation of content pre and post submission)

Identifying appropriate resources for generation of publications, according to priorities and Publications Plan or provide technical writing support as needed

Support coordination of review of publication drafts to ensure quality standards

Ensure update in a timely manner of all project management tools put in place by Global Pharma Company (iEnvision Datavision, tracking sheets, )

6. Provide technical writing support to specific publication deliverables as per plan and identified sourcing strategy

7. Coordinate publications management for Global Pharma Company Sponsored/Supported Studies 8. Support requirements for cross-asset congress and support TA publications team with guidance on requirements and technical support.

We are for a Female candidate to the post Journal publication assistant

Any degree

Good communication skill

Job Type: Full-time

Pay: ₹6, ₹10,000.00 per month

Experience:

• total work: 1 year (Preferred)

Overview:

Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.

If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.

Job Responsibilities:

• Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, manuscripts, pre & post congress and meetings materials, according to client needs with excellent attention to detail under the guidance of the scientific leads
• Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
• Effectively and proactively communicate with team members, authors/faculty, clients and vendors
• Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
• Attend client and other external meetings and supporting senior team members as needed
• Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
• You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
• Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
• Share best practices and client preferences, thereby contributing to skill development within the medical communications team

Requirements:

• 1-3 years of experience in relevant fields of scientific writing
• PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
• Should have experience working on publications
• Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
• Excellent communication skills, especially with the clients
• Ability to adapt writing style to different materials and target audiences
• Basic knowledge of biostatistics
• Literature reviewing and evaluation capabilities
• Very good working knowledge of MS Office

Application Process:

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, colour, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

• Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
• Documenting work that brings everyone on the same page.
• Maturity to choose between synchronous and asynchronous collaboration.
• Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About US:

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Riverbed, the leader in AI observability, helps organizations optimize their user's experiences by leveraging AI automation for the prevention, identification, and resolution of IT issues. With over 20 years of experience in data collection and AI and machine learning, Riverbed's open and
AI-powered observability platform
and solutions optimize digital experiences and greatly improves IT efficiency. Riverbed also offers industry-leading
Acceleration solutions
that provide fast, agile, secure acceleration of any app, over any network, to users anywhere. Together with our thousands of market-leading customers globally – including 95% of the FORTUNE 100 – we are empowering next-generation digital experiences.

Position
The Technical Publications team is seeking a skilled and detail-oriented Technical Publications Writer to create and maintain high-quality technical documentation for our enterprise products. This role is crucial in transforming complex technical information into clear, concise, and user-friendly content, including user guides, installation guides, deployment guides, hardware documentation, and API/CLI reference manuals. As a key member of the team, you will ensure that documentation is accurate, accessible, and integrated seamlessly with product development lifecycles, embracing a docs-as-code philosophy .

What You Will Do

• Collaborate with engineers, QA, product management, and subject matter experts to research, gather, and understand highly technical product information.
• Design, develop, and deliver comprehensive technical documentation for hardware and software, including user manuals, installation guides, configuration guides, command-line reference manuals, and online help systems.
• Implement and champion the docs-as-code paradigm, treating documentation as a version-controlled codebase using plain text formats (e.g., Markdown) and Git.
• Help architect and optimize a documentation toolchain for automated content generation, leveraging CI/CD pipelines to build and deploy documentation.
• Recommend, evaluate, and integrate tools for automation, content analysis, and potentially AI-driven enhancements for documentation processes.
• Ensure that documentation is accurate, consistent, and adheres to established style guides and terminology standards.
• Create and update diagrams, illustrations, and other visual aids to enhance clarity and user comprehension.
• Actively participate in documentation reviews and incorporate feedback from technical teams and end-users to continuously improve content quality and usability.

What Makes You An Ideal Candidate

• Proven technical writing experience with a strong portfolio of documentation samples for complex software and/or hardware products.
• Familiarity with the docs-as-code workflow, including experience with version control systems (e.g., Git) and plain text markup languages (e.g., Markdown).
• Experience using the Cursor IDE and appropriate extensions for Markdown rendering and linting.
• Experience with automated documentation build processes and static site generators (e.g., Sphinx).
• Proficiency with content creation tools and a willingness to adapt to new technologies and workflows (e.g. pandoc).
• Excellent written and verbal communication skills with the ability to translate complex technical concepts into clear, concise, and engaging content for diverse audiences.
• Strong research, analytical, and problem-solving abilities.
• Ability to work independently and collaboratively within an Agile development environment, managing multiple projects and meeting deadlines.
• Basic understanding of scripting languages (e.g., Python, Bash) to support automation efforts.

What Will Help You Further

• Knowledge of best practices for continuous integration/continuous deployment (CI/CD) pipelines in a documentation context.
• Experience in migrating documentation from traditional authoring tools (e.g., Adobe FrameMaker) to docs-as-code environments.
• Familiarity with API documentation tools (e.g., Swagger/OpenAPI).
• Experience with AI-powered tools for content review, editing, or generation.

What We Offer
Our employee benefits including flexible workplace policies, employee resource groups, learning and development resources, career progression pathways, and community engagement initiatives are some of the reasons why we have had great success in bringing in new talent. In addition, our global employee wellness programs are crafted to support the physical, emotional, and financial well-being of our employees.

Benefits & Perks vary by Country.

About Riverbed
With a 20-year history of innovation, Riverbed is agile, yet proven, and we are disrupting the market with differentiated solutions that enable our customers to deliver secure, seamless digital experiences and accelerate enterprise performance While we are a 'customer-first' company, we are all about our people with a shared commitment to creating a global impact. We bring our best selves to work and pursue excellence, trust, and respect for one another. We welcome and encourage transparency and open communication throughout the company. We strive to be an inclusive, fair, and enjoyable workplace for our people globally and care about their wellbeing. We are committed to our people, partners, and customers while supporting the communities where we work and live. It's the
Power of
WE
that binds us together.

Riverbed is an equal employment opportunity/Affirmative Action (EEO/AA) employer and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, gender, sexual orientation, gender identity or expression, national origin, age, physical disability (including HIV and AIDS), mental disability, medical condition, pregnancy or child birth (including breast feeding), sexual orientation, genetics, genetic information, marital status, veteran status or any other basis protected by and in accordance with applicable federal, state and local laws.

Check Us Out On

@LifeAtRiverbed

Tags

Job Title: Senior Technical Writer

Location:
Bangalore, India

Department:
Digital Buildings

Position Type:
Full-Time / Contract

Travel Required:
No

Position Overview:

We are seeking a detail-oriented and experienced 
Senior Technical Writer
 to support our NAM technical publications team. This role focuses on producing and managing high-quality technical content including documentation, test reports, and public release notes for our Connected Buildings solutions. The ideal candidate will have strong writing and organizational skills, a collaborative mindset, and the ability to translate complex technical information into clear, user-friendly content.

Key Responsibilities:

• Collaborate with engineering, QA, and product teams to gather and synthesize technical information.

• Assist in the creation, editing, and publication of:

• Test reports

• Public release notes

• Installation, configuration, and operation manuals

• Ensure consistency, clarity, and compliance with corporate standards across all documentation.

• Support the documentation lifecycle from planning to publication, including version control and updates.
• Help streamline and standardize existing documentation assets.
• Publish content to internal and external platforms, ensuring accessibility and usability.
• Work closely with Tech Pubs Team Lead and other stakeholders to meet project timelines and quality expectations.

Qualifications:

• Bachelor's degree in electrical engineering, Computer Science, Technical Communication, or related field.
• Minimum 15+ years of experience in technical writing, preferably in a high-tech or engineering environment.
• Proven ability to explain complex technical concepts in clear, concise language.
• Experience with documentation tools such as Adobe InDesign, Illustrator, Photoshop, and online help systems.
• Familiarity with hardware/software development processes and agile methodologies.
• Strong organizational skills and ability to manage multiple projects simultaneously.
• Excellent written and verbal communication skills in English and French.

Preferred Skills:

• Ability to convert technical workflows into diagrams and visual aids.
• Comfortable working in cross-functional and multicultural teams.
• Self-driven, detail-oriented, and adaptable to changing priorities.

Looking to make an IMPACT with your career?

When you are thinking about joining a new team, culture matters. At Schneider Electric, our values and behaviors are the foundation for creating a great culture to support business success. We believe that our  IMPACT values - Inclusion, Mastery, Purpose, Action, Curiosity, Teamwork - starts with us.

IMPACT is also your invitation to join Schneider Electric where you can contribute to turning sustainability ambition into actions, no matter what role you play. It is a call to connect your career with the ambition of achieving a more resilient, efficient, and sustainable world.

We are looking for IMPACT Makers; exceptional people who turn sustainability ambitions into actions at the intersection of automation, electrification, and digitization. We celebrate IMPACT Makers and believe everyone has the potential to be one.

Become an IMPACT Maker with Schneider Electric - apply today

€36 billion global revenue

+13% organic growth

employees in 100+ countries

You must submit an online application to be considered for any position with us. This position will be posted until filled.

Schneider Electric aspires to be the most inclusive and caring company in the world, by providing equitable opportunities to everyone, everywhere, and ensuring all employees feel uniquely valued and safe to contribute their best. We mirror the diversity of the communities in which we operate, and 'inclusion' is one of our core values. We believe our differences make us stronger as a company and as individuals and we are committed to championing inclusivity in everything we do.

At Schneider Electric, we uphold the highest standards of ethics and compliance, and we believe that trust is a foundational value. Our Trust Charter is our Code of Conduct and demonstrates our commitment to ethics, safety, sustainability, quality and cybersecurity, underpinning every aspect of our business and our willingness to behave and respond respectfully and in good faith to all our stakeholders. You can find out more about our Trust Charter here

Schneider Electric is an Equal Opportunity Employer. It is our policy to provide equal employment and advancement opportunities in the areas of recruiting, hiring, training, transferring, and promoting all qualified individuals regardless of race, religion, color, gender, disability, national origin, ancestry, age, military status, sexual orientation, marital status, or any other legally protected characteristic or conduct.

Objective:

To manage and control technical manuals and digital documentation for the Defense Aircraft, ensuring access to the latest revisions and maintaining compliance with OEM and regulatory documentation requirements.

Key Responsibilities:

1. Documentation Management:

• Maintain and update the physical and digital technical manual library (IETM, AMM, IPC, SRM, WDM, etc.).
• Ensure revision control and distribution of manuals to all relevant departments.

2. OEM Updates & Revision Control:

• Download and implement updates from Lockheed OEM portals.
• Log and track revisions in the Electronic Document Management System (EDMS).

3. Digital Access & Training:

• Manage access and user rights for IETM/IETP platforms.
• Provide user support and training for efficient use of digital documentation.

4. Compliance & Audit Readiness:

• Maintain revision logs and version control records for audits and regulatory inspections.

Deliverables:

• Up-to-date manual library and revision records
• IETM/IETP user access and usage reports
• Monthly update logs and distribution reports

Qualifications:

• Education: Diploma or Graduate (preferably in Library Science or Technical Publications)
• Experience: 36 years in technical publications or documentation within aviation/MRO
• Preferred: Familiarity with military aircraft manuals and EDMS tools

Key Competencies:

• Strong attention to detail and version control
• Proficiency in EDMS and IETM platforms
• Coordination skills for inter-departmental support
• Structured documentation management mindset

Overview:

Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.

If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.

Job Responsibilities:

• Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, manuscripts, pre & post congress and meetings materials, according to client needs with excellent attention to detail under the guidance of the scientific leads
• Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
• Effectively and proactively communicate with team members, authors/faculty, clients and vendors
• Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
• Attend client and other external meetings and supporting senior team members as needed
• Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
• You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
• Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
• Share best practices and client preferences, thereby contributing to skill development within the medical communications team

Requirements:

• 1-3 years of experience in relevant fields of scientific writing
• PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
• Should have experience working on publications
• Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
• Excellent communication skills, especially with the clients
• Ability to adapt writing style to different materials and target audiences
• Basic knowledge of biostatistics
• Literature reviewing and evaluation capabilities
• Very good working knowledge of MS Office

Application Process:

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, colour, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

• Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
• Documenting work that brings everyone on the same page.
• Maturity to choose between synchronous and asynchronous collaboration.
• Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About US:

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Overview:

Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.

If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.

Job Responsibilities:

• Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, manuscripts, pre & post congress and meetings materials, according to client needs with excellent attention to detail under the guidance of the scientific leads
• Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
• Effectively and proactively communicate with team members, authors/faculty, clients and vendors
• Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
• Attend client and other external meetings and supporting senior team members as needed
• Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
• You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
• Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
• Share best practices and client preferences, thereby contributing to skill development within the medical communications team

Requirements:

• 1-3 years of experience in relevant fields of scientific writing
• PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
• Should have experience working on publications
• Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
• Excellent communication skills, especially with the clients
• Ability to adapt writing style to different materials and target audiences
• Basic knowledge of biostatistics
• Literature reviewing and evaluation capabilities
• Very good working knowledge of MS Office

Application Process:

Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.

Equal Opportunity

Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, colour, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.

Accelerating from Anywhere

As a remote-first organization, these are essential attributes we look for in all our candidates.

• Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
• Documenting work that brings everyone on the same page.
• Maturity to choose between synchronous and asynchronous collaboration.
• Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.

About US:

At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.

Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.