Explore numerous writing job opportunities suitable for various skill levels. Writing roles encompass diverse fields, including 1,292 Writing jobs in India
Content Writing
Posted 20 days ago
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Job Description
Company Overview
TeachEdison is an innovative Education Technology Company that focuses on developing high-performance software solutions for educators. Our flagship product, EdisonOS, is a robust operating system designed to empower Knowledge Commerce. Based in Bangalore, our team comprises 11-50 dedicated employees committed to revolutionizing the educational landscape.
Job Overview
TeachEdison is seeking a passionate Content Writer to join our team in Coimbatore. As a fresher-level full-time position, this role is ideal for candidates with 0 to 1 year of work experience. The Content Writer will play a critical role in creating and improving content that enhances user experience and supports our products, including EdisonOS.
Qualifications and Skills
- Possess excellent communication skills with a strong command of written English.
- Demonstrate proficiency in content creation with the ability to produce engaging and informative content.
- Skilled in writing and developing comprehensive user manuals and product guides (Mandatory skill).
- Ability to deliver high-quality copywriting materials that align with brand messaging.
- Provide effective help desk support with a keen focus on addressing user queries.
- Exhibit strong grammar and proofreading skills to ensure content accuracy and readability.
- Capable of interpreting and simplifying complex information for diverse audiences.
- Detail-oriented with an ability to manage multiple projects and meet deadlines effectively.
Roles and Responsibilities
- Create, edit, and maintain product guides and user manuals to support our software products.
- Develop content that enhances user engagement and understanding of our educational solutions.
- Collaborate with product teams to ensure accuracy and clarity in documentation.
- Conduct research and gather information to develop relevant and up-to-date content.
- Assist in the preparation of training materials and guides for end-users.
- Provide assistance in help desk support by delivering comprehensive content solutions.
- Ensure the delivery of high-quality copy that is consistent with TeachEdisons brand voice.
- Continuously update and improve existing content based on feedback and technological advancements.
Content Writing
Posted 20 days ago
Job Viewed
Job Description
Who are WE ?
At Spyne, our mission is to revolutionize automotive retailing. Every year, 52 million cars are sold in the US, for a combined worth of $1700 billion, and, valuing the used-car market at $1000 billion. Our new-age, Generative AI-powered solutions are designed to transform the car visuals into premium studio visuals. Dealerships & marketplaces across the US & Europe, are able to better engage their online visitors, driving greater customer showroom visits, and eventually sales.
Spyne aims to expand into additional software segments within the used-car market, addressing the specific needs of dealerships. Leveraging our go-to-market strategy, we plan to cover all aspects of the dealer journey, from acquiring and appraising cars to listing, marketing, selling, and managing customer relationships.
The Spyne team, located in Gurugram, India, aims to be the leading software provider in the used-car market. Supported by top investors like Accel Partners and Storm Ventures, as well as experienced founders, we believe in revolutionizing Digital Production for greater efficiency and intelligence.
Know more about us here:
Yourstory -
Spyne x AWS -
Auto -
To get a preview of our product, download it from the Google Play store and iOS App Store.
What will be your key responsibilities?
- Writing long-form content (such as articles, blogs, and e-books) and short-form content (like product descriptions, and captions) tailored to target audiences.
- Revamp and optimize outdated content across various formats (blog posts, website copy) for enhanced relevance and engagement.
- Collaborate with the marketing team to refresh content, ensuring alignment with industry trends and brand guidelines.
- Experiment with formats and approaches to revamping old content, and monitoring metrics for optimization.
What you must have ?
- Strong command of the English language.
- Familiarity with Google Workspace (Docs, Sheets, Slides).
- Punctual and dedicated work ethic.
We Love to Enjoy!
- Unplugged Fridays: Monthly activities fun Friday activities where teams fuse creativity and competition, crowned with rewards for victory.
- Team Bashes: Regular gatherings to bring up appreciation, motivation, and relaxation.
- Birthday Bliss Bonanza: Monthly gatherings to celebrate the unique magic of each team member, turning birthdays into shared moments of joy.
- Festival Fiestas: Vibrant festivities with music, food, games, and more, creating memorable experiences
Why join Spyne?
- We are a young start up with an average age of employees as 25-26 yrs
- Even during the great resignation period, we had near-zero attrition that speaks volume about culture.
- With the rating of 4+ on glassdoor, we are one of the top rated AI Tech company
- Best Male-Female ratio among in the AI tech industry
- Have all best-in-class employee supportive policies, as per govt mandates
- We are obsessed about delivering best customer experience with utmost client delight
Associate Regulatory Writing
Posted today
Job Viewed
Job Description
Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what's known today.
**Roles & Responsibilities:**
+ Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information, in line with regulatory requirements and the agreed strategy defined by the cross functional team
+ Ensure consistent quality across documents, ensure submission readiness, and hand off for timely submission or posting
+ Collaborate with team members to resolve problems and escalate issues
+ Record and maintain written redaction strategy for the study and product
+ Manage timelines and coordinate work across team
+ Execute clinical trial disclosure business process and ensure deliverables and delivery timelines in compliance with regulations, Amgen policy and SOPs and guidance documents
+ Tactical point of contact for assigned areas of responsibility, completes assigned action items, and maintains documentation of assigned responsibilities
+ Assist/support trial disclosure audits and inspections
+ Serve as Process Administer for CTRS, support active CTRS users, system access, inquiries, and issue resolution
+ Generate /manage reports, trackers, portals and metric activities
**Required Skills:**
+ Experience understanding and interpreting data/information and its practical application
+ Self-motivated with developed skills in multi-tasking, attention to detail, and follow-through
+ Ability to follow controlled processes
+ Excellent spoken and written English
+ Project management skills, including ability to prioritize work in order to meet required deadlines
+ Problem solving ability
**Basic Qualifications:**
+ Bachelor's degree
+ Minimum of 1 year experience working with regulatory documents in a biotech/ pharmaceutical environment
+ Familiarity with clinical research and clinical regulatory documents
+ Knowledge of clinical trial disclosure regulations, guidelines, and best practices
**Preferred Qualifications:**
+ > One year experience preparing regulatory documents for public disclosure
+ Familiarity with Clinical Trial Registry System, NIH Protocol Registration System (PRS), ClinicalTrials.gov, EudraCT, EU CTIS, and other registries
+ Familiarity with redaction/anonymization of clinical trial documents
**EQUAL OPPORTUNITY STATEMENT**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with 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 an accommodation.
Associate Regulatory Writing
Posted today
Job Viewed
Job Description
Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what's known today.
**Roles & Responsibilities:**
+ Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information, in line with regulatory requirements and the agreed strategy defined by the cross functional team
+ Ensure consistent quality across documents, ensure submission readiness, and hand off for timely submission or posting
+ Collaborate with team members to resolve problems and escalate issues
+ Record and maintain written redaction strategy for the study and product
+ Manage timelines and coordinate work across team
+ Execute clinical trial disclosure business process and ensure deliverables and delivery timelines in compliance with regulations, Amgen policy and SOPs and guidance documents
+ Tactical point of contact for assigned areas of responsibility, completes assigned action items, and maintains documentation of assigned responsibilities
+ Assist/support trial disclosure audits and inspections
+ Serve as Process Administer for CTRS, support active CTRS users, system access, inquiries, and issue resolution
+ Generate /manage reports, trackers, portals and metric activities
**Required Skills:**
+ Experience understanding and interpreting data/information and its practical application
+ Self-motivated with developed skills in multi-tasking, attention to detail, and follow-through
+ Ability to follow controlled processes
+ Excellent spoken and written English
+ Project management skills, including ability to prioritize work in order to meet required deadlines
+ Problem solving ability
**Basic Qualifications:**
+ Bachelor's degree
+ Minimum of 1 year experience working with regulatory documents in a biotech/ pharmaceutical environment
+ Familiarity with clinical research and clinical regulatory documents
+ Knowledge of clinical trial disclosure regulations, guidelines, and best practices
**Preferred Qualifications:**
+ > One year experience preparing regulatory documents for public disclosure
+ Familiarity with Clinical Trial Registry System, NIH Protocol Registration System (PRS), ClinicalTrials.gov, EudraCT, EU CTIS, and other registries
+ Familiarity with redaction/anonymization of clinical trial documents
**EQUAL OPPORTUNITY STATEMENT**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with 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 an accommodation.
Associate Regulatory Writing
Posted today
Job Viewed
Job Description
Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what's known today.
**Roles & Responsibilities:**
+ Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information, in line with regulatory requirements and the agreed strategy defined by the cross functional team
+ Ensure consistent quality across documents, ensure submission readiness, and hand off for timely submission or posting
+ Collaborate with team members to resolve problems and escalate issues
+ Record and maintain written redaction strategy for the study and product
+ Manage timelines and coordinate work across team
+ Execute clinical trial disclosure business process and ensure deliverables and delivery timelines in compliance with regulations, Amgen policy and SOPs and guidance documents
+ Tactical point of contact for assigned areas of responsibility, completes assigned action items, and maintains documentation of assigned responsibilities
+ Assist/support trial disclosure audits and inspections
+ Serve as Process Administer for CTRS, support active CTRS users, system access, inquiries, and issue resolution
+ Generate /manage reports, trackers, portals and metric activities
**Required Skills:**
+ Experience understanding and interpreting data/information and its practical application
+ Self-motivated with developed skills in multi-tasking, attention to detail, and follow-through
+ Ability to follow controlled processes
+ Excellent spoken and written English
+ Project management skills, including ability to prioritize work in order to meet required deadlines
+ Problem solving ability
**Basic Qualifications:**
+ Bachelor's degree
+ Minimum of 1 year experience working with regulatory documents in a biotech/ pharmaceutical environment
+ Familiarity with clinical research and clinical regulatory documents
+ Knowledge of clinical trial disclosure regulations, guidelines, and best practices
**Preferred Qualifications:**
+ > One year experience preparing regulatory documents for public disclosure
+ Familiarity with Clinical Trial Registry System, NIH Protocol Registration System (PRS), ClinicalTrials.gov, EudraCT, EU CTIS, and other registries
+ Familiarity with redaction/anonymization of clinical trial documents
**EQUAL OPPORTUNITY STATEMENT**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with 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 an accommodation.
Associate Regulatory Writing
Posted today
Job Viewed
Job Description
Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what's known today.
**Roles & Responsibilities:**
+ Prepare clinical regulatory documents for public disclosure, including anonymization of personal data and redaction of commercially confidential information, in line with regulatory requirements and the agreed strategy defined by the cross functional team
+ Ensure consistent quality across documents, ensure submission readiness, and hand off for timely submission or posting
+ Collaborate with team members to resolve problems and escalate issues
+ Record and maintain written redaction strategy for the study and product
+ Manage timelines and coordinate work across team
+ Execute clinical trial disclosure business process and ensure deliverables and delivery timelines in compliance with regulations, Amgen policy and SOPs and guidance documents
+ Tactical point of contact for assigned areas of responsibility, completes assigned action items, and maintains documentation of assigned responsibilities
+ Assist/support trial disclosure audits and inspections
+ Serve as Process Administer for CTRS, support active CTRS users, system access, inquiries, and issue resolution
+ Generate /manage reports, trackers, portals and metric activities
**Required Skills:**
+ Experience understanding and interpreting data/information and its practical application
+ Self-motivated with developed skills in multi-tasking, attention to detail, and follow-through
+ Ability to follow controlled processes
+ Excellent spoken and written English
+ Project management skills, including ability to prioritize work in order to meet required deadlines
+ Problem solving ability
**Basic Qualifications:**
+ Bachelor's degree
+ Minimum of 1 year experience working with regulatory documents in a biotech/ pharmaceutical environment
+ Familiarity with clinical research and clinical regulatory documents
+ Knowledge of clinical trial disclosure regulations, guidelines, and best practices
**Preferred Qualifications:**
+ > One year experience preparing regulatory documents for public disclosure
+ Familiarity with Clinical Trial Registry System, NIH Protocol Registration System (PRS), ClinicalTrials.gov, EudraCT, EU CTIS, and other registries
+ Familiarity with redaction/anonymization of clinical trial documents
**EQUAL OPPORTUNITY STATEMENT**
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with 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 an accommodation.
Scientific Writing Intern
Posted 2 days ago
Job Viewed
Job Description
Key Responsibilities:
● Content Research & Curation: Identify, verify, and prepare relevant biotech/life science opportunities, updates, and resources for our audience.
● Article Writing: Create engaging career guidance articles tailored to students and professionals.
● News & Research Summaries: Curate and simplify the latest developments in biotechnology, life sciences, and allied fields.
● Creative & Media Support: Assist in designing presentations, brochures, posters, infographics, and social media creatives.
● Engagement & Outreach: Ensure all content is clear, accurate, and engaging to connect effectively with readers.
Digital Skills and Tools Utilization:
● Social Media Engagement: Utilize LinkedIn, Instagram, Facebook, and YouTube to increase visibility and engage relevant audiences.
● Email Marketing and Web Presence: Implement email marketing strategies and maintain an active website.
● Data Mining and Analysis: Employ analytical tools to gather information on target audiences, including email addresses and LinkedIn profiles, and trade show participation.
Educational Requirements:
● Bachelor’s or Master’s degree in life sciences, biotechnology, Chemistry, pharma or a related field.
● Proven passion and ability for writing and must be a voracious reader.
● Strong research skills and attention to detail.
● Knowledge of scientific writing and digital content creation.
● Familiarity with social media platforms and digital marketing concepts.
● Ability to work independently and in a team.
● Enthusiasm for learning about industry trends.
Benefits:
● Work with an international life sciences company and leading life sciences and
biotechnology news portal Biotecnika.
● Gain experience in scientific writing, journalism, and digital marketing.
● Exposure to the latest trends and developments in life sciences and
biotechnology.
● Networking opportunities with professionals and researchers.
● Certificate of completion at the end of the internship.
Duration: The internship will be for a period of six months, with the possibility of an
extension based on performance.
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Content writing Intern
Posted 2 days ago
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Job Description
Company Description
Bag2Bag is an innovative online accommodation booking platform offering short stays with the option to book hourly rooms and long stays for one or multiple days in hotels, homestays, service apartments, resorts, cottages, villas, and more, complete with food and beverages. The company operates in over 100 cities with more than 1000 properties, providing excellent services at affordable prices. Bag2Bag caters to diverse accommodation needs while enhancing travel experiences with pre-booked F&B offerings.
Role Description
This full-time role is for a Content Writing Intern located on-site in Bengaluru. The Content Writing Intern will be responsible for creating and managing web content, developing content strategies, and writing and organizing content. Day-to-day tasks include drafting, editing, and updating content for the company's digital platforms as well as collaborating effectively with other team members to ensure consistent and aligned messaging.
Qualifications
- Web Content Writing, Writing, and Content Management skills
- Experience in developing Content Strategy
- Strong Communication skills
- Excellent organizational and time management skills
- Ability to work collaboratively in a team setting
- Pursuing or completed a degree in English, Journalism, Communications, or a related field is preferred
Content Writing Intern
Posted 2 days ago
Job Viewed
Job Description
At Brightrays, we are at the forefront of integrating technology with creativity. Our mission is to provide insightful, engaging content across various fields using the latest generative AI tools (ChatGPT, Claude, etc).
If you have a flair for writing and a keen interest in AI technology, we invite you to apply for our Content Writer Internship.
Position: Content Writer Intern
Location: On-Site (Sector 16, Noida, Uttar Pradesh)
Duration: 3-month Internship
Stipend: INR 12,000 per month
Work Schedule: 5 days a week (Mon-Fri)
Dress Code: Smart Casuals or Semi-Formals
Job Description:
As a Generative AI Content Writer Intern, you will:
- Use cutting-edge AI tools to create 3-4 blog posts daily across various topics.
- Collaborate with our team to brainstorm innovative content ideas.
- Conduct research to ensure the accuracy and relevance of your content.
- Adapt content strategy based on analytics and user engagement.
We’re Looking For Someone Who:
- Currently enrolled in or having completed a graduation degree.
- Is proficient in English, with exceptional writing and editing skills.
- Has a strong interest in AI and its application in content creation.
- Can commit to producing high-quality content within tight deadlines.
- Has a basic understanding of SEO principles and digital marketing strategies.
If you are interested, kindly share your resume at
Content writing Interns
Posted 2 days ago
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Job Description
Job description
Company Description
FranchiseBAZAR is India's most trusted franchise business investment advisory, connecting entrepreneurs with over 4000 brands and franchisors. With a large network of serious business seekers, investors, and entrepreneurs, FranchiseBAZAR offers a platform for successful franchise expansion and recruitment. The company has been in operation for 22+ years and provides comprehensive franchise solutions for businesses looking to expand in India.
Role Description
This is a full-time (Mon-Sat 9.00 am to 6.00 pm) remote paid internship for a Content Writer located in India. The Content Writer will be responsible for web content writing, developing content strategies, conducting research, writing, and proofreading. The role will involve creating engaging content to attract potential franchisees and promote brands on various platforms.
Qualifications
- Web Content Writing and Writing skills
- Experience in developing content strategies and conducting research
- Proofreading skills
- Excellent written and verbal communication skills
- Ability to work independently and collaboratively
- Experience in the entrepreneurship, business writing, franchise or business development industry is a plus
- Bachelor's degree in English, Journalism, Communications, or related field
Responsibilities
- Writing one blog and 10 Quora answers every day around franchising, entrepreneurship, new business opportunities, and starting a new business.
- Researching given topics for writing original and meaningful content around franchising and entrepreneurship. So this is for content writers who want to dabble with business writing.
- Working closely with the Digital Marketing and SEO team for content creation.
- Write long-form content/articles on specific topics across various platforms that can engage entrepreneurs and investors looking at starting a new business in India and around the franchising industry segments and sub-segments, top brands, and more.
- Edit and fact-check pieces of content thoroughly and ensure zero grammar, and spelling mistakes independently.
- Keep the brand’s tone consistent across all articles. Ensure that the franchisebazar brand directory is optimized for every brand that is registered on the website.
Ideal Persona
- Graduates with excellent writing and editing skills, with a keen eye for detail and a passion for entrepreneurship.
- Ability to research and go into the depth of the matter.
- Candidates must know how to manage their time effectively.
Only those candidates can apply who:
1. are available for the work-from-home job/internship.
2. can start the work-from-home job/internship and can join immediately
3. are available for a min duration of 6 months
4. have relevant skills and interests
*professionals wanting to start/restart their careers can also apply.
Duration: 6 months
Stipend: There is a fixed Stipend of ₹5000 PM Plus Additional Incentives based on your manager's Ratings and your performance.
Interested candidates kindly Share your resume with
Perks
- Full time content writer role after completion of initial 6 months
- Get your blogs published on FranchiseBAZAR and IndiaFranchiseBlogs and create a rich portfolio in serious business writing. All blogs that we publish are done with the writers names, hence you get complete recognition.