The role can provide valuable exposure to global safety processes, regulatory requirements, adverse event evaluation, and structured medical documentation. It may be particularly suitable for graduates who want to build long-term careers in Medical Writing, Pharmacovigilance, Drug Safety, Medical Affairs, or Regulatory Writing.
Job Overview
| Particulars | Details |
|---|---|
| Position | MEDICAL WRITERS |
| Company | Wipro |
| Location | Pune |
| Job Type | Full-Time |
| Category / Department | Scientific Writer |
| Application Mode |
🏢 About Wipro
Wipro Limited is a global technology and business services organization headquartered in Bengaluru, India.
The company has evolved significantly since its establishment in 1945, when it began as Western India Vegetable Products Limited. Over the decades, Wipro transitioned from its original consumer products business into a global technology services company.
Today, its areas of work include cloud services, artificial intelligence, digital transformation, cybersecurity, data and analytics, and technology consulting.
The company's history reflects a major transformation from a consumer-focused business into an international IT and business services organization serving clients across multiple industries and geographies.
📌 COMPANY PROFILE
🏛️ Founded: 29 December 1945
📍 Headquarters: Bengaluru, Karnataka, India
👤 Executive Chairman: Rishad Premji
💻 Key Areas: Cloud, AI, Digital Transformation, Cybersecurity, Data & Analytics
🌍 Global Presence: International technology and business services operations
🚀 COMPANY JOURNEY
🔹 Early Years: The business originally operated in the consumer products sector, including cooking oils and other products.
🔹 Technology Transformation: During the late 20th century, the organization expanded into information technology and computing services.
🔹 Global Growth: Wipro developed into an international technology and business services provider.
🔹 Modern Direction: Its technology portfolio now spans areas such as cloud, AI, cybersecurity, digital engineering, and analytics.
💡 Editor's Note / Preparation Tip
📝 EDITORIAL NOTES
📌 This opportunity is relevant to M.Pharm and PharmD graduates interested in Medical Writing and Pharmacovigilance.
📌 Fresh graduates can consider applying if they meet the stated educational requirements.
📌 Candidates with relevant experience should clearly highlight their exposure to safety case processing or medical writing.
📌 Knowledge of MedDRA and pharmacovigilance regulations can strengthen a candidate's profile.
📌 Applicants should verify the current vacancy status and recruitment instructions before sending personal information.
📌 Use a clear and professional email subject line when submitting your resume.
📄 RESUME PREPARATION TIPS
1️⃣ Clearly mention M.Pharm or PharmD and your specialization at the beginning of your resume.
2️⃣ Highlight academic projects involving Pharmacovigilance, Drug Safety, Clinical Research, or Medical Writing.
3️⃣ Add relevant knowledge of MedDRA, adverse events, SAEs, literature review, and safety reporting.
4️⃣ Include internships, certifications, workshops, or training relevant to pharmacovigilance and medical writing.
5️⃣ Keep your resume concise, professional, keyword-rich, and easy for recruiters to scan.
🎯 INTERVIEW PREPARATION
1️⃣ Revise the fundamentals of Pharmacovigilance and Drug Safety.
2️⃣ Understand the purpose and basic structure of an ICSR and adverse event report.
3️⃣ Review MedDRA terminology, coding principles, and the difference between medical history and adverse events.
4️⃣ Prepare to explain how you would evaluate scientific literature for potential safety information.
5️⃣ Practice writing a short, accurate medical narrative using clear scientific language.
💡 PROFESSIONAL TIPS
🚀 Develop strong medical and scientific writing habits by practicing regularly.
📚 Keep yourself updated on global pharmacovigilance concepts and regulatory expectations.
🔍 Build excellent attention to detail because small errors can affect safety documentation.
🧠 Learn to simplify complex medical information without losing scientific accuracy.
📈 Consider developing expertise in areas such as Medical Writing, PV Case Processing, Signal Detection, Regulatory Writing, or Medical Communications.
📝 Job Description
🚨 WIPRO IS HIRING – MEDICAL WRITERS | PUNE 🧬📝
🎓 M.Pharm & PharmD | Freshers & Early-Career Professionals
Are you an M.Pharm or PharmD graduate looking to begin your career in Medical Writing, Pharmacovigilance, or Drug Safety?
Here is an opportunity to explore a Medical Writer position with Wipro in Pune. The role is suitable for freshers and candidates with up to 2 years of relevant experience who have an interest in scientific communication, safety reporting, biomedical literature, and pharmaceutical regulations.
If you enjoy working with scientific information and have a good understanding of pharmacology, MedDRA terminology, narrative writing, and pharmacovigilance concepts, this role could be a strong starting point for your professional journey. 🚀
📌 JOB DETAILS
🏢 Company: Wipro Limited
💼 Position: Medical Writer
📍 Location: Pune, Maharashtra
🎓 Qualification: M.Pharm / PharmD
💼 Experience: 0–2 Years
👤 Level: Freshers & Early-Career Professionals
🧪 Domain: Medical Writing / Pharmacovigilance / Drug Safety
📩 Application: Email
🎓 ELIGIBILITY & QUALIFICATION
✔ M.Pharm
✔ PharmD
💼 Experience:
Freshers can apply, and candidates with up to 2 years of experience in Medical Writing, Pharmacovigilance, or Drug Safety may also be considered.
🌟 WHY CONSIDER THIS OPPORTUNITY?
🌍 Exposure to projects involving global pharmaceutical clients
🧬 Opportunity to develop expertise in Pharmacovigilance and Drug Safety
📝 Practical experience in scientific and medical writing
📚 Exposure to international safety and regulatory reporting practices
📈 Potential career pathways in Medical Writing, Drug Safety, and Regulatory Writing
🤝 Opportunity to work in a professional, collaborative environment
⏰ General shift working environment, as indicated in the available job information
💰 ESTIMATED SALARY
💵 Indicative Range: ₹4,00,000 – ₹7,00,000 per annum (CTC)
The actual compensation may vary depending on the candidate's qualification, relevant skills, experience, and selection outcome. Candidates should confirm the final compensation details directly during the recruitment process.
📩 HOW TO APPLY
Interested candidates can share their updated resume with the recruitment contacts below:
📧 varsha.kamalapurkar@wipro.com
📧 priyanka.patra2@wipro.com
📧 riya.bhowmik@wipro.com
📌 Suggested Email Subject:
Application for Medical Writer – Pune – M.Pharm/PharmD
📢 Know someone who is looking for a career in Medical Writing or Pharmacovigilance? Tag them in the comments or share this opportunity with your network! 🤝
🎯 Key Responsibilities
- ✓ Review published scientific articles and biomedical literature for relevant safety information.
- ✓ Identify and assess individual and non-individual safety case information.
- ✓ Apply applicable regulatory requirements and internal procedures when evaluating potential safety cases.
- ✓ Prepare clear, concise, and scientifically accurate summaries based on published medical information.
- ✓ Perform appropriate coding of medical history, medications, and adverse events using MedDRA terminology.
- ✓ Review Serious Adverse Events (SAEs) and support accurate and timely processing.
- ✓ Prepare medical narratives and structured safety information for pharmacovigilance activities.
- ✓ Support the preparation of electronic regulatory documentation.
- ✓ Maintain high standards of accuracy, quality, compliance, and documentation.
- ✓ Collaborate with team members to complete assigned work within defined timelines.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This MEDICAL WRITERS role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
1️⃣ Who can apply for this Medical Writer position?
M.Pharm and PharmD graduates who meet the role requirements can apply. Freshers are also encouraged to explore the opportunity.
2️⃣ Is previous experience mandatory?
No. The available job information indicates an experience range of 0–2 years, making the role suitable for fresh graduates and early-career professionals.
3️⃣ What skills should candidates focus on?
Candidates should develop knowledge of Pharmacovigilance, MedDRA, medical writing, narrative writing, pharmacology, biomedical literature review, and regulatory concepts.
4️⃣ Where is the position located?
The position is listed for Pune, Maharashtra.
5️⃣ What is the estimated salary?
The indicative salary range is ₹4 LPA to ₹7 LPA, although the final compensation may depend on qualifications, skills, experience, and the employer's offer.
6️⃣ What career paths can this role lead to?
Experience in this area may help professionals progress toward careers in Medical Writing, Pharmacovigilance, Drug Safety, Regulatory Writing, Medical Communications, and related pharmaceutical functions.
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