Global technology and consulting giant Wipro Limited has officially re-opened recruitment pipelines for Medical Writers and Drug Safety Professionals.
This latest life sciences hiring drive offers an exceptional entry-level and early-career pathway for M.Pharm, PharmD, and life science graduates looking to build a high-paying corporate career in medical writing, narrative composition, and pharmacovigilance. Positions are primarily anchored at Wipro’s high-tech healthcare delivery hub in Pune, with temporary or hybrid remote flexible options available for select teams.
📋 Wipro Medical Writing Drive Overview
| Attribute | Details |
| Company Name | Wipro Limited / Wipro Life Sciences |
| Primary Job Roles | Medical Writer, Scientific Writer, Drug Safety Reviewer |
| Experience Scale | 0 to 2+ Years (Freshers and Experienced Professionals are both eligible) |
| Primary Job Location | Pune, Maharashtra, India (Currently extending hybrid/remote allocations) |
| Estimated Base CTC | ₹3.0 Lakhs to ₹7.0 Lakhs Per Annum (Based on experience & qualifications) |
| Shift Structural Norms | Standard General Shifts / Client-Aligned Work Patterns |
🎯 Target Educational Qualifications & Skill Matrix
Wipro maintains precise academic and domain competencies for its global healthcare project deployments:
1. Mandatory Qualifications
- For Medical Writers: Master of Pharmacy (M.Pharm – Pharmacology/Pharmaceutics preferred) or Doctor of Pharmacy (PharmD).
- For Allied Senior Profiles: MBBS / MD (Eligible for secondary Drug Safety Physician tracks within the same business unit).
2. Core Operational Capabilities Evaluated
- Scientific Document Compilations: Strong fundamentals in narrative summarizing, adverse event reporting, and clinical data interpretation.
- Industry Coding Glossaries: Preliminary or practical experience working with standard MedDRA terminology coding protocols for medical history and medications.
- Regulatory Framework Familiarity: Understanding baseline USFDA and EMA pharmacovigilance regulatory reporting compliance standards.
💻 Primary Job Responsibilities
Selected candidates will work directly with global pharmaceutical clients, executing the following baseline workflows:
- Reviewing published biomedical literature databases to extract valid safety cases.
- Drafting concise, error-free clinical scientific case summaries and individual case safety reports (ICSRs).
- Evaluating Serious Adverse Events (SAEs) and ensuring structural data alignment within pharmacovigilance tracking engines.
- Maintaining strict regulatory compliance goals and data confidentiality standards across matrix frameworks.
⚡ How to Submit Your Application (Step-by-Step Channels)
Because Wipro handles technical life sciences applications through specific talent acquisition desks, candidates are requested to follow this procedural pipeline:
1.Optimize and Sync Your CV:Step 1.
Update your single-page professional resume format. Ensure you explicitly highlight your final year academic projects, certifications in pharmacovigilance (if any), and core keywords like MedDRA, Narrative Writing, Pharmacology, and cGMP/GLP guidelines.
2.Submit Directly to Official HR Inboxes:Step 2.
Draft a professional cover note and route your PDF resume directly via email to the assigned Wipro Talent Acquisition Acquisition specialists:
- Email 1: [email protected]
- Email 2: [email protected]
- Email 3: [email protected]
- Subject Line Recommendation:
Application for Medical Writer Role - [Your Name] - [M.Pharm/PharmD] - Fresher/Experienced
3.Register on Wipro Careers Portal:Step 3.
Cross-reference and upload your formal details into the generalized corporate tracking database to ensure long-term visibility for global projects.
🔗 Official Verification & Apply Resource Nodes
- Official Corporate Interface Node: Verify Life Sciences Solutions via Wipro Dashboard
- Wipro Careers Database Portal: Explore and Track Active Openings at careers.wipro.com
