Are you a skilled Medical Writer with a passion for pharmacovigilance and scientific documentation? Here’s your opportunity to join Wipro, one of India’s leading global technology and consulting companies.
Wipro is inviting applications for Medical/Scientific Writing roles in the Pharmacovigilance domain. This role offers a chance to work with a global healthcare team and contribute to the preparation of high-quality regulatory and scientific documents that ensure patient safety and drug efficacy.
📌 Job Overview
Role: Medical Writer / Scientific Writer (Pharmacovigilance)
Company: Wipro Ltd.
Qualification: M.Pharm (Mandatory)
Experience: 2–4 Years
Location: Pune, India (3 Months Remote Work Option)
Employment Type: Full-time
Joining: Immediate joiners preferred
🧾 Key Responsibilities
- Prepare, review, and edit pharmacovigilance documents including case narratives, risk management plans, and safety reports.
- Ensure compliance with global regulatory requirements and internal quality standards.
- Collaborate with cross-functional teams to deliver high-quality scientific and regulatory content.
- Maintain accuracy, consistency, and scientific integrity in all deliverables.
- Participate in quality checks, audits, and continuous improvement initiatives within the medical writing function.
🎓 Qualifications and Skills
- M.Pharm degree (mandatory).
- 2–4 years of experience in pharmacovigilance or scientific writing.
- Strong understanding of drug safety regulations and clinical documentation.
- Excellent written and verbal communication skills.
- Detail-oriented, with the ability to work independently under deadlines.
💼 Why Join Wipro?
- Work with a global leader in IT and life sciences solutions.
- Exposure to international pharmacovigilance projects.
- Flexible hybrid model (3 months remote).
- Competitive salary and career development opportunities.
📧 How to Apply
Interested candidates can email their resumes to:
📩 varsha.kamalapurkar@wipro.com