PV Scientist – Medical Assessment Role for M.Pharm Graduates | Dr. Reddy’s Laboratories

M.Pharm Pharmacovigilance Job Vacancy at Dr. Reddy’s – Apply Now in Hyderabad

Apply now for PV Scientist – Medical Writing role in Hyderabad at Dr. Reddy’s Laboratories. Requires M.Pharm (Pharmacology) with 3–7 years’ experience.

PV Scientist – Medical Assessment Role for M.Pharm Graduates | Dr. Reddy’s Laboratories, Hyderabad

Looking to advance your career in Pharmacovigilance? Dr. Reddy’s Laboratories invites experienced M.Pharm graduates to apply for the PV Scientist – Medical Assessment (Medical Writing) role based in Hyderabad, India. This opportunity is ideal for professionals passionate about drug safety and medical documentation within a global pharmaceutical organization.

Why Work at Dr. Reddy’s?

Dr. Reddy’s Laboratories is a globally recognized pharmaceutical company that operates in over 66 countries with a strong presence in research, development, and manufacturing. With over 24,000 employees, Dr. Reddy’s is committed to providing affordable and innovative medicines, championing a culture of inclusion, sustainability, and professional growth.

Key Responsibilities

Signal Management

• Conduct and review signal alerts regularly using LifeSphere Signal Management System.
• Ensure timely detection and evaluation as per regulatory schedule.

Aggregate Safety Reporting & Risk Management

• Prepare and peer-review PSUR, PBRER, PADER, DSURs, and Health Hazard Evaluations.
• Support development of RMPs and REMS.
• Collaborate with PV physicians and affiliates on risk minimization.

Regulatory & Clinical Documentation

• Provide safety input for study protocols, SAP, CRFs, final reports, and dossier submissions.
• Assist in developing PV Medical Writing SOPs and reviewing cross-functional SOPs.

Medical Writing & Labeling

• Contribute to patient and investigator safety documents, including IBs and PILs.
• Assist with labeling reviews to ensure safety information accuracy.

Internal Communication and Compliance

• Coordinate responses to Regulatory Authority queries.
• Support PSMF updates, CAPA completion, deviation reporting, and database testing.

Desired Candidate Profile

Education Qualification

• M.Pharm (Pharmacology) or equivalent post-graduate degree.

Experience Required

• 3 to 7 years of experience in Pharmacovigilance, specifically with PV Medical Writing.

Key Competencies

• Good understanding of FDA, EU, and local PV regulations.
• Strong analytical, communication, and documentation skills.
• Proficiency in Microsoft Office and PV systems.

About the Department – GMO (Global Manufacturing Organisation)

Dr. Reddy’s GMO unit leads manufacturing excellence with 19 global facilities, producing high-quality APIs and formulations in key therapeutic areas. Recognized by the World Economic Forum, their Bachupally unit represents world-class pharma manufacturing.

Employee Benefits

• Competitive salary packages
• Relocation and joining assistance
• Family support (maternity, paternity)
• Health and life insurance
• Personalized learning and upskilling opportunities

Call to Action

If you are ready to contribute to global health with a company that prioritizes innovation and ethics, apply now and be part of a future-ready pharmaceutical team.

👉 Apply Now: Click here to apply

Quick Overview Table

Company Name	Current Vacancies in Departments
Dr. Reddy’s Laboratories	Medical Affairs – Pharmacovigilance (PV Scientist – Medical Writing)

Required Education	Experience Required
M.Pharm (Pharmacology)	3–7 years in Pharmacovigilance

Location: Hyderabad, India