Dr. Reddy’s Laboratories Regulatory Affairs Specialist Hiring at Hyderabad | Pharmacovigilance

Dr. Reddy’s Laboratories Regulatory Affairs Specialist Hiring at Hyderabad | Pharmacovigilance

About Dr. Reddy’s Laboratories

Dr. Reddy’s Laboratories Ltd. is a global pharmaceutical company committed to delivering affordable and innovative medicines. With operations spanning over 66 countries and a workforce of more than 24,000 employees, the company focuses on research, quality, and sustainable healthcare solutions. Driven by the mission of “Good Health Can’t Wait,” Dr. Reddy’s is a trusted name in the pharmaceutical industry.

Job Overview

Dr. Reddy’s Laboratories is looking for a Regulatory Affairs Specialist to join its team in Hyderabad, Telangana. This role requires an experienced professional who can oversee regulatory submissions, ensure compliance, and manage product lifecycle activities effectively.
Job Summary

they Looking for a Regulatory Affairs Specialist to oversee the preparation and publishing of regulatory submissions. This role is pivotal in managing activities pertaining to product lifecycle management, quality management. Collaboration with internal teams will be essential for supporting internal and external audits and implementing effective CAPA measures.

Roles & Responsibilities

• You will be responsible for preparation and publishing of the regulatory dossier.
• You will be responsible for delivering registration goals with minimum supervision.
• You will be responsible for regulatory program management. Collaborating with SMEs and PMO to track the documents required for dossier preparation.
• You will be responsible for product lifecycle management, including variations, renewals and post-approval commitments.
• You will be responsible for supporting internal and external audits and implementation of CAPA (Corrective and Preventive Actions).
• You will be responsible for developing and maintaining a good internal and external network.
• You will be responsible for performing other tasks and duties assigned by the immediate supervisor

Qualifications
Educational qualification: A Bachelor/Master of Science in life sciences or relevant
Minimum work experience: 8 to 10 years of experience in regulatory affairs, preferably with QA (Quality Assurance) and PV experience
Skills & attributes:

• • • Knowledge of FDA guidelines.
    • Proficiency in spoken and written English.
    • Proficiency in using a computer and its applications, specifically Google Applications and MS Excel.
    • Excellent interpersonal and communication skills.
    • Attention to detail and the ability to multi-task and meet strict deadlines.
    • Knowledge of Veeva vault will be added advantage.

How to Apply

Interested candidates can apply via LinkedIn: Dr. Reddy’s Laboratories Regulatory Affairs Specialist – LinkedIn

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