Are you a detail-oriented and experienced regulatory professional looking for a new challenge? Dr Reddy’s Laboratories Limited, a leading multinational pharmaceutical company, is seeking an Analyst in Regulatory Affairs to join their team in Bachupalle, Telangana. This is an excellent opportunity to work with a renowned company that is committed to accelerating access to affordable and innovative medicines.
🏢About Dr Reddy’s Laboratories
Dr Reddy’s Laboratories Ltd. is a global pharmaceutical company with a presence in over 66 countries. With a strong commitment to innovation, affordability, and accessibility, the company has established itself as a leader in the pharmaceutical industry. The company’s vision is to reach over 1.5 billion patients across the world by 2030, and it is driven by a purpose to make a positive impact on people’s lives.
💼Job Description
As an Analyst in Regulatory Affairs, you will play a critical role in overseeing Emerging Markets procedures, handling Marketing Authorisation Applications, and ensuring compliance with regulatory guidelines. Your responsibilities will include:
Managing chemistry, manufacturing, and controls (CMC) documentation for health authorities’ submissions
Addressing deficiency letters and responding to regulatory queries
Contributing to regulatory strategy development and facilitating effective communication with stakeholders
Reviewing critical quality and regulatory documents, such as specifications, stability protocols, and development reports
Providing launch support and interacting with internal and external stakeholders
⚙️Responsibilities
Handle end-to-end registration in ANZ and Emerging Markets
Prepare, review, and submit dossiers in ANZ and Emerging Markets
Author high-quality CMC documentation for health authorities’ submissions
Review and respond to deficiency letters
Prepare regulatory strategy notes, regulatory due diligence, and gap analysis
Evaluate and share regulatory affairs requirements with product development teams
Identify open issues and anticipated questions on regulatory submissions
Review and closure of change control notifications (CRNs)
Provide launch support and interact with internal and external stakeholders
🧠Qualifications
M Pharm degree
4-6 years of experience in ANZ Regulatory Affairs
Technical skills: knowledge of regulatory requirements, product development, manufacturing processes, intellectual property, and quality
Behavioural skills: excellent communication and interpersonal skills, efficient and good collaborator, effective planning, and a high level of performance orientation
🎁Benefits
Competitive salary and benefits package
Opportunity to work with a leading pharmaceutical company
Personalised learning programs and career growth opportunities
Medical coverage for yourself and your family
Life coverage
Joining and relocation support
Family support (maternity and paternity benefits)
💡Why Join Dr Reddy’s Laboratories?
Dr Reddy’s Laboratories is a company that values innovation, integrity, and sustainability. With a strong commitment to corporate governance and social responsibility, the company provides a work environment that is free from discrimination and is an equal opportunity employer. If you are a motivated and experienced regulatory professional looking for a new challenge, this is an excellent opportunity to join a team that is dedicated to making a positive impact on people’s lives.
📝 How to Apply
Apply now and take the next step in your regulatory career:
👉 Apply Here