Dr Reddys Laboratories Hiring Regulatory Associate in Hyderabad for experienced professionals with global regulatory submissions and lifecycle management expertise.
About the Company
Dr. Reddy’s Laboratories Limited is a leading global pharmaceutical company committed to providing affordable and innovative medicines. Founded in 1984, the organization operates across research, development, manufacturing, and commercialization in more than 60 countries.
With a strong presence in regulated markets such as the US and Europe, Dr. Reddy’s is known for its science-driven approach, robust compliance culture, and high regulatory standards. The company offers regulatory professionals long-term career stability, global exposure, and opportunities to work on complex product portfolios.
Job Details
- Job Title: Regulatory Associate
- Department: Regulatory Affairs
- Employment Type: Full-time
- Work Model: Onsite
- Job Location: Nacharam, Hyderabad, Telangana
- Experience Required: 4–8 years
Job Description
Dr. Reddy’s Laboratories is hiring a Regulatory Associate to support regulatory affairs operations in Hyderabad. This role is suited for experienced regulatory professionals who have hands-on exposure to product lifecycle management, regulatory submissions, compliance activities, and interactions with global health authorities.
The position plays a critical role in ensuring timely approvals, regulatory compliance, and uninterrupted market access for pharmaceutical products across regulated markets. Dr Reddys Laboratories Hiring Regulatory Associate
Skills / Qualifications
Required Education
Candidates must possess one of the following qualifications:
- M.Pharm
- M.Sc
- Industrial Pharmacy
- Registered Pharmacy Professional
Experience Requirement
- 4 to 8 years of experience in Regulatory Affairs
- Prior exposure to Quality Assurance (QA) and Pharmacovigilance (PV) activities is preferred
Required Skills & Attributes
- Strong knowledge of FDA, EMA, EU, and global regulatory guidelines
- Excellent written and verbal communication skills in English
- Proficiency in MS Excel, Google Applications, and regulatory documentation tools
- High attention to detail and ability to manage multiple submissions simultaneously
- Strong interpersonal skills and cross-functional collaboration abilities
Dr Reddys Laboratories Hiring Regulatory Associate
Key Responsibilities
- Prepare, compile, and submit regulatory dossiers to global health authorities
- Manage lifecycle activities including variations, renewals, and post-approval changes
- Support regulatory activities linked to quality systems and pharmacovigilance
- Coordinate with QA, PV, manufacturing, and other internal teams
- Respond to regulatory queries, deficiencies, and authority communications
- Develop, review, and implement regulatory SOPs and training materials
- Support internal and external audits and regulatory inspections
- Assist in compliance investigations and implementation of CAPA actions
- Ensure alignment with FDA, EMA, and other international regulatory requirements
Dr Reddys Laboratories Hiring Regulatory Associate
Benefits / Perks
- Exposure to global regulatory submissions and regulated markets
- Opportunity to work with established quality and compliance frameworks
- Long-term career growth in regulatory and leadership roles
- Stable work environment in a multinational pharmaceutical company
- Competitive compensation aligned with industry standards
Dr Reddys Laboratories Hiring Regulatory Associate
Why You Should Join
Building a regulatory career at Dr. Reddy’s Laboratories provides hands-on experience with complex global submissions, lifecycle management strategies, and interactions with major health authorities. The organization’s strong compliance culture and international footprint make it an ideal workplace for regulatory professionals seeking sustained growth and global exposure.
Dr Reddys Laboratories Hiring Regulatory Associate
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No. This position requires 4–8 years of regulatory affairs experience.
Does this role involve global regulatory exposure?
Yes. The role includes work aligned with FDA, EMA, and other international regulatory frameworks.
Is QA or PV experience mandatory?
QA and PV experience is preferred but not mandatory.
Is this an onsite role?
Yes. This is a full-time onsite position based in Hyderabad.
What is the career growth after this role?
Career progression may include Senior Regulatory Associate, Regulatory Manager, and global regulatory leadership roles.
Dr Reddys Laboratories Hiring Regulatory Associate
How to Apply
Eligible candidates can apply through the official LinkedIn job listing provided by Dr. Reddy’s Laboratories. Ensure all application details are complete and accurate before submission.
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