Clinical Research Jobs at Dr. Reddy’s Laboratories | MSc Graduates Apply Now for the Team Member Role
Dr. Reddy’s Laboratories is hiring for a Clinical Quality Assurance role to strengthen its global clinical research operations. This position offers an exciting opportunity to work on SOP management, vendor audits, risk assessments, and regulatory compliance, while contributing to the mission of making affordable and innovative medicines accessible worldwide. Join us in shaping the future of healthcare through quality, innovation, and purpose.
- Job Post: Team Member – Clinical DQA
- Location: Hyderabad
About the Company
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company driven by the purpose “Good Health Can’t Wait.” Established in 1984, the company has grown to over 24,000 employees across 66 countries. With strong foundations in science, innovation, and sustainability, Dr. Reddy’s continues to deliver affordable and innovative medicines to patients worldwide. By 2030, the goal is to impact 1.5+ billion patients, keeping sustainability and patient care at the core of its strategy.
Job Summary
We are seeking a highly motivated professional to join our Clinical Quality Assurance (CQA) team. The role involves reviewing SOPs, auditing BA/BE studies, conducting vendor risk assessments, and ensuring compliance with GCP and GLP guidelines.
Key Responsibilities
- Plan, perform, and document vendor qualifications for CROs, clinical sites, and central labs.
- Conduct audits of bioanalytical and bioequivalence studies across global teams.
- Perform self-inspections to ensure regulatory and internal compliance.
- Review deficiency responses and assist cross-functional teams with regulatory submissions.
- Support regulatory agency audits, develop CAPAs, and maintain QMS updates.
- Author, review, and approve SOPs for pre-clinical and clinical quality assurance.
- Provide training on GCP, quality principles, and regulatory requirements.
- Mentor junior team members and contribute to clinical QA strategies.
Qualifications
- Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, MSc in Clinical Research or related field (Master’s preferred).
- 3–5 years’ experience in bioanalytical method development or BE study audits.
- Strong knowledge of GCP, GLP, and global clinical research regulations.
- Technical expertise in SOP management, data integrity, and QA processes.
- Excellent communication, detail orientation, and problem-solving skills.
About the Department
Dr. Reddy’s operates 19 state-of-the-art facilities worldwide, producing APIs, injectables, and complex formulations. Recognized by the World Economic Forum’s Global Lighthouse Network, our facilities are benchmarks in innovation, sustainability, and operational excellence.
Work Culture & Benefits
At Dr. Reddy’s, employees thrive in a culture of empathy, diversity, and innovation. Benefits include:
- Competitive compensation and relocation support.
- Family support programs (maternity & paternity benefits).
- Comprehensive health and life coverage.
- Personalized learning and career development opportunities.
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