Dr. Reddy’s Hiring Pharma Graduates | Apply for Clinical DQA Position
Dr. Reddy’s Laboratories is inviting applications for the role of Team Member – Clinical DQA. This opportunity is ideal for professionals with experience in clinical quality assurance, audits, and regulatory compliance who want to contribute to one of the world’s leading pharmaceutical companies. Based in India, this role provides an opportunity to work in a purpose-driven, global organization that values innovation, sustainability, and patient-centric healthcare solutions.
- Job Position: Team Member – Clinical DQA
- Location: India
About the Company
Dr. Reddy’s Laboratories Ltd. is a multinational pharmaceutical company with a presence in 66 countries and a workforce of over 24,000 employees. Since 1984, the company has been committed to providing access, affordability, and innovation in healthcare. Guided by the credo Good Health Can’t Wait, Dr. Reddy’s is focused on building the future of healthcare through research, manufacturing excellence, and sustainability. Its vision is to impact over 1.5 billion patients worldwide by 2030.
Clinical Trials Job Description
The Team Member – Clinical DQA will play a critical role in ensuring the quality and compliance of clinical trials, bioequivalence (BE) studies, and vendor operations. The role involves auditing clinical CROs, reviewing SOPs, managing QMS updates, and supporting regulatory submissions. The ideal candidate should possess strong technical knowledge of GCP/GLP principles, hands-on experience in auditing, and excellent communication skills.
Key Responsibilities
- Conduct vendor qualification and re-qualification audits for CROs, clinical sites, and labs.
- Conduct audits of Central Labs and Bioanalytical components in accordance with established audit programs.
- Carry out post-study audits of BE studies across global clinical research teams.
- Review regulatory deficiency responses and provide cross-functional support.
- Prepare, host, and follow up on regulatory audits for clinical trials.
- Maintain and update the Quality Management System (QMS) for compliance.
- Develop, review, and approve SOPs for clinical and developmental QA processes.
- Train clinical research staff on quality assurance and GCP guidelines.
- Create and monitor quality metrics and KPIs for clinical QA.
- Mentor junior team members and contribute to continuous improvement.
Clinical Trials Job – Educational Qualifications
- Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, or related field.
- Master’s in Clinical Research or Pharmacy (preferred).
Experience and Skills
- 3–5 years of experience in the pharmaceutical industry with a focus on bioanalytical audits or BE studies.
- Strong knowledge of GCP, GLP, SOP management, and data integrity assurance.
- Excellent written and verbal communication skills.
- Attention to detail and adaptability to evolving regulatory requirements.
Keywords: Dr. Reddy’s careers, Clinical DQA jobs, Team Member, Clinical QA pharma, Pharmaceutical QA jobs, Clinical research quality assurance
