Are you passionate about ensuring pharmaceutical quality and compliance? Dr. Reddy’s Biologics, a leader in the global biosimilars market, is hiring a Quality Control Associate for its in-process team in Hyderabad, Telangana. This is an exciting opportunity to join a purpose-driven organization committed to accelerating access to affordable medicines. With a focus on innovation and sustainability, Dr. Reddy’s offers a dynamic work environment for professionals eager to grow in the pharmaceutical industry. Read on to explore this role, its responsibilities, qualifications, benefits, and how to apply.
Job Responsibilities
As a Quality Control Associate at Dr. Reddy’s Biologics, you will ensure the highest standards of product quality through meticulous testing and analysis. Key responsibilities include:
- Conducting quality control tests on raw materials, in-process samples, and finished products to meet regulatory standards.
- Operating and maintaining laboratory equipment to ensure accurate and reliable results.
- Performing data analysis and interpreting test results using statistical methods.
- Preparing detailed reports and maintaining precise documentation of quality control activities.
- Assisting in the development and enhancement of quality control procedures.
- Collaborating with cross-functional teams to resolve quality issues and implement corrective actions.
- Ensuring compliance with Good Manufacturing Practices (GMP) and regulatory requirements (FDA, EMA, etc.).
- Participating in internal audits and supporting external regulatory inspections.
- Contributing to continuous improvement initiatives in quality control processes.
Qualifications
To excel in this role, candidates should meet the following criteria:
- Education: Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or a related field.
- Experience: 1-3 years of experience in quality control, ideally in pharmaceuticals or biotechnology.
- Technical Skills: Proficiency in quality control techniques, statistical methods, and laboratory equipment operation.
- Regulatory Knowledge: Strong understanding of GMP and regulatory standards (FDA, EMA).
- Analytical Abilities: Excellent problem-solving skills with meticulous attention to detail.
- Documentation: Strong reporting and documentation skills for accurate record-keeping.
- Teamwork: Effective communication and collaboration skills for cross-functional teamwork.
- Additional Skills: Familiarity with Laboratory Information Management Systems (LIMS) is a plus.
- Multitasking: Ability to prioritize and manage workloads efficiently.
Benefits
Dr. Reddy’s Biologics offers a competitive benefits package designed to support your professional and personal growth:
- Career Development: Access to personalized learning programs to enhance your skills.
- Competitive Compensation: Salary range of INR 100,000–500,000 per month, commensurate with experience.
- Inclusive Culture: A diverse and discrimination-free workplace that values merit and inclusion.
- Industry-Leading Benefits: Comprehensive health, wellness, and professional development programs aligned with top industry standards.
- Purpose-Driven Mission: Contribute to Dr. Reddy’s goal of reaching 1.5 billion patients by 2030 through innovative and affordable medicines.
How to Apply
Ready to join a global leader in biosimilars? Apply for the Quality Control Associate position by visiting Dr. Reddy’s career portal at careers.drreddys.com. Submit your updated resume and a cover letter highlighting your qualifications and passion for quality control in pharmaceuticals. Applications are reviewed on a rolling basis, so apply by November 7, 2025, to be considered.
FAQs
Q: What is the work environment like at Dr. Reddy’s Biologics?
A: Dr. Reddy’s fosters an inclusive, purpose-driven culture with a focus on innovation, sustainability, and collaboration. Employees work on-site in Hyderabad, contributing to the mission of “Good Health Can’t Wait.”
Q: What qualifications are most important for this role?
A: A Bachelor’s degree in a relevant field, 1-3 years of quality control experience, and knowledge of GMP and regulatory standards are critical for success in this position.
