Microbiology Job at Dr. Reddy’s
Looking for a rewarding Microbiology Job in the pharmaceutical industry? Here’s an exciting opportunity from Dr. Reddy’s Laboratories, one of India’s leading global pharma companies. This QC Job in Hyderabad offers microbiology professionals the chance to work in a highly regulated laboratory environment while contributing to product quality, compliance, and patient safety. If you’re searching for a promising Dr. Reddy’s career opportunity and aiming to advance your life science journey, this opening deserves your attention.
About Dr. Reddy’s Laboratories
Dr. Reddy’s Laboratories is a leading multinational pharmaceutical company founded in 1984. Headquartered in Hyderabad, the company operates in over 66 countries and employs more than 24,000 professionals worldwide. The organization focuses on accelerating access to affordable and innovative medicines while maintaining the highest standards of quality, sustainability, and scientific excellence. A Dr. Reddy’s career is recognized globally for professional development, innovation, and employee growth.
Position Details
| Job Title | Team Member – QC (Microbiology) |
| Location | Hyderabad, Telangana, India |
| Function | Quality Control (QC) – Microbiology |
| Employment Type | Full-Time |
Role Overview
The Team Member – QC (Microbiology) is responsible for performing routine microbiological testing of raw materials, in-process samples, finished products, and environmental monitoring samples. The role ensures compliance with Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP), and applicable regulatory requirements.
The position supports quality assurance activities by conducting microbiological analyses, maintaining laboratory equipment, ensuring accurate documentation, and contributing to regulatory compliance across laboratory operations.
Key Responsibilities
Microbiological Testing
The selected candidate will:
- Perform routine microbiological analyses of raw materials, in-process samples, and finished products.
- Conduct:
- Total Viable Count (TVC)
- Microbial Limit Testing (MLT)
- Sterility Testing
- Endotoxin Testing (BET/LAL)
- Pathogen Testing (e.g., E. coli, Salmonella and other specified microorganisms)
- Prepare microbiological media and perform Growth Promotion Testing (GPT).
- Execute sterilization activities in accordance with laboratory procedures.
Environmental Monitoring
The role includes monitoring classified manufacturing and laboratory environments through:
- Active and passive air sampling.
- Surface monitoring using swabs and contact plates.
- Personnel monitoring programs.
- Recording, reviewing, and evaluating environmental monitoring results against established alert and action limits.
Instrument Operation and Maintenance
The candidate will be responsible for operating and maintaining laboratory equipment, including:
- Autoclaves
- Incubators
- Laminar Air Flow (LAF) systems
- Colony Counters
- Particle Counters (where applicable)
Additional responsibilities include:
- Ensuring equipment calibration compliance.
- Supporting preventive maintenance activities.
- Maintaining equipment usage and maintenance records.
Documentation and Regulatory Compliance
The selected candidate will:
- Maintain laboratory documentation in accordance with Good Documentation Practices (GDP).
- Accurately record observations and test results in:
- Laboratory logbooks
- Worksheets
- Laboratory Information Management Systems (LIMS), where applicable
- Follow approved SOPs, Standard Test Procedures (STPs), and laboratory guidelines.
- Ensure compliance with applicable regulatory requirements, including:
- US FDA
- EU GMP
- WHO Guidelines
- Internal Quality Management Systems
Educational Qualifications
Essential Qualification
- B.Sc. in Microbiology OR
- M.Sc. in Microbiology
Desired Skills and Competencies
Preferred candidates should possess:
- Strong understanding of microbiological testing techniques and laboratory practices.
- Knowledge of pharmaceutical quality control and microbiology laboratory operations.
- Familiarity with GLP, GDP, GMP, and regulatory compliance requirements.
- Experience in environmental monitoring and sterility assurance activities.
- Ability to operate laboratory instruments and maintain accurate documentation.
- Attention to detail and commitment to data integrity.
- Good communication and teamwork skills.
Why Join Dr. Reddy’s Laboratories?
Dr. Reddy’s offers an opportunity to work in a globally recognized pharmaceutical organization focused on innovation, quality, and patient impact. Employees contribute to advancing healthcare access while developing professionally in a collaborative, inclusive, and growth-oriented environment.
