Dr. Reddy’s Laboratories Ltd. is a globally recognized multinational pharmaceutical company committed to accelerating access to affordable and innovative medicines. Founded in 1984 with a vision to transform healthcare, the company now operates in 66 countries with 24,000+ employees.
Key Highlights:
- Mission: “Good Health Can’t Wait” – ensuring timely access to life-saving medicines.
- Global Presence: R&D centers, manufacturing facilities, and commercial operations worldwide.
- Sustainability Focus: Committed to ethical practices, environmental responsibility, and social impact.
- Diversity & Inclusion: An equal opportunity employer fostering a discrimination-free workplace.
Current Job Openings at Dr. Reddy’s
1. Team Member – QC Micro (Visakhapatnam)
Job Family: Quality | Sub Job Family: Microbiology
Experience: 3-6 Years | Business Unit: GMO
Job Description:
- Perform Environmental Monitoring (EM) in manufacturing areas and labs.
- Conduct microbial sampling for WFI, purified water, potable water, and pure steam.
- Operate autoclaves, steam sterilizers, and hot air ovens.
- Prepare water & EM trends (monthly/semi-annual/annual).
- Perform Microbial Limit Testing (MLT) and bioburden analysis.
- Use Vitek 2 system for microbial identification.
- Ensure compliance with SOPs, GMP, and safety protocols.
Qualifications:
- B.Sc/M.Sc in Microbiology
- 3-6 years in pharmaceutical QC Microbiology
2. Team Member – Quality Control (Baddi)
Job Family: Quality | Sub Job Family: Quality Control
Experience: 2-5 Years | Business Unit: GMO
Job Description:
- Conduct sampling & analysis of raw materials, packaging, and stability samples.
- Maintain SAP records, ROA (Record of Analysis), and COA (Certificate of Analysis).
- Ensure calibration & maintenance of lab instruments.
- Follow cGMP, SOPs, and safety protocols (PPE, JSA).
- Manage chemical/solvent storage & volumetric solutions.
Qualifications:
- B.Sc in Chemistry/Analytical Chemistry
- 2-5 years in pharmaceutical QC
3. Clinical Research Associate (Hyderabad)
Job Family: Clinical Development | Sub Job Family: Clinical Operations
Experience: 3-6 Years | Business Unit: Biologics
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Job Description:
- Manage clinical trial site activities (feasibility, initiation, monitoring).
- Ensure regulatory compliance (ICH-GCP, protocol adherence).
- Oversee IP (Investigational Product) accountability & reconciliation.
- Coordinate site contracts, payments, and vendor management.
- Maintain Trial Master File (TMF) for audit readiness.
Qualifications:
- M.Pharma/Life Sciences/Biotech/Clinical Research Diploma
- 2-5 years in clinical research
