Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).
Post : Team Member - Drug Substance
Job Description
Job summary
We are looking for an individual to execute downstream/upstream manufacturing unit operations, ensuring documentation and compliance within GMP (Good Manufacturing Practices), regulatory, and organizational guidelines. The objective is to produce products within defined volumes and timelines while maintaining compliance with quality standards, GMP, and other regulatory and statutory requirements, as per the schedule.
Roles & Responsibilities
• Execute unit operations within Downstream/Upstream according to the BPR (Batch Production Record).
• Conduct activities to support production schedules, obtain and stock supplies as required.
• Prepare media, buffers, and solutions necessary for unit operations.
• Perform routine cleaning and support activities in GMP Manufacturing areas.
• Perform routine process area cleaning, autoclave operation, manual cleaning and sterilization of components and parts.
• Monitor processes and results, suggesting methods to ensure process success, and interfacing with process automation systems.
• Issue discrepancies, collaborate with cross-functional departments to close them, implement corrective actions.
• Comply with GMP and safety standards for designated manufacturing equipment.
• Complete batch documentation in alignment with GMP, ensuring data collection and maintenance meet cGMPs (Current GMP), company standards, policies, and regulatory requirements.
• Support timely root cause investigations and CAPA (Corrective and Preventive Actions) completion.
• Maintain manufacturing equipment for correct functionality and calibration compliance.
• Operate within validated process parameters and support qualification and validation activities.
• Emphasize safety awareness and continuous improvement.
• Adhere to safety rules and promptly report unsafe matters and near misses/accidents.
Candidate Profile
Educational qualification : A Graduation in Chemical Engineering or Biotechnology, or a Post-Graduation in Science
Minimum work experience : 3 years of experience in working on Biosimilar Products
Technical Skills
• Comprehensive understanding of process manufacturing.
• Expertise in quality systems implementation and adherence to safety norms, ensuring compliance with industry standards.
• Practical experience and hands-on knowledge of Downstream and Upstream operations.
• Knowledge of equipment and processes, and proficiency in cleaning validation in the pharmaceutical manufacturing context.
• Understanding and knowledge of Clean-in-Place (CIP) and Sterilize-in-Place (SIP) systems.
Behavioural skills
• Possesses effective listening abilities, fostering clear communication and understanding.
• Pays meticulous attention to detail, ensuring precision in tasks and work.
• Prioritizes and is aware of deadlines, ensuring timely completion of tasks.
• Demonstrates analytical skills and the ability to troubleshoot effectively.
• Possesses strong interpersonal skills and collaborates effectively within a team.
Additional Information
Experience : 3 years
Qualification : A Graduation or a Post-Graduation
Location : Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 25th December 2025
Team Member : Apply here
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