Dr. Reddy’s Laboratories Hiring Biotech / Microbiology / Biochem For Team member – Drug Substance Post

Dr Reddy’s Latest Biotech Job – Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of their 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.

They started in 1984 with a modest investment, 20 employees and a bold vision. Today, they have research and development centers, manufacturing facilities, and a commercial presence in 66 countries.

Job Title: Team member – Drug Substance

Location: Dr. Reddy’s Laboratories · Hyderabad, Telangana, India

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

• You will execute unit operations within Cell Culture Downstream/Upstream according to the electronic/ paper 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, and perform routine cleaning and support activities

in GMP Manufacturing areas.

• You will perform routine autoclave operation, manual cleaning and sterilization of components and parts, monitoring processes and results, suggesting methods to ensure process success, and interfacing with process automation systems.

• You will issue discrepancies, collaborate with cross-functional departments to close them, implement corrective actions, and comply with GMP and safety standards, for designated manufacturing equipment.

• You will complete batch documentation in alignment with GMP, ensuring data collection and maintenance meet cGMPs (Current GMP), company standards, policies, and regulatory requirements, and supporting timely root cause investigations and CAPA (Corrective and Preventive Actions) completion.

• Your other responsibilities include maintaining manufacturing equipment for correct functionality and calibration compliance, operating within validated process parameters, and supporting qualification and validation activities.

• Emphasizing safety awareness and continuous improvement, you will actively adhere to safety rules and promptly report unsafe matters and near misses/accidents.

Qualifications

• Educational Qualification: A Graduation (B.Tech) in Biotechnology or a Post-Graduation in Science (Microbiology, biochemistry/ biotechnology)
• Minimum work experience: 2-6 years of experience working on Biosimilar Products

Skills & attributes:

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.

• Single-use technology

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.

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Additional Information

About the Department

Biologics

Currently operates in the Global Biosimilars business – a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon.

With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products.

With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation.

Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs.

We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure

Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date.

Benefits Offered – 

At Dr. Reddy’s we actively help to catalyze your career growth and professional development through personalized learning programs.

Dr Reddy’s Latest Biotech Job

The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself.