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Team Lead Drug Substance (Downstream)


Job Location:

Hyderabad - India

Monthly Salary: Not provided by the employer
Posted: 30 August 2026 (7 days ago)
Application Deadline: 27 November 2026
Vacancies: 1 Vacancy

Job Summary

Job summary
We are seeking an individual to lead the downstream manufacturing team and oversee the implementation of production schedules. The objective of this role is to produce products within defined volumes and timelines ensuring compliance with quality standards GMP (Good Manufacturing Practices) and other regulatory and statutory requirements as per the schedule.

Roles & Responsibilities
You will receive inputs from production planning oversee daily operations on the production floor (including scheduling staffing monitoring training and troubleshooting) ensure compliance with applicable BPRs/EBRs (Batch Production Record/Electronic Batch Record ) SOPs (Standard Operating Procedures) and safety guidelines and administer contract manpower.
Your responsibilities include issuing discrepancies collaborating with cross-functional departments to close discrepancies implementing corrective actions adhering to GMP safety standards and SOPs for designated manufacturing equipment and completing batch documentation in compliance with GMP.
You will maintain manufacturing equipment functionality and calibration compliance operate equipment within validated process parameters actively promote safety awareness and improvements engage in continuous improvement activities and report unsafe matters and near misses/accidents.
You will actively promote safety awareness and improvements be involved in goal setting and performance reviews providing training and coaching to employees effectively manage employee performance issues and corrective actions and recognize employee contributions.


Qualifications :

Educational qualification: A Graduation in Chemical Engineering or a Post-Graduation in Science

Minimum work experience: 12 years of experience in working on Biosimilar Products

Skills & attributes:

Technical Skills

Comprehensive understanding of process manufacturing.
Understanding of Quality Systems and the regulatory environment with the ability to integrate quality standards into manufacturing processes.
In-depth knowledge of Current Good Manufacturing Practices (cGMP) and safety regulations.
Knowledge in mammalian cell culture techniques.
Expertise in operating bioreactors proficiency in using control systems familiarity with data acquisition and storage 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 :

About the Department
Biologics

Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 1015-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 900000 patients having benefited from our products till date.

Benefits Offered
At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddys 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.

Our Work Culture
Ask any employee at Dr. Reddys why they come to work every day and theyll say because Good Health Cant Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations but as a means to help patients lead healthier lives and were always attuned to the new and the next to empower people to stay fit. And to do this we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system they can make magic.
For more details please visit our career website at


Remote Work :

No


Employment Type :

Full-time


About Company

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Dr. ReddyÂ’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 CanÂ’t Wa ... View more

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