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Team Member Production Sterile
Posted on Aug. 26, 2026
- Ts, India
- 0 - 0 USD (yearly)
- Full Time
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Company Description
Job Description
Job Summary
This role is for a Manufacturing Operator responsible for executing production operations as per batch records (BMR/BPR) and SOPs, ensuring quality and safety compliance. The position involves machine maintenance, calibration, inventory management, and contemporaneous documentation in GMP systems. You will contribute to operational excellence by adhering to safety norms, participating in toolbox talks (TBTs), reporting near-misses, and supporting CAPA implementation. The role emphasizes continuous improvement through Kaizen and 5S, while ensuring coordination with seniors, co-workers, and cross-functional teams to achieve production goals.
Roles & Responsibilities
Qualifications
Educational qualification: Diploma/ Graduation in Science, Pharmacy, Pharmaceutical Sciences, Industrial Engineering, or a related field is mandatory.
Minimum work experience:
2+ / 4+ / 6+ years of experience
Skills & attributes &Critical exposures
Functional Skills
Additional Information
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.
We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.
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).
‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency
Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.
Job Description
Job Summary
This role is for a Manufacturing Operator responsible for executing production operations as per batch records (BMR/BPR) and SOPs, ensuring quality and safety compliance. The position involves machine maintenance, calibration, inventory management, and contemporaneous documentation in GMP systems. You will contribute to operational excellence by adhering to safety norms, participating in toolbox talks (TBTs), reporting near-misses, and supporting CAPA implementation. The role emphasizes continuous improvement through Kaizen and 5S, while ensuring coordination with seniors, co-workers, and cross-functional teams to achieve production goals.
Roles & Responsibilities
- You will be responsible for executing manufacturing operations as per plan, ensuring quality and safety compliance.
- You will be responsible for performing shop floor activities as per BMR/BPR and SOP instructions.
- You will be responsible for machine maintenance, calibration, inventory management, and ensuring material availability for batch production.
- You will be responsible for making online entries in GMP documents to ensure contemporaneous documentation.
- You will be responsible for following safety norms, participating in toolbox talks (TBTs), and reporting near-misses or unsafe conditions.
- You will be responsible for executing operations without quality deviations, maintaining compliance at all times.
- You will be responsible for supporting continuous improvement through Kaizen and implementing 5S at the workplace.
- You will be responsible for coordinating with seniors, co-workers, subordinates, and cross-functional teams to ensure smooth operations.
Qualifications
Educational qualification: Diploma/ Graduation in Science, Pharmacy, Pharmaceutical Sciences, Industrial Engineering, or a related field is mandatory.
Minimum work experience:
2+ / 4+ / 6+ years of experience
Skills & attributes &Critical exposures
Functional Skills
- Aseptic Processing
- Batch Production
- Cleanrooms
- Equipment Maintenance
- Incident Reporting
- Pharmaceutical Batch Documentation
- Pharmaceutical Manufacturin
- Quality Management
- Current Good Manufacturing Practices (cGMPS)
- Total Productive Maintenance
- Digital Literacy
- Good Documentation Practices
- Lean Methodologies
- Safety-first mindset with strong compliance and regulatory alignment
- Collaborative across shop floor, engineering, and cross-functional teams
- Continuous improvement orientation with problem-solving and innovation
- Experience in the setup and operation of equipment used in the manufacturing of sterile products, aseptic filling, lyophilization, and cleanroom operations is desired
- Experience in PA/PR, operator exposure bands (OE/OL bands), 7QC tools used in sterile manufacturing processes, such as isolators, RABS, automated visual inspection systems, and sterilization equipment (autoclaves, depyrogenation tunnels), is desired.
- Exposure in the manufacturing of oncology and anti-cancer drugs, expertise in high-containment facilities, handling highly potent active pharmaceutical ingredients (HPAPIs) using split-phase butterfly valves (SFBV), and in-process QA/QC is preferred.
- Exposure to digital systems, material handling, inventory accuracy, adherence to contamination control protocols, and safety protocols in handling hazardous materials is preferred.
Additional Information
Benefits Offered
At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs.
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.
Our Work Culture
Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t 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 we’re 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 https://careers.drreddys.com/#!/
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