Team Member

6 months ago

Telangana, India Dr Reddy's Laboratories Limited Full time

**Company Description**
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 Summary**

**Roles & Responsibilities**
- You will be responsible for handling line operations, specifically manufacturing activities like CIP (Cleaning-in-place), SIP (Sterilizing-in-place), and batch manufacturing.
- You will be responsible for handling equipment like Steam Sterilizer, Dry heat sterilizer, HVAC (Heating, Ventilation, and Air Conditioning), water system, compressed air, Nitrogen system, etc.
- You will be responsible for process validation for Sterilization, Washing, Aseptic filling, and cleaning procedures.
- You will evaluate change controls, deviation, and incident, out of specification, out of trend, and risk management.
- You will prepare the production process SOPs (Standard Operating Procedures) and batch records.
- You will provide training on goods manufacturing practices.
- You will respond to queries and questions regarding regulatory audits such as US FDA (Food and Drug Administration).

**Qualifications**
**Educational qualification**:A Bachelor's or Master’s degree in Pharmaceutical Sciences, Chemical Engineering, or a related field

**Minimum work experience**: 10 years of experience in pharmaceutical manufacturing operations, with a focus on batch manufacturing, and process validation

**Skills & attributes**:
***
**Technical Skills**
- Expertise in line operations, especially in manufacturing activities like CIP, SIP, and batch manufacturing.
- Proficiency in understanding equipment such as Steam Sterilizer, Dry heat sterilizer, HVAC, water system, compressed air, Nitrogen system, etc.
- Understanding of Process Validation for Sterilization, Washing, Aseptic filling, and cleaning procedures.
- Knowledge for evaluation of change control, deviation, incident, out of specification, out of trend, and risk management.
- Experience in preparing production process SOPs and batch records.
- Hands-on experience in regulatory audits, particularly with agencies like the US FDA.

**Behavioural Skills**
- Capacity to provide training on good manufacturing practices and other relevant areas.
- Demonstrates a proactive approach to identifying and solving challenges in manufacturing processes.
- Exhibits a keen attention to detail in handling complex manufacturing activities, ensuring precision and accuracy.
- Collaborates seamlessly with cross-functional teams, promoting a cooperative and inclusive work environment.
- Efficiently manages time to meet production schedules and deadlines without compromising quality.
- Displays a willingness to stay updated on industry trends, regulations, and emerging technologies, contributing to ongoing professional development.
- Knowledge of working in regulatory environment like USFDA, MHRA, TGA.
- Should have good understanding of cGM, cGDP, and good laboratories practice.
- Must have hands-on experience in sophisticated manufacturing machine and equipment.
- Effective communication and training skills for user departments and service providers.

**Additional Information** About the Department**
**Global Manufa

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