Team Member

**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.
**Job Description** Job Summary**

**Roles & Responsibilities**
- Responsible for executing the production targets of the packing as per the packing plan.
- To implement and follow the policies and procedures for efficient functioning of the machines.
- Responsible for strict adherence to entry and exit procedure as per respective SOP’s.
- Responsible for strict adherence to the standard operating procedures and cGMP.
- Responsible for implementation online documentation (Batch packing record, MES entries, logbook entries).
- To execute the batch packing activity as per the instruction of e-BPR and workflow in Rockwell software as part of manufacturing execution system.
- Responsible for batch coding, serialization of the product as per respective SOP’s.
- Responsible for supervising the packing (Vial, bottle and blister) line as per production plan.
- Responsible for implementing the productivity improvement measures.
- Responsible for guiding of sub-ordinates and new joinees.
- To ensure the discipline is maintained at the shop floor.
- Responsible for co-ordination with supporting departments for smooth production operation.
- Responsible for production SAP related transactions.
- Responsible for setup, operation and cleaning, line clearance, maintenance, of machines as per the operating instructions and standard cleaning procedures.
- Responsible for carrying out the in-process checks as per the instructions in the batch production record.
- To perform reconciliation of the product as per respective SOP or batch packing record.
- Responsible for performing the change overs.
- Responsible for dispensing of packing materials, packing lines as per production plan.
- Responsible for manpower management and scheduling.
- Responsible for meeting the daily production schedule.
- Responsible for implementation of simplification in packing areas.
- Responsible for audit preparation.
- Responsible for maintaining all the parameters in Safety, Quality and productivity.

**Qualifications**
**Educational qualification**:A Diploma or Bsc degree in Pharmaceutical Sciences, Chemical Engineering, or a related field

**Minimum work experience**: 2-6 years of experience in pharmaceutical packing operations (Vial, bottle and blister) and packing validation

**Skills & attributes**:
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**Technical Skills**
- Expertise in line operations, especially in packing activities like Secondary packing and Track and Trace.
- Proficiency in understanding equipment such Labelling machine, Autocartonator, Serialization etc.
- Understanding of Packing Validation for Oral Solid Product and Injectables 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 packing processes.
- Exhibits a keen attention to detail in handling complex packing activities, ensuring precision and accuracy.
- Collaborates seamlessly with cross-functi