Team Member Manufacturing (Granulation)

Purpose of the Role

To execute granulation manufacturing activities in accordance with approved Batch Manufacturing Records (BMRs) Standard Operating Procedures (SOPs) cGMP requirements and safety standards ensuring consistent production of high-quality pharmaceutical products while meeting productivity compliance and quality objectives.

Key Roles & Responsibilities

Raw Material Handling & Dispensing

• Verify availability and status of raw materials before batch execution.
• Receive and transfer dispensed materials as per BMR requirements.
• Check material identity quantity batch number and status labels before use.
• Ensure proper handling and storage of materials during manufacturing.

Granulation Operations

• Perform sifting dispensing dry mixing wet granulation drying milling and blending activities as per approved procedures.
• Operate pharmaceutical manufacturing equipment such as:
  • Rapid Mixer Granulator (RMG)
  • Fluid Bed Dryer (FBD)
  • Fluid Bed Processor (FBP)
  • Multi Mill
  • Cone Mill
  • Vibro Sifter
  • Octagonal Blender / Bin Blender
• Monitor critical process parameters during manufacturing.
• Ensure product quality and process consistency throughout batch execution.

Equipment Operation & Maintenance

• Conduct machine startup operation shutdown and cleaning activities.
• Perform pre-operation and post-operation equipment checks.
• Report equipment abnormalities and breakdowns immediately.
• Support preventive maintenance activities as required.
• Ensure equipment is used and maintained according to approved SOPs.

Batch Documentation

• Record manufacturing activities accurately in Batch Manufacturing Records (BMRs).
• Maintain equipment logbooks and operational records.
• Follow Good Documentation Practices (GDP) and Data Integrity requirements.
• Record process parameters yields and observations accurately and contemporaneously.
• Ensure all entries are complete and compliant with regulatory expectations.

In-Process Controls & Quality Compliance

• Perform and document in-process checks as defined in BMRs and SOPs.
• Monitor granulation quality parameters during processing.
• Coordinate with IPQA for line clearance and stage-wise approvals.
• Report deviations non-conformances and process abnormalities immediately.
• Support investigation activities by providing accurate data and observations.

Line Clearance & Area Compliance

• Perform line clearance before starting manufacturing operations.
• Verify cleanliness and readiness of equipment and manufacturing areas.
• Ensure proper status labeling of equipment accessories and materials.
• Prevent product mix-ups and cross-contamination.

Cleaning & Housekeeping

• Perform equipment cleaning and area cleaning as per approved cleaning procedures.
• Maintain housekeeping standards and 5S practices in production areas.
• Handle and dispose of manufacturing waste according to SOPs.
• Ensure manufacturing areas remain audit-ready and inspection-ready.

cGMP & Regulatory Compliance

• Adhere to cGMP guidelines and site quality systems.
• Follow approved SOPs BMRs and manufacturing instructions.
• Comply with regulatory requirements including USFDA MHRA WHO-GMP and EU-GMP standards.
• Participate in internal audits and regulatory inspections.
• Ensure compliance with data integrity and quality systems.

Qualifications :

Experience

• 0-3 years for entry-level Team Member positions.
• Experience in Oral Solid Dosage (OSD) manufacturing is preferred.
• Hands-on exposure to granulation operations and GMP manufacturing environments is desirable.

Required Knowledge & Skills

Technical Skills

• Knowledge of pharmaceutical granulation processes.
• Understanding of RMG FBD Multi Mill Vibro Sifter and Blending Operations.
• Knowledge of cGMP GDP and Data Integrity requirements.
• Understanding of Batch Manufacturing Records (BMRs).
• Knowledge of line clearance and contamination control practices.
• Basic troubleshooting and equipment operation skills.
• Awareness of in-process quality controls and yield management

Additional Information :

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 Work :

No

Employment Type :

Full-time