DPI Manufacturing Operator 18816

The DPI Manufacturing Operator's responsibilities include:

• Proficiency in granulation and spray jet drying (FBD Dryer).
• Handling granulation equipment transfer, loading, and unloading.
• Safely lifting heavy weights using ergonomic techniques.
• Supervising granulation operations to maintain quality standards.
• Precisely blending powdered ingredients according to formulas.
• Monitoring ingredient batches for weight and measurement compliance.
• Ensuring cleanliness in manufacturing rooms per SOP.
• Mixing and granulating powdered ingredients using machinery.
• Adhering to cGMP and documenting tasks in SOPs and logbooks.
• Making safety and quality-related decisions, including line stoppage.
• Completing raw material and equipment checklists.
• Weighing and managing product transfers.
• Inspecting machine parts and operating pharmaceutical equipment.
• Conducting quality checks and submitting product samples.
• Maintaining batch, room, and equipment records.
• Assisting in validation batch runs.
• Monitoring production efficiency, making adjustments, and reporting accurately.
• Assisting with machine adjustments, repairs, and troubleshooting.
• Following safety protocols and immediately reporting concerns.
• Performing line cleaning, waste segregation, and material return.
• Disassembling, cleaning, and reassembling equipment according to SOPs.
• Participating in safety programs and adhering to safety regulations.
• Complying with CIPLA's Safety, Health, and Environmental policies.
• Completing other duties as assigned by Manufacturing Management.

Requirements:

• Prior experience as a Manufacturing Operator in a Pharma or Nutraceutical unit.
• Proficiency in supporting Granulation, Blending, Compression, Coating, and Encapsulation processes.
• Strong emphasis on Granulation expertise.
• Knowledge of current Good Manufacturing Practices (cGMP), Standard Operating Procedures and Food and Drug Administration (FDA) regulations
• Ability to communicate effectively and clearly, both written and verbally in English
• Comply with safety and quality regulatory standards.
• Ensure products are Manufacture in accordance with CIPLA/InvaGen standards.

Shift Timings:

• 1st Shift: 7:00 am - 3:30 pm
• 2nd Shift: 3:00 pm - 11:30 pm