DPI Manufacturing Operator 18816
Staffworthy
DPI Manufacturing Operator
New York, New York, United States
About the Job
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
Vacancy posted 4 days ago
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