DPI Manufacturing Operator 18816

StaffWorthy; New York (NY); On-site; USD 45,000 - 60,000; Full time

Job summary

A pharmaceutical company in New York is seeking a Manufacturing Operator to oversee granulation processes, ensure compliance with cGMP, and manage the blending of ingredients. The ideal candidate has prior experience in the Pharma or Nutraceutical industry and must communicate effectively. This position emphasizes safety and cleanliness, requiring knowledge of FDA regulations. Join us to play a crucial role in maintaining high-quality manufacturing standards.

Qualifications

• Prior experience as a Manufacturing Operator in a Pharma or Nutraceutical unit.
• Proficiency in supporting Granulation, Blending, Compression, Coating, and Encapsulation processes.
• Knowledge of current Good Manufacturing Practices (cGMP) and FDA regulations.

Responsibilities

• Oversee granulation operations to ensure quality standards.
• Handle blending and mixing of powdered ingredients using machinery.
• Adhere to cGMP while documenting tasks in SOPs.

Skills

Granulation expertise

Effective communication

cGMP knowledge

Safety compliance

Job description

About the job 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.