Compression Operator I

Role Summary

Compression Operator I is an entry-level role in the Compression Department responsible for the setup and operation of compression machinery in accordance with SOPs and cGMP standards to support the production of high-quality pharmaceutical products.

Responsibilities

• Responsible for conducting in-process checks including average weight, thickness, hardness, friability, and individual tablet weight, among others.
• Initiates 'B' and 'A' level cleaning of compression rooms and ensures compliance with IPQA procedures.
• Accurately identifies and segregates rejected blends and tablets, ensures required quality checks are completed, and upholds cleanliness and organization of the compression room and equipment to maintain compliance and operational efficiency.
• Promptly notifies the Supervisor of any machine abnormalities or expired calibration status. Ensures weighing scales are kept clean and orderly for accurate calibration checks.
• Verifies ingredients weighed in Mixing & Granulation against entries in the Production Batch Record (PBR), reporting any discrepancies to the Supervisor or designee. Responsible for real-time documentation across all Compression operations and for reviewing batch records to ensure accuracy.

Qualifications

• Education:
  • High School or GED General HS Curriculum - Preferred
• Experience:
  • 1 year or more in Experience in Pharmaceutical Manufacturing Environment

Skills

• Ability to read, write, and communicate in English. - Intermediate
• High school level math and mechanical skills. - Intermediate
• Ability to work as part of a team. - Intermediate
• Attention to detail and accuracy. - Intermediate
• Basic computer literacy with the ability to use web browsers, typing applications, Microsoft Office, and related communication tools. - Intermediate

Specialized Knowledge

• High speed Compression Machine set up preferred.