LEAD STICK PACK OPERATOR (C Shift FRI-SUN 5:00am-5:30pm)

Prinova Nutrition, LLCSpring Hill, TN
51m

About The Position

The Lead Stick Pack Machine Operator is responsible for leading the daily production activities of filling Stick Packs and packing them out for the respective shift. Also, the Lead assists in developing training, promoting safety, and fostering good communication, and leads the team to produce quality product in the most efficient manner according to cGMPs and SOPs.

Requirements

  • 0 -1 year of experience in a manufacturing production line facility
  • Minimum High School Education or equivalent
  • Basic math, communication, and problem solving skills
  • Must be able to understand, verify, and convert between grams and kilograms on scales
  • Basic computer skills in Microsoft Office and Outlook
  • Ability to follow GMP and SOP guidelines
  • Ability to work alone and in a team environment
  • Ability to follow detailed instructions to perform daily tasks efficiently and independently
  • Self-starter/Multi-tasker
  • Attention to detail.

Responsibilities

  • Knowledge of all processes and equipment related to the Stick Pack production, including: room and equipment cleanliness, machinery setup, product verification (before, during, and after product run)
  • Organizes work for smooth operations, which includes maintaining clean and orderly work areas
  • Ensures all functions of the Stick Pack area are performed accurately and with the utmost quality
  • Follows cGMP guidelines and processes as established in department SOPs
  • Provides accurate and timely recording of materials received, process parameters, product produced, scrap, and excess on specified documents
  • Ensures proper use and care of equipment and materials issued to work area
  • Ensures that established policies, rules, regulations, and procedures are followed
  • Accountable for the quality of the product made
  • Verifies that all documentation is completed in an accurate and timely manner, and files them appropriately
  • Continuously looks for opportunities to improve current processes
  • Follow cGMP guidelines and processes as established in department SOPs
  • Perform other duties as deemed necessary.
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