Mfg Operator PC - TEMP

Noven Pharmaceuticals•Miami, FL

About The Position

The Mfg Operator PC is responsible for activities related to the manufacturing and packaging of potential and existing products. The role operates and maintains small production equipment and weighs, measures, and checks raw materials to ensure manufactured batches contain the correct ingredients and quantities. The operator maintains records and cleanliness in compliance with cGMP, SOP, and safety protocols. Work includes manufacturing, packaging, punching, and pouching products; setting up equipment; inspecting labels, patches, and pouches; and supporting special packaging for clinical studies. The operator also cleans equipment and manufacturing rooms according to established policies and regulatory requirements, assists with shipping, receiving, and warehousing, and performs related duties and assigned special projects.

Requirements

  • High school diploma or technical training.
  • At least two years of professional experience with knowledge of manufacturing processes related to the pharmaceutical industry, or one to three years of work experience in another industry with demonstrated ability to learn new processes and procedures quickly.
  • Good communication skills.
  • Strong organizational skills and attention to detail.
  • Visual acuity and manual dexterity to operate machinery as necessary.
  • Ability to regularly lift and carry objects weighing up to 50 pounds.

Responsibilities

  • Process products in strict compliance with cGMP and SOPs.
  • Operate and maintain production equipment.
  • Participate in manufacturing, packaging, punching, and pouching activities.
  • Clean equipment and manufacturing rooms in compliance with established policies and regulatory requirements.
  • Set up equipment for operation, labeling, patch and pouch inspection, and special packaging for clinical studies.
  • Assist with shipping, receiving, and warehousing.
  • Perform related duties and special projects as assigned.
  • Weigh, measure, and check raw materials to ensure batches contain the proper ingredients and quantities.
  • Maintain records and cleanliness in compliance with cGMP, SOP, and safety protocols.
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