Production Operator I

Lupin
Onsite

About The Position

The Production Operator I is responsible for verifying dispensed raw materials, staging components, assembling production equipment, and executing all tasks in accordance with Batch Records, SOPs, and cGMP requirements. This role involves accurate documentation of operational parameters, weighing and recording materials, performing in-process testing, monitoring production lines, and packaging finished goods. The operator will also handle waste disposal, clean production areas and equipment, and support Quality Assurance operations. Maintaining GMP-compliant storage and control of tooling and materials is crucial. The role requires performing granulation, compounding, batch manufacturing, filling, and packaging activities, along with conducting room and equipment inspections. Adherence to all cGMP, regulatory, and company compliance requirements, as well as Health & Safety policies, is mandatory. The operator must properly use required Personal Protective Equipment (PPE) and maintain a clean, safe, and organized work environment, operating in alignment with the company’s Code of Conduct and Business Ethics. Additional duties may be assigned by Manufacturing Management.

Requirements

  • High school diploma.
  • Minimum of 5 years of experience and/or training; or equivalent combination of education and experience within a Production cGMP Environment.
  • Knowledge of FDA, cGMP, GDP and SOPs related to job requirements.
  • Ability to read and interpret documents in English such as safety rules, Standard Operating Procedures, batch records, and cleaning procedures.
  • Proficient in English to sign and complete batch record documentation.
  • Ability to speak and understand English effectively.
  • Ability to add, subtract, multiply and divide using different units of measure to include averages of whole numbers, common fractions, and decimals.
  • Ability to apply common sense thinking and understanding to carry out detailed written instructions.
  • Experience in batch manufacturing, filling, and packaging operations for DPI or MDI products.
  • Proficient in cleaning, setup, and operation of DPI or MDI related equipment, including: TRV blenders, Mixers and compounding systems, Manufacturing vessels, Filling machines, Blister filling and packaging lines, Filling and final packaging line assemblies.
  • Understanding of blending uniformity, powder handling, and environmental controls required for DPI or MDI manufacturing.
  • Ensures adherence to SOPs, batch records, and regulatory requirements throughout the production process.

Responsibilities

  • Verify dispensed raw materials for each batch, ensuring accuracy and compliance with batch records and SOPs.
  • Stage components and assemble production equipment required for manufacturing and packaging operations.
  • Perform daily equipment checks and document usage in appropriate logbooks.
  • Execute all tasks in accordance with Batch Records, SOPs, and cGMP requirements, ensuring proper documentation at all stages.
  • Accurately document all operational parameters and process steps within batch manufacturing records.
  • Weigh and record components, in-process materials, and finished product quantities.
  • Perform routine in-process testing and inspections to ensure product quality and consistency.
  • Monitor production lines for accuracy, stability, conformity, and product defects; take corrective actions when necessary.
  • Assemble, stage, and distribute materials required for manufacturing and packaging activities.
  • Package finished goods, including placing products into shipping containers and labeling shipments appropriately.
  • Handle and properly dispose of production waste in compliance with SOPs at the completion of each batch.
  • Palletize and transport finished goods within the facility using carts or pallet jacks, including movement to and from refrigerated storage areas.
  • Clean production areas and equipment, maintaining proper documentation in cleaning logs.
  • Support Quality Assurance (QA) and Laboratory operations as needed.
  • Maintain GMP-compliant storage, issuance, and control of tooling and materials.
  • Prepare and return partial raw material containers to the warehouse; properly deface and dispose of empty containers per SOPs.
  • Verify the accuracy of materials received from dispensing and prior processing stages.
  • Perform granulation, compounding, batch manufacturing, filling, and packaging activities using appropriate equipment.
  • Conduct room and equipment inspections and maintain complete and accurate documentation.
  • Adhere to all cGMP, regulatory, and company compliance requirements.
  • Follow all Health & Safety policies, procedures, and training guidelines.
  • Properly use required Personal Protective Equipment (PPE) at all times.
  • Maintain a clean, safe, and organized work environment.
  • Operate in alignment with the company’s Code of Conduct and Business Ethics.
  • Perform additional duties as assigned by Manufacturing Management.
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