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Operator II, Manufacturing

Thermo Fisher ScientificLenexa, KS
Onsite

About The Position

The Manufacturing Operations team produces single-use bioproprocessing products in a cGMP manufacturing environment. Operators work collaboratively to support safe, efficient, and compliant manufacturing processes while delivering high-quality products to our customers. As an Operator II, you will perform manufacturing activities that directly support the production of products used in the pharmaceutical and biotechnology industries. Your work will ensure products are manufactured safely, efficiently, and in compliance with quality and regulatory requirements.

Requirements

  • High School Diploma or GED
  • 1- 2 years’ experience in manufacturing, production, operations, laboratory, or a related environment.
  • Experience working in a cleanroom environment.
  • Ability to lift product up to 50lbs
  • Communicate effectively in English, both verbal and written
  • Understand and perform basic math
  • Knowledge of cGMP, Good Documentation Practices (GDP), and Standard Operating Procedures (SOPs).
  • Ability to operate manufacturing equipment, follow detailed work instructions, and accurately complete production documentation.
  • Strong communication, teamwork, problem-solving, and organizational skills with the ability to work independently in a fast-paced manufacturing environment.
  • Ability to stand, walk, bend, reach, and perform repetitive tasks throughout the work shift.
  • Ability to lift, push, and pull up to 50 pounds with or without reasonable accommodation.
  • Ability to wear required personal protective equipment (PPE) and work in a cleanroom and cGMP manufacturing environment.

Nice To Haves

  • Experience in a cGMP manufacturing environment preferred.

Responsibilities

  • Perform manufacturing activities including equipment setup, cleaning, hose changes, assembly, operation of production equipment, and material handling following approved SOPs and cGMP requirements.
  • Complete production documentation, SAP transactions, and batch records accurately while following Good Documentation Practices (GDP).
  • Monitor equipment and manufacturing processes, identify and report issues, and work with Production, Quality, Engineering, and Maintenance teams to support continuous improvement and operational excellence.

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