Manufacturing Operations Associate

TekWissen•Lenexa, KS
•Onsite

About The Position

The Manufacturing Operations Associate supports the production of high-quality microbiological culture media in a regulated manufacturing environment. The role involves operating production equipment, performing aseptic manufacturing processes, inspecting products, and maintaining accurate documentation while following Quality System Regulations (QSR), current Good Manufacturing Practices (cGMP), and Standard Operating Procedures (SOPs). This is a temporary, onsite assignment in Lenexa, Kansas, scheduled Monday through Friday from 10:00 PM to 6:30 AM, for a duration of six months. Additional overtime may be required.

Requirements

  • Must be at least 18 years of age.
  • High school diploma or equivalent required.
  • Ability to communicate effectively in English, verbally and in writing.
  • Basic mathematical skills for measurements, calculations, and production documentation.
  • Ability to read, understand, and follow SOPs, work instructions, and safety procedures.
  • Ability to accurately complete manufacturing and quality documentation.
  • Strong attention to detail, organizational skills, and commitment to product quality.
  • Ability to distinguish colors for product inspection and manufacturing activities.
  • Ability to stand for extended periods and lift up to 50 pounds.
  • Ability to work independently and collaboratively in a fast-paced manufacturing environment.
  • Willingness to work the stated shift and overtime as needed.

Nice To Haves

  • 0–1 year of experience in manufacturing or a regulated environment preferred.
  • Familiarity with aseptic techniques preferred.
  • Experience in pharmaceutical, medical device, biotechnology, or microbiology manufacturing preferred.

Responsibilities

  • Manufacture and package microbiological culture media according to established SOPs, cGMP, and quality standards.
  • Operate assigned manufacturing machinery safely and efficiently, perform basic maintenance, and report equipment malfunctions.
  • Perform aseptic manufacturing processes, including dispensing, inspection, and packaging.
  • Monitor production processes and inspect products for compliance with quality specifications.
  • Measure and document in-process parameters, including weight, time, pH, and other required readings.
  • Complete production records and documentation accurately and promptly.
  • Follow production schedules, coordinate batches, and ensure materials are available to meet production targets.
  • Retrieve and verify required materials from warehouse or staging areas.
  • Identify and escalate process deviations, discrepancies, equipment issues, and quality concerns to leadership.
  • Maintain a clean, organized, and safe work environment and consistently wear required personal protective equipment (PPE).
  • Follow written and verbal instructions and collaborate with team members and other departments.
  • Support training and mentoring of coworkers as needed.
  • Maintain productivity and quality standards with minimal supervision.
  • Work scheduled hours and additional overtime as required.
  • Perform other duties as assigned.
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