About The Position

As a Quality Control Technician – Environmental Monitoring, you will be a vital member of the site Quality team, ensuring the safety and compliance of our manufacturing environment. In this role, you will be responsible for the routine and non-routine monitoring of cleanroom air, surfaces, and critical utilities to support sterile production and regulatory excellence. Elanco is a global leader in animal health, dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. Elanco fosters a diverse and inclusive work environment, believing that diversity drives innovation, creativity, and business success.

Requirements

  • High School Diploma or GED with 5 years of relevant experience, or a Bachelor’s degree in Microbiology, Biological Sciences, Pharmaceutical Sciences, or a closely related field.
  • Demonstrated experience in a laboratory or technical environment with a focus on microbiology.
  • Advanced technical proficiency in aseptic technique and sterile gowning.
  • Excellent organizational and documentation skills.

Nice To Haves

  • Prior experience in a cGMP-regulated environment with specialized knowledge of FDA, USDA, and ISO requirements for pharmaceutical or veterinary biologics.
  • Proven expertise in sterility testing, mycoplasma analysis, and water system monitoring.
  • Experience with analytical method development, validation protocols, and the use of specialized instrument software to obtain results.
  • Strong technical writing skills for the creation of quality procedures and investigation reports.
  • Ability to succeed in a physically demanding role that requires long hours on your feet and the movement of heavy laboratory materials in a cross-functional team environment.

Responsibilities

  • Perform routine and non-routine environmental monitoring (air and surface sampling) and utility testing (WFI, USP water, pure steam, and clean compressed air) to ensure manufacturing environments meet strict quality standards.
  • Conduct complex microbiology-based analysis on raw materials, in-process samples, and final products, including endotoxin, bioburden, TOC/Conductivity, and sterility testing.
  • Provide critical production support by participating in aseptic process simulations and production fills, maintaining gown qualification to operate within sterile manufacturing environments.
  • Lead laboratory stewardship activities, including growth promotion of culture media, microbial identification, equipment calibration support, and maintaining meticulous inventory and safety standards.
  • Support site quality systems by assisting in OOS/OOT investigations, drafting and revising SOPs, and preparing method validation protocols and analytical study reports.

Benefits

  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • Up to 6% 401K matching
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