Skilled Validation Engineer

Job Summary:

This position is in the Quality Engineering organization at the aseptic pharmaceutical manufacturing facility. The incumbent will work individually, supporting another engineer, or as part of a team, experienced in chemistry laboratory instrumentation, specifically, an osmometer. MUST NOT BE ALLERGIC TO PENICILLIN OR CEPHALOSPORINS.


  • The individual will be responsible for supporting a range of validation disciplines which may include equipment, facility, software, cleaning, and process validations.
  • In addition, the individual may be requested to execute feasibility, evaluation, or exploratory studies to support new products or processes.
  • The individual will be responsible for collecting requirements, developing a project validation plan, and executing to completion.


  • Minimum of a BA or BS preferably in the Life Sciences/Engineering/Chemistry or other job-related discipline.
  • A minimum of 2 years previous experience with a pharmaceutical or biotech company.
  • At least 1 year of validation experience
  • Experience with equipment (water and utilities), including familiarity with basic microbiological and chemical water testing a plus.
  • Must have the ability to prioritize and execute multiple project tasks.
  • Knowledge of the basic principles of validation across multiple disciplines
  • Ability to solve routine validation issues with minimal assistance.
  • Ability to learn quickly through multiple channels.
  • Must be able to work as a collaborative team member.
  • Ability to clearly communicate with respect to technical or project management issues, both verbally and in written form.
  • Must possess strong documentation skills and be able to follow specific instructions.


  • Team Player
  • Excellent Communication


Location Round Lake, IL
Workload 40 hours/week , 100% onsite
Expected start date ASAP
Expected end date Open
Necessary languages English
Necessary skills BA, CHEMISTRY, ENGINEER, Management, Validation

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