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Eurofins - Columbia, MO

posted about 2 months ago

Full-time
Columbia, MO
10,001+ employees
Professional, Scientific, and Technical Services

About the position

The position involves performing various tasks and analyses of bio/pharmaceutical ingredients and products, ensuring quality data is delivered to clients while adhering to GMP and GLP regulations. The role requires independent operation of laboratory equipment, process improvements, and effective communication with clients and team members.

Responsibilities

  • Perform various tasks and analyses of bio/pharmaceutical ingredients and products.
  • Review or prepare standards and samples for analysis.
  • Run a variety of equipment or instrumentation independently.
  • Ensure quality data by reviewing laboratory data for accuracy and adherence to GMP and/or GLP regulations.
  • Evaluate current systems and suggest process improvements.
  • Initiate and assist in completing investigations.
  • Apply GMP/GLP in all areas of responsibility.
  • Demonstrate strong client service skills, teamwork, and collaboration.
  • Proactively plan and multitask to maximize productivity.
  • Meet all quality and productivity metrics.
  • Perform laboratory operations with good dexterity and high accuracy.
  • Perform/review preparations of reagents, samples, and standards according to procedures.
  • Document testing, observations, deviations, and results clearly and completely.
  • Understand and perform calculations as required by test methods.
  • Utilize computers for information access, calculations, and report preparation/review.
  • Read and understand analytical procedures and internal SOPs.
  • Demonstrate technical writing skills.
  • Process/review data, generate/review reports, and evaluate data.
  • Communicate effectively, both orally and in writing.
  • Perform laboratory maintenance as required.
  • Support LEAN initiatives.
  • Conduct all activities in a safe and efficient manner.

Requirements

  • Bachelor's degree in chemistry, biology, biochemistry, or related degree concentration.
  • Some previous laboratory experience.
  • Ability to read and understand Standard Operating Procedures (SOPs) and method/protocol documents.
  • Demonstrate documentation practices appropriate for a regulatory environment.

Benefits

  • Health, Dental, and Vision Insurance
  • 401(k) matching
  • PTO and Holidays
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