Pharmaceutical Equipment Qualification/Validation

Kansas City, KS

Job ID: 128596 Industry: Pharma

 

Pharmaceutical Equipment Qualification/Validation

Project Description:

Our client is a biologics company operating as a multiproduct cGMP facility. They are in need of a validation engineer to perform the validation, qualification and commissioning of existing and new equipment.

  Day to Day Responsibilities:

The consultant will be responsible for the validation, qualification and commissioning of equipment in an aseptic manufacturing environment. They will also be responsible for executing protocols and writing summary reports. This person must have experience working with freezers, bioreactors and refrigerators along with basic utilities such as; hot water and compressed air. They are currently performing a sterilization qualification, so this experience would also be very helpful along with commissioning related work.

 

Required Skills:
  • Aseptic Manufacturing
  • Equipment Qualification (IOQ)
  • Freezers, refrigerator, bioreactor, basic utilities (hot water, compressed air)
  • Write/Execute protocols, summary reports
  • Sterilization Qualification
  • Commissioning

Job Type: Contract

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