Pharmaceutical Quality Systems CSV SME

New York City, NY

Job ID: 131108 Industry: Pharma
Pharmaceutical Quality Systems CSV SME

Overview:  Our client is a pharmaceutical company looking for a quality systems and computer software validation expert.


Responsibilities: The consultant will be responsible for doing the GXP validation for their quality systems. This will include writing validation plans and protocols including IQ, OQ, PQ. This consultant must have excellent writing and communication skills. The consultant will be responsible for the technical execution and writing of test scripts. They must have extensive experience with SDLC (Software Development Life Cycle) and the deliverables required at each stage. They will be responsible for not only the execution of validation protocols but the validation master plan writing and development.

  • CSV/Quality Systems
  • Lab Systems, Enterprise Systems
  • Manufacturing
  • Periodic Review
  • IQ OQ PQ
  • SDLC
  • Excellent Writing and communication skills

Job Type: Contract  

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