Pharmaceutical Quality Systems CSV SME

New York City, NY

Job ID: 129136 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.

Required:
  • CSV
  • Quality Systems
  • IQ OQ PQ
  • SDLC
  • Excellent Writing and communication skills

 Job Type: Contract  

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