Senior Validation Specialist

1 week ago


Columbia, South Carolina, United States Avance Consulting Full time
Job Overview

Avance Consulting is seeking a highly skilled Validation Engineer to support the performance of FAT, SAT, CSV, and CQV, as well as the development of applicable protocols and summary reports.

Key Responsibilities
  • Provide support in the performance of FAT, SAT, CSV, and CQV
  • Develop applicable protocols and summary reports
  • Work in a pharmaceutical CGMP environment with knowledge of CGMP validation and qualification requirements and approaches
  • Experience in sterile drug manufacturing is preferred
Requirements
  • Knowledge of Current Good Manufacturing Practice (GMP)
  • Experience in equipment and/or computer system validation/qualification processes
  • Strong analytical and problem-solving skills
  • Strong technical writing ability
  • Excellent written and verbal communication skills
  • Bachelor's degree in Engineering or a related field
  • 3 - 5 years experience in the pharmaceutical, biotechnology, or medical device industries


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