Epicareer Might not Working Properly
Learn More
E

Computer System Validation (CSV) Specialist

Salary undisclosed

Checking job availability...

Original
Simplified

Job Description: Computer System Validation (CSV) Specialist

Location: Iselin, NJ / Princeton Junction, NJ
Industry: Life Sciences
Experience Required: 8-10 years


Key Responsibilities:

  • Develop and execute validation protocols for computer systems.
  • Ensure compliance with regulatory requirements and industry standards.
  • Create detailed validation documentation, including plans, reports, and scripts.
  • Conduct risk assessments and impact analyses related to computer systems.
  • Coordinate and supervise testing activities.
  • Collaborate with cross-functional teams to maintain and improve system validation processes.
  • Monitor and report on validation project progress.
  • Provide training and support to staff regarding validation processes and requirements.

Requirements:

  • 8-10 years of experience in Computer System Validation (CSV) within the Life Sciences industry.
  • Strong understanding of regulatory frameworks and industry standards.
  • Excellent communication skills to collaborate effectively with stakeholders and teams.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job

Job Description: Computer System Validation (CSV) Specialist

Location: Iselin, NJ / Princeton Junction, NJ
Industry: Life Sciences
Experience Required: 8-10 years


Key Responsibilities:

  • Develop and execute validation protocols for computer systems.
  • Ensure compliance with regulatory requirements and industry standards.
  • Create detailed validation documentation, including plans, reports, and scripts.
  • Conduct risk assessments and impact analyses related to computer systems.
  • Coordinate and supervise testing activities.
  • Collaborate with cross-functional teams to maintain and improve system validation processes.
  • Monitor and report on validation project progress.
  • Provide training and support to staff regarding validation processes and requirements.

Requirements:

  • 8-10 years of experience in Computer System Validation (CSV) within the Life Sciences industry.
  • Strong understanding of regulatory frameworks and industry standards.
  • Excellent communication skills to collaborate effectively with stakeholders and teams.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job