Demo

Computer System Validation (CSV)

Katalyst CRO
Jersey, NJ Contractor
POSTED ON 3/13/2025
AVAILABLE BEFORE 4/10/2025
Responsibilities

  • Have a strong understanding of CSV, as well as CAPA's, investigations, deviations.
  • Help manage projects from concept through to completion, ensuring timely delivery of milestones and results.
  • Utilize strong problem-solving skills to address technical challenges and support team members.
  • Stay updated with industry trends and advancements, applying relevant knowledge to e rnhance project outcomes.
  • Ensure compliance with all relevant regulations, safety standards, and best practices.
  • Contribute to the creation and execution of project plans, timelines, and budgets.
  • Communicate project updates and results effectively to internal stakeholders and external partners.

Requirements:

  • 5-10 years of experience in the biotechnology or life sciences industry.
  • Strong background in CSV.
  • Some experience in Project Management.
  • Excellent communication and organizational skills.
  • Demonstrated ability to work in a fast-paced, collaborative environment.
  • Strong problem-solving and analytical skills.
  • "Go -Getter” personality: Willing to ask for more work, or reach out to others to get what they need to keep things moving and finish their work on time.
  • Our client is seeking a highly skilled and experienced CSV resource to join their dynamic team.
  • The ideal candidate will have 5-10 years of experience in CSV in the biotechnology field and some experience in project management.
  • This candidate will play a pivotal role in driving key projects forward.

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