Senior Validation Specialist
Master Compliance - Grand Forks, ND
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Role: CSV Professional Duration: 6 Months Onsite/Hybrid/Remote: Fully Onsite Rate: Open My Client is seeking a skilled CSV professional with 8-10 years of experience in Computer System Validation (CSV) within biotechnology, along with some project management experience. This role is key in driving projects to successful completion. Responsibilities: Manage CSV processes, including CAPAs, investigations, and deviations. Lead projects from initiation to completion, ensuring on-time delivery. Resolve technical challenges and support team members. Develop and manage project plans, timelines, and budgets. Communicate project updates to stakeholders and partners. Qualifications: 8-10 years in biotechnology or life sciences. Strong CSV background with project management experience. Excellent communication and organizational skills. Ability to thrive in a fast-paced, collaborative environment. Strong problem-solving skills and proactive attitude.
Created: 2025-02-21