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Senior Validation Specialist

MasterCompliance LLC
Boston, MA Full Time
POSTED ON 2/26/2025
AVAILABLE BEFORE 5/23/2025

Role : CSV ProfessionalDuration : 6 MonthsOnsite / Hybrid / Remote : Fully OnsiteRate : OpenMy 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.

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