Description

You will manage validation activities within a pharmaceutical manufacturing environment, ensuring strict compliance and system reliability.

Responsibilities

• Execute Computer System Validation (CSV) protocols to ensure regulatory compliance.
• Manage validation lifecycles using Application Lifecycle Management (ALM) tools.
• Support process validation requirements for manufacturing systems.
• Integrate and validate webMethods within the production environment.

Required Skills

• 5+ years of experience in manufacturing systems validation.
• Deep expertise in Computer System Validation (CSV).
• Hands-on experience with ALM frameworks.
• Practical knowledge of pharmaceutical manufacturing processes.
• Experience working with webMethods.
• Proven background in process validation.

Preferred Skills

• Bachelor's degree or equivalent graduate-level education.

Key Skills

Education

ANY GRADUATE