equipment, facilities, and systems are qualified, validated, and maintained in compliance with regulatory standards. You will work closely with operations, engineering teams, and regulatory bodies to uphold product quality and patient safety. This is an exciting opportunity to contribute to a critical phase of a large-scale manufacturing project in a collaborative and fast-paced environment.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Oversee validation and qualification activities to ensure GMP equipment, facilities, and systems remain in a validated state.
• Schedule and manage tasks for yourself and Level 1 team members as directed by the Validation Manager.
• Conduct change control assessments for GMP equipment, facilities, and systems to ensure regulatory compliance.
• Develop validation protocols based on validation plans, if applicable.
• Review and approve SOPs, validation protocols, reports, change controls, deviations, and CAPAs.
• Perform quality system activities,