Validation Specialist

Join us in changing lives at OXB, a quality and innovation-led viral vector CDMO. As a Validation Specialist, you will participate in high-value projects, working alongside cross-functional teams to deliver company goals and ensure regulatory compliance for GMP systems.

Requirements

• Degree in Science/Engineering or related discipline
• Experience in laboratory systems qualification, including automated systems
• Strong background on validation of systems with CSV component
• Proven experience within the generation/execution of equipment validation lifecycle documents (URS, DQ, IQ, OQ, PQ, RQ & RTM)
• Working knowledge of current standards, GMP regulations and industry guidelines as they relate to qualification/validation of GMP systems
• Experience of working within a GMP Quality Management System

Benefits

• Competitive total reward packages
• Wellbeing programmes that support your mental and physical health
• Career development opportunities
• Supportive, inclusive, and collaborative culture
• State-of-the-art labs and manufacturing facilities