Validation Specialist

Overview

OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 30 years of experience in viral vectors; the driving force behind the majority of gene therapies.

OXB collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.

We’re currently recruiting for a Validation Specialist to join our Validation Equipment team. In this role, you will have the opportunity to participate in high value projects, working alongside cross-functional teams to deliver company goals, contribute to the delivery of major customer projects and the ensuring of regulatory compliance for GMP systems, playing a key part in advancing our mission and making a real difference.

• Preparation and execution of validation deliverables for GMP systems.
• Providing SME support from Validation for project activities related to GMP systems.
• Active participation in cross-functional meetings and discussions to provide validation support to both internal and customer SMEs.
• Ownership of quality records (Deviations, Change Controls and CAPAs) on behalf of the Validation Department.
• Supporting Validation activities during Technology Transfer of new systems.
• Contributing to the maintenance of overall department KPIs relating to validation of equipment, facilities, utilities, processes and computerised systems.

• A degree (or equivalent) in a Science / Engineering or related discipline.
• Experience in laboratory systems qualification, including automated systems.
• Strong background on validation of systems with CSV component.
• Proven experience with in the generation/execution of equipment validation lifecycle documents (URS, DQ, IQ, OQ, PQ, RQ & RTM).
• A working knowledge of the 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.
• Highly organised individual with a proven ability for problem-solving, thoroughness and good teamwork.
• Demonstrable effective oral, written & interpersonal skills.
• The ability to adapt to changes in priorities and meeting timelines.
• Highly motivated individual with ability to identify and implement continuous improvement activities.

• 💸Competitive total reward packages
• 🧘Wellbeing programmes that support your mental and physical health
• 🚀Career development opportunities to help you grow and thrive
• 🤝Supportive, inclusive, and collaborative culture
• 🧪State-of-the-art labs and manufacturing facilities
• 🌍A company that lives its values:
  Responsible, Responsive, Resilient, Respect

We want you to feel inspired every day. At OXB, we’re future-focused and growing fast. We succeed together—through passion, commitment, and teamwork.

Collaborate. Contribute. Change lives.