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- Tasks: Join our Validation Equipment team to ensure compliance and support life-changing therapies.
- Company: OXB, a pioneering viral vector CDMO with a mission to transform healthcare.
- Benefits: Wellbeing programmes, career development, and a supportive, inclusive culture.
- Why this job: Make a real difference in advancing innovative therapies while growing your career.
- Qualifications: Degree in Science/Engineering and experience in GMP systems validation.
- Other info: Dynamic environment with state-of-the-art facilities and collaborative teams.
The predicted salary is between 36000 - 60000 ÂŁ per year.
At OXB, our people are at the heart of everything we do. We’re on a mission to enable life‑changing therapies to reach patients around the world—and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.
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.
Your responsibilities in this role would be:
- 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.
We are looking for:
- 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 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.
- Demonstratable effective oral, written & interpersonal skills.
- The ability to adapt to changes in priorities and meet timelines.
- Highly motivated individual with ability to identify and implement continuous improvement activities.
About Us:
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.
Why Join Us?
- 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.
Validation Specialist employer: Oxford Biomedica
Contact Detail:
Oxford Biomedica Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Specialist
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching OXB and understanding their mission and values. Tailor your responses to show how you embody being Responsible, Responsive, Resilient, and Respectful—these traits are key!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online resources to refine your answers. Focus on articulating your experience with GMP systems and validation processes clearly.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in joining the OXB team and contributing to life-changing therapies.
We think you need these skills to ace Validation Specialist
Some tips for your application 🫡
Show Your Passion: When you're writing your application, let your enthusiasm for the role shine through! We want to see how your values align with ours—Responsible, Responsive, Resilient, and Respectful. Make it personal and relatable!
Tailor Your CV: Don’t just send a generic CV! Highlight your experience in validation and GMP systems specifically. Use keywords from the job description to show us you’re the perfect fit for the Validation Specialist role.
Be Clear and Concise: Keep your application straightforward and to the point. We appreciate clarity, so make sure your skills and experiences are easy to read and understand. Avoid jargon unless it’s relevant to the role!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team!
How to prepare for a job interview at Oxford Biomedica
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and the specific regulations that apply to validation systems. Being able to discuss these confidently will show that you’re not just familiar with the terms, but that you understand their importance in ensuring compliance.
✨Showcase Your Problem-Solving Skills
Prepare examples from your past experiences where you successfully tackled challenges related to validation processes or equipment. Highlighting your problem-solving abilities will demonstrate your resilience and capability to adapt to changing priorities, which is key for this role.
✨Engage in Cross-Functional Discussions
Since the role involves active participation in cross-functional meetings, practice discussing how you would contribute to team discussions. Think about how you can provide validation support and be ready to share insights on how collaboration can enhance project outcomes.
✨Prepare Quality Records Examples
Be ready to discuss your experience with quality records like Deviations, Change Controls, and CAPAs. Having specific examples of how you’ve managed these documents will illustrate your organisational skills and attention to detail, both of which are crucial for a Validation Specialist.
