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- Tasks: Ensure quality assurance in life-changing therapies and support manufacturing teams.
- Company: Join OXB, a pioneer in cell and gene therapy with a mission to change lives.
- Benefits: Competitive rewards, wellbeing programmes, and career development opportunities.
- Why this job: Make a real impact in advancing innovative therapies for patients worldwide.
- Qualifications: Experience in GMP-regulated environments and strong communication skills.
- Other info: Collaborative culture with state-of-the-art facilities and growth potential.
The predicted salary is between 40000 - 50000 £ per year.
Join us in changing lives. At OXB, our people are at the heart of everything we do. We are on a mission to enable life-changing therapies to reach patients around the world and we are looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.
We are currently recruiting for a Senior Quality Assurance Officer to join our Quality Assurance team. In this role, you will provide expert QA support for OXB Manufacturing Operations, playing a key part in advancing our mission and making a real difference. Your responsibilities in this role would be:
- Reviewing and approving deviations, CAPAs and change controls within defined timelines.
- Supporting manufacturing teams as a QA partner to ensure GMP compliance during production activities.
- Reviewing batch documentation and supporting preparation for Qualified Person batch disposition.
- Participating in investigations, root cause analysis and risk assessments for quality events.
- Reviewing and approving SOPs, protocols, reports and other GMP documentation.
- Supporting implementation of new manufacturing processes for incoming client programs.
- Contributing to continuous improvement initiatives to strengthen quality systems and operational processes.
We are looking for:
- Experience in a GMP-regulated pharmaceutical, biotechnology or similar manufacturing environment.
- Significant experience managing quality events such as deviations, CAPAs and change controls.
- Strong understanding of GMP regulations and regulatory expectations (FDA / EMA).
- Ability to work independently, make sound quality decisions and manage multiple priorities.
- Strong communication skills and the ability to collaborate closely with manufacturing and technical teams.
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?
- 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 are future-focused and growing fast. We succeed together through passion, commitment, and teamwork. Ready to Make a Difference? Collaborate. Contribute. Change lives.
Senior QA Officer in Oxford employer: Oxford BioMedica Limited
Contact Detail:
Oxford BioMedica Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QA Officer in Oxford
✨Tip Number 1
Network like a pro! Reach out to current employees at OXB on LinkedIn or other platforms. Ask them about their experiences and any tips they might have for landing the Senior QA Officer role. Personal connections can make a huge difference!
✨Tip Number 2
Prepare for the interview by brushing up on your GMP knowledge. Make sure you can discuss specific examples of how you've handled deviations, CAPAs, and change controls in the past. We want to see your expertise shine!
✨Tip Number 3
Show us your passion for quality assurance! During interviews, share why you love working in QA and how it aligns with OXB's mission to change lives. Your enthusiasm can set you apart from other candidates.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at OXB.
We think you need these skills to ace Senior QA Officer in Oxford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Senior QA Officer role. Highlight your experience in GMP-regulated environments and any relevant quality events you've managed. We want to see how you embody our core values!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance and how you can contribute to our mission at OXB. Be sure to mention specific examples of your past work that relate to the responsibilities listed in the job description.
Showcase Your Communication Skills: Strong communication is key for this role, so make sure your application reflects that. Whether it's through clear language in your CV or a well-structured cover letter, we want to see how you can collaborate effectively with teams.
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 keen on joining our team at OXB!
How to prepare for a job interview at Oxford BioMedica Limited
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of GMP regulations and how they apply to the pharmaceutical and biotechnology sectors. Be ready to discuss specific examples from your past experience where you've ensured compliance or handled quality events like deviations and CAPAs.
✨Showcase Your Problem-Solving Skills
Prepare to talk about your experience with investigations and root cause analysis. Think of a couple of scenarios where you successfully identified issues and implemented solutions, as this will demonstrate your ability to manage quality events effectively.
✨Communicate Like a Pro
Strong communication skills are key in this role. Practice articulating your thoughts clearly and concisely, especially when discussing complex topics like batch documentation or SOPs. You might even want to do a mock interview with a friend to get comfortable.
✨Emphasise Team Collaboration
OXB values teamwork, so be prepared to share examples of how you've collaborated with manufacturing and technical teams in the past. Highlight your ability to work independently while also being a supportive QA partner during production activities.