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- Tasks: Ensure quality assurance in manufacturing and support life-changing therapies.
- Company: Join OXB, a leader in viral vector development and manufacturing.
- Benefits: Competitive rewards, wellbeing programmes, and career growth opportunities.
- Why this job: Make a real difference in patients' lives through innovative therapies.
- Qualifications: Experience in GMP-regulated environments and strong communication skills.
- Other info: Collaborative culture with state-of-the-art facilities and a focus on values.
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'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 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're future-focused and growing fast. We succeed together through passion, commitment, and teamwork.
Ready to Make a Difference? Collaborate. Contribute.
Senior QA Officer 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
✨Tip Number 1
Get to know the company! Research OXB's mission and values, and think about how your experience aligns with them. This will help you stand out during interviews and show that you're genuinely interested in being part of the team.
✨Tip Number 2
Network like a pro! Reach out to current or former employees on LinkedIn to get insider tips about the company culture and the role. A personal connection can sometimes give you the edge you need to land that interview.
✨Tip Number 3
Prepare for common interview questions related to quality assurance and GMP compliance. Think of specific examples from your past experiences that demonstrate your skills and how you've handled challenges in similar environments.
✨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 proactive and serious about joining OXB.
We think you need these skills to ace Senior QA Officer
Some tips for your application 🫡
Read the Job Description Thoroughly: Before you start your application, take a good look at the job description. It’s packed with info about what we’re looking for in a Senior QA Officer, so make sure you understand the key responsibilities and qualifications. This will help you tailor your application to show us you’re the perfect fit!
Showcase Your Relevant Experience: When writing your application, highlight your experience in GMP-regulated environments and managing quality events like deviations and CAPAs. We want to see how your background aligns with our needs, so don’t hold back on sharing specific examples that demonstrate your expertise.
Be Clear and Concise: Keep your application clear and to the point. Use straightforward language and avoid jargon unless it’s relevant to the role. We appreciate a well-structured application that makes it easy for us to see your qualifications and enthusiasm for the position.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the details you need about the role and our company culture right there!
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 experience where you've ensured compliance or managed quality events like deviations and CAPAs.
✨Showcase Your Problem-Solving Skills
Prepare to share instances where you've participated in investigations or root cause analyses. Highlight your ability to make sound quality decisions under pressure, as this will demonstrate your resilience and responsiveness—qualities that OXB values highly.
✨Communicate Effectively
Since strong communication skills are essential for this role, practice articulating your thoughts clearly and concisely. Think about how you can collaborate with manufacturing and technical teams, and be ready to discuss how you've done this in past roles.
✨Embrace Continuous Improvement
OXB is all about strengthening quality systems and operational processes. Come prepared with ideas or examples of how you've contributed to continuous improvement initiatives in your previous positions. This shows that you're not just a fit for the role, but also aligned with their mission to innovate.