At a Glance
- Tasks: Ensure quality assurance in life-changing therapies and support manufacturing operations.
- Company: Join OXB, a pioneer in cell and gene therapy with over 30 years of experience.
- Benefits: Competitive rewards, wellbeing programmes, and career development opportunities.
- Other info: Collaborative culture with state-of-the-art facilities and a focus on growth.
- Why this job: Make a real difference in patients' lives through innovative therapies.
- Qualifications: Experience in GMP-regulated environments and strong quality management skills.
The predicted salary is between 40000 - 50000 £ per year.
OXB is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, OXB has more than 30 years of experience in viral vectors, the driving force behind the majority of gene therapies.
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're currently recruiting for a Senior Quality Assurance Officer to join our Quality Assurance team on a 12 month fixed-term contract. 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. Please note, this role will be 5 days a week onsite at our Cowley facility.
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 support 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.
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. Change lives.
Senior QA Officer - 12 Month FTC in Banbury employer: Oxford BioMedica (UK) Limited
At OXB, we pride ourselves on being a leading employer in the biotechnology sector, offering a supportive and inclusive work culture that prioritises employee wellbeing and professional growth. Our state-of-the-art facilities in Cowley provide an inspiring environment where passionate individuals can thrive, collaborate, and contribute to life-changing therapies. With competitive rewards and a commitment to our core values of being Responsible, Responsive, Resilient, and Respectful, OXB is dedicated to empowering our team members to make a meaningful impact in the world of gene therapy.
Contact Details:
Oxford BioMedica (UK) Limited Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Senior QA Officer - 12 Month FTC in Banbury
✨Get Familiar with Temporary Roles in Pharma
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Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
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We think you need these skills to ace Senior QA Officer - 12 Month FTC in Banbury
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at Oxford BioMedica (UK) Limited.
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at Oxford BioMedica (UK) Limited. This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at Oxford BioMedica (UK) Limited
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with Oxford BioMedica (UK) Limited.
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help Oxford BioMedica (UK) Limited achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
