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- Tasks: Ensure quality compliance in GMP testing and support QA processes.
- Company: Join Oxford Biomedica, a leader in viral vector development for life-changing therapies.
- Benefits: Enjoy wellbeing programs, career growth opportunities, and a supportive culture.
- Why this job: Be part of a mission-driven team that values innovation and collaboration.
- Qualifications: A level or National Certificate in Science; understanding of GMP is essential.
- Other info: Work in state-of-the-art labs with a focus on continuous improvement.
The predicted salary is between 36000 - 60000 £ 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.
The purpose of the role is to provide QA support to the Good Manufacturing Practice (GMP) analytical laboratory facilities. Oxford Biomedica’s Quality Assurance (QA) team is responsible for the company’s quality processes and systems, in compliance with GMP guidelines. The team is accountable for ensuring quality compliance of analytical functions within the company. This includes, but is not limited to:
- Product testing operations
- Stability testing operations
- Method and equipment validations
- Ensuring compliance via the conduction of internal audits
Your responsibilities in this role would be:
- Oversee quality of GMP testing operations to ensure adequate and timely release of GMP compliant product.
- Ensure that all documentation and quality records are reviewed and approved.
- Review quality systems documentation including Deviations, Change Controls, and CAPAs, and provide QA support to resolve compliance issues.
- Perform walk rounds/inspections in the GMP laboratory areas at appropriate and quality-critical stages of the testing process to ensure the testing is performed to GMP standards.
- Undertake continuous quality and process improvement for efficient ways of working and to meet current regulations.
- Liaise with stakeholders, e.g., laboratory/production managers, internal customers, to provide appropriate QA support and guidance to ensure compliance with GxP quality standards and any other regulatory standards.
- Communicate updates on activities to management to ensure tasks are progressing and completed in a timely manner.
We are looking for:
- A level or National Certificate in a Science discipline.
- Higher National Certificate or Degree in a science discipline (desirable).
- Understanding of GMP and pharmaceutical industry QA requirements.
- Excellent attention to detail.
- Experience working in an ATMP / Biologics environment (preferable).
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. As one of the pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors, driving the majority of gene therapies. OXB collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing expertise in viral vector development and manufacturing, including lentivirus, adeno-associated virus (AAV), and adenoviral vectors. Our capabilities span from early-stage development to commercialization, supported by robust quality assurance systems, analytical methods, and regulatory expertise.
Why Join Us?
- Wellbeing programs 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, Respectful
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.
QA Officer employer: Oxford Biomedica
Contact Detail:
Oxford Biomedica Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Officer
✨Tip Number 1
Familiarise yourself with GMP guidelines and the specific QA processes used in the pharmaceutical industry. Understanding these standards will not only help you in interviews but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the QA field, especially those who work in ATMP or biologics environments. Engaging with industry experts can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss your attention to detail and problem-solving skills during interviews. Think of specific examples from your past experiences where you successfully identified and resolved compliance issues.
✨Tip Number 4
Research Oxford Biomedica’s recent projects and collaborations. Being knowledgeable about their work will show your genuine interest in the company and how you can contribute to their mission.
We think you need these skills to ace QA Officer
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the responsibilities and requirements of the QA Officer position. Tailor your application to highlight how your skills and experiences align with these specific needs.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous experience you have in quality assurance, particularly in GMP environments or the pharmaceutical industry. Use specific examples to demonstrate your attention to detail and compliance knowledge.
Showcase Your Qualifications: Make sure to mention your educational background, especially if you have a qualification in a science discipline. If you have any additional certifications related to quality assurance or GMP, include those as well.
Craft a Compelling Cover Letter: Write a personalised cover letter that reflects your passion for the role and the company. Discuss why you want to work at Oxford Biomedica and how you embody their core values: Responsible, Responsive, Resilient, and Respectful.
How to prepare for a job interview at Oxford Biomedica
✨Understand GMP Standards
Make sure you have a solid grasp of Good Manufacturing Practice (GMP) standards. Be prepared to discuss how these guidelines apply to quality assurance in the pharmaceutical industry, as this will demonstrate your knowledge and commitment to compliance.
✨Showcase Attention to Detail
As a QA Officer, attention to detail is crucial. During the interview, provide examples from your past experiences where your meticulous nature helped identify issues or improve processes. This will highlight your suitability for the role.
✨Prepare for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills in a QA context. Think about potential compliance issues you might encounter and how you would address them, showcasing your proactive approach to quality assurance.
✨Emphasise Collaboration Skills
Since the role involves liaising with various stakeholders, be ready to discuss your experience working in teams. Highlight instances where you successfully collaborated with laboratory or production managers to ensure compliance, demonstrating your ability to work effectively in a team environment.