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For Companies At a Glance
- Tasks: Ensure compliance in manufacturing processes and support quality assurance efforts.
- Company: Join a pioneering company in cell and gene therapy with over 25 years of experience.
- Benefits: Competitive rewards, wellbeing programmes, and career development opportunities.
- Why this job: Make a real difference in life-changing therapies while working in a supportive environment.
- Qualifications: Experience in GMP environments and strong attention to detail required.
- Other info: Collaborative culture with state-of-the-art facilities and a focus on innovation.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Join Us in Changing Lives
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 25 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.
Role
We’re currently recruiting for a Process Compliance Officer to join our Manufacturing team. In this role, you will work alongside the GMP Manufacturing teams to ensure the timely completion of batch-related tasks, playing a key part in advancing our mission and making a real difference.
Responsibilities
- Supporting investigations and root cause analysis into process and facility deviations
- Identifying and implementing effective Corrective and Preventative Actions (CAPAs)
- Conducting regular self-inspections of the Manufacturing department
- Leading updates to batch and facility documentation to capture new learnings and best practices
- Leading and promoting process improvement ideas to increase the department’s efficiency
- Acting as the key link between the QA department and the Manufacturing department
Qualifications
- Experience of working within a GMP pharmaceutical/biotechnology environment.
- Experience with documentation such as SOPs, Deviations, Change Controls, Risk Assessments and CAPAs
- Familiarity with Root Cause Analysis techniques and the ability to amalgamate and interpret complex data in an investigative capacity would be an advantage
- Organised, self-motivated, pragmatic, and have an excellent attention to detail.
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.
We offer: Oxford Biomedica 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, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies.
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Process Compliance Officer employer: OXB
Contact Detail:
OXB Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Process Compliance Officer
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at OXB. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Brush up on GMP practices and be ready to discuss how your experience aligns with the role of Process Compliance Officer. We want to see your passion for quality and compliance!
✨Tip Number 3
Showcase your problem-solving skills! Be ready to share examples of how you've tackled challenges in past roles, especially around CAPAs and root cause analysis. We love candidates who can think on their feet!
✨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 serious about joining our mission to change lives.
We think you need these skills to ace Process Compliance Officer
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Process Compliance Officer role. Highlight your experience in GMP environments and any relevant documentation skills. We want to see how you can contribute to our mission!
Showcase Your Attention to Detail: In this role, attention to detail is key! Use specific examples in your application that demonstrate your ability to manage complex data and conduct thorough investigations. This will help us see your fit for the position.
Be Clear and Concise: When writing your application, keep it clear and to the point. Avoid jargon unless it's relevant to the role. We appreciate straightforward communication that gets to the heart of your qualifications and experiences.
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, you’ll find all the details you need about the position there!
How to prepare for a job interview at OXB
✨Know Your GMP Basics
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Understand the key principles and how they apply to the role of a Process Compliance Officer. This will show that you're not just familiar with the terminology but can also apply it in real-world scenarios.
✨Prepare for Root Cause Analysis Questions
Expect questions around root cause analysis and CAPAs. Be ready to discuss specific examples from your past experience where you identified issues and implemented solutions. This will demonstrate your problem-solving skills and your ability to think critically under pressure.
✨Showcase Your Organisational Skills
As this role requires excellent attention to detail and organisation, prepare to discuss how you manage documentation and ensure compliance. Bring examples of how you've successfully handled complex data or documentation processes in previous roles.
✨Emphasise Team Collaboration
Since you'll be acting as a link between QA and Manufacturing, highlight your teamwork experiences. Share stories that illustrate your ability to collaborate effectively with different departments, showing that you can bridge gaps and promote a culture of quality and compliance.
