Process Compliance Officer
UK Visa Sponsorship Analytics
Analytics are greyed out due to low classification confidence (59.0%).
Occupation Type
Quality assurance and regulatory professionals
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£48,200
(£24.72 per hour)
Occupation rate applies
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Description
Location:
Oxford, GB
Company: oxfordbiom
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 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 quality records, playing a key part in advancing our mission and making a real difference.
Your responsibilities in this role would be:
Oxford, GB
Company: oxfordbiom
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 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 quality records, playing a key part in advancing our mission and making a real difference.
Your responsibilities in this role would be:
- 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
- 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
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
Ready to Make a Difference?
Collaborate. Contribute. Change lives.