Process Compliance Officer

Oxford Biomedica; Oxford; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading biotechnology company in Oxford is seeking a Process Compliance Officer to ensure the timely completion of batch-related activities. The role requires collaboration with GMP Manufacturing teams, proficiency in documentation like SOPs and Deviations, and experience in a pharmaceutical environment. Join a company committed to life-changing therapies, where you can enhance processes and contribute significantly.

Benefits

Competitive total reward packages

Wellbeing programmes

Career development opportunities

Supportive, inclusive culture

Qualifications

• Experience of working within a GMP pharmaceutical/biotechnology environment.
• Familiarity with documentation such as SOPs, Deviations, Change Controls, and CAPAs.
• Organised, self-motivated, and pragmatic.

Responsibilities

• Support investigations and root cause analysis into process deviations.
• Identify and implement effective Corrective and Preventative Actions (CAPAs).
• Conduct regular self-inspections of the Manufacturing department.

Skills

GMP pharmaceutical/biotechnology experience

Documentation management (SOPs, Deviations, CAPAs)

Root Cause Analysis

Attention to detail

Job description

Overview

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, 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

Requirements

• 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.

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 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.

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.