Quality Systems Officer at oxfordbiom

Oxford, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

10 Apr, 26

Salary

0.0

Posted On

10 Jan, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Management Systems, GMP Compliance, Pharmaceutical Regulations, Quality Audits, Root Cause Analysis, Change Control Processes, Computer Systems Validation, Electronic Quality Management Systems, Microsoft Office, Supplier Management, Training Delivery, Continuous Improvement, Metrics Monitoring, Deviation Review, CAPA Review, Supplier Complaints Review

Industry

Pharmaceutical Manufacturing

Description

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 are currently recruiting for a Quality Systems Officer, responsible for maintaining the Quality Management Systems and promoting continuous improvements to meet the business needs Your responsibilities in this role would be: Provide primary Quality Systems support for, materials, suppliers and services providers Maintain supplier and internal audit schedules Provide Quality Systems input to annual Quality Reports Facilitate updates into Quality/Technical Agreements Review Deviations, CAPAs, Change Controls and Supplier Complaints Review Computer Systems Validation (CSV) documents Identify and lead QMS improvements Monitor and produce metrics for GMP compliance Deliver training on QMS We are looking for: A-Level education in (science preferred) or equivalent experience Experience working within a GMP-regulated environment Knowledge of pharmaceutical regulations and compliance requirements Experience within Quality within a pharmaceutical’s environment Hands-on experience using electronic Quality Management Systems (eQMS) to GMP standards. An understanding and awareness of Computer Systems Validation (CSV) An understanding of Quality audits, investigations, and root cause analysis and change Control Processes Proficient in Microsoft Office (Word, Excel, Outlook, PowerPoint) Proven knowledge and application of GMP and wider pharmaceutical Quality standards. Awareness of Quality Systems with the ability to support and improve them effectively 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

Responsibilities

The Quality Systems Officer is responsible for maintaining Quality Management Systems and promoting continuous improvements. Key tasks include providing support for materials and suppliers, maintaining audit schedules, and reviewing deviations and complaints.