Senior Manager, Quality Systems and Compliance

Location:

Durham, NC, US

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.

Following the expansion of our US footprint with the acquisition of a new commercial-scale viral vector facility in Durham, North Carolina we have some new opportunities to join us.

We’re currently recruiting for a Senior Manager, Quality Systems & Compliance to join our Quality team . In this role, you will be a key leader within the Quality organization, responsible for overseeing and strengthening site quality compliance and quality systems to ensure ongoing adherence to established quality standards and regulatory requirements, playing a key part in advancing our mission and making a real difference.

Your responsibilities in this role would be:

• Lead and oversee site Quality Systems to ensure compliant, effective, and inspection-ready execution of deviation management, CAPA, change control, quality metrics, Quality Council governance, and health authority inspection readiness within a commercial cell and gene therapy manufacturing environment.
• Continuously optimize quality system infrastructure, processes, and procedures to support scalable commercial operations, advanced therapy manufacturing complexity, and evolving regulatory expectations.
• Partner with Corporate Quality Services & Compliance to ensure alignment and effective deployment of global Quality programs, standards, and continuous improvement initiatives at the site level.
• Ensure sustained compliance with applicable U.S. and EU cGMP regulations, global regulatory requirements, and industry standards relevant to advanced therapy medicinal products (ATMPs).
• Lead site inspection readiness activities, maintaining a constant state of readiness and serving as the primary site coordinator for corporate, client, and regulatory inspections, including preparation, execution, and follow-up.
• Provide quality leadership for cross-functional risk assessments, including evaluation of product, process, and system risks inherent to cell and gene therapy manufacturing.
• Lead and support site gap assessments to proactively identify compliance risks, drive remediation, and strengthen quality system robustness.
• Chair or support the site Quality Council, delivering timely, data-driven insights on quality system performance to site leadership and management review forums.
• Provide strategic site-level input to support the continuous improvement and evolution of corporate quality systems for commercial advanced therapy operations.
• Proactively identify and resolve quality and compliance risks through collaborative, solutions-oriented engagement with cross-functional stakeholders.
  
  

We are Looking For:

• Bachelor’s degree in a scientific or technical discipline with a minimum of 7–10 years of progressive experience in Quality Assurance and/or Quality Control, including direct involvement in compliance activities and health authority inspections.
• Experience in, or working knowledge of, cell therapy and/or gene therapy manufacturing, including material collection, processing, and upstream manufacturing, preferred but not required.
• Strong working knowledge of GxP regulations, global regulatory requirements, quality systems, and applicable guidance documents, including ICH guidelines.
• Demonstrated ability to manage complex quality initiatives with strong organizational and project management skills, effectively balancing multiple priorities in a fast-paced, highly regulated environment.
• Proven experience communicating complex quality and compliance issues clearly and effectively, with the ability to influence outcomes and build productive relationships across site-level and global functions.
• Experience applying quality risk management principles, including impact and risk assessment tools, process mapping, and continuous improvement methodologies.
• Willingness and ability to travel domestically and internationally (up to 15%) as required to support business and quality objectives.
  
  

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.

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 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 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, 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?

Nearest Major Market: Durham

Nearest Secondary Market: Raleigh