Automation Engineer IV

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 Automation Engineer III to join our Manufacturing team. In this role, you will support cGMP manufacturing by working with process equipment, control systems, and instrumentation throughout all project phases, playing a key part in advancing our mission and making a real difference.

Your responsibilities in this role would be:

• Planning, execution, and monitoring of Automation systems utilized on site for cGMP manufacturing and facility utilities.
• Provide technical support for automation projects, including automation system design, control system hardware, equipment design, control panel design, alarm management, and instrumentation start-up and troubleshooting.
• Support development of technical standards, guidelines, and procedures in accordance with industry best practices.
• Support automation system design and integration, including hardware/software design specification development, user / functional requirement development, integration, and validation in conjunction with IT Computer Systems Validation & QA Validation leads.
• Develop P&IDs and loop descriptions for various processes, and/or equipment.
• Partner with automation system service providers, contract resources and Instrument/Electrical technicians ensuring safe, compliant maintenance and project execution.  Maintain current contacts as needed for system support.
• Support automation issue identification, communication, and resolution, including all compliance aspects such as Deviation investigation, Change Control, Corrective and Preventative Action (CAPA).
• Provide technical support for troubleshooting, improving, or optimizing ongoing manufacturing operations, including being on-call for after-hours remote support.
• Support the design, configuration, administration and maintenance activities of the sites manufacturing computer and automation systems, including process control systems, building automation systems, manufacturing execution systems, and data historians. 
• Ability to evaluate automation systems from a compliance perspective and ensure adherence to applicable standards (i.e. 21CFR Part 11, EU Annex 11).
• Troubleshooting experience, both hardware and software, at a manufacturing cGMP operation with flexibility to support operations on off hours. 

We are Looking For:

• Requires a BS/MS in Engineering or related field.
• Must have 5+ years of experience working in a biotechnology company, with focus on cross functional support for cGMP manufacturing.
• 5+ years of experience in the execution of the automation discipline in a regulated manufacturing environment.
• Strong understanding of GMPs and good engineering practice (GEP), including ISA S88, GAMP, ASTM E2500, ISPE guidance, etc.
• Experience with HMI/SCADA packages such as: Rockwell RSView, FactoryTalk.
• Experience with OSI PI.
• Experience with PLCs such as: Rockwell, Siemens.
• Experience owning SOPs, deviations, change controls, and CAPAs to support operations.
• Experience in plant start up, equipment commissioning, and qualification is a plus.
• Experience with recipe design and qualification for bioreactors or chromatography skids is a plus.

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 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 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?