OXB
Process Engineer I
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Process Engineer I
role at
OXB . 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 new opportunities to join us.
We’re currently recruiting for a
Process Engineer
to join our Engineering team. In this role, you will provide operational support and equipment support from selection to initial design through delivery and qualification, playing a key part in advancing our mission and making a real difference.
Responsibilities
Lead site projects from inception to completion ensuring safety, regulatory and quality compliance
Support equipment and utilities detailed design, commissioning, and qualification activities
Support department quality events (change control, corrective action/preventative action, deviations, etc.)
Support the development and maintenance of equipment drawings (P&IDs, PFDs, etc) and equipment lifecycle (URSs)
Provide support to Facilities/Maintenance team for development of a spare parts program and identify spare parts for incoming equipment
Ensure potential safety hazards are identified/shared and effective actions are rapidly implemented
Must be willing to have a flexible schedule to support 24x7 manufacturing activities
Qualifications
BS/MS in Engineering or a related field
Experience in pharmaceutical/biotech manufacturing is a plus
Familiar with FDA and EU regulations and GMP standards is a plus
Prior cGMP cell or gene therapy manufacturing experience is a plus
Willingness to take on other tasks as needed to support site, engineering, and facilities 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. We collaborate with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, AAV, and adenoviral vectors. Our world‑class capabilities span from early‑stage development to commercialization, supported by robust quality‑assurance systems, analytical methods, and depth of regulatory expertise.
Benefits
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, Respectful
Location: Durham, NC
#J-18808-Ljbffr
Process Engineer I
role at
OXB . 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 new opportunities to join us.
We’re currently recruiting for a
Process Engineer
to join our Engineering team. In this role, you will provide operational support and equipment support from selection to initial design through delivery and qualification, playing a key part in advancing our mission and making a real difference.
Responsibilities
Lead site projects from inception to completion ensuring safety, regulatory and quality compliance
Support equipment and utilities detailed design, commissioning, and qualification activities
Support department quality events (change control, corrective action/preventative action, deviations, etc.)
Support the development and maintenance of equipment drawings (P&IDs, PFDs, etc) and equipment lifecycle (URSs)
Provide support to Facilities/Maintenance team for development of a spare parts program and identify spare parts for incoming equipment
Ensure potential safety hazards are identified/shared and effective actions are rapidly implemented
Must be willing to have a flexible schedule to support 24x7 manufacturing activities
Qualifications
BS/MS in Engineering or a related field
Experience in pharmaceutical/biotech manufacturing is a plus
Familiar with FDA and EU regulations and GMP standards is a plus
Prior cGMP cell or gene therapy manufacturing experience is a plus
Willingness to take on other tasks as needed to support site, engineering, and facilities 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. We collaborate with some of the world's most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, AAV, and adenoviral vectors. Our world‑class capabilities span from early‑stage development to commercialization, supported by robust quality‑assurance systems, analytical methods, and depth of regulatory expertise.
Benefits
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, Respectful
Location: Durham, NC
#J-18808-Ljbffr