OXB
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Process Engineer II (MSAT)
role at
OXB .
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 Engineer II
to join our
Manufacturing Sciences and Technology Team (MSAT) . In this role, you will be responsible for leading the assessment and technology transfer of new manufacturing processes that support clinical and commercial manufacturing, playing a key part in advancing our mission and making a real difference.
Your responsibilities
Serve as the downstream (clarification, chromatography, TFF, sterile fill/finish) technical support for the vector manufacturing process in the MSAT team.
Technology Transfer Technical Leader for cross‑functional team.
Lead the introduction of new manufacturing processes and methods to facilitate clinical and commercial manufacturing of multiple cell and gene therapy platform drug substances and products.
Lead the information transfer and gap assessment of new process and method transfers.
Support MSAT and Manufacturing documentation drafting/review with a strong understanding of equipment, critical process parameters, in‑process testing, etc.
Provide guidance and lead facility fit assessments of manufacturing processes in production suites and use FMEA or similar risk‑based approaches to troubleshoot processing issues.
Author and execute tech transfer plans, engineering studies, risk assessments, technical reports, change controls, and process validation plans/protocols.
Provide guidance in the documentation of events and deviations during cGMP manufacturing production.
Provide guidance for process equipment onboarding.
May support other tasks as determined by management.
Qualifications
BS/MS in Engineering or a related field or Biological Science or related field with 0‑3 years of experience in a technical engineering role or related areas (or a combination of education and experience).
Requires 0‑3 years of experience in the pharmaceutical or biologics industry in process development or manufacturing operations.
Experience in implementing special projects related to operational process improvement.
Strong leadership, relationship management, and organizational planning.
Ability and willingness to learn and adapt skillsets for various areas of MSAT.
Knowledge of cGMP compliance around bioprocess drug substance manufacturing.
Experience with bioprocess drug substance manufacturing process development and CGMP manufacturing.
Experience in monoclonal antibody production and purification process development is a plus.
Technical expertise in upstream/downstream operations including equipment knowledge and processes (disposable technologies, clarification, chromatography skids, TFFs, formulation processes, final fill, etc.).
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 commercialization. These capabilities are supported by robust quality‑assurance systems, analytical methods, and depth of regulatory expertise.
Why Join Us
Competitive total reward packages
Well‑being 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
Ready to Make a Difference? 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.
#J-18808-Ljbffr
Process Engineer II (MSAT)
role at
OXB .
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 Engineer II
to join our
Manufacturing Sciences and Technology Team (MSAT) . In this role, you will be responsible for leading the assessment and technology transfer of new manufacturing processes that support clinical and commercial manufacturing, playing a key part in advancing our mission and making a real difference.
Your responsibilities
Serve as the downstream (clarification, chromatography, TFF, sterile fill/finish) technical support for the vector manufacturing process in the MSAT team.
Technology Transfer Technical Leader for cross‑functional team.
Lead the introduction of new manufacturing processes and methods to facilitate clinical and commercial manufacturing of multiple cell and gene therapy platform drug substances and products.
Lead the information transfer and gap assessment of new process and method transfers.
Support MSAT and Manufacturing documentation drafting/review with a strong understanding of equipment, critical process parameters, in‑process testing, etc.
Provide guidance and lead facility fit assessments of manufacturing processes in production suites and use FMEA or similar risk‑based approaches to troubleshoot processing issues.
Author and execute tech transfer plans, engineering studies, risk assessments, technical reports, change controls, and process validation plans/protocols.
Provide guidance in the documentation of events and deviations during cGMP manufacturing production.
Provide guidance for process equipment onboarding.
May support other tasks as determined by management.
Qualifications
BS/MS in Engineering or a related field or Biological Science or related field with 0‑3 years of experience in a technical engineering role or related areas (or a combination of education and experience).
Requires 0‑3 years of experience in the pharmaceutical or biologics industry in process development or manufacturing operations.
Experience in implementing special projects related to operational process improvement.
Strong leadership, relationship management, and organizational planning.
Ability and willingness to learn and adapt skillsets for various areas of MSAT.
Knowledge of cGMP compliance around bioprocess drug substance manufacturing.
Experience with bioprocess drug substance manufacturing process development and CGMP manufacturing.
Experience in monoclonal antibody production and purification process development is a plus.
Technical expertise in upstream/downstream operations including equipment knowledge and processes (disposable technologies, clarification, chromatography skids, TFFs, formulation processes, final fill, etc.).
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 commercialization. These capabilities are supported by robust quality‑assurance systems, analytical methods, and depth of regulatory expertise.
Why Join Us
Competitive total reward packages
Well‑being 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
Ready to Make a Difference? 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.
#J-18808-Ljbffr