OXB
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Analyst II, Quality Control
role at
OXB
Location: Durham, NC, US Company: oxfordbiom
Overview 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 .
Responsibilities
Perform cGMP analytical testing (Cell based Assays, flow cytometry, qPCR, ddPCR, ELISAs, and UPLC)
Review and evaluate raw data from a peer or technical review level of all analytical methods, as well as sample authorization.
Author, review, and/or approve SOPs/policies and technical reports with general guidance.
Support laboratory deviations and investigations (IA, OOS, AR).
Support operational systems (equipment/instrument maintenance/calibration, equipment alarm monitoring, sample handling/tracking, data integrity/control, cGMP documentation, LIMS, laboratory audit, and method training).
Execute phase-appropriate test method validation protocols as needed.
Qualifications
BS with 3+ years in a biotechnology discipline.
3+ years of experience in a cGMP/GxP environment is preferred.
Hands on experience in flow cytometry, quantitative PCR, and other bioanalytical methods such as ELISA and UPLC methods.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.
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-
#J-18808-Ljbffr
Analyst II, Quality Control
role at
OXB
Location: Durham, NC, US Company: oxfordbiom
Overview 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 .
Responsibilities
Perform cGMP analytical testing (Cell based Assays, flow cytometry, qPCR, ddPCR, ELISAs, and UPLC)
Review and evaluate raw data from a peer or technical review level of all analytical methods, as well as sample authorization.
Author, review, and/or approve SOPs/policies and technical reports with general guidance.
Support laboratory deviations and investigations (IA, OOS, AR).
Support operational systems (equipment/instrument maintenance/calibration, equipment alarm monitoring, sample handling/tracking, data integrity/control, cGMP documentation, LIMS, laboratory audit, and method training).
Execute phase-appropriate test method validation protocols as needed.
Qualifications
BS with 3+ years in a biotechnology discipline.
3+ years of experience in a cGMP/GxP environment is preferred.
Hands on experience in flow cytometry, quantitative PCR, and other bioanalytical methods such as ELISA and UPLC methods.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.
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-
#J-18808-Ljbffr