JMD Technologies Inc.
Shift Details: Initial Training: Mon–Fri (first 2 weeks), then move to 4x10 shift schedule
Responsibilities
Provide QA floor support for cell/gene therapy manufacturing Perform
batch record and QC data review
for product disposition Review/approve deviations, CAPAs, and manufacturing documentation Support compliance walkthroughs, inspection readiness, and continuous improvement Qualifications
Bachelor’s degree in science or allied health (Master’s preferred) 3–5 years of QA operations in
cell/gene therapy Experience with
commercial QA, lot disposition, and QA on the floor Strong knowledge of GMPs, aseptic processing, and ATMP regulatory considerations Seniority level
Mid-Senior level Employment type
Contract Job function
Quality Assurance Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
Provide QA floor support for cell/gene therapy manufacturing Perform
batch record and QC data review
for product disposition Review/approve deviations, CAPAs, and manufacturing documentation Support compliance walkthroughs, inspection readiness, and continuous improvement Qualifications
Bachelor’s degree in science or allied health (Master’s preferred) 3–5 years of QA operations in
cell/gene therapy Experience with
commercial QA, lot disposition, and QA on the floor Strong knowledge of GMPs, aseptic processing, and ATMP regulatory considerations Seniority level
Mid-Senior level Employment type
Contract Job function
Quality Assurance Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr