MOI/QCCB Lead Operator
Johnson & Johnson · Raritan, NJ
Manufacturing OperationsFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Lead operator role in a cGMP manufacturing environment for MOI and Quality Control Cell Bank preparation of autologous CAR-T products. Responsible for executing manufacturing procedures, maintaining compliance standards, and supporting production scheduling in a cleanroom facility.
What they're looking for
- High school diploma with 6 years biotech/pharmaceutical experience, or equivalent industry experience
- Bachelor's degree in Life Sciences or Engineering with 2 years biotech/pharmaceutical experience preferred
- Working knowledge of cGMP requirements and manufacturing compliance regulations
- Proficiency with data entry systems including SAP and electronic batch records
- Ability to read, interpret, and document manufacturing procedures and batch records
- Experience with cell culturing, purification, aseptic processing, or cryopreservation techniques
What you'll be doing
- Lead and independently execute MOI and QCCB CAR-T manufacturing processes according to standard operating procedures
- Perform manufacturing unit operations and accurately record production data following Good Documentation Practices
- Maintain compliance with cGMP requirements and quality standards across all assigned tasks
- Support continuous improvement initiatives and contribute to process development and documentation
- Collaborate with cross-functional teams to meet production schedules and troubleshoot routine manufacturing processes
Privacy & handoff
This role links to Johnson & Johnson's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.