Lentiviral Vector Support Operator

J&J FAMILY OF COMPANIES

Raritan, New Jersey, United States
Base: $36,750.00 - $59,167.50; bonus/equity: not s...
Onsite
Cgmp cleanroom environment
Aseptic processing support
Production data recording
Johnson & Johnson is seeking a Lentiviral Vector Support Operator in Raritan, New Jersey, to join their manufacturing operations team. The role involves providing operational support in a cGMP cleanroom environment for the production of Lentiviral vector products essential for CAR-T clinical and commercial operations

Job Summary

  • Be part of the manufacturing operations team responsible for production of Lentiviral vector products for autologous CAR-T clinical and commercial operation in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment.
  • Perform support operations function according to standard operating procedures and batch records, and record production data and information in a clear, concise, format according to Good Documentation Practices (GDP).
  • Employees are eligible for a comprehensive benefits package including vacation, sick time, parental leave, and participation in retirement and long-term incentive programs.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Lentiviral Vector Support Operator in Raritan, New Jersey, to join their manufacturing operations team. The role involves providing operational support in a cGMP cleanroom environment for the production of Lentiviral vector products essential for CAR-T clinical and commercial operations.

Salary

Base: $36,750.00 - $59,167.50; Bonus/Equity: Not specified; Benefits: Retirement plans, vacation, sick time, parental leave, and other paid time off

Skills & Requirements

Must-have

  • cGMP cleanroom environment
  • aseptic processing support
  • production data recording
  • Good Documentation Practices
  • team-based manufacturing operations
  • Microsoft Office proficiency
  • lifting and standing capability

Nice-to-have

  • continuous improvement mindset
  • cross-functional teamwork
  • operational excellence
  • process optimization
  • regulatory compliance awareness
  • detail-oriented
  • self-awareness

Key Requirements

  • High School diploma or Associate’s degree
  • Minimum one year related work experience
  • Experience in manufacturing or quality areas preferred
  • Knowledge of cGMP preferred
  • Experience in Pharmaceuticals or Biopharmaceuticals preferred
  • Proficiency in English verbal and written
  • Availability to work day shift and other shifts as needed

Work Rights

Not specified

Tailored Resume

Cover Letter