Lentiviral Vector Support Operator

Johnson & Johnson Johnson & Johnson · Pharma · Raritan, NJ +1

Operates and supports manufacturing processes for Lentiviral vector products in a cGMP cleanroom environment, focusing on cell culturing, aseptic processing, downstream, and fill finish operations. Requires adherence to SOPs, GDP, and safety policies. Involves restocking, material preparation, cleaning, and continuous improvement initiatives. Requires a High School diploma/Associate's or 1 year of related experience, with preferred experience in manufacturing, pharmaceuticals, aseptic environments, and cGMP knowledge.

What you'd actually do

  1. 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.
  2. Provide operational support to associates engaged in production activities related to cell culturing, aseptic processing, downstream and fill finish process.
  3. 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).
  4. Perform tasks on time in a manner consistent with the safety policies, quality systems and cGMP requirements.
  5. Execute production support activities such as restocking, picking, transferring, cleaning, wiping material for production use and related processes.

Skills

Required

  • High School diploma or an Associate’s or a minimum of one (1) years of related work experience
  • Proficiency in English (verbal and written)
  • good communication skills
  • Ability to lift a minimum of 25 lbs.
  • Ability to stand for a long period of time
  • Basic proficiency with Microsoft Office tools (Word, Excel, PowerPoint and Outlook)
  • Availability to work in a day shift
  • Ability to accommodate changes in the schedule including working in other shifts as per operational needs

Nice to have

  • Experience in manufacturing, maintenance, quality, testing, or engineering areas
  • Knowledge of current Good Manufacturing Practices (cGMP)
  • Experience in the Pharmaceuticals or Biopharmaceuticals industry
  • Experience in an aseptic and manufacturing environment

What the JD emphasized

  • cGMP
  • Good Documentation Practices (GDP)
  • aseptic
  • cleanroom environment