Lentivirus Manufacturing Operator - Johnson & Johnson : Job Details

Lentivirus Manufacturing Operator

Johnson & Johnson

Job Location : Raritan,NJ, USA

Posted on : 2024-11-25T08:28:20Z

Job Description :

Johnson & Johnson is currently seeking a lentivirus Manufacturing Operator in Raritan, NJ.

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world's most pressing healthcare challenges.

We know that the success of our business - and our ability to deliver meaningful solutions - depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

As the LVV Manufacturing Operator, CAR-T, you will:

* Be part of the manufacturing operations team responsible for production of Lentivirus vector for the autologous CAR-T products in a controlled current Good Manufacturing Practice (cGMP) cleanroom environment.

* Perform process unit operations 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).

* Perform tasks on time in a manner consistent with the safety policies, quality systems and cGMP requirements.

* Execute production activities common to cell culture in shake flasks and wave bioreactor, cell counting methods (i.e. Vi-Cell), thawing, passaging, aseptic technique/processing, chromatography columns or filtration(TFF, DF), filter integrity test, GE AKTA systems and/or microfiltration/ultrafiltration systems, purification, automated filler (i.e.FP50) and sterile filling using appropriate techniques.

* Perform tasks related to single use bioreactor operations including bioreactor setup, sampling and monitoring, and disassembly.

* Work in a team based, cross-functional environment to complete production tasks required by shift schedule.

* Aid in the development of manufacturing processes including appropriate documentation.

* Drive continuous improvement of manufacturing operations leveraging own observation as well as input of team members.

* Handle virus and human derived materials in containment areas.

Apply Now!

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