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About Innovative Medicine  

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. 

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. 

Learn more at  https://www.jnj.com/innovative-medicine 

We are searching for the best talent for Lentivirus Manufacturing Operator.

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. 

Duties / Responsibilities

• 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. 

Qualifications / Requirements: 

EDUCATION AND EXPERIENCE: 

• A High School diploma with a 1-2 years of related work experience

OR

• An Associate’s or Bachelor's degree in a related field (i.e. Chemical Engineering, Biological Sciences, Chemistry or Biochemistry) is required. 
• Experience in manufacturing, maintenance, quality, testing, or engineering areas is preferred. 
• Knowledge of current Good Manufacturing Practices (cGMP) is preferred. 
• Experience in the Pharmaceuticals or Biopharmaceuticals industry is preferred. 
• Experience in an aseptic and manufacturing environment is preferred. 
• Proficiency in English (verbal and written), as well as, good communication skills are required. 
• Ability to lift a minimum of 25 lbs. and to stand for a long period of time are required. 
• Basic proficiency with Microsoft Office tools (Word, Excel, PowerPoint and Outlook) is required. 
• Availability to work in a day shift is required. 
• Ability to accommodate changes in the schedule including working in other shifts as per operational needs is required. 
• This position will be based in Raritan, NJ and requires up to ten percent (10%) of domestic travel. 

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center  ([email protected]) or contact AskGS to be directed to your accommodation resource. 

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