Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Manufacturing Specialist, CAR-T.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal. Janssen Biotech, Inc. is part of the Janssen Pharmaceutical Companies.
Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy. This innovative strategic partnership is designed to combine the strengths and expertise of two companies to advance the promise of an immunotherapy CAR T platform and investigational treatment
As the Manufacturing Specialist, CAR-T, you will:
* Be part of the manufacturing operations team responsible for production of autologous CAR-T products for clinical and commercial operation 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 culturing, purification, aseptic processing and cryopreservation using appropriate techniques. * 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 human derived materials in containment areas.
* A High School diploma with at least eight (8) years of related work experience OR an Associate's degree with at least six (6) years of related experience OR a Bachelor's degree with at least four (4) years of related experience is required. * Experience in manufacturing, maintenance, quality, testing, or engineering areas is required. * Experience in the Pharmaceuticals or Biopharmaceuticals industry is preferred. * Knowledge of current Good Manufacturing Practices (cGMP) is required. * Experience in an aseptic manufacturing environment is preferred. * Experience handling complex manufacturing issues and providing guidance to Associates is preferred. * Proficiency in English (verbal and written) and 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 (1st or 2nd 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 Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.