Operator I, Manufacturing - Raritan, NJ, United States - Johnson & Johnson

    Johnson & Johnson
    Johnson & Johnson Raritan, NJ, United States

    1 month ago

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    Full time
    Description

    Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Manufacturing Operator, CAR-T to be located in Raritan, NJ.

    At Johnson & Johnson, we believe health is everything.

    Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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.

    As the Manufacturing Support Operator, CAR-T ( Lenti Dept), you will:

    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.

    Provide operational support to associates engaged in production activities related to cell culturing, aseptic processing, downstream and fill finish process .

    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).

    Perform tasks on time in a manner consistent with the safety policies, quality systems and cGMP requirements.
    Execute production support activities such as restocking, picking, transferring, cleaning, wiping material for production use and related processes.
    Work in a team based, cross-functional environment to complete production tasks required by shift schedule.
    Aid in the development of streamlining the support operation process 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 or an Associate's or a minimum of one (1) years of related work experience is required
    Experience in manufacturing, maintenance, quality, testing, or engineering areas is preferred.
    Experience in the Pharmaceuticals or Biopharmaceuticals industry is preferred.
    Proficiency in English (verbal and written), as well as, good communication skills 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.
    Schedule will be Monday - Friday 7:30m - 4:00pm
    This position is overtime eligible
    This position is eligible for a shift differential.
    Holiday pay, including Floating Holidays – up to 13 days per calendar year

    The Company may however extend this time-period, in which case the posting will remain available on to accept additional applications.

    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.

    For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit