Lentiviral Vector Support Operator

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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. Learn more at https://www.jnj.com/. 

We are searching for the best talent for a Lentiviral Vector Support Operator.

Duties / Responsibilities

• 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.

Qualifications / Requirements:

• 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.

• 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.

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 & 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 contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

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