Sr. Supervisor, Operations CAR-T

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 Med Tech, 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  

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

** Job Function:*
* Supply Chain Manufacturing

** Job Sub*
* ** Function:*
* Manufacturing Pharmaceutical Process Operations

** Job Category:*
* People Leader

** All Job Posting Locations:*
* Raritan, New Jersey, United States of America

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* Job Description:

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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 *
* We are searching for the best talent for a Sr. Supervisor, Operations CAR-T to join our team in Raritan, NJ.

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* Summary:

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* The Sr. Supervisor is an exempt-level position within Operations responsible for directing the daily production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Their job duties will be performed within a team-based environment.  
** This role will support the Monday-Friday 2nd shift schedule 4:00pm-12:30am.*
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* Key Responsibilities:

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* + Lead and provide oversight for off-shift manufacturing activities within one or multiple unit operations in the CAR-T process.

+ Lead daily shift operations meetings (Tier Meeting) where you would assign individuals their daily production task to complete and ensure compliance and successful completion of work-related tasks.

+ Work closely with operations personnel on the production floor to provide clear guidance and perform production tasks as needed to help the team, in a manner consistent with safety policies, quality systems, and cGMP requirements.

+ Support manufacturing investigations and the implementation of subsequent corrective actions.

+ Work with Process Area Owners to help oversee the development of production personnel, provide input on personnel performance.

+ Build positive relationships with Manufacturing, Engineering, and Quality to ensure seamless execution of daily production tasks and work as part of a cross-functional team to address production issues as the first point of contact for operators on the production floor.

+ Support the development of manufacturing processes and work with cross-functional teams to drive continuous improvements and efficiencies within cell therapy Operations.

+ Participate in various department projects and handle challenging priorities in a fast paced and dynamic environment

+ Support the growth and development of supervisors and operations personnel within the Value Stream through coaching, hiring support, performance management, and talent development.

+ Maintain a state of permanent inspection readiness and actively support internal and regulatory inspections.

+ Supports the operational unit assigned as a process subject matter expert in addition being able to fully support the

Functional Area

Manager as a delegate in decision making for the operational unit.

** Qualifications*
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* Education:

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* + A minimum of a Bachelor's degree is required, preferably with a focus in Science or Engineering.

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* Experience and Skills:

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* Required:

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* + Minimum five (5) years of manufacturing experience in a Good Manufacturing Practices (GMP) environment.

+ Extensive experience managing direct…