Senior Scientist, External Manufacturing MS&T (CAR-T)

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

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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 are searching for the best talent for a Senior Scientist External Manufacturing MS&T (CAR-T) to be in Raritan NJ.

Purpose:

The Senior Scientist External Manufacturing MS&T (CAR-T) supports manufacturing activities for the Advanced Therapies Supply Chain organization within the third-party manufacturing site. This includes executing robust strategies to maintain the validated state of cell and gene therapy processes while implementing lifecycle management initiatives related to new technologies automation technology transfer etc. This role serves as a person-in-plant in support of routine manufacturing aids in change management activities at the third-party manufacturing site and supports complex deviations. This is a critical role supporting the sites technical supply and compliance related objectives. This position supports/participates in the virtual plant team and actively collaborates with Quality Supply Chain and Growth & Partnerships functions.

You will be responsible for:

• Provide manufacturing floor support investigations of major/critical process deviations impact assessments process monitoring/continued process verification and process improvement projects.

• Act as receiving site for any lifecycle process technology transfers including process qualification/comparability campaigns process risk assessments process control strategies and new process training.

• Provide technical support to regulatory filings regulatory inspections and health authority questions.

• In collaboration with other functions supports the development and implementation of fit-for-purpose effective systems and business processes to assure compliance with corporate guidelines for deviation investigations technology transfer process monitoring and other relevant areas.

• Support process monitoring and process data analysis troubleshooting facility fit assessments of new processes into the existing manufacturing plant assessments and writing of technical documents and technical optimization/implementation projects

• Translate strategic product roadmaps to detailed execution plans for programs to deliver on target outcomes to enhance the lifecycle of the product.

• Drive continuous improvement and foster an operational excellence culture to enhance productivity and efficiency of operations

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QUALIFICATIONS:

• A Bachelors Degree or Masters Degree in Science/Engineering or Equivalent with 4-6 years of Biotech/ Pharmaceutical experience or equivalent industry experience.

• Prior work experience in a manufacturing environment

• Knowledge of good manufacturing practices (GMP) and documentation.

• Ability to work in a cleanroom laboratory and office setting

• Excellent judgment. able to prioritize and decide appropriate courses of actions.

• Effective at implementing decisions troubleshooting and problem-solving skills in a fast-paced environment.

• Hands-on experience and knowledge in manufacturing sciences and operations support technology transfer process comparability process monitoring change management cGMP compliance and advanced therapies (i.e. cell/gene therapy products vaccines) product regulatory and validation requirements

• Experience in a Cell/Gene Therapy cGMP manufacturing setting

• Working knowledge of Lean/Continuous improvement concepts

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 () or contact AskGS to be directed to your accommodation resource.

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

The anticipated base pay range for this position is :

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