This job posting is anticipated to close on May 13 2026. We may however extend this time period, in which case the posting will remain available on www.careers.jnj.com to accept additional applications.
Description
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 jnj.com
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 ManufacturingJob Sub Function:
Manufacturing Pharmaceutical Process OperationsJob Category:
Business Enablement/SupportAll Job Posting Locations:
Raritan, New Jersey, United States of AmericaJob Description:
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 https://www.jnj.com/innovative-medicine
Learn more and apply to this exciting new role!
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.
An internal pre-identified candidate for consideration has been identified. However, all applicants will be considered.
This role will Lead, coach and deliver a holistic, effective process qualification program for Operations trainees who support daily clinical production and strategically prepare for commercial supply of a CAR-T product.
Key Responsibilities:
Manages, plans, coordinates, prepares and performs hands-on process training curriculum for specific unit operation qualification.
Prepares and maintains training lab, materials, and equipment.
Conducts Observation, Side-by-Side, and Process Qualification activities for new trainees.
Assess technical qualifications of new Operations trainees.
Conducts knowledge and skill checks for Operations.
Work with Operations Management to assess and report on new trainee development.
Work with Operations Management to develop streamlines and robust qualification process.
Helps write or revise Operations training procedures, practices, and skills assessments.
Performs training assessments for new and updated procedures.
Identifies technical training needs and expectations, monitors progress, addresses and resolves gaps in training requirements for Operations.
Supports evaluation of appropriate compliance courses for Operations.
Optimizes the effectiveness and efficiency of training program in delivery of qualified personnel.
Supports investigations and evaluates improvement opportunities for effective compliant training performance leading to sustained right first-time execution.
Knowledge of LMS system.
Supports the maintenance and reporting of quality training metrics.
Support daily manufacturing activities when necessary.
Qualifications
Education:
A minimum of a Bachelor’s Degree in a Life Sciences field or equivalent technical discipline/experience is required.
Experience and Skills:
Required:
A minimum 4 years of relevant work experience is required.
Experience working within an aseptic manufacturing facility, preferably in training/system applications, quality systems, or learning management systems.
Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell based products as well as knowledge of Good Tissue Practices.
Experience with training methodology, adult learning theory, instructional design and Train-the-Trainer programs.
Curriculum and module design experience.
Advanced computer skills and practical knowledge of MS Office Suite, SharePoint, and other related systems.
Excellent organizational skills.
Ability to effectively prioritize and execute tasks in a fast-paced environment.
Works well in a team-oriented, collaborative environment.
The candidate must be highly organized and capable of working in a team environment with a positive attitude under minimal supervision.
Proactive and continuous improvement oriented.
Ability to lead with influence.
cGMP manufacturing experience
Able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members.
Strong analytical, problem solving and critical thinking skills.
Other:
Ability to work a flexible schedule due to business needed and project timelines
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.]
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, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
Required Skills:
Preferred Skills:
Agile Manufacturing, Analytics Dashboards, Chemistry, Manufacturing, and Control (CMC), Communication, Data Compilation, Data Savvy, Execution Focus, Gap Analysis, Good Manufacturing Practices (GMP), Issue Escalation, Operational Excellence, Pharmaceutical Industry, Plant Operations, Proactive Behavior, Problem Solving, Process Optimization, Project Administration, Quality AuditingThe anticipated base pay range for this position is :
$63,000.00 - $101,430.00Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).Positions Represented by CBA: Please use the following language:
This position is eligible for benefits to include medical, dental, vision and time off, as well as any others as provided for in the applicable Collective Bargaining Agreement.
The following link to general company benefits information MUST also be included in the posting: Please use the following language:
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
This position is eligible to participate in the Company’s long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
