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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

Job Function:

Supply Chain Manufacturing

Job Sub** **Function:

Manufacturing Deployment

Job Category:

Professional

All Job Posting Locations:

New Brunswick, New Jersey, United States of America

Job 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

We are searching for the best talent for a **Senior Scientist, Process Validation** to be based New Brunswick, New Jersey. Alternative locations include Raritan, New Jersey.

Our Global Focus in Advanced Therapies

Advanced therapy medicinal products (ATMPs), including CAR-T and viral vector-based treatments, represent a transformative approach to patient care. As a global organization, we strive to harmonize validation strategies, ensuring consistency, compliance, and innovation throughout our manufacturing network.

The Process Validation Center of Excellence

The CoE provides strategic leadership for validation activities and governance standards to drive accountability across partners. We define standard processes, drive harmonization, and enable technology adoption to ensure robust, validated processes that meet regulatory expectations and deliver life-changing therapies to patients worldwide.

Role Summary

The Senior Scientist serves as a key member of the global Life Cycle Management team, responsible for developing, implementing, and governing validation strategies across the Advanced Therapies network. This role focuses on global alignment, standardization of validation approaches, and strategic oversight of Tech Transfer, PPQ campaigns, CPV programs, and digital readiness. This role partners closely with regional MSAT, R&D, Quality, Regulatory, and Engineering teams to ensure consistent, compliant, and innovative validation practices globally.

Operational Excellence & Governance

+ Define and maintain global Validation Master Plans and governance frameworks for ATMP processes.

+ Drive global implementation of risk-based validation approaches aligned with ICH Q8/Q9/Q10, Annex 15, and FDA/EMA guidance.

+ Author harmonized validation standards and templates across the global network.

+ Provide strategic oversight for PPQ campaigns implemented at multiple sites, ensuring consistency and compliance.

+ Support global CPV strategy, apply data analytics, statistical tools, and risk management principles to evaluate process capability and drive data-informed decisions.

+ Support lifecycle improvement initiatives and evaluate digital tools for process monitoring.

+ Partner with regional and site teams to assess validation readiness for new technologies and platforms.

+ Support and author regulatory submissions with globally aligned validation documentation and strategies.

Cross-Functional Leadership & Communication

+ Act as an inspiring leader, mentoring teams and influencing global validation policy and innovation.

+ Facilitate collaboration and communicate program goals, progress, risks, and results to senior leadership and technical teams with clarity and influence.

_Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s)_

_United States -_** **_Requisition Number: R-048421_

_Belgium - Requisition Number: R-049802_

_Ireland - Requisitions Number: R-049778_

_Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission._

Required Qualifications:

Education:

+ Bachelor's degree in biology, biotechnology, or related scientific field is required; advanced degree or equivalent experience preferred.

Skills & Experience:

+ 7+ years proven experience within a regulated biologics or pharma industry

+ Experience in global process validation strategy, governance, and regulatory compliance for ATMPs.

+ Strong understanding of risk-based validation principles and Health Authority expectations.

+ Demonstrate the ability to work effectively in cross-functional environment and influence global teams

Preferred Qualifications:

+ Prior experience in cell culture or viral vector commercial manufacturing is highly desired.

+ Knowledge in statical process control and analytical data modeling.

+ Experience in digital solution implementation and deployment.

+ Knowledge in data management platforms and data governance

Other Requirements:

+ International travel to partner sites and global meetings, up to 20% of the time. Flexibility to work remotely when not travelling.

+ Language requirements – fluency in English required; additional languages preferred.

+ The anticipated compensation rage for this position is 94,000-144,500

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 ([email protected]) 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 www.careers.jnj.com .

Required Skills:

Preferred Skills:

Agile Manufacturing, Business Process Design, Coaching, Communication, Critical Thinking, Good Manufacturing Practices (GMP), Innovation, Manufacturing Engineering, Manufacturing Flow Management, Manufacturing Processes, Plant Operations, Proactive Behavior, Problem Solving, Product Development Lifecycle, Production Operations, Profit and Loss Responsibility, Robotic Automation, Structural Fabrication, Sustainability

The anticipated base pay range for this position is :

94,000-144,500

Additional Description for Pay Transparency:

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 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 Condolence Leave – 30 days for an immediate family member: 5 days for an extended family member Caregiver Leave – 10 days Volunteer Leave – 4 days Military Spouse Time-Off – 80 hours Additional information can be found through the link below. https://www.careers.jnj.com/employee-benefits