Senior Facility Manufacturing Engineer

• Job title Senior Facility Manufacturing Engineer
• Function Supply Chain Engineering
• Sub function Facilities Engineering
• Category Senior Engineer, Facilities Engineering (ST6)
• Location Raritan / United States of America
• Date posted Aug 17 2026
• Requisition number R-089960
• Work pattern Fully Onsite

This job posting is anticipated to close on Aug 24 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.

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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 https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Senior Facility Manufacturing Engineer to join our team in Raritan, NJ.

Summary:

The Senior Facility Manufacturing Engineer is a key engineering role responsible for driving facility reliability, project execution, and operational excellence within a regulated pharmaceutical manufacturing environment. This role leads cross-functional initiatives that support manufacturing operations, utilities, and facility systems while ensuring compliance with cGMP, safety, quality, and regulatory requirements. The successful candidate combines strong technical expertise, project leadership, and stakeholder management skills to deliver sustainable improvements in equipment performance, operational efficiency, and site readiness.

Key Responsibilities:

This role is responsible for leading and governing site-wide projects and equipment improvement initiatives to ensure safety, reliability, regulatory compliance, operational effectiveness, and cost efficiency. The successful candidate will be proficient in project management , including Microsoft Office applications, Microsoft Project, and quality systems such as Non-Conformance (NC) and CAPA reporting platforms.

• Lead the planning, scheduling, coordination, and execution of projects to ensure compliance with regulatory, quality, and operational requirements.

• Serve as the primary governance lead for projects and initiatives impacting the Raritan Manufacturing site, overseeing decision gates, execution readiness, and implementation activities, including site shutdowns and slowdowns.

• Establish, maintain, and continuously improve project governance frameworks, including approval processes, roles and responsibilities, documentation requirements, escalation pathways, and execution controls.

• Drive effective change management by ensuring appropriate change control processes, milestone reviews, and risk assessments are completed to safeguard manufacturing operations, utilities, warehouse, quality control, and production areas.

• Partner cross-functionally with Operations, Quality, Engineering, EHS, Supply Chain, and external contractors to ensure alignment, transparency, and readiness before project execution.

• Conduct impact assessments, resource planning, and execution sequencing reviews to minimize operational disruptions and ensure appropriate contingency and recovery plans are established.

• Oversee project readiness activities, including commissioning, qualification, testing, training, documentation, and verification activities prior to implementation.

• Monitor project governance metrics, schedules, and performance indicators; facilitate post-implementation reviews, capture lessons learned, and drive continuous improvement initiatives.

• Support regulatory inspections, internal audits, and compliance initiatives by ensuring project documentation and execution practices meet applicable standards and requirements.

• Act as the escalation point for governance-related issues and facilitate risk-based go/no-go decisions, ensuring appropriate stakeholder alignment, approvals, and documented mitigation plans.

• Provide training, coaching, and communication to site personnel and contractors regarding project governance processes

• Lead reliability and continuous improvement initiatives that enhance safety, productivity, compliance, and overall facility performance.

Qualifications

Education

• A minimum of a Bachelor's degree is required. Focused degree in Engineering (i.e., Chemical, Mechanical, Biomedical, Manufacturing/Production, or related fields) is preferred.

Required:

• Minimum of four (4) years of experience in Engineering, Maintenance, Facilities, or a related technical environment.

• Experience working in a manufacturing environment, with a strong background in cGMP compliance and documentation. Experience within the pharmaceutical or biologics industry is preferred.

• Experience supporting operations in aseptic and/or cleanroom environments.

• Proven project management skills, with the ability to successfully lead projects from initiation through completion.

• Experience supporting capital projects, maintenance programs, and/or manufacturing operations.

• Strong analytical, troubleshooting, and problem-solving abilities.

• Demonstrated ability to collaborate effectively across cross-functional teams, including contractors and internal subject matter experts, to drive project execution and operational success.

• Strong communication and stakeholder management skills, with the ability to coordinate resources and align diverse teams toward common objectives.

Preferred:

• Demonstrated ability to resolve complex technical and operational issues through effective root cause analysis and sustainable solutions.

• Proven contractor management leadership experience, including directing and coordinating external resources to achieve project objectives.

• Working knowledge of Process Excellence, Lean, Six Sigma, or continuous improvement methodologies and tools.

• Experience driving process improvements that enhance operational efficiency, reliability, and compliance.

Other

• This position supports a 24/7 dynamic biological manufacturing environment, working in mechanical spaces and on utility systems

• Up to 10% domestic/international travel may be 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, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

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