Senior Facility Manufacturing Engineer

6062-Janssen Pharmaceuticals, Inc. Legal Entity

Raritan (NJ)

On-site

USD 94,000 - 152,000

Full time

7 days ago

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Job summary

Johnson & Johnson in Raritan, NJ, seeks a Senior Facility Manufacturing Engineer to drive facility reliability and project execution within a regulated pharmaceutical environment. The role leads cross-functional initiatives supporting manufacturing, utilities, and facility systems while ensuring cGMP, safety, quality, and regulatory standards are met.

The candidate will manage governance, milestones, and risk assessments, coordinating with Operations, Quality, Engineering, EHS, Supply Chain and

Qualifications

Bachelor's degree in Engineering required.
Minimum of four (4) years of experience in Engineering, Maintenance, Facilities, or a related technical environment.
Experience in manufacturing with strong cGMP compliance and documentation.
Experience in pharmaceutical or biologics industry preferred and aseptic/cleanroom exposure.
Proven project management skills with ability to lead projects from initiation through completion.

Responsibilities

Lead and govern site-wide projects and equipment improvements to ensure safety, reliability, regulatory compliance, operational effectiveness, and cost efficiency.
Proficient in project management tools including Microsoft Office and project management software; manage NC and CAPA reporting.
Plan, schedule, coordinate, and execute projects to meet regulatory, quality, and operational requirements.
Serve as governance lead for projects impacting the Raritan site, overseeing gates, readiness, and implementation activities.
Establish and improve project governance frameworks, including roles, documentation requirements, escalation paths, and controls.
Drive change management with proper change control, milestone reviews, and risk assessments across manufacturing operations and utilities.
Collaborate with Operations, Quality, Engineering, EHS, Supply Chain, and contractors for alignment and readiness.
Conduct impact assessments, resource planning, sequencing reviews to minimize disruption and ensure contingency plans.
Oversee readiness activities: commissioning, qualification, testing, training, documentation, verification.
Monitor governance metrics, schedules, and performance; lead post-implementation reviews and lessons learned.
Support regulatory inspections and internal audits with compliant documentation and practices.
Provide training and coaching on project governance to site personnel and contractors.
Lead reliability and continuous improvement initiatives to enhance safety, productivity, and compliance.

Skills

Project management

Cross-functional collaboration

Communication

Education

Bachelor's degree in Engineering

Tools

Microsoft Office

Microsoft Project

Non-Conformance (NC) reporting

CAPA systems

Job description

About Johnson & Johnson

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions 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 and Details

Job Function: Supply Chain Engineering
Job Sub Function: Facilities Engineering
Job Category: Scientific/Technology
All Job Posting Locations: Raritan, New Jersey, United States of America

Job Description

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 Experience:
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 Experience:
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 Information

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.

Equal Opportunity Statement

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. Johnson & Johnson is an Equal Employment 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.

Salary and Benefits

The anticipated base pay range for this position is : $94,000.00 - $151,800.00

Additional 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)).

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