Exp Engineer- Process Engineering System Owner

Johnson Johnson; Wilson (NC); On-site; USD 110,000 - 150,000; Full time

Job summary

Johnson & Johnson in the United States seeks a System Owner for GMP biotherapeutics process systems. You will manage design through turnover, partnering with design, construction, commissioning, manufacturing, quality, and external vendors to ensure systems are delivered safely, on schedule, and in alignment with GMP requirements.

The position will own approximately $10–$20 million of process equipment packages and provide ongoing support during qualification batches, GMP readiness activities,

Qualifications

• Minimum 5 years of process or plant engineering in commercial biologics facilities.
• Experience in GMP-regulated environments.
• Experience delivering equipment from construction through commissioning, qualification, turnover.
• Ability to lead or support cross‑functional teams in a matrixed project environment.
• Strong communication, collaboration, problem‑solving, and decision‑making skills.
• Ability to manage multiple priorities and support multiple project activities simultaneously.

Responsibilities

• Lead system delivery: provide engineering design and startup support for GMP biotherapeutics manufacturing facility systems and equipment.
• Drive right‑first‑time execution: apply integrated equipment, utility, and facility engineering expertise with an operational focus to support successful startup.
• Manage equipment packages: lead vendor equipment packages to ensure delivery on schedule, within budget, and in accordance with approved specifications.
• Support construction execution: coordinate with the construction management team to resolve system clashes, address field issues, and maintain construction progress.
• Coordinate system readiness: lead owner walkdowns, ensure punch list closure, and approve systems as ready for commissioning.
• Oversee commissioning and qualification: review and approve commissioning and qualification protocols before and after execution.
• Resolve issues and manage change: drive issue resolution during commissioning and create project change approval requests when needed.
• Ensure successful handover: accountable for on‑time commissioning completion, approval for GMP operation, and system handover to the end user.

Skills

Cross-functional teams

Communication

Problem solving

Decision making

Multitasking

Education

Bachelor's in Chemical/Mechanical Eng

Master's degree preferred

Job 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 Engineering

Job Sub Function

Process Engineering

Job Category

Scientific/Technology

All Job Posting Locations

Wilson, North Carolina, United States of America

Job Description

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

The System Owner serves as the project manager and technical owner for assigned process systems and equipment packages from design through turnover to the end user. In this role, you will partner closely with design, construction, commissioning and qualification, manufacturing, quality, and external vendors to ensure systems are delivered safely, on schedule, within budget, and in alignment with GMP requirements.

This position will own approximately $10 million to $20 million of process equipment packages and associated field-installed scope within the production building. Following turnover, the System Owner will continue to provide technical support during qualification batches, GMP readiness activities, and audit preparation.

Key Responsibilities

• Lead system delivery: Provide engineering design and startup support for GMP biotherapeutics manufacturing facility systems and equipment.
• Drive right-first-time execution: Apply integrated equipment, utility, and facility engineering expertise with an operational focus to support successful startup.
• Manage equipment packages: Lead vendor equipment packages to ensure delivery on schedule, within budget, and in accordance with approved specifications.
• Support construction execution: Coordinate with the construction management team to resolve system clashes, address field issues, and maintain construction progress.
• Coordinate system readiness: Lead owner walkdowns, ensure punch list closure, and approve systems as ready for commissioning.
• Oversee commissioning and qualification: Review and approve commissioning and qualification protocols before and after execution.
• Resolve issues and manage change: Drive issue resolution during commissioning and create project change approval requests when needed.
• Ensure successful handover: Accountable for on-time commissioning completion, approval for GMP operation, and system handover to the end user.

Qualifications

Education

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, Bioprocess Engineering, or a related technical field.
• Master's degree, MBA; preferred

Experience and Skills

Required

• A minimum 5 years of process or plant engineering experience in commercial biologics manufacturing facilities
• Experience in process engineering, plant engineering, equipment delivery, or manufacturing support within a GMP-regulated environment.
• Experience supporting the implementation of new equipment from construction through commissioning, qualification, and turnover.
• Demonstrated ability to lead or support cross‑functional teams in a matrixed project environment.
• Strong communication, collaboration, problem‑solving, and decision‑making skills.
• Ability to manage multiple priorities and support multiple project activities simultaneously.

Preferred

• Experience with large-scale monoclonal antibody production equipment, such as low-pressure liquid chromatography, inline conditioning or dilution, axial compression chromatography columns, solution preparation and storage, tangential flow filtration, washers, autoclaves, or clean-in-place systems.
• Experience working with external partners such as architecture and engineering firms, construction firms, and equipment vendors to develop, organize, and execute project plans.
• Startup, commissioning, qualification, or GMP readiness experience for a new or expanded manufacturing facility.
• Strong understanding of GMPs, regulatory expectations, business requirements, risk management, and proj