Process Engineer I

• Job title Process Engineer I
• Function Supply Chain Manufacturing
• Sub function Manufacturing Product & Packaging Operations
• Category Analyst, Manufacturing Product & Packaging Operations (P4 - N23)
• Location Irving / United States of America
• Date posted Aug 28 2025
• Requisition number R-030676
• Work pattern Fully Onsite

This job posting is anticipated to close on Sep 05 2025. 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

Job Function:

Supply Chain Manufacturing

Job Sub Function:

Manufacturing Product & Packaging Operations

Job Category:

Professional

All Job Posting Locations:

Irving, Texas, United States of America

Job Description:

About MedTech

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at

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 .

We are searching for the best talent for Process Engineer I.

JOB SUMMARY

• Provides process engineering and controls support. Plans and conducts activities related to the development of new processes including researching current and emerging technologies, evaluating process cost, quality, and capability alternatives, and performing process characterization and optimization using designed experiments, and problem solving and decision-making tools.
• Responsible to identify process improvement initiatives and develops proposals for problem solving improvement or optimization.
• Support process improvement projects that have the objectives of developing more cost efficient and quality enhanced processes.
• Establish machine and process standards and overall equipment efficiency.
• Assist in the development of more effective operational control systems.
• Evaluate data generated through studies using statistical analytical methods.
• Responsible for the development and/or revision of production standards and standard work documents.
• Develops, writes and implements engineering studies, design of experiments, and IQ/OQ/PQ protocols and reports.

DUTIES & RESPONSIBILITIES

Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Works on optimization of process output and throughput, equipment utilization, equipment downtime, waste reduction/yield improvements, budget management, standard cost and capital investment management.
• Provides technical support to the production areas evaluating process deficiencies, process changes, modifications and equipment failure. Defines, analyzes, reviews and evaluates problems for prompt solutions.
• Figures out, adapts, and modifies methods and standards to control all aspects of assigned projects or portions of major projects.
• Coordinates phases of work with other departments within the company and with other Medical Device divisions.
• Perform Investigation and writes NC reports following established timelines.
• Routes and follows up on NC reports through the evaluation, review and approval processes to follow the established timeline.
• Coordinates and participates in Cross Functional Investigations (CFI)
• Revise and maintain engineering and equipment procedures.
• Follows Standard Operating Procedures (SOP), Good Manufacturing Practices (GMPs), Company Policies and Federal, State and Local Government Regulations.
• Map processes and analyze current status and potential future states with improvements. Define and quantify improvements to further analyze the gains. Use tools from Lean and Six Sigma to create and execute CIP projects.
• Participates in GMP audits regarding equipment recording and machine performance.
• Coordinates communications and interfaces with end users, machine manufacturers and/or suppliers.
• Participates in projects involving other departments and activities (CIM, QIP, CFM, etc.).
• Writes, develops and implements validation procedures.
• Comply J&J Safety Requirements and ensure safe working conditions and practices in the department.
• Reviews and analyzes data, understanding of statistics and the application of statistical data, able to determine normal and non-normal data along with probable causes of non-normal results.
• Demonstrate independent understanding and application of core GMP fundamentals, including but not limited to: Data Integrity (DI), Good Manufacturing Practices (GMP), and Good Documentation Practices (GDPs).
• Responsible for communicating business related issues or opportunities to next management level
• Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
• Performs other duties assigned as needed

EXPERIENCE AND EDUCATION

• Bachelor's degree in engineering discipline.
• 0-2 years' work experience in engineering in a medical device environment preferred.

REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES and AFFILIATIONS

• Advanced computer skills and use of software applications. Strong computer background (MS Office, MS Project Management, PowerPoint, Word, Excel, Outlook etc.)
• Experience in a manufacturing environment developing manufacturing standards.
• Proven ability to anticipate and solve problems.
• Ability to prioritize multiple commitments and technical problem-solving duties.
• Experience or knowledge in short and long-term project management.
• Provides technical support to the production areas evaluating process deficiencies, process changes, modifications and equipment failure. Defines, analyzes, reviews and evaluates problems for prompt solutions.
• Self-motivated and capable of completing job duties with limited supervision.
• Capable of serving as back up Facilitator when Facilitator is not available.
• Strong Organizational, interpersonal, oral and written communication skills.

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, please contact us via or contact AskGS to be directed to your accommodation resource.

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