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Product​/Process Engineer

Job in Jacksonville, Duval County, Florida, 32232, USA
Listing for: J&J Family of Companies
Full Time position
Listed on 2026-06-12
Job specializations:
  • Engineering
    Process Engineer, Quality Engineering, Manufacturing Engineer, Biomedical Engineer
Job Description & How to Apply Below
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 Med Tech, 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  () .

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:*
* Jacksonville, Florida, United States of America

*
* Job Description:

*
* Johnson & Johnson is recruiting a  
** Product/Process Engineer** , to join our Vision team in Jacksonville, FL.

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

Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that's reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs - from the pediatric to aging eye - in a patient's lifetime.

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

*
* Purpose:

*
* The Engineer plans, schedules, and executes moderately complex engineering activities and projects within an assigned manufacturing value stream and/or technical function (e.g., Process, Packaging, Materials/Supplier, Equipment/Validation). The role provides technical leadership to improve safety, quality, delivery, and cost, and supports new product introductions, product/process changes, and compliance commitments in a regulated (GMP/ISO/FDA) environment.

The Engineer leads and/or supports change control, equipment/process/packaging qualification and validation activities (IQ/OQ/PQ as applicable), technical investigations, and continuous improvement initiatives. The role interfaces directly with cross‑functional partners (Operations, Quality, Engineering, Supply Chain, and external vendors) to deliver business objectives and ensure robust, compliant solutions.

Responsibilities and accountabilities may vary by site. Applicable procedures and quality systems (e.g., QUMAS/eDMS where applicable) define responsibilities and may supersede elements of this position description.

*
* Key Responsibilities:

*
* ** 1. Project Delivery & Technical Leadership*
* - Plans and executes moderately complex engineering and/or change control projects requiring conceptual evaluation, design, and validation.

- Applies standard project management methodologies to plan work, manage scope, and deliver milestones.

- Participates in technical design reviews and translates requirements into manufacturing, product, or equipment specifications.

- Supports capital and expense project justification as applicable.

** 2. Qualification, Validation & Change Control*
* - Plans and executes qualification of new or modified equipment, controls, systems, and/or processes; supports vendor and site acceptance testing as required.

- Leads and/or supports validation activities (IQ/OQ/PQ), protocol execution, and reporting.

- Authors and reviews technical documentation in accordance with GDP and internal standards.

** 3. Process / Equipment / Packaging / Materials Improvements*
* - Identifies and implements equipment, process, packaging, and/or materials enhancements to improve efficiency, yield, reliability, and safety.

- Designs and executes…
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