Package Engineer

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:

R&D Product Development

Job Sub Function:

Biomedical Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Jacksonville, Florida, United States of America

Job Description:

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 https://www.jnj.com/medtech

An internal pre-identified candidate for consideration has been identified. However, all applications will be considered.

We are searching for the best talent for Package Engineer.

JOB POSITION SUMMARY

Provides technical expertise and participates as an independent and integral contributor to cross-functional teams responsible for designing, developing, production scale-up and executing package testing of new packaging components, systems, and processes, as well as packaging equipment process validations. Leads projects with guidance of an experienced Packaging Engineer.

DUTIES & RESPONSIBILITIES

• Design, develop, and optimize packaging for new product launches and existing products throughout all stages of product development from concept to launch, including clinical trials, global and limited market releases, as well as key operations initiatives
• Generate and execute design of experiments (DOE) for process validations.
• Apply appropriate industry standards such as ISO 11607-2, to specify and validate packaging equipment and packaging manufacturing processes to determine appropriate sourcing, purchasing, installation planning and specifications.
• Identify, develop, and participate in packaging operations projects (e.g., cost improvements, qualifying new suppliers and product transfers).
• Validates package components and packaging processes.
• Develops package testing plans and interprets results as required for various projects.
• Supports activities associated with manufacturing and testing.
• Provides troubleshooting in the resolution of packaging related issues in manufacturing and the field.
• Participates in process improvement or task teams.
• Participates and advises in decisions involving equipment, package design, cost saving and source reduction.
• Determines and coordinates physical testing to ensure product and package integrity for manufacturing through end users.
• Builds technical competencies in packaging materials and processes used in all manufacturing processes.
• Participates and provides technical expertise for risk assessment and compliance assurance programs.
• Assure delivery of robust, cost effective, fully compliant packaging solutions that meet current and evolving customers’ needs.

• Knows and follows all laws and policies that apply to one's job, and maintains the highest levels of professionalism, ethics, and compliance at all times.
• Promotes and nurtures the highest standards of professionalism, ethics and compliance and actively supports our compliance program-related initiatives and activities.
• Participate as an independent and integral contributor to cross-functional teams responsible for designing, developing, testing, and executing package testing, as well as packaging equipment process validations.

EXPERIENCE & EDUCATION

• Bachelor’s degree in engineering or equivalent Technical Degree required.
• 2-4 years work experience
• Medical device or regulated industry experience preferred.

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

• Fluency in English is required.
• Team Player with a creative attitude.
• Problem solving skills and ability to work independently is required.
• Strong attention to detail, critical thinking, and problem-solving skills
• Familiar with ASTM and ISTA test methods, ISO 11607-1, ISO 11607-2, 21 CFR Part 820, ISO 13485
• GDP - Good Documentation Practices
• Good communication (e.g., written and verbal) and interpersonal skills.
• Ability to work on multiple projects in a fast-paced environment.
• Good understanding of processes and equipment used in assigned work.
• Ability to interact professionally with all organizational levels.
• Ability to develop good technical writing skills.
• Ability to develop/strengthen critical thinking skills.

LOCATION & TRAVEL REQUIREMENTS

This position has one location supporting Johnson & Johnson:

• Vision Care (Jacksonville, FL)
• May require some travel

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 and 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 email the Employee Health Support Center ([email protected]) or contact AskGS to be directed to your accommodation resource

#LI-Onsite 

 

 

Required Skills:

 

 

Preferred Skills:

Bioinformatics, Biological Engineering, Biological Sciences, Biostatistics, Data Reporting, Data Savvy, Design of Experiments (DOE), Detail-Oriented, Execution Focus, Feasibility Studies, Preclinical Research, Problem Solving, Process Oriented, Prototyping, Report Writing, Research and Development, Researching, SAP Product Lifecycle Management, Technologically Savvy