Senior Packaging Engineer

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

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Fueled by innovation at the intersection of biology and technology were 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 are searching for the best talent for Senior Packaging Engineer to be in Irving TX.

A pre-identified candidate for consideration has been identified. However all applications will be considered.

JOB SUMMARY

• The Senior Engineer Package Development provides technical expertise in the areas of design development testing and production scale-up of new packaging components systems and processes.
• They lead complex engineering assignments and works independently.
• This position supports Mentor Medical Systems B.V. at Leiden The Netherlands

DUTIES & RESPONSIBILITIES

In accordance with all applicable federal state and local laws/regulations and Corporate Johnson & Johnson procedures and guidelines this position:

• Collaborates with research and development product management stability regulatory and quality process among other functions to ensure all package design requirements are met.
• Leads some aspects of the product / package portfolio to develop business strategies for continuous improvement related to design process and validation
• Work with Packaging Engineering contractors and full time engineers on a dotted line project specific basis.
• Has full technical responsibility for interpreting organizing executing and coordinating assignments. Determines and coordinates physical testing to ensure product and package integrity for manufacturing through end users.
• Contributes to resolution of packaging related issues in manufacturing compliance and the field. Develops recommendations on general packaging guidelines and standards for processes and functional requirements and ensures regulatory requirements are satisfied.
• Contributes to the company with inventions new designs processes or techniques which are significant to the solution of important problems. Continually evaluates new packaging solutions and alternatives to improve operating efficiency generate market differentiators and add sources of revenue.
• Promotes and nurtures the highest standards of integrity ethics and compliance and actively supports our compliance program-related initiatives and activities.

EXPERIENCE AND EDUCATION

• Bachelors Degree in Package Engineering or other Technical Degree (Mechanical Chemical Biomedical Engineering etc.)
• 4-6 years of experience

REQUIRED KNOWLEDGE SKILLS ABILITIES CERTIFICATIONS/LICENSES and AFFILIATIONS

Required:

• Experience with new product development and commercialization of products in a regulated industry as an engineer
• Experience as a package development engineer or a strong understanding of the package development process and responsibilities
• Experience as a technical lead of projects
• Proficiency in computers technology including MS office applications

Preferred:

• Experience working with medical device package development
• Knowledge of sterile barrier packaging systems and design verification including ASTM or ISTA test methods.
• Knowledge of Package Assembly and Manufacturing processes.
• Knowledge and experience with ISO11607
• Medical Device and/or pharmaceutical industry experience.
• Understanding of sterilization modes used in medical devices.
• Project management skills.

Reporting:

• This position reports to the LCM Manager
• Below is a list of potential internal interfaces required:
  • R&D PM LCM Labeling Quality Regulatory Sterility Stability Advanced Evaluation Marketing Medical Affairs Lab personnel Manufacturing Engineering

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 () or contact AskGS to be directed to your accommodation resource.

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