Device Lifecycle Engineer Co-Op

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 https://www.jnj.com

Job Function:
Career Programs

Job Sub Function:
Non-LDP Intern/Co-Op

Job Category:
Career Program

All Job Posting Locations:
Titusville, New Jersey, United States of America

Job Description:

The Device & Primary Container Team, within the MSAT organization of Johnson & Johnson & Johnson Innovative Medicine (JJIM) is recruiting for a Device Lifecycle Engineer Co-Op.

This position is located in Titusville, NJ.

Medical Device and Packaging solutions are becoming an increasingly meaningful component in delivering innovative medicines to our patients.

The Device Lifecycle Engineer Co-Op will work in a multi-functional setting, responsible for lifecycle engineering and technical support for the device constituents of Synthetics combination products in the JJIM network.

They will lead and support product and process quality improvement and reliability projects, and be the key point of contact for their area of responsibility.

Key Responsibilities:



* Well-documented design change control processes that may include assessments, risk analyses, and implementation plans.


* Detailed documentation demonstrating compliance with regulatory standards, including effective technical assessment reports.

Qualifications

Education:



* Co-Op will be pursuing a degree in Engineering or Science (Biomedical, Mechanical, or Materials Science preferred).

Experience and Skills

Required:



* Effective problem-solving to assess supplier changes to commercial products within multi-functional teams.


* Excellent organizational and planning skills, able to balance multiple priorities.


* Shown ability to respond to complex inquiries from all levels of employees or external sources, strong communication and interpersonal skills.


* Technical writing skills to efficiently document device design control.


* Awareness of and willingness to learn medical device regulatory and quality system requirements.


* Strong interpersonal and decision-making skills, ability to operate with professionalism, confidentiality and in a dynamic environment.


* Intermediate to advanced digital literacy, including document management systems, word processing, spreadsheets, project planning, and database applications.

Preferred, but not Required:



* Experience working within a quality system, experience in the medical industry, or syringe manufacturing/engineering experience.

Other:



* Requires proficiency ...