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 DESCRIPTION:

The Sterilmed Inc. business, a member of Johnson & Johnson’s Family of Companies, is currently recruiting for a Senior Systems & Equipment Development Engineer, located in Plymouth, MN.
We are excited to announce an excellent opportunity for an Engineer who will work directly with equipment vendors to develop new processes and enhance existing ones. This role involves close collaboration with our R&D team to create tabletop equipment concepts that focus on simple automation and vision systems. Familiarity with programming languages and Programmable Logic Controllers (PLCs) will be beneficial.
As a Technical Life Cycle Management member, you will collaborate with design team members to design intricate mechanisms and lightweight structures. Your responsibilities will include both conceptual and detailed Computer-Aided Design (CAD) drawings, along with related documentation and design specifications. You will focus on creating innovative designs that align with user needs and product requirements.
In the role of Development Engineer, you will contribute to the expansion of capabilities and services within the TLCM department. You will thrive in a fast-paced environment, designing, ordering, and qualifying tooling and capital equipment for reprocessing medical devices. This position requires engagement with Operations and R&D teams to define design criteria that optimize quality and improve efficiency.
Effective communication is crucial, as you will need to convey ideas clearly, both verbally and in writing, to team members who may not have technical backgrounds. Partnering with the Quality team will involve addressing Corrective and Preventive Actions (CAPAs), non-conformances, and conducting root cause investigations. Collaboration with Sterilmed’s external manufacturers to plan facility changes will also be a key aspect of the role, along with coordinating with construction contractors to ensure the smooth introduction of processes and developed product lines.
You will participate in comprehensive engineering initiatives, developing and implementing effective, high-quality processes and design guidelines throughout the division. This includes conducting design reviews, providing feedback for improvements in manufacturability, and seeing opportunities for cost reductions. You will define equipment, materials, and process performance requirements and perform vendor evaluations to ensure they can produce high-quality products in vital quantities at competitive costs.
Facilitating experiments and capability studies, you will develop detailed process specifications and design and procure process tools. Evaluating and recommending suitable equipment will be critical for achieving efficient performance and balance in production lines. Furthermore, you will analyze new processes, systems, and equipment with the goal of driving continuous improvement. Proposing process improvements to a diverse audience and editing/publishing process documentation and training materials will be part of your responsibilities. It’s also important to ensure that all new equipment and systems stay in sync with environmental, health, and safety standards.

MINIMUM QUALIFICATIONS

• Bachelor’s degree in a relevant field such as mechanical, electrical, materials, or biosystems engineering or equivalent experience
• Proven experience with process scale-up and development
• Minimum of six years of related work experience
• Must have good technical writing skills for presentations of engineering studies and other investigative initiatives.

PREFERRED REQUIREMENTS

• Experience in a R&D design, process development and/or manufacturing engineering role in the medical device industry.
• Proficient experience with PLCs, visions systems, optics, and automation
• Proficiency with Solidworks or other CAD programs
• Proven track record working well and leading in a team environment and learning from others
• Outstanding communication, presentation, and interpersonal skills working within all levels of the organization required
  Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.
  We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Please refer the Job description for details