Process Engineer

Johnson & Johnson•Manatí, PR

4d•Onsite

About The Position

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: Supply Chain Engineering Job Sub Function: Process Engineering Job Category: Scientific/Technology All Job Posting Locations: Manatí, Puerto Rico, United States of America Job Description: Fueled by innovation at the intersection of biology and technology, we’re 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 https://www.jnj.com/medtech Responsible for providing Base Business Support. Responsible to identify process improvement initiatives and develops proposals for problem solving, improvement or optimization. Support process improvement projects that have the objectives of developing more cost efficient and quality enhanced processes. Establish the machine hour’s standards and Overall equipment efficiency. Assist in the development of more effective operational control system. Evaluate data generated through studies using statistical analytical methods Responsible for the development and/or revision of production standards and Manufacturing/Packaging process to assure utilization of best process. Performs duties encompassing all process transfers and other projects in an assigned engineering specialization for the development, manufacture, installation, operation and maintenance of products, production processes and/or equipment, packaging and other related activities. Coordinates work in conjunction with personnel assigned to specific projects.

Requirements

Bachelor’s degree in Engineering required.
Relevant work experience is required.
Functional knowledge of English language, must be able to read, write and converse in English and Spanish is required.
Advanced computer skills and use of software application(s) including MS Office.
Proven ability to anticipate and solve problems.
Able to manage multiple priorities.
Experience and working knowledge in short and long term project management.

Nice To Haves

Experience with automated assembly and packaging equipment in the medical device manufacturing environment preferred.
Experience in developing manufacturing standards a plus.
Process Excellence (Green Belt or Black Belt) and Lean certifications are preferred.

Responsibilities

The Process Engineer works in the optimization of process output and through put, equipment utilization, equipment downtime, waste reduction/yield improvements, budget management, standard cost and capital investment management.
Provides technical support to the Production areas in evaluating process deficiencies, process changes, modifications and equipment failure.
Defines, analyzes, reviews and evaluates problems for prompt solutions.
Determines, adapts, and modifies methods and standards to control all aspects of assigned projects or portions of major projects.
Coordinates phases of work with other departments within the company (San Lorenzo or Manati) and with other Ethicon divisions.
Perform Investigation and writes NC Reports following the established timeline.
Routes and follows up the NC Reports through the evaluation, review and approval processes to comply with the established timeline.
Coordinates and participates on Cross Functional Investigation (CFI).
Performs and evaluates established Production Operation metrics for Manufacturing and Packaging Areas.
Supports manufacturing in the day-to-day troubleshooting of equipments.
Leads mitigations to determine the root cause, provide recommendations and may lead NCR’s and CAPA depending on the need or root cause.
Revise and maintain engineering, equipments and process procedure.
Participates in GMP audits regarding equipment recording and machine performance.
Performs other duties assigned as needed