Job Title: Process Engineer
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.
Role Overview
This Process Engineer role is based in Limerick, Ireland, one of two global production facilities at Johnson & Johnson Vision (JJV). The site produces a range of contact lens medical devices and holds a strong position with a large portion of the global contact lens market.
Main Responsibilities
* Provide technical leadership within a production value stream.
* Work within the NPI process to complete process characterization work, process challenge testing, and process capability and stability runs to qualify new products and processes.
* Identify and implement process-related continuous improvement activities that improve product quality and grow overall equipment efficiency.
* Engage with personnel in the identification and resolution of corrective/preventative actions for process quality-related manufacturing issues.
* Solve problems systematically and use data to support decision making.
* Ensure the delivery of high-quality, innovative products to customers in a timely and cost-effective manner across multiple product value streams.
* Lead process redesign projects, complete proof of principle activity, and assist in the development and installation and qualification of new process equipment.
* Manage and coordinate multiple projects within an exciting environment.
* Apply troubleshooting expertise to resolve complex equipment, systems, and process problems using strong statistical and analytical methodologies.
* Communicate findings throughout the organization.
* Stay up-to-date on the latest process engineering developments and technologies.
Requirements
* Minimum Level 8 B.Sc. or B.Eng. honours degree qualification in Physics/Chemistry/Biological Science or Mechanical/Material/Process Engineering.
* Minimum of two years' work experience in a manufacturing environment or similar.
* Previous experience in the use of statistical techniques (DOE, Process Capability Analysis, Hypothesis Test methods) and problem-solving methodologies is advantageous.
* Familiarity with equipment validation in an FDA environment is a plus.
* Good Project Management skills with a proven record of leading multi-functional teams effectively.
* Strong interpersonal skills and ability to relate well to peers.