Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Senior Process Engineer

Posted Oct 24, 2025
Job ID: JJJP00023930
Location
Limerick
Hours/week
40 hrs/week
Timeline
1 year
Payrate range
Unknown

Senior Process Engineer


Location: Limerick, site based

Duration: 12 months

Hours: 39 hours per week

Imagine your next project providing technical leadership within a production value stream to drive continuous process improvement, solve complex technical issues, and support product transfers in a fast-paced GMP environment.

As a member of the process engineering team, you will work within an assigned value stream with specific accountability for process improvement, providing technical support to solve process issues, and supporting internal and inter site product transfers.


Roles and Responsibilities

You will be responsible for providing technical leadership within a production value stream and supporting/leading the following initiatives. This will involve:

  • Responsible for providing technical leadership within a production value stream and support/lead the following:

    • Identification and implementation of process related continuous improvement activities that improve product quality and grow overall equipment effectiveness.

    • Engage with personnel in the identification and resolution of corrective/preventative actions that address any process quality related manufacturing issues.

    • Systematically solve problems and use data in support of your decision making. You will enjoy taking the initiative and yet possess the collaborative and influencing skills needed to be a key contributor to cross-functional teams.

    • Ensure the delivery of high quality, new and innovative products to our customers, in a timely -and cost-effective manner across multiple product value streams

    • Project management, planning and co-ordination of multiple projects, within a matrix environment, including change management via quality systems.

    • Apply troubleshooting expertise to resolve complex equipment, systems and process problems using strong statistical and analytical methodologies.

    • Communicate details of findings throughout the organization.

  • Process validation of products on new and/or existing production lines.

  • Keep up-to-date on the latest process engineering developments and technologies and will leverage breakthrough ideas that set new performance standards.

  • Engage with the appropriate personnel in the identification and resolution of corrective/preventative actions that address quality, technical, and manufacturing issues.


How to Succeed

You will be a highly motivated self-starter with a strong statistical and analytical background who can lead cross-functional teams to solve complex problems. You will also bring:

Essential:

  • Minimum a Level 8. B.Sc. or B.Eng. honors degree qualification in Physics/Chemistry/Biological Science or Mechanical/Material/Process Engineering, with a demonstrable track record of delivering results.

  • Minimum of 7 years experience working in a GMP environment as an Engineer.


Desirable:

  • Good Project Management skills, FPx or other, are required with a demonstrated ability to lead cross functional team effectively.

  • Good interpersonal skills and ability to relate well to people both individually and in a team environment

  • Good problem-solving methodology and able to manage multiple activities at one time

  • High level of self-motivation required.

  • Possess the collaborative and influencing skills needed to be a key contributor to cross-functional teams.

  • Has a good working knowledge of MS Office suite.

  • Previous experience in the use of 'black belt' type statistical techniques (DOE, Process Capability Analysis, Hypothesis Test methods) and problem-solving methodologies (DMAIC).

  • Familiarity with Process validation in a regulated medical device / pharmaceutical environment.


Benefits

This role offers a very competitive hourly rate. This contract will run for 12 months

You Are Welcome Here

Johnson & Johnson is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

About Johnson & Johnson Vision

Johnson & Johnson Vision brings together cutting-edge insights, science, technology and people. We partner with eye care professionals and help more people around the world preserve and restore sight. Our portfolio includes the best selling contact lens brand in the world, ACUVUE, plus consumer eye health solutions, dry eye treatments, refractive (Lasik) and cataract products. Contribute to the next healthcare breakthrough, create a world connected by SIGHT with your next project at Johnson & Johnson Vision.

Application Process

We are looking to process the first round of applications within the next 2 working days. We do not accept applications via email.

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.

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