Process Engineer - Blarney
Cork (County Cork) Design / Civil engineering / Industrial engineering
Job description
A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
Your Role
Reporting to the new facility Senior Process Engineer, the Process Engineer will be responsible for managing project and process engineering requirements through technology transfer and commercialization in a new manufacturing facility. They will initiate, co-ordinate and complete assigned projects within, using structured approach and detailed planning to deliver projects that meet or exceed stakeholder expectations and that are delivered Right First Time, safely, on schedule and within budget. While providing process inputs to the design/ URS’s for process equipment and ensure transferred processes are designed for manufacture, automated, innovative, cost effective and meet all Quality and EHS regulatory requirements.
Other Duties include:
· Complete Process / Product Validations in conjunction with Quality/Validation group.
· Support Equipment Validations, in conjunction with Quality/Validation group.
· Conduct process feasibility trials / process DOE’s to determine appropriate/robust process windows.
· Prepare & execute OQ / PQ protocols for process / material changes as needed.
· Work in conjunction with the Quality & Validation group to determine appropriate validation sampling and acceptance criteria.
· Liaise with operations and other departments to prepare plan for validation builds.
· Co-ordinate the execution of OQ / PQ builds.
· Prepare OQ / PQ validation reports and deviations as required.
· Conduct process capability analysis using Minitab.
· Maintain and develop manufacturing process documentation and procedures. All process changes and modifications to be documented and tracked closely.
· Provide Technical/Engineering support to manufacturing.
· Lead and coordinate the troubleshooting of various manufacturing process issues.
· Responsible for dealing with process, product and quality issues to achieve long term solutions.
Who you are?
· Education: Degree in Mechanical / Production Engineering or equivalent.
· Experience: minimum of 3 years relevant experience, preferably within Medical Device industry or other regulated environments. (candidates coming from an automotive/ semiconductor / electronics or other GMP / FDA regulated background will also be considered)
· Working knowledge of validation systems.
· Moulding experience an advantage.
Note: This role involves travel to the US, in some cases for extended periods
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences.
We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology.
We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons.
Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!
Job Requisition ID: 255066
Location: Carrigtwohill
Career Level: C - Professional (1-3 years)
Working time model: full-time .buttontext3bd8dd742c10cffa a{ border: 1px solid transparent; } .buttontext3bd8dd742c10cffa a:focus{ border: 1px dashed #eb3c96 !important; outline: none !important; }
North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request. You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.
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