Development Engineer

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At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

Position Summary

About you:

Do you want to spend your working time making a difference in the world around you? Are you passionate about supporting the medical and pharmaceutical industries? Do you care about keeping patients and people safe? If so, then a career with Steris AST could be a great fit for you.

About Us:

At Steris AST we are the trusted experts in neutral sterilization offering includes radiation and gas technologies.

We offer electron beam, gamma, X-ray, ethylene oxide and vaporized hydrogen peroxide technologies for the purpose of product sterilization. Whether that product be a single use medical instrument, a hospital environment, cosmetics and toiletries, or food products, we make sure that everything that makes its way to an end user is safe for use or consumption.

We are currently recruiting for a Development Engineer vacancy. This is an excellent opportunity to join the business at a skilled professional level.

This role is positioned within the engineering team based at the STERIS Galway laboratory. The site provides testing and other technical services to the medical device and pharma industries.

Duties

• Manages multiple complex customer testing projects simultaneously
• Leads device and packaging testing projects for medical device and pharma customers
• Interfaces with Customers and sales team to assess feasibility and costings of new projects
• Develops and agrees project plans, test protocols and test methods with Customers
• Coordinates staff and schedules equipment resources to execute testing and reporting of results
• Designs and documents test jigs and fixtures
• Working with the validation team to conduct Test Method Validation studies
• Assess equipment specifications and suitability for test method
• Develops URS for laboratory equipment procurement
• Support Quality team with investigations, procedure updates and audits
• Engage in lean and continuous improvements onsite
  
  

Duties - cont'd

Education Degree

• Bachelor's Degree
  
  

Required Experience

• Medical device verification and validation / regulatory submission project experience
• Experience working in highly regulated environment
• Customer facing experience
• Proven project management track record
• CAD and Minitab software experience an advantage
  
  

Skills

Preferred Experience

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 18,000 associates and Customers in more than 100 countries.

STERIS strives to be an Equal Opportunity Employer.Seniority level

• Seniority levelAssociate

Employment type

• Employment typeFull-time

Job function

• IndustriesMedical Equipment Manufacturing and Hospitals and Health Care

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