Validation Engineer

Posted 06 March 2023
LocationCounty Offaly
Job type Permanent
Contact NameEugene O’Rourke

Job description

What you need to know

Our client a provider of sterilisation services to many of the world’s largest medical device manufacturers is currently seeking a Validation Engineer. This role is a new and exciting position, and the company is experiencing unprecedented growth. This role would suit someone with a strong background in validations, Microbiological testing, document controlling or technical writing and is willing to take the next step into a Validation Engineer position.

You will report directly to the Validation Supervisor, and you will work with them to ensure that validation processes are followed and that customer requirements are consistently met.

There will be a big emphasis on training in relation to projects that in turn ensures a strong relationship with the client’s customers and that clients requirements are met.

This is a permanent role with an excellent salary and package

Your new job

Key duties & responsibilities include:

  • Liaise with customers and provide technical support regularly interacting with the customers to ensure that validation expectations are being met to ISO 11135 and ISO 13485 standards while additionally adhering to GMP standards

  • Involvement in Technical writing through reporting and protocoling and provide input and recommendations in the technical writing being carried out

  • Provide a dynamic approach to managing continuous improvement projects

  • Collaborate with quality, operations planning, laboratory and customer service teams to co-ordinate customers validation and projects

  • Support harmonisation and share best practise within the technical team to achieve common objectives

  • Prepare and provide audit support to the Quality department during internal, customer and regulatory audits

  • Comply with Health and Safety policies and procedures

What are we looking for?

  • Diploma/Degree in Science or Engineering with a minimum of 1 year of industrial experience.

  • Working knowledge of ISO11135 and ISO13485 process validation and Microbiological/chemical testing is desirable

  • Exposure to technical writing in a med device/pharma environment would be a necessary

  • Customer focused and always remaining committed to meet the needs and expectations of the customer

  • A self-starter that has a proactive approach to carrying out their duties while always maintaining a positive attitude

  • Possess the ability to work effectively in a team and be able to liaise with other departments effectively

  • A strong multitasker with the ability to take on several projects at a time

Apply for this job now with a Word version of your CV or get in touch with Eugene at 087 407 5822

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