Validation Engineer
- Posted 06 March 2023
- LocationCounty Offaly
- Job type Permanent
- DisciplineEngineering
- Reference9808
- 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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